Layered ammonium vanadate has become a promising cathode material for aqueous zinc ion batteries(ZIBs)due to its small mass and large ionic radius of ammonium ions as well as the consequent large layer spacing and hig...Layered ammonium vanadate has become a promising cathode material for aqueous zinc ion batteries(ZIBs)due to its small mass and large ionic radius of ammonium ions as well as the consequent large layer spacing and high specific capacity.However,the irreversible de-ammoniation caused by N·H···O bonds damaged would impair cycle life of ZIBs and the strong electrostatic interaction between Zn^(2+)and V-O frame could slower the mobility of Zn^(2+).Furthermore,the thermal instability of ammonium vanadate also limits the use of common carbon coating modification method to solve the problem.Herein,V_(2)CT_(X)MXene was innovatively selected as a bifunctional source to in-situ derivatized(NH_(4))_(2)V_(8)O_(20)·x H_(2)O with amorphous carbon-coated(NHVO@C)via one-step hydrothermal method in relatively moderate temperature.The amorphous carbon shell derived from the V_(2)CT_(X)MXene as a conductive framework to effectively improve the diffusion kinetics of Zn^(2+)and the robust carbon skeleton could alleviate the ammonium dissolution during long-term cycling.As a result,zinc ion batteries using NHVO@C as cathode exhibit superior electrochemical performance.Moreover,the assembled foldable or high loading(10.2 mg/cm^(2))soft-packed ZIBs further demonstrates its practical application.This study provided new insights into the development of the carbon cladding process for thermally unstable materials in moderate temperatures.展开更多
The present work aims to stabilize the room temperature allotropic transition of ammonium nitrate(AN)particles utilizing a microencapsulation technique,which involves solvent/non-solvent in which nitrocellulose(NC)has...The present work aims to stabilize the room temperature allotropic transition of ammonium nitrate(AN)particles utilizing a microencapsulation technique,which involves solvent/non-solvent in which nitrocellulose(NC)has been employed as a coating agent.The SEM micrographs revealed distinct features of both pure AN and NC,contrasting with the irregular granular surface topography of the coated AN particles,demonstrating the adherence of NC on the AN surface.Structural analysis via infrared spectroscopy(IR)demonstrated a successful association of AN and NC,with slight shifts observed in IR bands indicating interfacial interactions.Powder X-ray Diffraction(PXRD)analysis further elucidated the structural changes induced by the coating process,revealing that the NC coating altered the crystallization pattern of its pure form.Thermal analysis demonstrates distinct profiles for pure and coated AN,for which the coated sample exhibits a temperature increase and an enthalpy decrease of the room temperature allotropic transition by 6℃,and 36%,respectively.Furthermore,the presence of NC coating alters the intermolecular forces within the composite system,leading to a reduction in melting enthalpy of coated AN by~39%compared to pure AN.The thermal decomposition analysis shows a two-step thermolysis process for coated AN,with a significant increase in the released heat by about 78%accompanied by an increase in the activation barrier of NC and AN thermolysis,demonstrating a stabilized reactivity of the AN-NC particles.These findings highlight the synergistic effect of NC coating on AN particles,which contributed to a structural and reactive stabilization of both AN and NC,proving the potential application of NC-coated AN as a strategically advantageous oxidizer in composite solid propellant formulations.展开更多
A series of multi-hydroxyl bis-(quaternary ammonium)ionic liquids(Ils1‒7)was prepared as bifunctional catalysts for the chemical fixation of CO_(2).All these ionic liquid compounds were efficient for the catalytic syn...A series of multi-hydroxyl bis-(quaternary ammonium)ionic liquids(Ils1‒7)was prepared as bifunctional catalysts for the chemical fixation of CO_(2).All these ionic liquid compounds were efficient for the catalytic synthesis of cyclic carbonates and oxazolidinones via the cycloaddition reactions between CO_(2) and epoxides or aziridines with excellent yield and high selectivity in the absence of co-catalyst,metal and solvent.Due to the synergistic effects of hydroxyl groups and halogen anion,the cycloaddition reactions proceeded smoothly either at atmospheric pressure or room temperature.The selectivity for substituted oxazolidinones at 5-and 4-positions can be tuned via changing the reaction conditions.Finally,possible mechanisms including the activation of both CO_(2) and epoxide or aziridines were proposed based on the literatures and experimental results.展开更多
This study investigates the compatibility and efficacy of combining ammonium molybdate(AM)with antagonistic bacteria Bacillus amyloliquefaciens B10W10 and Pseudomonas sp.B11W11 for brown rot control(Monilinia laxa).In...This study investigates the compatibility and efficacy of combining ammonium molybdate(AM)with antagonistic bacteria Bacillus amyloliquefaciens B10W10 and Pseudomonas sp.B11W11 for brown rot control(Monilinia laxa).In vitro experiments reveal variable mycelial growth inhibition rates compared to untreated controls,with B11W11+0.5%AM and B10W10+2%AM displaying the highest inhibition rates after 5 days.After 10 days,the 2%AM+B10W10 combination exhibits the highest inhibition rate.Microscopic observations show structural alterations in mycelium within inhibition zones,marked by vacuolization.The antagonistic bacteria,alone or with different ammonium molybdate concentrations,significantly impact M.laxa spore germination,with the B10W10 cell filtrate+2%ammonium molybdate combination achieving the most substantial inhibition.Conversely,the 0.5%ammonium molybdate treatment has the lowest inhibition rate while the combination of AM and bacteria is giving better results compared to the use of bacteria alone.Fruits treated with various antagonistic bacteria and ammonium molybdate combinations demonstrate a significant reduction in disease severity.The 0.5%AM+B10W10 combination exhibits the lowest severity.FT-IR spectra analysis identifies shifts in fungal biomass functional groups,with reduced lignin-related bands and increased phenols,lipids,polysaccharides,and carbohydrates.This highlights the structural modifications caused by the biological treatments.The study also evaluates the effects on fruit quality parameters.The 2%ammonium molybdate treatment yields the lowest weight loss.TSS levels are affected by salt concentration,while acid content remains consistent across treatments.All treatments influence fruit firmness compared to controls.These findings emphasize the potential of combining ammonium molybdate and antagonistic bacteria for effective brown rot control,highlighting their compatibility and effects on disease severity,fungal biomass,spore germination,and fruit quality.展开更多
Modified activated carbons(AS)were fabricated through the oxidation effect of ammonium persulfate and applied to the dynamic adsorption of different acrylate gas.The pore structures,surface chemical properties and sur...Modified activated carbons(AS)were fabricated through the oxidation effect of ammonium persulfate and applied to the dynamic adsorption of different acrylate gas.The pore structures,surface chemical properties and surface morphology of AS were respectively characterized by N2 adsorption,Boehm titration,X-ray Photoelectron Spectroscopy(XPS)and scanning electron microscopy(SEM)techniques.After modification,the specific surface area increased from 954 to 1154 m^(2)·g^(-1).The contents of oxygen-containing functional groups on the AS surface increase obviously and have a great effect on the adsorption behavior of acrylate gases.According to the results of dynamic adsorption,the adsorption capacities of acrylates are as the following order:methyl acrylate(461.9 mg·g^(-1))>methyl methacrylate(436.9 mg·g^(-1))>butyl acrylate(381.8 mg·g^(-1)),which is attributed to the size adaptability of AS pores and acrylates.The adsorption behavior of AS for acrylate gases conforms to the Bangham model and the Temkin model.展开更多
Lepidolite,feldspar,and quartz are silicate minerals with similar chemical properties,complicating their flotation separation.Current collector systems require strong acidic conditions for effective separation but sti...Lepidolite,feldspar,and quartz are silicate minerals with similar chemical properties,complicating their flotation separation.Current collector systems require strong acidic conditions for effective separation but still face challenges related to low separation efficiency and recovery rates.This study proposed a novel collector,ammonium dodecylsulfate(ALS),to selectively extract lepidolite from feldspar and quartz using highly selective flotation methods.Microflotation experiments showed that ALS significantly outperforms other collectors in collecting lepidolite compared to feldspar and quartz.At pH 7,lepidolite recovery reached 95%,while flotation recoveries for both feldspar and quartz were below 10%.Mixed pure mineral flotation tests revealed that at pH 7 and ALS concentration of 2.5×10^(-4) mol·L^(−1),the Li_(2)O content in the concentrate was 4.21%,with a recovery rate of 95.01%.Separation efficiency and Gaudin selectivity index values were recorded.Solution chemical analyses showed that at pH 7,ALS completely ionizes into NH_(4)^(+)and CH_(3)(CH_(2))_(11)OSO_(3)^(−).Various analytical techniques,including high-speed photography imaging,contact angle measurements,Fourier transform infrared spectroscopy,zeta potential analysis,and X-ray photoelectron spectroscopy,confirmed that the anion CH_(3)(CH_(2))_(11)OSO_(3)^(−)adsorbs chemically onto aluminum sites on lepidolite's surface,while the cation NH_(4)+binds through electrostatic interactions and hydrogen bonding.The combined adsorption of these ions on lepidolite's surface enhanced its hydrophobicity.In contrast,ALS showed minimal adsorption on feldspar and quartz surfaces,which remained hydrophilic,enabling efficient selective flotation separation of lepidolite from both feldspar and quartz.展开更多
Anaerobic ammonium oxidation coupled to iron(III)reduction(Feammox)process has recently been recognized as an important pathway for removing ammonium in various natural habitats.However,our understanding for Feammox i...Anaerobic ammonium oxidation coupled to iron(III)reduction(Feammox)process has recently been recognized as an important pathway for removing ammonium in various natural habitats.However,our understanding for Feammox in river–estuary continuum is limited.In this study,stable isotope tracers and high-throughput amplicon sequencing were employed to determine Feammox rates and identify associated microbial communities in sediments along the Yangtze river–estuary continuum.Feammox rates averaged 0.0058±0.0069 mg N/(kg·d)and accounted for approximately 22.3%of the ammonium removed from the sediments.Sediment Fe(III),ammonium(NH_(4)^(+)),total organic carbon(TOC),and pH were identified as important factors influencing Feammox rates.Additionally,Spirochaeta,Caldilineaceae_uncultured,and Ignavibacterium were found potentially associated with Feammox,which had not been documented as Feammox-associated microbial taxa previously.This study demonstrates that Feammox plays a vital role in ammonium removal within the Yangtze river–estuary continuum,providing greater insight into nitrogen removal and cycling in aquatic ecosystems.展开更多
The purity of electronic-grade chemicals significantly impacts electronic components.Although crystallization has been used to purify cerium ammonium nitrate(CAN),the impurity removal mechanism underlying different cr...The purity of electronic-grade chemicals significantly impacts electronic components.Although crystallization has been used to purify cerium ammonium nitrate(CAN),the impurity removal mechanism underlying different crystallization parameters remains unclear.Traditional analytical methods of inductively coupled plasma mass spectrometry(ICP-MS)have problems in detecting trace Fe accurately,because of the high concentration of Ce and interference of polyatomic ions.Therefore,this study developed a new method integrating the standard addition and internal standard methods and explored the role of the kinetic energy discrimination mode.This new approach effectively overcomes Ce-related matrix interference and fills the gap in ultra-trace impurity detection.Furthermore,the study investigated the effects of cooling rate,seed mass loading and seed size on the removal of Fe impurity.The seed mass loading affects the average crystal size through regulating secondary nucleation and crystal growth.The removal of Fe in CAN is determined by surface adsorption and agglomeration.Under the condition of the cooling rate of 0.2 K·min^(-1),and addition of 0.5%(mass)600-680 μm seeds,the Fe content is the lowest,at only 0.24 mg·L^(-1),and the Fe removal rate reaches 92.28%.展开更多
Aqueous-phase reactions between carbonyls and reduced nitrogen compounds play a considerable role in the formation of secondary organic aerosols and brown carbon in the atmosphere.However,the reported reaction rate co...Aqueous-phase reactions between carbonyls and reduced nitrogen compounds play a considerable role in the formation of secondary organic aerosols and brown carbon in the atmosphere.However,the reported reaction rate constants for these reactions have largely been limited to bulk aqueous-phase simulations,which may not accurately represent the real state of atmospheric cloud droplets.We employed an integration of optical tweezers and Raman spectroscopy to manipulate and analyze simulated cloud droplets(size range8000-10,000 nm),comprising a mixture of glyoxal and ammonium sulfate.This approach enabled us to delve into the intricate realm of their reaction kinetics at individual droplet level mimicking cloud droplets.Raman spectroscopy provided high temporal resolution(20 s)measurements of the changes in the amount of nitrogen-containing organics(or NOCs as represented by the C-N bond)within the droplets.The results indicate that the reaction follows first-order kinetics throughout the monitoring over 80-400 min.The average reaction rate constant for the formation of NOCs within the single droplet was determined to be(6.77±0.98)×10^(-5)s^(-1),up to three orders of magnitude higher than those through the bulk aqueous-phase simulations,especially at lower p H levels.Additionally,the reaction rate constant in single droplet increases with increasing p H,consistent with the trend previously reported for the bulk aqueous-phase simulations.The results highlight the difference of the reaction rate constant between bulk aqueous-phase and droplets,which would improve our understanding on the formation and impacts of secondary organic aerosols and brown carbon in atmospheric aqueous phase.展开更多
Ammonium level in body fluids serves as one of the critical biomarkers for healthcare,especially those relative to liver diseases.The continuous and real-time monitoring in both invasive and noninvasive manners is hig...Ammonium level in body fluids serves as one of the critical biomarkers for healthcare,especially those relative to liver diseases.The continuous and real-time monitoring in both invasive and noninvasive manners is highly desired,while the ammonium concentrations vary largely in different body fluids.Besides,the sensing reliability based on ion-selective biosensors can be significantly interfered by potassium ions.To tackle these challenges,a flexible and biocompatible sensing patch for wireless ammonium level sensing was reported with an ultrawide linear range for universal body fluids including blood,tears,saliva,sweat and urine.The as-prepared biocompatible sensors deliver a reliable sensitivity of 58.7 mV decade-1 in the range of 1-100 mM and a desirable selectivity coefficient of 0.11 in the interference of potassium ions,attributed to the cross-calibration within the sensors array.The sensor’s biocompatibility was validated by the cell growth on the sensor surface(>80%),hemolysis rates(<5%),negligible cellular inflammatory responses and weight changes of the mice with implanted sensors.Such biocompatible sensors with ultrawide linear range and desirable selectivity open up new possibility of highly compatible biomarker analysis via different body fluids in versatile approaches.展开更多
The organic pollutants,such as quaternary ammonium compounds,in high salinity flowback water from shale gas extraction may pose a severe risk to public health.Conventional biological technologies have limited effectiv...The organic pollutants,such as quaternary ammonium compounds,in high salinity flowback water from shale gas extraction may pose a severe risk to public health.Conventional biological technologies have limited effectiveness in the treatment of high-salt wastewaters,whereas electrocatalytic oxidation has shown potential for treating organic pollutants in high-salt flowback water.This study developed a carbon nanotubes(CNTs)doped Ru/Ir oxide coated Ti electrode CNTs-(Ru_(x)Ir_(y)O_(2))/Ti,which exhibited enhanced electrocatalytic performance for the treatment of quaternary ammonium compound in high-salt wastewater compared to the control metal oxide coated Ti anode(Ru_(x)Ir_(y)O_(2))/Ti,with pseudofirst-order reaction rate constant improved from 7.36×10^(-3) to 1.12×10^(-2) min−1.Moreover,the CNTs-(Ru_(x)Ir_(y)O_(2))/Ti anode electrocatalytic oxidation system exhibited excellent cycling stability.Mechanism studies indicated that the CNTs-(Ru_(x)Ir_(y)O_(2))/Ti electrode enhanced singlet oxygen(^(1)O_(2))generation,which played a major role in pollutant degradation.Furthermore,the formation of high concentrations of HClO and H_(2)O_(2) further facilitated the generation of ^(1)O_(2).This study may provide an efficient and green technology for the treatment of organic pollutants in high-salt shale gas flowback water.展开更多
To explore high-performance cathode materials for aqueous ammonium ion batteries(AAIBs),vanadium-based Prussian blue analogue composites(VFe-PBAs)were prepared by hydrothermal coprecipitation method to enhance the rev...To explore high-performance cathode materials for aqueous ammonium ion batteries(AAIBs),vanadium-based Prussian blue analogue composites(VFe-PBAs)were prepared by hydrothermal coprecipitation method to enhance the reversible storage of NH_(4)^(+).Benefiting from the stable three-dimensional structure and spacious gap position,VFe-PBAs-2 cathode displays excellent electrochemical activity and rate performance,achieving a high specific capacity of 84.3 mA·h/g at a current density of 1000 mA/g.In addition,VFe-PBAs-2 cathode also shows impressive long-term cycle durability with 85.2% capacity retention after 3×10^(4) cycles at 5000 mA/g.The synthesized cathode materials combined with the high electrochemical activity of vanadium ions significantly promote the rapid transfer of NH_(4)^(+).Furthermore,NH_(4)^(+)embedding/extraction mechanism of VFe-PBAs-2 cathode was revealed by electrochemical kinetics tests and advanced ex-situ characterizations.The experimental results demonstrate that vanadium-modified VFe-PBAs-2 as a cathode material can remarkably improve the capacity,electrochemical activity and cycling stability of AAIBs to achieve high performance NH_(4)^(+)storage.展开更多
A biodegradable and green organic compound octadecyl dimethyl benzyl amm-onium chloride(ODBAC)was used as an efficient inhibitor for cold rolled steel(CRS)in phosphoric acid(H_(3)PO_(4)).The mechanism of adsorption an...A biodegradable and green organic compound octadecyl dimethyl benzyl amm-onium chloride(ODBAC)was used as an efficient inhibitor for cold rolled steel(CRS)in phosphoric acid(H_(3)PO_(4)).The mechanism of adsorption and film formation of ODBAC on CRS was studied through experimental and theoretical calculations.The weight loss method shows that the inhibition efficiency of ODBAC can reach 92.01%at a concentration of 10 mg·L^(-1).The adsorption of ODBAC on the CRS surface conforms to the Langmuir isotherm model,which is a mixed adsorption mainly based on physical adsorption.The X-ray photoelectron spectroscopy(XPS)and contact angle results confirmed the existence of the ODBAC film and steel surface's hydrophobicity has been significantly enhanced.Electrochemical test results reveal that the film's formation mainly inhibits the cathodic corrosion reaction and effectively increases the charge transfer resistance.Quantum chemical calculations have found that N18 in ODBAC and C24 and C25 on the benzene ring are the key active adsorption sites.Molecular dynamics simulation results indicate that ODBAC can sharply reduce the free fraction volume to 8%and inhibit the diffusion of corrosion particles,meaning that the formed ODBAC film makes it difficult for corrosion particles to penetrate,thus improving the corrosion resistance of CRS in H_(3)PO_(4).展开更多
Inverted perovskite solar cells(PSCs)have stood out in recent years for their great potential in offering low-temperature compatibility,long-term stability and tandem cell suitability.However,challenges persist,partic...Inverted perovskite solar cells(PSCs)have stood out in recent years for their great potential in offering low-temperature compatibility,long-term stability and tandem cell suitability.However,challenges persist,particularly concerning the use of nickel oxide nanoparticles(NiO_(x)NPs)as the hole transport material,where issues such as low conductivity,impurity-induced aggregation and interface redox reactions significantly hinder device performance.In response,this study presents a novel synthesis method for NiO_(x)NPs,leveraging the introduction of ammonium salt dopants(NH_(4)Cl and NH_(4)SCN),and the solar cell utilizing the doped NiO_(x)substrate exhibits much enhanced device performance.Furthermore,doped solar cells reach 23.27%power conversion efficiency(PCE)when a self-assembled monolayer(SAM)is further employed.This study provides critical insights into the synthesis and growth pathways of NiO_(x)NPs,propelling the development of efficient hole transport materials for high-performance PSCs.展开更多
Aqueous rechargeable ammonium-ion batteries(AIBs)have drew considerable attention because of their capacity for high rates,low cost,and high safety.However,developing desired electrodes requiring stable structure in t...Aqueous rechargeable ammonium-ion batteries(AIBs)have drew considerable attention because of their capacity for high rates,low cost,and high safety.However,developing desired electrodes requiring stable structure in the aqueous fast ammoniation/de-ammoniation becomes urgent.Herein,an ammonium ion full battery using Cu_(3)[Fe(CN)_(6)]_(2)(CuHCF)acting to be a cathode and barium vanadate(BVO)acting to be an anode is described.Its excellent electrochemical behavior of Prussian blue analogs and the perfectly matched lattice structure of NH_(4)^(+)is expected.And the open structure of vanadium compounds satisfies the fast ammoniation/de-ammoniation of NH4+is also achieved.As a result of these synergistic effects,the BVO//CuHCF full cell retains 80.5 percent of its capacity following 1000 cycling.These achievements provide new ideas for developing low-cost and long-life AIBs.展开更多
Reasonable nitrogen(N) application is a promising strategy for reducing crop cadmium(Cd) toxicity. However, the specific form of N and the required amount that affect Cd tolerance and accumulation in rice remain uncle...Reasonable nitrogen(N) application is a promising strategy for reducing crop cadmium(Cd) toxicity. However, the specific form of N and the required amount that affect Cd tolerance and accumulation in rice remain unclear. This study explored the influence of different N-fertilizer forms(NH_(4)NO_(3), NH_4Cl, and KNO_(3)) and dosages on Cd tolerance and uptake in Cd-stressed N-sensitive and N-insensitive indica rice accessions. The results indicated that the Cd tolerance of N-sensitive indica accessions is more robust than that of N-insensitive ones. Furthermore, the shoot Cd content and Cd translocation rate in both N-sensitive and N-insensitive indica accessions decreased with an appropriate supply of NH_(4)NO_(3) and NH_4Cl, whereas they were comparable or slightly increased with increased KNO_(3). Unfortunately, we did not find significant and regular differences in Cd accumulation or translocation between N-sensitive and N-insensitive rice accessions. Consistent with the reduction of shoot Cd content, the addition of NH_(4)NO_(3) and NH_4Cl also inhibited the instantaneous root Cd^(2+) uptake. The expression changes of Cd transport-related genes under different N forms and dosages suggested that the decreased shoot Cd content, caused by the increased supply of NH_(4)NO_(3) and NH_4Cl, is likely achieved by reducing the transcription of OsNRAMP1 and OsIRT1. In summary, our findings reveal that an appropriate supply of NH_(4)NO_(3) and NH_4Cl could reduce Cd uptake and transport in rice seedlings, suggesting that rational N management could reduce the Cd risk in rice production.展开更多
Defect engineering is an effective strategy for modifying the energy storage materials to improve their electrochemical performance.However,the impact of oxygen defect and its content on the electrochemical performanc...Defect engineering is an effective strategy for modifying the energy storage materials to improve their electrochemical performance.However,the impact of oxygen defect and its content on the electrochemical performances in the burgeoning aqueous NH_(4)^(+)storage field remains explored.Therefore,for the first time in this work,an oxygen-defective ammonium vanadate[(NH_(4))_(2)V_(10)O_(25)·8H_(2)O,denoted as Od-NHVO]with a novel 3D porous flower-like architecture was achieved via the reduction of thiourea in a mild reaction condition,which is a facile method that can realize the intention to regulate the oxygen defect content,with the capability of mass-production.The as-prepared Od_M-NHVO with moderate oxygen defect content can deliver a stable specific capacitance output(505 F g^(-1),252 mAh g^(-1)at 0.5 A g^(-1)with~80% capacitance retention after 10,000 cycles),which benefits from extra active sites,unimpeded NH_(4)^(+)-migration path and relatively high structure integrity.In contrast,low oxygen defect content will lead to the torpid electrochemical reaction kinetics while too high content of it will reduce the chargestorage capability and induce structural disintegration.The superior NH_(4)^(+)-storage behavior is achieved with the reversible intercalation/deintercalation process of NH_(4)^(+)accompanied by forming/breaking of hydrogen bond.As expected,the assembled flexible OdM-NHVO//PTCDI quasi-solid-state hybrid supercapacitor(FQSS HSC)also exhibits high areal capacitance,energy density and reliable flexibility.This work provides a new avenue for developing materials with oxygen-deficient structure for application in various aqueous non-metal cation storage systems.展开更多
In this work,a variety of Cu_(x)Ni_(2-x)Fe(CN)_(6)(x=0,0.4,0.8,1.2,1.6,2)cathodes for ammonium ion batteries are prepared and their electrochemical performances are investigated.During the introduction of copper in ni...In this work,a variety of Cu_(x)Ni_(2-x)Fe(CN)_(6)(x=0,0.4,0.8,1.2,1.6,2)cathodes for ammonium ion batteries are prepared and their electrochemical performances are investigated.During the introduction of copper in nickel hexacyanoferrate,the electrochemical performance varies without changing the structure of nickel hexacyanoferrate.The increase of Cu content in nickel hexacyanoferrate leads to the enhancement of reaction potential and capacity.Electrochemical results suggest that the substitution of Cu for Ni has a positive effect on improving the cycling stability and rate capacity of nickel hexacyanoferrate when x in Cu_(x)Ni_(2-x)Fe(CN)_(6)is less than 0.4.Therefore,Cu_(0.4)Ni_(1.6)Fe(CN)_(6)exhibits the best cycling per-formance(capacity retention of 97.54%at 0.3 C)and the highest rate capacity(41.4 mAh g^(-1)at 10 C)in Cu_(x)Ni_(2-x)Fe(CN)_(6).Additionally,the X-ray diffraction(XRD)and X-ray photoelectron spectroscopy(XPS)tests also reveal that the structural evolution of Cu_(0.4)Ni_(1.6)Fe(CN)_(6)is highly reversible upon NH_(4)^(+)storage.Therefore,this work proposes a candidate material for ammoniumion batteries and offers a novel avenue for adjusting the operating potential of the material.展开更多
Electrochemical corrosion of AZ31 magnesium alloy in the NH_(4)^(+)-SO_(4)2−-Cl−environment is studied.Effect of NH_(4)^(+)overshadows that of Cl−as the(NH_(4))_(2)SO_(4) concentration is 0.005 M or higher,yielding an...Electrochemical corrosion of AZ31 magnesium alloy in the NH_(4)^(+)-SO_(4)2−-Cl−environment is studied.Effect of NH_(4)^(+)overshadows that of Cl−as the(NH_(4))_(2)SO_(4) concentration is 0.005 M or higher,yielding an evolution from localized corrosion to uniform corrosion.Acceleration effect of NH_(4)^(+)can be attributed to that(i)NH_(4)^(+)dissolves the inner MgO and hinders the precipitation of Mg(OH)_(2) and(ii)the buffering ability of NH_(4)^(+)provides H+,enhances the hydrogen evolution,and expedites the corrosion process.The latter is demonstrated as the dominant factor with the results in unbuffered and buffered environments.The severe corrosion and hydrogen process in NH_(4)^(+)-containing solution results in a high Hads coverage and yields an inductive loop within the low frequency.Meanwhile,SO_(4)^(2−)is helpful in generating cracked but partially protective corrosion products,while Cl−could broaden the corrosion area beneath the corrosion product.展开更多
Vanadium-based cathode materials are attractive for aqueous zinc-ion batteries(AZIBs)owing to the high capacity from their open frameworks and multiple valences.However,the cycle stability and rate capability are stil...Vanadium-based cathode materials are attractive for aqueous zinc-ion batteries(AZIBs)owing to the high capacity from their open frameworks and multiple valences.However,the cycle stability and rate capability are still restricted by the low electrical conductivity and trapped diffusion kinetics.Here,we propose an organic-inorganic co-intercalation strategy to regulate the structure of ammonium vanadate(NH_(4)V_(4)O_(10),NVO).The introduction of Al^(3+)and polyaniline(PANI)induces the optimized layered structure and generation of urchin-like hierarchical construction(AP-NVO),based on heterogeneous nucleation and dissolution-recrystallization growth mechanism.Owing to these favorable features,the AP-NVO electrode delivers a desirable discharge capacity of 386 mA h g^(-1) at 1.0 A g^(-1),high-rate capability of 263 mA h g^(-1 )at 5.0 A g^(-1) and excellent cycling stability with 80.4%capacity retention over 2000 cycles at 5.0 A g^(-1).Such satisfactory electrochemical performance is believed to result from the enhanced reaction kinetics provided by the stable layered structure and a high intercalation pseudo-capacitance reaction.These results could provide enlightening insights into the design of layered vanadium oxide cathodematerials.展开更多
基金financially supported by the National Natural Science Foundation of China(Nos.52402271,22005167 and52302273)the Youth Innovation Team Project for Talent Introduction and Cultivation in Universities of Shandong Province(No.2024KJH129)+2 种基金the Taishan Scholar Project of Shandong Provinceof China(Nos.tsqn202211160,tsqn202312199)Shandong Provincial Natural Science Foundation of China(Nos.ZR2022QE003 and ZR2023QE176)China Postdoctoral Science Foundation(No.2023M741810)。
文摘Layered ammonium vanadate has become a promising cathode material for aqueous zinc ion batteries(ZIBs)due to its small mass and large ionic radius of ammonium ions as well as the consequent large layer spacing and high specific capacity.However,the irreversible de-ammoniation caused by N·H···O bonds damaged would impair cycle life of ZIBs and the strong electrostatic interaction between Zn^(2+)and V-O frame could slower the mobility of Zn^(2+).Furthermore,the thermal instability of ammonium vanadate also limits the use of common carbon coating modification method to solve the problem.Herein,V_(2)CT_(X)MXene was innovatively selected as a bifunctional source to in-situ derivatized(NH_(4))_(2)V_(8)O_(20)·x H_(2)O with amorphous carbon-coated(NHVO@C)via one-step hydrothermal method in relatively moderate temperature.The amorphous carbon shell derived from the V_(2)CT_(X)MXene as a conductive framework to effectively improve the diffusion kinetics of Zn^(2+)and the robust carbon skeleton could alleviate the ammonium dissolution during long-term cycling.As a result,zinc ion batteries using NHVO@C as cathode exhibit superior electrochemical performance.Moreover,the assembled foldable or high loading(10.2 mg/cm^(2))soft-packed ZIBs further demonstrates its practical application.This study provided new insights into the development of the carbon cladding process for thermally unstable materials in moderate temperatures.
文摘The present work aims to stabilize the room temperature allotropic transition of ammonium nitrate(AN)particles utilizing a microencapsulation technique,which involves solvent/non-solvent in which nitrocellulose(NC)has been employed as a coating agent.The SEM micrographs revealed distinct features of both pure AN and NC,contrasting with the irregular granular surface topography of the coated AN particles,demonstrating the adherence of NC on the AN surface.Structural analysis via infrared spectroscopy(IR)demonstrated a successful association of AN and NC,with slight shifts observed in IR bands indicating interfacial interactions.Powder X-ray Diffraction(PXRD)analysis further elucidated the structural changes induced by the coating process,revealing that the NC coating altered the crystallization pattern of its pure form.Thermal analysis demonstrates distinct profiles for pure and coated AN,for which the coated sample exhibits a temperature increase and an enthalpy decrease of the room temperature allotropic transition by 6℃,and 36%,respectively.Furthermore,the presence of NC coating alters the intermolecular forces within the composite system,leading to a reduction in melting enthalpy of coated AN by~39%compared to pure AN.The thermal decomposition analysis shows a two-step thermolysis process for coated AN,with a significant increase in the released heat by about 78%accompanied by an increase in the activation barrier of NC and AN thermolysis,demonstrating a stabilized reactivity of the AN-NC particles.These findings highlight the synergistic effect of NC coating on AN particles,which contributed to a structural and reactive stabilization of both AN and NC,proving the potential application of NC-coated AN as a strategically advantageous oxidizer in composite solid propellant formulations.
文摘A series of multi-hydroxyl bis-(quaternary ammonium)ionic liquids(Ils1‒7)was prepared as bifunctional catalysts for the chemical fixation of CO_(2).All these ionic liquid compounds were efficient for the catalytic synthesis of cyclic carbonates and oxazolidinones via the cycloaddition reactions between CO_(2) and epoxides or aziridines with excellent yield and high selectivity in the absence of co-catalyst,metal and solvent.Due to the synergistic effects of hydroxyl groups and halogen anion,the cycloaddition reactions proceeded smoothly either at atmospheric pressure or room temperature.The selectivity for substituted oxazolidinones at 5-and 4-positions can be tuned via changing the reaction conditions.Finally,possible mechanisms including the activation of both CO_(2) and epoxide or aziridines were proposed based on the literatures and experimental results.
基金supported by the Phytopathology Unit of the Department of Plant Protection(ENA-Meknes,Morocco).
文摘This study investigates the compatibility and efficacy of combining ammonium molybdate(AM)with antagonistic bacteria Bacillus amyloliquefaciens B10W10 and Pseudomonas sp.B11W11 for brown rot control(Monilinia laxa).In vitro experiments reveal variable mycelial growth inhibition rates compared to untreated controls,with B11W11+0.5%AM and B10W10+2%AM displaying the highest inhibition rates after 5 days.After 10 days,the 2%AM+B10W10 combination exhibits the highest inhibition rate.Microscopic observations show structural alterations in mycelium within inhibition zones,marked by vacuolization.The antagonistic bacteria,alone or with different ammonium molybdate concentrations,significantly impact M.laxa spore germination,with the B10W10 cell filtrate+2%ammonium molybdate combination achieving the most substantial inhibition.Conversely,the 0.5%ammonium molybdate treatment has the lowest inhibition rate while the combination of AM and bacteria is giving better results compared to the use of bacteria alone.Fruits treated with various antagonistic bacteria and ammonium molybdate combinations demonstrate a significant reduction in disease severity.The 0.5%AM+B10W10 combination exhibits the lowest severity.FT-IR spectra analysis identifies shifts in fungal biomass functional groups,with reduced lignin-related bands and increased phenols,lipids,polysaccharides,and carbohydrates.This highlights the structural modifications caused by the biological treatments.The study also evaluates the effects on fruit quality parameters.The 2%ammonium molybdate treatment yields the lowest weight loss.TSS levels are affected by salt concentration,while acid content remains consistent across treatments.All treatments influence fruit firmness compared to controls.These findings emphasize the potential of combining ammonium molybdate and antagonistic bacteria for effective brown rot control,highlighting their compatibility and effects on disease severity,fungal biomass,spore germination,and fruit quality.
基金Funded by the National Natural Science Foundation of China(No.51873167)the Self-determined and Innovative Research Funds of WUT(No.2024-CL-B1-02)。
文摘Modified activated carbons(AS)were fabricated through the oxidation effect of ammonium persulfate and applied to the dynamic adsorption of different acrylate gas.The pore structures,surface chemical properties and surface morphology of AS were respectively characterized by N2 adsorption,Boehm titration,X-ray Photoelectron Spectroscopy(XPS)and scanning electron microscopy(SEM)techniques.After modification,the specific surface area increased from 954 to 1154 m^(2)·g^(-1).The contents of oxygen-containing functional groups on the AS surface increase obviously and have a great effect on the adsorption behavior of acrylate gases.According to the results of dynamic adsorption,the adsorption capacities of acrylates are as the following order:methyl acrylate(461.9 mg·g^(-1))>methyl methacrylate(436.9 mg·g^(-1))>butyl acrylate(381.8 mg·g^(-1)),which is attributed to the size adaptability of AS pores and acrylates.The adsorption behavior of AS for acrylate gases conforms to the Bangham model and the Temkin model.
基金supported by the Project of the National Natural Science Foundation of China(No.52274263)the Key Research and Development Program of Jiangxi Province(No.20214BBG74001)the Major Science and Technology Innovation Project of Yichun(No.2023ZDKJGG03).
文摘Lepidolite,feldspar,and quartz are silicate minerals with similar chemical properties,complicating their flotation separation.Current collector systems require strong acidic conditions for effective separation but still face challenges related to low separation efficiency and recovery rates.This study proposed a novel collector,ammonium dodecylsulfate(ALS),to selectively extract lepidolite from feldspar and quartz using highly selective flotation methods.Microflotation experiments showed that ALS significantly outperforms other collectors in collecting lepidolite compared to feldspar and quartz.At pH 7,lepidolite recovery reached 95%,while flotation recoveries for both feldspar and quartz were below 10%.Mixed pure mineral flotation tests revealed that at pH 7 and ALS concentration of 2.5×10^(-4) mol·L^(−1),the Li_(2)O content in the concentrate was 4.21%,with a recovery rate of 95.01%.Separation efficiency and Gaudin selectivity index values were recorded.Solution chemical analyses showed that at pH 7,ALS completely ionizes into NH_(4)^(+)and CH_(3)(CH_(2))_(11)OSO_(3)^(−).Various analytical techniques,including high-speed photography imaging,contact angle measurements,Fourier transform infrared spectroscopy,zeta potential analysis,and X-ray photoelectron spectroscopy,confirmed that the anion CH_(3)(CH_(2))_(11)OSO_(3)^(−)adsorbs chemically onto aluminum sites on lepidolite's surface,while the cation NH_(4)+binds through electrostatic interactions and hydrogen bonding.The combined adsorption of these ions on lepidolite's surface enhanced its hydrophobicity.In contrast,ALS showed minimal adsorption on feldspar and quartz surfaces,which remained hydrophilic,enabling efficient selective flotation separation of lepidolite from both feldspar and quartz.
基金supported by the National Natural Science Foundation of China(Nos.U2040201,32201334,92251304,and 42271126),the Project of Southern Marine Science and Engineering Guangdong Laboratory(Guangzhou,No.GML20220017),the Outstanding Postdoctoral Project in Jiangsu Province(No.2022ZB455),the Chinese Postdoctoral Science Foundation(No.2022M721661)and the Project of State Key Laboratory of Lake Science and Environment(No.2022SKL019).
文摘Anaerobic ammonium oxidation coupled to iron(III)reduction(Feammox)process has recently been recognized as an important pathway for removing ammonium in various natural habitats.However,our understanding for Feammox in river–estuary continuum is limited.In this study,stable isotope tracers and high-throughput amplicon sequencing were employed to determine Feammox rates and identify associated microbial communities in sediments along the Yangtze river–estuary continuum.Feammox rates averaged 0.0058±0.0069 mg N/(kg·d)and accounted for approximately 22.3%of the ammonium removed from the sediments.Sediment Fe(III),ammonium(NH_(4)^(+)),total organic carbon(TOC),and pH were identified as important factors influencing Feammox rates.Additionally,Spirochaeta,Caldilineaceae_uncultured,and Ignavibacterium were found potentially associated with Feammox,which had not been documented as Feammox-associated microbial taxa previously.This study demonstrates that Feammox plays a vital role in ammonium removal within the Yangtze river–estuary continuum,providing greater insight into nitrogen removal and cycling in aquatic ecosystems.
基金the National Natural Science Foundation of China(22308358,22208346,22421003)IPE Project for Frontier Basic Research(QYJC-2023-05)+1 种基金National Key Research and Development Program(2022YFC3902701)CAS Project for Young Scientists in Basic Research(YSBR-038).
文摘The purity of electronic-grade chemicals significantly impacts electronic components.Although crystallization has been used to purify cerium ammonium nitrate(CAN),the impurity removal mechanism underlying different crystallization parameters remains unclear.Traditional analytical methods of inductively coupled plasma mass spectrometry(ICP-MS)have problems in detecting trace Fe accurately,because of the high concentration of Ce and interference of polyatomic ions.Therefore,this study developed a new method integrating the standard addition and internal standard methods and explored the role of the kinetic energy discrimination mode.This new approach effectively overcomes Ce-related matrix interference and fills the gap in ultra-trace impurity detection.Furthermore,the study investigated the effects of cooling rate,seed mass loading and seed size on the removal of Fe impurity.The seed mass loading affects the average crystal size through regulating secondary nucleation and crystal growth.The removal of Fe in CAN is determined by surface adsorption and agglomeration.Under the condition of the cooling rate of 0.2 K·min^(-1),and addition of 0.5%(mass)600-680 μm seeds,the Fe content is the lowest,at only 0.24 mg·L^(-1),and the Fe removal rate reaches 92.28%.
基金supported by the National Natural Science Foundation of China(Nos.42222705,42377097,and 22361162668)the National Key Research and Development Program of China(No.2022YFC3701101)+1 种基金the Youth Innovation Promotion Association CAS(No.2021354)Guangdong Foundation for Program of Science and Technology Research(No.2023B1212060049)。
文摘Aqueous-phase reactions between carbonyls and reduced nitrogen compounds play a considerable role in the formation of secondary organic aerosols and brown carbon in the atmosphere.However,the reported reaction rate constants for these reactions have largely been limited to bulk aqueous-phase simulations,which may not accurately represent the real state of atmospheric cloud droplets.We employed an integration of optical tweezers and Raman spectroscopy to manipulate and analyze simulated cloud droplets(size range8000-10,000 nm),comprising a mixture of glyoxal and ammonium sulfate.This approach enabled us to delve into the intricate realm of their reaction kinetics at individual droplet level mimicking cloud droplets.Raman spectroscopy provided high temporal resolution(20 s)measurements of the changes in the amount of nitrogen-containing organics(or NOCs as represented by the C-N bond)within the droplets.The results indicate that the reaction follows first-order kinetics throughout the monitoring over 80-400 min.The average reaction rate constant for the formation of NOCs within the single droplet was determined to be(6.77±0.98)×10^(-5)s^(-1),up to three orders of magnitude higher than those through the bulk aqueous-phase simulations,especially at lower p H levels.Additionally,the reaction rate constant in single droplet increases with increasing p H,consistent with the trend previously reported for the bulk aqueous-phase simulations.The results highlight the difference of the reaction rate constant between bulk aqueous-phase and droplets,which would improve our understanding on the formation and impacts of secondary organic aerosols and brown carbon in atmospheric aqueous phase.
基金supported by the National Natural Science Foundation of China(62201243)Natural Science Foundation of Guangdong Province(2022A1515011928)+2 种基金Shenzhen Science and Technology Program(Grant No.RCYX20231211090432060,JSGGZD20220822095600001)Postgraduate Scientific Research Innovation Project of Hunan Province(CX20231306)the technical support from the Southern University of Science and Technology Core Research Facilities(SUSTech CRF)。
文摘Ammonium level in body fluids serves as one of the critical biomarkers for healthcare,especially those relative to liver diseases.The continuous and real-time monitoring in both invasive and noninvasive manners is highly desired,while the ammonium concentrations vary largely in different body fluids.Besides,the sensing reliability based on ion-selective biosensors can be significantly interfered by potassium ions.To tackle these challenges,a flexible and biocompatible sensing patch for wireless ammonium level sensing was reported with an ultrawide linear range for universal body fluids including blood,tears,saliva,sweat and urine.The as-prepared biocompatible sensors deliver a reliable sensitivity of 58.7 mV decade-1 in the range of 1-100 mM and a desirable selectivity coefficient of 0.11 in the interference of potassium ions,attributed to the cross-calibration within the sensors array.The sensor’s biocompatibility was validated by the cell growth on the sensor surface(>80%),hemolysis rates(<5%),negligible cellular inflammatory responses and weight changes of the mice with implanted sensors.Such biocompatible sensors with ultrawide linear range and desirable selectivity open up new possibility of highly compatible biomarker analysis via different body fluids in versatile approaches.
基金supported by the National Natural Science Foundation of China(Nos.52200186 and 52070025)Chongqing Natural Science Foundation(No.CSTB2024NSCQ-MSX0407)+1 种基金the National Key Research and Development Program of China(No.2019YFC1805502)Chongqing Municipal Human Resources and Social Security Bureau(No.2309013519935095).
文摘The organic pollutants,such as quaternary ammonium compounds,in high salinity flowback water from shale gas extraction may pose a severe risk to public health.Conventional biological technologies have limited effectiveness in the treatment of high-salt wastewaters,whereas electrocatalytic oxidation has shown potential for treating organic pollutants in high-salt flowback water.This study developed a carbon nanotubes(CNTs)doped Ru/Ir oxide coated Ti electrode CNTs-(Ru_(x)Ir_(y)O_(2))/Ti,which exhibited enhanced electrocatalytic performance for the treatment of quaternary ammonium compound in high-salt wastewater compared to the control metal oxide coated Ti anode(Ru_(x)Ir_(y)O_(2))/Ti,with pseudofirst-order reaction rate constant improved from 7.36×10^(-3) to 1.12×10^(-2) min−1.Moreover,the CNTs-(Ru_(x)Ir_(y)O_(2))/Ti anode electrocatalytic oxidation system exhibited excellent cycling stability.Mechanism studies indicated that the CNTs-(Ru_(x)Ir_(y)O_(2))/Ti electrode enhanced singlet oxygen(^(1)O_(2))generation,which played a major role in pollutant degradation.Furthermore,the formation of high concentrations of HClO and H_(2)O_(2) further facilitated the generation of ^(1)O_(2).This study may provide an efficient and green technology for the treatment of organic pollutants in high-salt shale gas flowback water.
基金supported by the National Natural Science Foundation of China(No.52374301)the Hebei Provincial Natural Science Foundation,China(No.E2024501010)+2 种基金the Shijiazhuang Basic Research Project,China(No.241790667A)the Fundamental Research Funds for the Central Universities,China(No.N2423054)the Performance Subsidy Fund for Key Laboratory of Dielectric and Electrolyte Functional Material of Hebei Province,China(No.22567627H).
文摘To explore high-performance cathode materials for aqueous ammonium ion batteries(AAIBs),vanadium-based Prussian blue analogue composites(VFe-PBAs)were prepared by hydrothermal coprecipitation method to enhance the reversible storage of NH_(4)^(+).Benefiting from the stable three-dimensional structure and spacious gap position,VFe-PBAs-2 cathode displays excellent electrochemical activity and rate performance,achieving a high specific capacity of 84.3 mA·h/g at a current density of 1000 mA/g.In addition,VFe-PBAs-2 cathode also shows impressive long-term cycle durability with 85.2% capacity retention after 3×10^(4) cycles at 5000 mA/g.The synthesized cathode materials combined with the high electrochemical activity of vanadium ions significantly promote the rapid transfer of NH_(4)^(+).Furthermore,NH_(4)^(+)embedding/extraction mechanism of VFe-PBAs-2 cathode was revealed by electrochemical kinetics tests and advanced ex-situ characterizations.The experimental results demonstrate that vanadium-modified VFe-PBAs-2 as a cathode material can remarkably improve the capacity,electrochemical activity and cycling stability of AAIBs to achieve high performance NH_(4)^(+)storage.
基金support from National Natural Science Foundation of China(52161016)Joint Key Project of Agricultural Fundamental Research in Yunnan Province(202101BD070001-017)+2 种基金Yunnan Provincial Academician Workstation(202305AF150009)Special Project of“Top Young Talents”of Yunnan Ten Thousand Talents Plan(51900109)Special Project of“Leading Talents of Industrial Technology”of Yunnan Ten Thousand Talents Plan(80201408)are acknowledged.
文摘A biodegradable and green organic compound octadecyl dimethyl benzyl amm-onium chloride(ODBAC)was used as an efficient inhibitor for cold rolled steel(CRS)in phosphoric acid(H_(3)PO_(4)).The mechanism of adsorption and film formation of ODBAC on CRS was studied through experimental and theoretical calculations.The weight loss method shows that the inhibition efficiency of ODBAC can reach 92.01%at a concentration of 10 mg·L^(-1).The adsorption of ODBAC on the CRS surface conforms to the Langmuir isotherm model,which is a mixed adsorption mainly based on physical adsorption.The X-ray photoelectron spectroscopy(XPS)and contact angle results confirmed the existence of the ODBAC film and steel surface's hydrophobicity has been significantly enhanced.Electrochemical test results reveal that the film's formation mainly inhibits the cathodic corrosion reaction and effectively increases the charge transfer resistance.Quantum chemical calculations have found that N18 in ODBAC and C24 and C25 on the benzene ring are the key active adsorption sites.Molecular dynamics simulation results indicate that ODBAC can sharply reduce the free fraction volume to 8%and inhibit the diffusion of corrosion particles,meaning that the formed ODBAC film makes it difficult for corrosion particles to penetrate,thus improving the corrosion resistance of CRS in H_(3)PO_(4).
基金supported by the Open Research Fund of Songshan Lake Materials Laboratory(No.2021SLABFK09)the National Natural Science Foundation of China(No.22109093)+1 种基金the Program for Professor of Special Appointment(Eastern Scholar)at Shanghai Institutions of Higher Learning and the Shanghai Rising-Star Program(No.19QA1403800)the Project of Innovative Development Agency of Republic of Uzbekistan(No.FZ-20200929177)and Shanghai Technical Service Computing Center of Science and Engineering,Shanghai University.
文摘Inverted perovskite solar cells(PSCs)have stood out in recent years for their great potential in offering low-temperature compatibility,long-term stability and tandem cell suitability.However,challenges persist,particularly concerning the use of nickel oxide nanoparticles(NiO_(x)NPs)as the hole transport material,where issues such as low conductivity,impurity-induced aggregation and interface redox reactions significantly hinder device performance.In response,this study presents a novel synthesis method for NiO_(x)NPs,leveraging the introduction of ammonium salt dopants(NH_(4)Cl and NH_(4)SCN),and the solar cell utilizing the doped NiO_(x)substrate exhibits much enhanced device performance.Furthermore,doped solar cells reach 23.27%power conversion efficiency(PCE)when a self-assembled monolayer(SAM)is further employed.This study provides critical insights into the synthesis and growth pathways of NiO_(x)NPs,propelling the development of efficient hole transport materials for high-performance PSCs.
基金Joint Funds of the National Natural Science Foundation of China(No.U22A20140)the Independent Cultivation Program of Innovation Team of Ji'nan City(No.2019GXRC011)the Natural Science Foundation of Shandong Province,China(No.ZR2021MA073)。
文摘Aqueous rechargeable ammonium-ion batteries(AIBs)have drew considerable attention because of their capacity for high rates,low cost,and high safety.However,developing desired electrodes requiring stable structure in the aqueous fast ammoniation/de-ammoniation becomes urgent.Herein,an ammonium ion full battery using Cu_(3)[Fe(CN)_(6)]_(2)(CuHCF)acting to be a cathode and barium vanadate(BVO)acting to be an anode is described.Its excellent electrochemical behavior of Prussian blue analogs and the perfectly matched lattice structure of NH_(4)^(+)is expected.And the open structure of vanadium compounds satisfies the fast ammoniation/de-ammoniation of NH4+is also achieved.As a result of these synergistic effects,the BVO//CuHCF full cell retains 80.5 percent of its capacity following 1000 cycling.These achievements provide new ideas for developing low-cost and long-life AIBs.
基金supported by the National Natural Science Foundation of China (Grant No.31971872)the Open Research Fund of State Key Laboratory of Hybrid Rice, China (Grant No.2022KF02)+3 种基金the National Natural Science Foundation of China (Grant Nos.32101755 and 32188102)the Zhejiang Provincial Natural Science Foundation, China (Grant No.LY22C130005)the Key Research and Development Program of Zhejiang Province, China (Grant No.2021C02056)the ‘Pioneer’ and ‘Leading Goose’ R&D Program of Zhejiang, China (Grant No.2023C02014)。
文摘Reasonable nitrogen(N) application is a promising strategy for reducing crop cadmium(Cd) toxicity. However, the specific form of N and the required amount that affect Cd tolerance and accumulation in rice remain unclear. This study explored the influence of different N-fertilizer forms(NH_(4)NO_(3), NH_4Cl, and KNO_(3)) and dosages on Cd tolerance and uptake in Cd-stressed N-sensitive and N-insensitive indica rice accessions. The results indicated that the Cd tolerance of N-sensitive indica accessions is more robust than that of N-insensitive ones. Furthermore, the shoot Cd content and Cd translocation rate in both N-sensitive and N-insensitive indica accessions decreased with an appropriate supply of NH_(4)NO_(3) and NH_4Cl, whereas they were comparable or slightly increased with increased KNO_(3). Unfortunately, we did not find significant and regular differences in Cd accumulation or translocation between N-sensitive and N-insensitive rice accessions. Consistent with the reduction of shoot Cd content, the addition of NH_(4)NO_(3) and NH_4Cl also inhibited the instantaneous root Cd^(2+) uptake. The expression changes of Cd transport-related genes under different N forms and dosages suggested that the decreased shoot Cd content, caused by the increased supply of NH_(4)NO_(3) and NH_4Cl, is likely achieved by reducing the transcription of OsNRAMP1 and OsIRT1. In summary, our findings reveal that an appropriate supply of NH_(4)NO_(3) and NH_4Cl could reduce Cd uptake and transport in rice seedlings, suggesting that rational N management could reduce the Cd risk in rice production.
基金partially supported by the Large Instrument and Equipment Open Foundation of Dalian University of Technology and Fundamental Research Funds for the Central Universities(DUT21LK34)。
文摘Defect engineering is an effective strategy for modifying the energy storage materials to improve their electrochemical performance.However,the impact of oxygen defect and its content on the electrochemical performances in the burgeoning aqueous NH_(4)^(+)storage field remains explored.Therefore,for the first time in this work,an oxygen-defective ammonium vanadate[(NH_(4))_(2)V_(10)O_(25)·8H_(2)O,denoted as Od-NHVO]with a novel 3D porous flower-like architecture was achieved via the reduction of thiourea in a mild reaction condition,which is a facile method that can realize the intention to regulate the oxygen defect content,with the capability of mass-production.The as-prepared Od_M-NHVO with moderate oxygen defect content can deliver a stable specific capacitance output(505 F g^(-1),252 mAh g^(-1)at 0.5 A g^(-1)with~80% capacitance retention after 10,000 cycles),which benefits from extra active sites,unimpeded NH_(4)^(+)-migration path and relatively high structure integrity.In contrast,low oxygen defect content will lead to the torpid electrochemical reaction kinetics while too high content of it will reduce the chargestorage capability and induce structural disintegration.The superior NH_(4)^(+)-storage behavior is achieved with the reversible intercalation/deintercalation process of NH_(4)^(+)accompanied by forming/breaking of hydrogen bond.As expected,the assembled flexible OdM-NHVO//PTCDI quasi-solid-state hybrid supercapacitor(FQSS HSC)also exhibits high areal capacitance,energy density and reliable flexibility.This work provides a new avenue for developing materials with oxygen-deficient structure for application in various aqueous non-metal cation storage systems.
基金supported by the Ningbo Natural Science Founda-tion(No.2022J064)the NSAF Joint Fund(No.U1830106)the National Natural Science Foundation of China(No.22209082).
文摘In this work,a variety of Cu_(x)Ni_(2-x)Fe(CN)_(6)(x=0,0.4,0.8,1.2,1.6,2)cathodes for ammonium ion batteries are prepared and their electrochemical performances are investigated.During the introduction of copper in nickel hexacyanoferrate,the electrochemical performance varies without changing the structure of nickel hexacyanoferrate.The increase of Cu content in nickel hexacyanoferrate leads to the enhancement of reaction potential and capacity.Electrochemical results suggest that the substitution of Cu for Ni has a positive effect on improving the cycling stability and rate capacity of nickel hexacyanoferrate when x in Cu_(x)Ni_(2-x)Fe(CN)_(6)is less than 0.4.Therefore,Cu_(0.4)Ni_(1.6)Fe(CN)_(6)exhibits the best cycling per-formance(capacity retention of 97.54%at 0.3 C)and the highest rate capacity(41.4 mAh g^(-1)at 10 C)in Cu_(x)Ni_(2-x)Fe(CN)_(6).Additionally,the X-ray diffraction(XRD)and X-ray photoelectron spectroscopy(XPS)tests also reveal that the structural evolution of Cu_(0.4)Ni_(1.6)Fe(CN)_(6)is highly reversible upon NH_(4)^(+)storage.Therefore,this work proposes a candidate material for ammoniumion batteries and offers a novel avenue for adjusting the operating potential of the material.
基金support of National Natural Science Foundation of China(No.U2106216)the National Science and Technology Resources Investigation Program of China(No.2019FY101400)the Youth Innovation Plan of Shandong Province(2019KJD001).
文摘Electrochemical corrosion of AZ31 magnesium alloy in the NH_(4)^(+)-SO_(4)2−-Cl−environment is studied.Effect of NH_(4)^(+)overshadows that of Cl−as the(NH_(4))_(2)SO_(4) concentration is 0.005 M or higher,yielding an evolution from localized corrosion to uniform corrosion.Acceleration effect of NH_(4)^(+)can be attributed to that(i)NH_(4)^(+)dissolves the inner MgO and hinders the precipitation of Mg(OH)_(2) and(ii)the buffering ability of NH_(4)^(+)provides H+,enhances the hydrogen evolution,and expedites the corrosion process.The latter is demonstrated as the dominant factor with the results in unbuffered and buffered environments.The severe corrosion and hydrogen process in NH_(4)^(+)-containing solution results in a high Hads coverage and yields an inductive loop within the low frequency.Meanwhile,SO_(4)^(2−)is helpful in generating cracked but partially protective corrosion products,while Cl−could broaden the corrosion area beneath the corrosion product.
基金financially supported by the National Natural Science Foundation of China(U21A2077)the Taishan Scholar Project Foundation of Shandong Province(ts20190908)the Natural Science Foundation of Shandong Province(ZR2022MB084 and ZR2021ZD05).
文摘Vanadium-based cathode materials are attractive for aqueous zinc-ion batteries(AZIBs)owing to the high capacity from their open frameworks and multiple valences.However,the cycle stability and rate capability are still restricted by the low electrical conductivity and trapped diffusion kinetics.Here,we propose an organic-inorganic co-intercalation strategy to regulate the structure of ammonium vanadate(NH_(4)V_(4)O_(10),NVO).The introduction of Al^(3+)and polyaniline(PANI)induces the optimized layered structure and generation of urchin-like hierarchical construction(AP-NVO),based on heterogeneous nucleation and dissolution-recrystallization growth mechanism.Owing to these favorable features,the AP-NVO electrode delivers a desirable discharge capacity of 386 mA h g^(-1) at 1.0 A g^(-1),high-rate capability of 263 mA h g^(-1 )at 5.0 A g^(-1) and excellent cycling stability with 80.4%capacity retention over 2000 cycles at 5.0 A g^(-1).Such satisfactory electrochemical performance is believed to result from the enhanced reaction kinetics provided by the stable layered structure and a high intercalation pseudo-capacitance reaction.These results could provide enlightening insights into the design of layered vanadium oxide cathodematerials.
