In addition to sequestering carbon in soil,biochars can also play a role in changing the potassium equilibration and dynamics of the soil.Nowadays,acidification of biochar is commonly used to improve its properties,wh...In addition to sequestering carbon in soil,biochars can also play a role in changing the potassium equilibration and dynamics of the soil.Nowadays,acidification of biochar is commonly used to improve its properties,which can impact the potassium content in the soil.Simultaneous application of acidified biochar and sodium bentonite can complicate this effect.In the present study,the effects of adding two types of biochars prepared from municipal waste and used coffee grounds and their acidified types,along with sodium bentonite at three levels(0.00%,1.00%,and 2.00%),on soil physical-chemical properties(pH,salinity,cation exchange capacity,concentration of soluble cations and their ratio,and sodium adsorption ratio)and the release of potassium from a calcareous soil were investigated.The results showed that the addition of coffee ground biochar increased the concentration of soluble potassium and decreased the ratio of calcium to potassium,while the acidified coffee ground biochar decreased the amount of soluble potassium and increased the ratio of calcium to potassium.Alkaline and acidified municipal waste biochars had no effect on soluble potassium and soluble cations ratio.Application of bentonite increased the amount of soluble calcium and sodium and the ratio of calcium to potassium.Addition of bentonite also increased the amount of exchangeable potassium and exchangeable sodium percentage,but use of different biochars reduced negative effect of bentonite.Use of bentonite also caused an increase in the exchangeable potassium and a decrease in the non-exchangeable potassium contents.Alkaline and acidified coffee ground biochars increased the amount of exchangeable,non-exchangeable,and total potassium,but this effect was greater by alkaline biochar.Application of municipal waste biochar did not affect the amount of exchangeable potassium but increased the amount of non-exchangeable and total potassium,with no significant difference observed between alkaline and acidified biochars.Potassium saturation percentage was not affected by bentonite,but coffee ground biochar increased its amount and municipal waste biochar had no effect on it.Acidified and alkaline coffee ground biochars were able to release more potassium from the soil(475 and 71 mg/kg,respectively),while alkaline municipal waste biochar did not affect it and acidified municipal waste biochar reduced it by 113 mg/kg.In general,it can be concluded that alkaline biochars in calcareous soils can improve potassium fertility by reduction of the ratio of calcium to potassium and increasing its various forms,while acidified biochars and bentonite may aggravate potassium deficiency in these soils.Considering the lack of significant change in the pH of calcareous soils with the use of different biochars,it is suggested to use alkaline biochars,which can improve the potassium status of the soil while reducing the costs associated with biochar modification.展开更多
Thanks to its abundant reserves,relatively high energy density,and low reduction potential,potassium ion batteries(PIBs)have a high potential for large-scale energy storage applications.Due to the large radius of pota...Thanks to its abundant reserves,relatively high energy density,and low reduction potential,potassium ion batteries(PIBs)have a high potential for large-scale energy storage applications.Due to the large radius of potassium ions,most conventional anode materials undergo severe volume expansion,making it difficult to achieve stable and reversible energy storage.Therefore,developing high-performance anode materials is one of the critical factors in developing PIBs.In this sense,antimony(Sb)-based anode materials with high theoretical capacity and safe reaction potentials have a broad potential for application in PIBs.However,overcoming the rapid capacity decay induced by the large radius of potassium ions is still an issue that needs to be focused on.This paper reviews the latest research on different types of Sb-based anode materials and provides an in-depth analysis of their optimization strategies.We focus on material selection,structural design,and storage mechanisms to develop a detailed description of the material.In addition,the current challenges still faced by Sb-based anode materials are summarized,and some further optimization strategies have been added.We hope to provide some insights for researchers developing Sb-based anode materials for next-generation advanced PIBs.展开更多
Potassium-ion batteries(PIBs)are considered as a promising energy storage system owing to its abundant potassium resources.As an important part of the battery composition,anode materials play a vital role in the futur...Potassium-ion batteries(PIBs)are considered as a promising energy storage system owing to its abundant potassium resources.As an important part of the battery composition,anode materials play a vital role in the future development of PIBs.Bismuth-based anode materials demonstrate great potential for storing potassium ions(K^(+))due to their layered structure,high theoretical capacity based on the alloying reaction mechanism,and safe operating voltage.However,the large radius of K^(+)inevitably induces severe volume expansion in depotassiation/potassiation,and the sluggish kinetics of K^(+)insertion/extraction limits its further development.Herein,we summarize the strategies used to improve the potassium storage properties of various types of materials and introduce recent advances in the design and fabrication of favorable structural features of bismuth-based materials.Firstly,this review analyzes the structure,working mechanism and advantages and disadvantages of various types of materials for potassium storage.Then,based on this,the manuscript focuses on summarizing modification strategies including structural and morphological design,compositing with other materials,and electrolyte optimization,and elucidating the advantages of various modifications in enhancing the potassium storage performance.Finally,we outline the current challenges of bismuth-based materials in PIBs and put forward some prospects to be verified.展开更多
Recently,potassium-ion batteries(PIBs)have received significant attention in the energy storage field owing to their high-power output,fast charging capability,natural abundance,and environmental sustainability.Herein...Recently,potassium-ion batteries(PIBs)have received significant attention in the energy storage field owing to their high-power output,fast charging capability,natural abundance,and environmental sustainability.Herein,we comprehensively review recent advancements in the design and development of carbon-based anode materials for PIBs anodes,covering graphite,hard carbon,alloy and conversion materials with carbon,and carbon host for K metal deposition.Chemical strategies such as structural engineering,heteroatom-doping,and surface modifications are highlighted to improve electrochemical performances as well as to resolve technical challenges,such as electrode instability,low initial Coulombic efficiency,and electrolyte compatibility.Furthermore,we discuss the fundamental understanding of potassium-ion storage mechanisms of carbon-based materials and their correlation with electrochemical performance.Finally,we present the current challenges and future research directions for the practical implementation of carbon-based anodes to enhance their potential as next-generation energy storage materials for PIBs.This review aims to provide our own insights into innovative design strategies for advanced PIB's anode through the chemical and engineering strategies.展开更多
Graphdiyne(GDY)is a two-dimensional carbon allotrope with exceptional physical and chemical properties that is gaining increasing attention.However,its efficient and scalable synthesis remains a significant challenge....Graphdiyne(GDY)is a two-dimensional carbon allotrope with exceptional physical and chemical properties that is gaining increasing attention.However,its efficient and scalable synthesis remains a significant challenge.We present a microwave-assisted approach for its continuous,large-scale production which enables synthesis at a rate of 0.6 g/h,with a yield of up to 90%.The synthesized GDY nanosheets have an average diameter of 246 nm and a thickness of 4 nm.We used GDY as a stable coating for potassium(K)metal anodes(K@GDY),taking advantage of its unique molecular structure to provide favorable paths for K-ion transport.This modification significantly inhibited dendrite formation and improved the cycling stability of K metal batteries.Full-cells with perylene-3,4,9,10-tetracarboxylic dianhydride(PTCDA)cathodes showed the clear superiority of the K@GDY anodes over bare K anodes in terms of performance,stability,and cycle life.The K@GDY maintained a stable voltage plateau and gave an excellent capacity retention after 600 cycles with nearly 100%Coulombic efficiency.This work not only provides a scalable and efficient way for GDY synthesis but also opens new possibilities for its use in energy storage and other advanced technologies.展开更多
Carbon materials are considered as prospective anode candidates for potassium ion batteries(PIBs).However,the low-rate capability is hampered by slow K+diffusion kinetics and obstructed electron transport of carbon-ba...Carbon materials are considered as prospective anode candidates for potassium ion batteries(PIBs).However,the low-rate capability is hampered by slow K+diffusion kinetics and obstructed electron transport of carbon-based anodes.In this work,calcium D-gluconate derived mesoporous carbon nanosheets(CGC)were interpenetrated into the architecture of reduced graphene oxides(RGO)to form the composites of two-dimensional(2D)/2D graphene/mesoporous carbon nanosheets(RGO@CGC).CGC as a rigid skeleton can prevent the graphene layers from restacking and maintain the structural stability of the 2D/2D carbon composites of RGO@CGC.The mesopores in CGC can shorten the path of ion diffusion and facilitate the penetration of electrolytes.RGO possesses the high surface-to-volume ratio and superior electron transport capability in the honeycomb-like 2D network consisting of sp^(2)-hybridized carbon atoms.Especially,theπ-πstacking interaction between CGC and RGO enhances stable composite structure formation,expedites interlayer-electron transfer,and establishes three-dimensional(3D)ion transportation pathways.Owing to these unique structure,RGO@CGC exhibits fast and stable potassium storage capability.Furthermore,the effects of binders and electrolytes on the electrochemical performance of RGO@CGC were investigated.Finally,Prussian blue was synthesized as a positive electrode to explore the possibility of RGO@CGC as a full battery application.展开更多
With the rapid development of electric vehicles,hybrid electric vehicles and smart grids,people's demand for large-scale energy storage devices is increasingly intense.As a new type of secondary battery,potassium ...With the rapid development of electric vehicles,hybrid electric vehicles and smart grids,people's demand for large-scale energy storage devices is increasingly intense.As a new type of secondary battery,potassium ion battery is promising to replace the lithium-ion battery in the field of large-scale energy storage by virtue of its low price and environmental friendliness.At present,the research on the anode materials of potassium ion batteries mainly focuses on carbon materials and the design of various nanostructured metal-based materials.Problems such as poor rate performance and inferior cycle life caused by electrode structure comminution during charge and discharge have not been solved.Quantum dots/nanodots materials are a new type of nanomaterials that can effectively improve the utilization of electrode materials and reduce production costs.In addition,quantum dots/nanodots materials can enhance the electrode reaction kinetics,reduce the stress generated in cycling,and effectively alleviate the agglomeration and crushing of electrode materials.In this review,we will systematically introduce the synthesis methods,K+storage properties and K+storage mechanisms of carbon quantum dots and carbon-based transition metal compound quantum dots composites.This review will have significant references for potassium ion battery researchers.展开更多
In recent years,metal phosphosulfides have attracted great attention as the promising anode materials in sodium/potassium batteries because of their incorporation of the advantages of metal phosphides and sulfides.How...In recent years,metal phosphosulfides have attracted great attention as the promising anode materials in sodium/potassium batteries because of their incorporation of the advantages of metal phosphides and sulfides.However,they are also confronted with the problem of unstable battery performance due to the heavy volume expansion and sluggish ion reaction kinetics.Herein,yolk-shell cobalt phosphosulfide nanocrystals encapsulating into multi-heterogeneous atom(N,P,S)-doped carbon framework(Co_(9)S_(8)/CoP@NPSC)were constructed by employing dodecahedral ZIF-67 as precursor and a polymer as carbon sources through simultaneous sulfidation and phosphorization processes.The synergistic effect of Co_(9)S_(8)and CoP component and the yolk-shell structure greatly improve the bettery performance and structural stability.In addition,the multiple hetero-atoms doped carbon frameworks enhance the conductivity of the electrode materials and increase the spacing of carbon layers to supply sufficient active sites and facilitate the Na^(+)/K^(+)transport.The electrochemical results demonstrated that Co_(9)S_(8)/CoP@NPSC exhibited the pleasant reversible capacity(360.47 mAh/g at 1 A/g)after 300 cycles and an unpredictable cycling stability(103.22 mAh/g after 1000 cycles)in the SIBs application.The ex-situ XRD and XPS analyses were further applied to study the sodium ion storage mechanism and the multi-step phase transition reaction of the yolk-shell heterogeneous structure.This work provides new perspectives for the preparation of novel structure metal phosphosulfide and their applications in anode materials for sodium/potassium batteries and other secondary batteries.展开更多
The central nervous system, information integration center of the body, is mainly composed of neurons and glial cells. The neuron is one of the most basic and important structural and functional units of the central n...The central nervous system, information integration center of the body, is mainly composed of neurons and glial cells. The neuron is one of the most basic and important structural and functional units of the central nervous system, with sensory stimulation and excitation conduction functions. Astrocytes and microglia belong to the glial cell family, which is the main source of cytokines and represents the main defense system of the central nervous system. Nerve cells undergo neurotransmission or gliotransmission, which regulates neuronal activity via the ion channels, receptors, or transporters expressed on nerve cell membranes. Ion channels, composed of large transmembrane proteins, play crucial roles in maintaining nerve cell homeostasis. These channels are also important for control of the membrane potential and in the secretion of neurotransmitters. A variety of cellular functions and life activities, including functional regulation of the central nervous system, the generation and conduction of nerve excitation, the occurrence of receptor potential, heart pulsation, smooth muscle peristalsis, skeletal muscle contraction, and hormone secretion, are closely related to ion channels associated with passive transmembrane transport. Two types of ion channels in the central nervous system, potassium channels and calcium channels, are closely related to various neurological disorders, including Alzheimer's disease, Parkinson's disease, and epilepsy. Accordingly, various drugs that can affect these ion channels have been explored deeply to provide new directions for the treatment of these neurological disorders. In this review, we focus on the functions of potassium and calcium ion channels in different nerve cells and their involvement in neurological disorders such as Parkinson's disease, Alzheimer's disease, depression, epilepsy, autism, and rare disorders. We also describe several clinical drugs that target potassium or calcium channels in nerve cells and could be used to treat these disorders. We concluded that there are few clinical drugs that can improve the pathology these diseases by acting on potassium or calcium ions. Although a few novel ion-channelspecific modulators have been discovered, meaningful therapies have largely not yet been realized. The lack of target-specific drugs, their requirement to cross the blood–brain barrier, and their exact underlying mechanisms all need further attention. This review aims to explain the urgent problems that need research progress and provide comprehensive information aiming to arouse the research community's interest in the development of ion channel-targeting drugs and the identification of new therapeutic targets for that can increase the cure rate of nervous system diseases and reduce the occurrence of adverse reactions in other systems.展开更多
To address challenges related to the intermittency of renewable energy sources,aqueous potassium-ion batteries(AKIBs)are a promising and sustainable alternative to conventional systems for large-scale energy storage.T...To address challenges related to the intermittency of renewable energy sources,aqueous potassium-ion batteries(AKIBs)are a promising and sustainable alternative to conventional systems for large-scale energy storage.To enable their practical application,maximizing energy density and longevity while minimizing production and material costs is a key goal.In this work,we propose an AKIB consisting only of abundant and cost-efficient materials,which delivers a high energy density of more than 70 Wh kg^(-1).We combine simple strategies to stabilize the Mn-rich Prussian blue analog cathode by Fe-doping,improving the crystallinity,and tuning the electrolyte composition without employing expensive water-in-salt electrolytes.Using a mixed 2.5 M Ca(NO_(3))_(2)+1.5 M KNO_(3)electrolyte,we assemble a novel AKIB with a Fe-doped manganese hexacyanoferrate cathode and an organic poly(naphthalene-4-formylethylenediamine)anode.Besides a high energy density,the full cell delivers a specific capacity of approximately 60 mAhg^(-1),a power density of 5000 W kg^(-1),and 80% capacity retention after 600 cycles.展开更多
A comparative study of products of thermal and thermocatalytic cracking of polypropylene(PP) in the presence of potassium polytitanate(PPT) synthesized by treatment of TiO_(2)(rutile) powder with molten mixture of KOH...A comparative study of products of thermal and thermocatalytic cracking of polypropylene(PP) in the presence of potassium polytitanate(PPT) synthesized by treatment of TiO_(2)(rutile) powder with molten mixture of KOH and KNO_(3) taken in a weight ratio of 30∶30∶40 has been carried out.It was shown that the studied type of PPT powder exhibits catalytic properties in the reaction of thermal decomposition of PP,compared to the effect of commercial zeolite catalyst CBV-780 traditionally used for this purpose.Based on the analysis performed,the differences in the mechanism of catalytic action of PPT and the zeolite were considered.The reasons for the observed differences in the composition of PP cracking products and in the rate of coke formation on the surface of studied catalysts were analyzed.Considering the obtained results,it has been proposed that the CBV-780 catalyst promoted more intensive production of the gaseous hydrocarbons compared to PPT,due to higher specific surface area(internal surface) accessible for relatively light and small-sized hydrocarbon products of cracking.However,intensive coke formation on the outer surface of the microporous zeolite contributes to the blocking of transport channels and the rapid loss of catalytic action.At the same time,PPT,which initially has a smaller specific surface area,retains its catalytic activity significantly longer due to slit-shaped flat pores and higher transport accessibility of the inner surface.展开更多
Aiming at the problems of complex process and high cost in the production of potassium bromide at present,the solubility data and the phase diagram of the quaternary system KBr-MgBr_(2)-K_(2)SO_(4)-MgSO_(4)-H_(2)O at ...Aiming at the problems of complex process and high cost in the production of potassium bromide at present,the solubility data and the phase diagram of the quaternary system KBr-MgBr_(2)-K_(2)SO_(4)-MgSO_(4)-H_(2)O at 298.15 K were studied using the isothermal dissolution equilibrium method.The results showed that there are eight invariant points,sixteen univariant curves,and nine crystallization regions in the phase diagram which is complex and contains two double salts(K_(2)SO_(4)·MgSO_(4)·6H_(2)O and KBr·MgBr_(2)·6H_(2)O)and a metastable phase(MgSO_(4)·5H_(2)O).On the basis of the Pitzer model and HW model,the solubilities of the quaternary system were calculated,with which the corresponding phase diagram was plotted.By comparison,the evaluated phase diagram is in accordance with the measured one.Through analysis,the phase diagrams of the quaternary system at(298.15 and 323.15)K were combined to put forward a process to separate KBr from the system by evaporation and crystallization,which realized the full circulation of the mother solution.展开更多
Potassium is one of the macro minerals necessary for the cellular functions,obtained from foods.Excessive amounts of potassium can cause health problems.Determination of potassium in various samples,especially food an...Potassium is one of the macro minerals necessary for the cellular functions,obtained from foods.Excessive amounts of potassium can cause health problems.Determination of potassium in various samples,especially food and drug samples,is an important task.In this study,we developed a new potentiometric sensor selective to potassium ions.The sensor had a detection limit of 8.64×10^(-5) M in the concentration range of 1.0×10^(-1)-1.0×10^(-4) M and a near-Nernstian behavior of 49.0±4.32 mV/decade.The sensor exhibited a response time of 10 s,as well as good selectivity,good repeatability,and a wide pH working range(4.0-11.0).The developed sensor was successfully applied to a drug sample and different water samples with very high recoveries(>91.20%).展开更多
Mn-rich layered oxides are appealing cathodes for potassium ion batteries(PIBs)in view of their comprehensive virtues such as low cost,high energy density and mature craftsmanship.However,the insufficient covalency be...Mn-rich layered oxides are appealing cathodes for potassium ion batteries(PIBs)in view of their comprehensive virtues such as low cost,high energy density and mature craftsmanship.However,the insufficient covalency between transition metal(TM)and O usually induces irreversible structural evolution and cation migration during repeated insertion and extraction of K^(+),resulting in capacity loss,voltage fading and sluggish kinetics.Herein,an anion substitution strategy is proposed for a stable operation of layered oxide cathode by adjusting the valence electron layer structure between TM and O.The resultant strong TM−O skeleton can inhibit the occurrence of side effects derive from Ni^(4+)during the deep depotassium process,so as to achieve a gentle structural transition.Consequently,stable cycling performance of K_(0.39)Mn_(0.77)Ni_(0.23_O_(1.9)F_(0.1)(KMNOF)cathode is achieved with 77%capacity retention over 350 cycles at 100mA/g,yielding high discharge capacity 93.5 mAh/g at 20mA/g and significantly improved rate capability of 50.1 mAh/g at 500 mA/g,whereas irreversible structural evolution and rapid capacity fade with KMNO cathode.Finally,in situ/ex situ characterizations and theoretical computations sheds light on the charge transfer and structure evolution mechanisms of KMNOF.展开更多
Oxygen-rich porous carbons are promising candidates for the carbon-based cathodes of zinc ion hybrid capacitors(ZIHCs).Potassium activation is a traditional and effective way to prepare oxygen-rich porous carbons.Effi...Oxygen-rich porous carbons are promising candidates for the carbon-based cathodes of zinc ion hybrid capacitors(ZIHCs).Potassium activation is a traditional and effective way to prepare oxygen-rich porous carbons.Efficient potassium activation is the key to develop high-performance oxygen-rich porous carbon cathodes.Herein,the alkali lignin,extracted from eucalyptus wood by geopolymer-assisted low-alkali pretreatment,is used to prepare oxygen-rich lignin-derived porous carbons(OLPCs)through KOH activation and K_(2)CO_(3)activation at 700-900℃.KOH activation constructs a hierarchical micro-mesoporous structure,while K_(2)CO_(3)activation constructs a microporous structure.Furthermore,K_(2)CO_(3)activation could more efficiently construct active oxygen(C=O)species than KOH activation.The OLPCs prepared by KOH/K_(2)CO_(3)activations at 800℃show the highest microporosity(78.4/87.7%)and C=O content(5.3/8.0 at.%).Due to that C=O and micropore adsorb zinc ions,the OLPCs prepared by K_(2)CO_(3)activation at 800℃with higher C=O content and microporosity deliver superior capacitive performance(256 F g^(-1)at 0.1 A g^(-1))than that by KOH activation at 800℃(224 F g^(-1)at 0.1 A g^(-1)),and excellent cycling stability.This work provides a new insight into the sustainable preparation of oxygenrich porous carbon cathodes through efficient potassium activation for ZIHCs.展开更多
In the post-lithium-ion battery era,potassium-ion batteries(PIBs)show great potential due to their high energy density and economic competitiveness from abundant potassium resources.In comparison with traditional orga...In the post-lithium-ion battery era,potassium-ion batteries(PIBs)show great potential due to their high energy density and economic competitiveness from abundant potassium resources.In comparison with traditional organic electrolytes,aqueous electrolytes bring lower costs,higher safety,and more environmentally friendly preparation processes for PIBs.Against this background,aqueous PIBs(APIBs)have gradually become a research hotspot in the past few years.Cathodes,a critical component of APIBs,directly affect energy density,safety,and stability.Herein,this review systematically summarizes the research progress of typical APIB cathode materials,some breakthrough investigations of which are highlighted.Meanwhile,material synthesis methods,electrolyte design strategies,electrochemical performance optimization pathways,and electrochemical reaction mechanisms are introduced briefly.Finally,the current challenges and corresponding improvement strategies are proposed to provide a reference for further development.展开更多
BACKGROUND The use of proton pump inhibitors(PPIs)with the intent of reducing gastric acidity to the desired therapeutic level for treating bleeding peptic ulcer still has several limitations.AIM To compare intravenou...BACKGROUND The use of proton pump inhibitors(PPIs)with the intent of reducing gastric acidity to the desired therapeutic level for treating bleeding peptic ulcer still has several limitations.AIM To compare intravenous PPIs and oral potassium competitive acid blockers(PCABs)administered prior to endoscopic treatment of bleeding peptic ulcers.METHODS This retrospective study involved 105 consecutive patients with non-variceal upper gastrointestinal bleeding(treated August 2023 to February 2024).Prior to emergency endoscopy,patients received either intravenous PPI(pantoprazole 80 mg bolus)or oral PCAB(tegoprazan 50 mg single-dose).Severity of bleeding was assessed using the Glasgow-Blatchford,Rockall,and AIMS65 scoring systems.Patients with severe comorbidities were excluded.Primary outcomes included need for therapeutic endoscopic intervention and occurrence of re-bleeding.Multivariate logistic regression was performed to adjust for potential confounding factors.RESULTS Total of the 105 patients,61 received intravenous PPI injection and 44 received oral PCAB prior to emergency endoscopy.To minimize selection bias,bleeding severity was assessed using the Glasgow-Blatchford,Rockall and AIMS65 scores,with no statistically significant differences observed between the two groups.During emergency endoscopy performed within 48 hours,ulcer bed status was classified according to the Forrest classification.The proportion of lesions graded IIa or higher was significantly lower in the PCAB group(P<0.001),as was the frequency of therapeutic endoscopy intervention(odds ratio=0.272,95%confidence interval:0.111-0.665,P=0.004).The frequency of re-bleeding events was statistically significantly higher in the PPI group(odds ratio=0.141,95%confidence interval:0.024-0.844,P=0.032).CONCLUSION Pre-endoscopic PCAB administration is more effective than PPI injection for upper gastrointestinal bleeding and may reduce ulcer bleeding mortality.展开更多
Highly dispersed noble metals are acknowledged for its pivotal role in influencing the efficiency of catalysts during the HCHO oxidation process.Interestingly,in this work,an innovative approach was employed to augmen...Highly dispersed noble metals are acknowledged for its pivotal role in influencing the efficiency of catalysts during the HCHO oxidation process.Interestingly,in this work,an innovative approach was employed to augmenting the stabilization of noble metals on irreducible carriers supported noble metal catalyst(Pd/SiO_(2))by adding alkali metal potassium(K).A formidable promotion effect was observed when the K doping to Pd/SiO_(2) catalysts.It achieves a conversion rate of 93%for 270 ppmV of HCHO to harmless CO_(2) and H_(2)O at a weight hourly space velocity(WHSV)of 300,000 mL/(g·hr)at 25℃.Multiple characterization results illustrated that a strong interaction between added K and Pd species was formed after K addition,which not only stabilized Pd species on the carrier surface but alsomarkedly enhanced its dispersal on the SiO_(2) carrier.The increasing Pd dispersion induced more oxygen vacancies on the surfaces of the Pd/SiO_(2) catalysts.The formation of these oxygen vacancies can be attributed to the phenomenon of hydrogen spillover,which also contributed to elevating the electron density on the Pd sites.Meanwhile,the oxygen vacancies favored the O_(2) activation to formmore reactive oxygen species participating in the HCHO oxidation reaction,thus improving the performance of Pd/SiO_(2) catalysts displayed for HCHO oxidation.This study provides a simple strategy to design high-performance irreducible carriers supported noble metal catalysts for HCHO catalytic oxidation.展开更多
Organic electrode materials(OEMs)constitute an attractive class of energy storage materials for potassium-ion batteries,but their application is severely hindered by sluggish kinetics and limited capacities.Herein,ino...Organic electrode materials(OEMs)constitute an attractive class of energy storage materials for potassium-ion batteries,but their application is severely hindered by sluggish kinetics and limited capacities.Herein,inorganic molecules covalent combination strategy is proposed to drive advanced potassium organic batteries.Specifically,molecular selenium,possessing high potential of conductivity and electroactivity,is covalently bonded with organic matrix,that is symmetrical selenophene-annulated dipolyperylene diimide(PDI2-2Se),is designed to verify the feasibility.The inorganic-anchored OEM(PDI2-2Se)can be electrochemically activated to form organic(PDI2 matrix)–inorganic(Se)hybrids during initial cycles.Stateof-the-art 3D tomography reveals that a“mutual-accelerating”effect was realized,that is,the 10-nm Se quantum dots,possessing high conductivity,facilitate charge transfer in organics as well store K^(+)-ions,and organic PDI2 matrix benefits the encapsulation of Se,thereby suppressing shuttle effect and volume fluctuation during cycling,endowing resulting PDI2/Se hybrids with both high-rate capacities and longevity.The concept of inorganicconfigurated OEM through covalent bonds,in principle,can also be extended to design novel functional organic-redox electrodes for other high-performance secondary batteries.展开更多
In order to study the effects of nitrogen fertilizer application methods and nitrogen fertilizer regulation with straw-return on wheat yield and potassium forms in the soil, field experiment was arranged in Pinyuan Co...In order to study the effects of nitrogen fertilizer application methods and nitrogen fertilizer regulation with straw-return on wheat yield and potassium forms in the soil, field experiment was arranged in Pinyuan County, and the effects of the regulation of different ratios of basal to topdressed nitrogen on the yield of wheat and the contents of different forms of potassium in the soil were studied. The re- sults indicated that in the condition of straw-return, the yield of wheat was the high- est after the treatments of the ratios of basal to topdressed nitrogen of 7：3 and 6：4. As to the contents of different forms of potassium, the contents of water-soluble potassium, exchangeable potassium and total potassium treated by the ratios of basal to topdressed nitrogen of 7：3 and 6：4 were the highest, and the differences of non-exchangeable potassium among all treatments were not significant. Under the experiment condition, the ratios of basal to topdressed nitrogen of 7：3 and 6：4 were the best treatments, they can increase the wheat yield and the contents of available potassium and total potassium in the soil.展开更多
文摘In addition to sequestering carbon in soil,biochars can also play a role in changing the potassium equilibration and dynamics of the soil.Nowadays,acidification of biochar is commonly used to improve its properties,which can impact the potassium content in the soil.Simultaneous application of acidified biochar and sodium bentonite can complicate this effect.In the present study,the effects of adding two types of biochars prepared from municipal waste and used coffee grounds and their acidified types,along with sodium bentonite at three levels(0.00%,1.00%,and 2.00%),on soil physical-chemical properties(pH,salinity,cation exchange capacity,concentration of soluble cations and their ratio,and sodium adsorption ratio)and the release of potassium from a calcareous soil were investigated.The results showed that the addition of coffee ground biochar increased the concentration of soluble potassium and decreased the ratio of calcium to potassium,while the acidified coffee ground biochar decreased the amount of soluble potassium and increased the ratio of calcium to potassium.Alkaline and acidified municipal waste biochars had no effect on soluble potassium and soluble cations ratio.Application of bentonite increased the amount of soluble calcium and sodium and the ratio of calcium to potassium.Addition of bentonite also increased the amount of exchangeable potassium and exchangeable sodium percentage,but use of different biochars reduced negative effect of bentonite.Use of bentonite also caused an increase in the exchangeable potassium and a decrease in the non-exchangeable potassium contents.Alkaline and acidified coffee ground biochars increased the amount of exchangeable,non-exchangeable,and total potassium,but this effect was greater by alkaline biochar.Application of municipal waste biochar did not affect the amount of exchangeable potassium but increased the amount of non-exchangeable and total potassium,with no significant difference observed between alkaline and acidified biochars.Potassium saturation percentage was not affected by bentonite,but coffee ground biochar increased its amount and municipal waste biochar had no effect on it.Acidified and alkaline coffee ground biochars were able to release more potassium from the soil(475 and 71 mg/kg,respectively),while alkaline municipal waste biochar did not affect it and acidified municipal waste biochar reduced it by 113 mg/kg.In general,it can be concluded that alkaline biochars in calcareous soils can improve potassium fertility by reduction of the ratio of calcium to potassium and increasing its various forms,while acidified biochars and bentonite may aggravate potassium deficiency in these soils.Considering the lack of significant change in the pH of calcareous soils with the use of different biochars,it is suggested to use alkaline biochars,which can improve the potassium status of the soil while reducing the costs associated with biochar modification.
基金financially supported by the National Natural Science Foundation of China(No.22209057)the Guangzhou Basic and Applied Basic Research Foundation(No.2024A04J0839)。
文摘Thanks to its abundant reserves,relatively high energy density,and low reduction potential,potassium ion batteries(PIBs)have a high potential for large-scale energy storage applications.Due to the large radius of potassium ions,most conventional anode materials undergo severe volume expansion,making it difficult to achieve stable and reversible energy storage.Therefore,developing high-performance anode materials is one of the critical factors in developing PIBs.In this sense,antimony(Sb)-based anode materials with high theoretical capacity and safe reaction potentials have a broad potential for application in PIBs.However,overcoming the rapid capacity decay induced by the large radius of potassium ions is still an issue that needs to be focused on.This paper reviews the latest research on different types of Sb-based anode materials and provides an in-depth analysis of their optimization strategies.We focus on material selection,structural design,and storage mechanisms to develop a detailed description of the material.In addition,the current challenges still faced by Sb-based anode materials are summarized,and some further optimization strategies have been added.We hope to provide some insights for researchers developing Sb-based anode materials for next-generation advanced PIBs.
基金supported by the National Natural Science Foundation of China(22209057)the Guangzhou Basic and Applied Basic Research Foundation(2024A04J0839).
文摘Potassium-ion batteries(PIBs)are considered as a promising energy storage system owing to its abundant potassium resources.As an important part of the battery composition,anode materials play a vital role in the future development of PIBs.Bismuth-based anode materials demonstrate great potential for storing potassium ions(K^(+))due to their layered structure,high theoretical capacity based on the alloying reaction mechanism,and safe operating voltage.However,the large radius of K^(+)inevitably induces severe volume expansion in depotassiation/potassiation,and the sluggish kinetics of K^(+)insertion/extraction limits its further development.Herein,we summarize the strategies used to improve the potassium storage properties of various types of materials and introduce recent advances in the design and fabrication of favorable structural features of bismuth-based materials.Firstly,this review analyzes the structure,working mechanism and advantages and disadvantages of various types of materials for potassium storage.Then,based on this,the manuscript focuses on summarizing modification strategies including structural and morphological design,compositing with other materials,and electrolyte optimization,and elucidating the advantages of various modifications in enhancing the potassium storage performance.Finally,we outline the current challenges of bismuth-based materials in PIBs and put forward some prospects to be verified.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(No.RS-2024-00453815)Korea Institute of Energy Technology Evaluation and Planning(KETEP)grant funded by the Korea government(MOTIE)(20228510070100)。
文摘Recently,potassium-ion batteries(PIBs)have received significant attention in the energy storage field owing to their high-power output,fast charging capability,natural abundance,and environmental sustainability.Herein,we comprehensively review recent advancements in the design and development of carbon-based anode materials for PIBs anodes,covering graphite,hard carbon,alloy and conversion materials with carbon,and carbon host for K metal deposition.Chemical strategies such as structural engineering,heteroatom-doping,and surface modifications are highlighted to improve electrochemical performances as well as to resolve technical challenges,such as electrode instability,low initial Coulombic efficiency,and electrolyte compatibility.Furthermore,we discuss the fundamental understanding of potassium-ion storage mechanisms of carbon-based materials and their correlation with electrochemical performance.Finally,we present the current challenges and future research directions for the practical implementation of carbon-based anodes to enhance their potential as next-generation energy storage materials for PIBs.This review aims to provide our own insights into innovative design strategies for advanced PIB's anode through the chemical and engineering strategies.
基金supported by National Natural Science Foundation of China(52302034,52402060,52202201,52021006)Beijing National Laboratory for Molecular Sciences(BNLMS-CXTD202001)+1 种基金Shenzhen Science and Technology Innovation Commission(KQTD20221101115627004)China Postdoctoral Science Foundation(2024T170972)。
文摘Graphdiyne(GDY)is a two-dimensional carbon allotrope with exceptional physical and chemical properties that is gaining increasing attention.However,its efficient and scalable synthesis remains a significant challenge.We present a microwave-assisted approach for its continuous,large-scale production which enables synthesis at a rate of 0.6 g/h,with a yield of up to 90%.The synthesized GDY nanosheets have an average diameter of 246 nm and a thickness of 4 nm.We used GDY as a stable coating for potassium(K)metal anodes(K@GDY),taking advantage of its unique molecular structure to provide favorable paths for K-ion transport.This modification significantly inhibited dendrite formation and improved the cycling stability of K metal batteries.Full-cells with perylene-3,4,9,10-tetracarboxylic dianhydride(PTCDA)cathodes showed the clear superiority of the K@GDY anodes over bare K anodes in terms of performance,stability,and cycle life.The K@GDY maintained a stable voltage plateau and gave an excellent capacity retention after 600 cycles with nearly 100%Coulombic efficiency.This work not only provides a scalable and efficient way for GDY synthesis but also opens new possibilities for its use in energy storage and other advanced technologies.
基金the financial support from the National Natural Science Foundation of China(No.92163124)Foundation for the Sichuan University and Zigong City Joint research project(No.2021CDZG-2)+1 种基金Foundation for the Sichuan University and Yibin City Strategic Cooperation Project(No.2020CDYB-32)Guangxi Key Laboratory of Low Carbon Energy Material(No.2020GKLLCEM02)。
文摘Carbon materials are considered as prospective anode candidates for potassium ion batteries(PIBs).However,the low-rate capability is hampered by slow K+diffusion kinetics and obstructed electron transport of carbon-based anodes.In this work,calcium D-gluconate derived mesoporous carbon nanosheets(CGC)were interpenetrated into the architecture of reduced graphene oxides(RGO)to form the composites of two-dimensional(2D)/2D graphene/mesoporous carbon nanosheets(RGO@CGC).CGC as a rigid skeleton can prevent the graphene layers from restacking and maintain the structural stability of the 2D/2D carbon composites of RGO@CGC.The mesopores in CGC can shorten the path of ion diffusion and facilitate the penetration of electrolytes.RGO possesses the high surface-to-volume ratio and superior electron transport capability in the honeycomb-like 2D network consisting of sp^(2)-hybridized carbon atoms.Especially,theπ-πstacking interaction between CGC and RGO enhances stable composite structure formation,expedites interlayer-electron transfer,and establishes three-dimensional(3D)ion transportation pathways.Owing to these unique structure,RGO@CGC exhibits fast and stable potassium storage capability.Furthermore,the effects of binders and electrolytes on the electrochemical performance of RGO@CGC were investigated.Finally,Prussian blue was synthesized as a positive electrode to explore the possibility of RGO@CGC as a full battery application.
基金financial support from the Doctoral Foundation of Henan University of Engineering(No.D2022025)National Natural Science Foundation of China(No.U2004162)+1 种基金National Natural Science Foundation of China(No.52302138)Key Project for Science and Technology Development of Henan Province(No.232102320221)。
文摘With the rapid development of electric vehicles,hybrid electric vehicles and smart grids,people's demand for large-scale energy storage devices is increasingly intense.As a new type of secondary battery,potassium ion battery is promising to replace the lithium-ion battery in the field of large-scale energy storage by virtue of its low price and environmental friendliness.At present,the research on the anode materials of potassium ion batteries mainly focuses on carbon materials and the design of various nanostructured metal-based materials.Problems such as poor rate performance and inferior cycle life caused by electrode structure comminution during charge and discharge have not been solved.Quantum dots/nanodots materials are a new type of nanomaterials that can effectively improve the utilization of electrode materials and reduce production costs.In addition,quantum dots/nanodots materials can enhance the electrode reaction kinetics,reduce the stress generated in cycling,and effectively alleviate the agglomeration and crushing of electrode materials.In this review,we will systematically introduce the synthesis methods,K+storage properties and K+storage mechanisms of carbon quantum dots and carbon-based transition metal compound quantum dots composites.This review will have significant references for potassium ion battery researchers.
基金supported by National Natural Science Foundation of China(Nos.52472194,52101243)Natural Science Foundation of Guangdong Province,China(No.2023A1515012619)the Science and Technology Planning Project of Guangzhou(No.202201010565)。
文摘In recent years,metal phosphosulfides have attracted great attention as the promising anode materials in sodium/potassium batteries because of their incorporation of the advantages of metal phosphides and sulfides.However,they are also confronted with the problem of unstable battery performance due to the heavy volume expansion and sluggish ion reaction kinetics.Herein,yolk-shell cobalt phosphosulfide nanocrystals encapsulating into multi-heterogeneous atom(N,P,S)-doped carbon framework(Co_(9)S_(8)/CoP@NPSC)were constructed by employing dodecahedral ZIF-67 as precursor and a polymer as carbon sources through simultaneous sulfidation and phosphorization processes.The synergistic effect of Co_(9)S_(8)and CoP component and the yolk-shell structure greatly improve the bettery performance and structural stability.In addition,the multiple hetero-atoms doped carbon frameworks enhance the conductivity of the electrode materials and increase the spacing of carbon layers to supply sufficient active sites and facilitate the Na^(+)/K^(+)transport.The electrochemical results demonstrated that Co_(9)S_(8)/CoP@NPSC exhibited the pleasant reversible capacity(360.47 mAh/g at 1 A/g)after 300 cycles and an unpredictable cycling stability(103.22 mAh/g after 1000 cycles)in the SIBs application.The ex-situ XRD and XPS analyses were further applied to study the sodium ion storage mechanism and the multi-step phase transition reaction of the yolk-shell heterogeneous structure.This work provides new perspectives for the preparation of novel structure metal phosphosulfide and their applications in anode materials for sodium/potassium batteries and other secondary batteries.
基金supported by the National Natural Science Foundation of China,Nos.81901098(to TC),82201668(to HL)Fujian Provincial Health Technology Project,No.2021QNA072(to HL)。
文摘The central nervous system, information integration center of the body, is mainly composed of neurons and glial cells. The neuron is one of the most basic and important structural and functional units of the central nervous system, with sensory stimulation and excitation conduction functions. Astrocytes and microglia belong to the glial cell family, which is the main source of cytokines and represents the main defense system of the central nervous system. Nerve cells undergo neurotransmission or gliotransmission, which regulates neuronal activity via the ion channels, receptors, or transporters expressed on nerve cell membranes. Ion channels, composed of large transmembrane proteins, play crucial roles in maintaining nerve cell homeostasis. These channels are also important for control of the membrane potential and in the secretion of neurotransmitters. A variety of cellular functions and life activities, including functional regulation of the central nervous system, the generation and conduction of nerve excitation, the occurrence of receptor potential, heart pulsation, smooth muscle peristalsis, skeletal muscle contraction, and hormone secretion, are closely related to ion channels associated with passive transmembrane transport. Two types of ion channels in the central nervous system, potassium channels and calcium channels, are closely related to various neurological disorders, including Alzheimer's disease, Parkinson's disease, and epilepsy. Accordingly, various drugs that can affect these ion channels have been explored deeply to provide new directions for the treatment of these neurological disorders. In this review, we focus on the functions of potassium and calcium ion channels in different nerve cells and their involvement in neurological disorders such as Parkinson's disease, Alzheimer's disease, depression, epilepsy, autism, and rare disorders. We also describe several clinical drugs that target potassium or calcium channels in nerve cells and could be used to treat these disorders. We concluded that there are few clinical drugs that can improve the pathology these diseases by acting on potassium or calcium ions. Although a few novel ion-channelspecific modulators have been discovered, meaningful therapies have largely not yet been realized. The lack of target-specific drugs, their requirement to cross the blood–brain barrier, and their exact underlying mechanisms all need further attention. This review aims to explain the urgent problems that need research progress and provide comprehensive information aiming to arouse the research community's interest in the development of ion channel-targeting drugs and the identification of new therapeutic targets for that can increase the cure rate of nervous system diseases and reduce the occurrence of adverse reactions in other systems.
基金Deutsche Forschungsgemeinschaft(DFG,German Research Foundation)under Germany’s Excellence Strategy-EXC 2089/1-390776260(e-conversion)for fundingfinancial support from TUM Innovation Network for Artificial Intelligence powered Multifunctional Material Design(ARTEMIS)。
文摘To address challenges related to the intermittency of renewable energy sources,aqueous potassium-ion batteries(AKIBs)are a promising and sustainable alternative to conventional systems for large-scale energy storage.To enable their practical application,maximizing energy density and longevity while minimizing production and material costs is a key goal.In this work,we propose an AKIB consisting only of abundant and cost-efficient materials,which delivers a high energy density of more than 70 Wh kg^(-1).We combine simple strategies to stabilize the Mn-rich Prussian blue analog cathode by Fe-doping,improving the crystallinity,and tuning the electrolyte composition without employing expensive water-in-salt electrolytes.Using a mixed 2.5 M Ca(NO_(3))_(2)+1.5 M KNO_(3)electrolyte,we assemble a novel AKIB with a Fe-doped manganese hexacyanoferrate cathode and an organic poly(naphthalene-4-formylethylenediamine)anode.Besides a high energy density,the full cell delivers a specific capacity of approximately 60 mAhg^(-1),a power density of 5000 W kg^(-1),and 80% capacity retention after 600 cycles.
文摘A comparative study of products of thermal and thermocatalytic cracking of polypropylene(PP) in the presence of potassium polytitanate(PPT) synthesized by treatment of TiO_(2)(rutile) powder with molten mixture of KOH and KNO_(3) taken in a weight ratio of 30∶30∶40 has been carried out.It was shown that the studied type of PPT powder exhibits catalytic properties in the reaction of thermal decomposition of PP,compared to the effect of commercial zeolite catalyst CBV-780 traditionally used for this purpose.Based on the analysis performed,the differences in the mechanism of catalytic action of PPT and the zeolite were considered.The reasons for the observed differences in the composition of PP cracking products and in the rate of coke formation on the surface of studied catalysts were analyzed.Considering the obtained results,it has been proposed that the CBV-780 catalyst promoted more intensive production of the gaseous hydrocarbons compared to PPT,due to higher specific surface area(internal surface) accessible for relatively light and small-sized hydrocarbon products of cracking.However,intensive coke formation on the outer surface of the microporous zeolite contributes to the blocking of transport channels and the rapid loss of catalytic action.At the same time,PPT,which initially has a smaller specific surface area,retains its catalytic activity significantly longer due to slit-shaped flat pores and higher transport accessibility of the inner surface.
基金supported by the National Natural Science Foundation of China (22008049 and 22478095)Hebei Provincial Key Research Projects (22374101D)+3 种基金Central Guidance Project for Local Science and Technology Development from S&T Program of Hebei (246Z1009G)Special Proof-of-concept Project on Basic Research from S&T Program of Hebei (E2024402143)Science and Technology Project of Hebei Education Department (CXY2023004)Hebei University of Engineering Doctoral Scientific Research Start-up Foundation (SJ2401002210).
文摘Aiming at the problems of complex process and high cost in the production of potassium bromide at present,the solubility data and the phase diagram of the quaternary system KBr-MgBr_(2)-K_(2)SO_(4)-MgSO_(4)-H_(2)O at 298.15 K were studied using the isothermal dissolution equilibrium method.The results showed that there are eight invariant points,sixteen univariant curves,and nine crystallization regions in the phase diagram which is complex and contains two double salts(K_(2)SO_(4)·MgSO_(4)·6H_(2)O and KBr·MgBr_(2)·6H_(2)O)and a metastable phase(MgSO_(4)·5H_(2)O).On the basis of the Pitzer model and HW model,the solubilities of the quaternary system were calculated,with which the corresponding phase diagram was plotted.By comparison,the evaluated phase diagram is in accordance with the measured one.Through analysis,the phase diagrams of the quaternary system at(298.15 and 323.15)K were combined to put forward a process to separate KBr from the system by evaporation and crystallization,which realized the full circulation of the mother solution.
文摘Potassium is one of the macro minerals necessary for the cellular functions,obtained from foods.Excessive amounts of potassium can cause health problems.Determination of potassium in various samples,especially food and drug samples,is an important task.In this study,we developed a new potentiometric sensor selective to potassium ions.The sensor had a detection limit of 8.64×10^(-5) M in the concentration range of 1.0×10^(-1)-1.0×10^(-4) M and a near-Nernstian behavior of 49.0±4.32 mV/decade.The sensor exhibited a response time of 10 s,as well as good selectivity,good repeatability,and a wide pH working range(4.0-11.0).The developed sensor was successfully applied to a drug sample and different water samples with very high recoveries(>91.20%).
基金financially supported by the National Natural Science Foundation of China(No.51902090)Henan Key Research Project Plan for Higher Education Institutions(No.24A150019)the Doctoral Start-Up Foundation(No.QD2022017).
文摘Mn-rich layered oxides are appealing cathodes for potassium ion batteries(PIBs)in view of their comprehensive virtues such as low cost,high energy density and mature craftsmanship.However,the insufficient covalency between transition metal(TM)and O usually induces irreversible structural evolution and cation migration during repeated insertion and extraction of K^(+),resulting in capacity loss,voltage fading and sluggish kinetics.Herein,an anion substitution strategy is proposed for a stable operation of layered oxide cathode by adjusting the valence electron layer structure between TM and O.The resultant strong TM−O skeleton can inhibit the occurrence of side effects derive from Ni^(4+)during the deep depotassium process,so as to achieve a gentle structural transition.Consequently,stable cycling performance of K_(0.39)Mn_(0.77)Ni_(0.23_O_(1.9)F_(0.1)(KMNOF)cathode is achieved with 77%capacity retention over 350 cycles at 100mA/g,yielding high discharge capacity 93.5 mAh/g at 20mA/g and significantly improved rate capability of 50.1 mAh/g at 500 mA/g,whereas irreversible structural evolution and rapid capacity fade with KMNO cathode.Finally,in situ/ex situ characterizations and theoretical computations sheds light on the charge transfer and structure evolution mechanisms of KMNOF.
基金supported by the National Natural Science Foundation of China(22408061 and 22468005)Program for Introducing High-Level Talents from Guangxi University,and Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology(2023Z014).
文摘Oxygen-rich porous carbons are promising candidates for the carbon-based cathodes of zinc ion hybrid capacitors(ZIHCs).Potassium activation is a traditional and effective way to prepare oxygen-rich porous carbons.Efficient potassium activation is the key to develop high-performance oxygen-rich porous carbon cathodes.Herein,the alkali lignin,extracted from eucalyptus wood by geopolymer-assisted low-alkali pretreatment,is used to prepare oxygen-rich lignin-derived porous carbons(OLPCs)through KOH activation and K_(2)CO_(3)activation at 700-900℃.KOH activation constructs a hierarchical micro-mesoporous structure,while K_(2)CO_(3)activation constructs a microporous structure.Furthermore,K_(2)CO_(3)activation could more efficiently construct active oxygen(C=O)species than KOH activation.The OLPCs prepared by KOH/K_(2)CO_(3)activations at 800℃show the highest microporosity(78.4/87.7%)and C=O content(5.3/8.0 at.%).Due to that C=O and micropore adsorb zinc ions,the OLPCs prepared by K_(2)CO_(3)activation at 800℃with higher C=O content and microporosity deliver superior capacitive performance(256 F g^(-1)at 0.1 A g^(-1))than that by KOH activation at 800℃(224 F g^(-1)at 0.1 A g^(-1)),and excellent cycling stability.This work provides a new insight into the sustainable preparation of oxygenrich porous carbon cathodes through efficient potassium activation for ZIHCs.
基金financially supported by the National Natural Science Foundation of China(52201259,52202286,52002094)the Education Department of Liaoning Province(JYTQN2023285)+5 种基金the Shenyang University of Technology(QNPY202209-4)the Key Laboratory of Functional Inorganic Material Chemistry(Heilongjiang University,Ministry of Education)the Science and Technology Department of Liaoning Province(2024-BSLH-172,JYTMS20231216)the Natural Science Foundation of Zhejiang Province(LY24B030006)the Science and Technology Plan Project of Wenzhou Municipality(ZG2024055)the Shenzhen Science and Technology Innovation Program(RCBS20210706092218040)。
文摘In the post-lithium-ion battery era,potassium-ion batteries(PIBs)show great potential due to their high energy density and economic competitiveness from abundant potassium resources.In comparison with traditional organic electrolytes,aqueous electrolytes bring lower costs,higher safety,and more environmentally friendly preparation processes for PIBs.Against this background,aqueous PIBs(APIBs)have gradually become a research hotspot in the past few years.Cathodes,a critical component of APIBs,directly affect energy density,safety,and stability.Herein,this review systematically summarizes the research progress of typical APIB cathode materials,some breakthrough investigations of which are highlighted.Meanwhile,material synthesis methods,electrolyte design strategies,electrochemical performance optimization pathways,and electrochemical reaction mechanisms are introduced briefly.Finally,the current challenges and corresponding improvement strategies are proposed to provide a reference for further development.
文摘BACKGROUND The use of proton pump inhibitors(PPIs)with the intent of reducing gastric acidity to the desired therapeutic level for treating bleeding peptic ulcer still has several limitations.AIM To compare intravenous PPIs and oral potassium competitive acid blockers(PCABs)administered prior to endoscopic treatment of bleeding peptic ulcers.METHODS This retrospective study involved 105 consecutive patients with non-variceal upper gastrointestinal bleeding(treated August 2023 to February 2024).Prior to emergency endoscopy,patients received either intravenous PPI(pantoprazole 80 mg bolus)or oral PCAB(tegoprazan 50 mg single-dose).Severity of bleeding was assessed using the Glasgow-Blatchford,Rockall,and AIMS65 scoring systems.Patients with severe comorbidities were excluded.Primary outcomes included need for therapeutic endoscopic intervention and occurrence of re-bleeding.Multivariate logistic regression was performed to adjust for potential confounding factors.RESULTS Total of the 105 patients,61 received intravenous PPI injection and 44 received oral PCAB prior to emergency endoscopy.To minimize selection bias,bleeding severity was assessed using the Glasgow-Blatchford,Rockall and AIMS65 scores,with no statistically significant differences observed between the two groups.During emergency endoscopy performed within 48 hours,ulcer bed status was classified according to the Forrest classification.The proportion of lesions graded IIa or higher was significantly lower in the PCAB group(P<0.001),as was the frequency of therapeutic endoscopy intervention(odds ratio=0.272,95%confidence interval:0.111-0.665,P=0.004).The frequency of re-bleeding events was statistically significantly higher in the PPI group(odds ratio=0.141,95%confidence interval:0.024-0.844,P=0.032).CONCLUSION Pre-endoscopic PCAB administration is more effective than PPI injection for upper gastrointestinal bleeding and may reduce ulcer bleeding mortality.
基金supported by the Youth Innovation Promotion Association,CAS(No.2020310)Sanming University(No.23YG05).
文摘Highly dispersed noble metals are acknowledged for its pivotal role in influencing the efficiency of catalysts during the HCHO oxidation process.Interestingly,in this work,an innovative approach was employed to augmenting the stabilization of noble metals on irreducible carriers supported noble metal catalyst(Pd/SiO_(2))by adding alkali metal potassium(K).A formidable promotion effect was observed when the K doping to Pd/SiO_(2) catalysts.It achieves a conversion rate of 93%for 270 ppmV of HCHO to harmless CO_(2) and H_(2)O at a weight hourly space velocity(WHSV)of 300,000 mL/(g·hr)at 25℃.Multiple characterization results illustrated that a strong interaction between added K and Pd species was formed after K addition,which not only stabilized Pd species on the carrier surface but alsomarkedly enhanced its dispersal on the SiO_(2) carrier.The increasing Pd dispersion induced more oxygen vacancies on the surfaces of the Pd/SiO_(2) catalysts.The formation of these oxygen vacancies can be attributed to the phenomenon of hydrogen spillover,which also contributed to elevating the electron density on the Pd sites.Meanwhile,the oxygen vacancies favored the O_(2) activation to formmore reactive oxygen species participating in the HCHO oxidation reaction,thus improving the performance of Pd/SiO_(2) catalysts displayed for HCHO oxidation.This study provides a simple strategy to design high-performance irreducible carriers supported noble metal catalysts for HCHO catalytic oxidation.
基金supported by the National Natural Science Foundation of China(NSFC,21975194,22175134,22209127 and 52072282)Natural Science Foundation of Hubei Province(No.2023AFA014)+2 种基金the research fund for distinguished young scholars of Hubei Province(2019CFA042)the generous start-up funds from the Wuhan University of Technology(nos.2182022132)the Fundamental Research Funds for the Central Universities(195220009).
文摘Organic electrode materials(OEMs)constitute an attractive class of energy storage materials for potassium-ion batteries,but their application is severely hindered by sluggish kinetics and limited capacities.Herein,inorganic molecules covalent combination strategy is proposed to drive advanced potassium organic batteries.Specifically,molecular selenium,possessing high potential of conductivity and electroactivity,is covalently bonded with organic matrix,that is symmetrical selenophene-annulated dipolyperylene diimide(PDI2-2Se),is designed to verify the feasibility.The inorganic-anchored OEM(PDI2-2Se)can be electrochemically activated to form organic(PDI2 matrix)–inorganic(Se)hybrids during initial cycles.Stateof-the-art 3D tomography reveals that a“mutual-accelerating”effect was realized,that is,the 10-nm Se quantum dots,possessing high conductivity,facilitate charge transfer in organics as well store K^(+)-ions,and organic PDI2 matrix benefits the encapsulation of Se,thereby suppressing shuttle effect and volume fluctuation during cycling,endowing resulting PDI2/Se hybrids with both high-rate capacities and longevity.The concept of inorganicconfigurated OEM through covalent bonds,in principle,can also be extended to design novel functional organic-redox electrodes for other high-performance secondary batteries.
基金Supported by the Project of National Science and Technology Support Plan-"Integration and Demonstration ration of Straw Resources Recycling Technologies in Huang-HuaiHai Plain Area"(2012BAD14B07)the Project of Major Application Technology Innovation of Agriculture in Shandong Province-"Study on Recycling Technology of Waste Resourcization in Large-scale Farm"+1 种基金the Foundation for Outstanding Young Scientist in Shandong Province-"Study on the Mechanism of the Effect of Drip Irrigation with Saline Water on Soil Environment and Its Crop Response"(BS2011NY017)the Project of National Natural Science Foundation-"Study on the Allocation Pattern and Interface Control of Salinity under the Condition of Brackish Water Irrigation"(51209130)~~
文摘In order to study the effects of nitrogen fertilizer application methods and nitrogen fertilizer regulation with straw-return on wheat yield and potassium forms in the soil, field experiment was arranged in Pinyuan County, and the effects of the regulation of different ratios of basal to topdressed nitrogen on the yield of wheat and the contents of different forms of potassium in the soil were studied. The re- sults indicated that in the condition of straw-return, the yield of wheat was the high- est after the treatments of the ratios of basal to topdressed nitrogen of 7：3 and 6：4. As to the contents of different forms of potassium, the contents of water-soluble potassium, exchangeable potassium and total potassium treated by the ratios of basal to topdressed nitrogen of 7：3 and 6：4 were the highest, and the differences of non-exchangeable potassium among all treatments were not significant. Under the experiment condition, the ratios of basal to topdressed nitrogen of 7：3 and 6：4 were the best treatments, they can increase the wheat yield and the contents of available potassium and total potassium in the soil.
