The deposition of ultrafine single-atom nickel particles on Nb_(2)C(MXene)was successfully achieved using a wet chemistry method to synthesize Ni@Nb_(2)C composite.This study explored the effect of Ni@Nb_(2)C on the h...The deposition of ultrafine single-atom nickel particles on Nb_(2)C(MXene)was successfully achieved using a wet chemistry method to synthesize Ni@Nb_(2)C composite.This study explored the effect of Ni@Nb_(2)C on the hydrogen absorption and desorption properties of MgH_(2) through theoretical calculations and experimental investigations.Under the catalytic action of Ni@Nb2C,the initial dehydrogenation temperature of MgH_(2) was reduced by 121℃,with approximately 4.26 wt.% of H_(2) desorbed at 225℃ in 100 min.The dehydrogenation activation energy of the MgH_(2)+Ni@Nb_(2)C composite dropped to 86.7 kJ·mol^(-1),a reduction of 60.5 kJ·mol^(-1) compared to pure MgH_(2).Density functional theory calculations indicated that the incorporation of Ni@Nb_(2)C enhanced the performance of MgH_(2) performance by improving interactions among Nb_(2)C,Ni,Mg,and H atoms.In the Ni@Nb_(2)C+MgH_(2) system,the lengths of Mg-H bonds(1.91-1.99 A)were found to be longer than those observed in pure MgH_(2)(1.71 A).The dehydrogenation energy for this system(1.08 eV)was lower than that for Nb_(2)C(1.52 eV).These findings suggest that the synergistic effect of Ni and Nb2C significantly enhances the hydrogenation/dehydrogenation kinetics of MgH_(2),thereby introducing a novel approach for catalytic modification of solid hydrogen storage materials through synergistic actions.展开更多
An ionic liquid assisted hydrogel modified silica was synthesized using a one-pot polymerization and physical coating technique and subsequently applied to mixed-mode liquid chromatography.Analytical techniques,includ...An ionic liquid assisted hydrogel modified silica was synthesized using a one-pot polymerization and physical coating technique and subsequently applied to mixed-mode liquid chromatography.Analytical techniques,including Fourier transform infrared spectroscopy(FT-IR),X-ray photoelectron spectroscopy(XPS),and elemental analysis,etc.,confirmed the successful prepared of this innovative stationary phase.The unique combination of amide,long alkyl chain,and imidazole ring in the hydrogel coating enables the stationary phase to function effectively in hydrophilic/reversed-phase/ion exchange liquid chromatography.Notably,the stationary phase exhibited superior separation performance owing to the synergistic effect of the ionic liquid and hydrogel.This was particularly evident when analyzing various analytes such as organic acids,nucleosides/bases,polycyclic aromatic hydrocarbons(PAHs)and anions.Furthermore,under our operating conditions,an excellent column efficiency of 53,642.9 plates/m was achieved for theobromine.In summary,we have proposed a straightforward strategy to enhance the separation performance of hydrogel coatings in liquid chromatography,thereby broadening the potential applications of hydrogels in the field of separation.展开更多
Polyvinyl chloride(PVC)is one of the most widely used plastic materials worldwide,particularly in long-life applications such as construction materials.However,recycling options for PVC waste remain limited,as convent...Polyvinyl chloride(PVC)is one of the most widely used plastic materials worldwide,particularly in long-life applications such as construction materials.However,recycling options for PVC waste remain limited,as conventional methods often degrade material quality or generate environmentally hazardous byproducts.In this study,we demonstrate an efficient process to convert PVC into new polymers with variable aromatic groups,using triethylsilane as the reductant in different solvents.This approach enables the production of polymers analogous to functionalized polyethylene(PE),which are typically challenging to obtain through conventional copolymerization or direct post-modification of C-H bonds in PE.The resulting polymers exhibit tunable thermal and mechanical properties depending on the introduced aromatic groups,which not only enhance the sustainable valorization of PVC waste,but also provide an opportunity for the synthesis of new functionalized polymers.展开更多
Platinum-based(Pt)catalysts are notoriously susceptible to deactivation in industrial chemical processes due to carbon monoxide(CO)poisoning.Overcoming this poisoning deactivation of Pt-based catalysts while enhancing...Platinum-based(Pt)catalysts are notoriously susceptible to deactivation in industrial chemical processes due to carbon monoxide(CO)poisoning.Overcoming this poisoning deactivation of Pt-based catalysts while enhancing their catalytic activity,selectivity,and durability remains a major challenge.Herein,we propose a strategy to enhance the CO tolerance of Pt clusters(Pt_n)by introducing neighboring functionalized vip single atoms(such as Fe,Co,Ni,Cu,Sb,and Bi).Among them,antimony(Sb)single atoms(SAs)exhibit significant performance enhancement,achieving 99%CO selectivity and 33.6%CO_(2)conversion at 450℃,Experimental results and density functional theory(DFT)calculations indicate the optimization arises from the electronic interaction between neighboring functionalized Sb SAs and Pt clusters,leading to optimal 5d electron redistribution in Pt clusters compared to other functionalized vip single atoms.The redistribution of 5d electrons weaken both theσdonation andπbackdonation interactions,resulting in a weakened bond strength with CO and enhancing catalyst activity and selectivity.In situ environmental transmission electron microscopy(ETEM)further demonstrates the exception thermal stability of the catalyst,even under H_(2)at 700℃.Notably,the functionalized Sb SAs also improve CO tolerance in various heterogenous catalysts,including Co/CeO_(2),Ni/CeO_(2),Pt/Al_(2)O_(3),and Pt/CeO_(2)-C.This finding provides an effective approach to overcome the primary challenge of CO poisoning in Pt-based catalysts,making their broader applications in various industrial catalysts.展开更多
The growing demands for energy storage systems,electric vehicles,and portable electronics have significantly pushed forward the need for safe and reliable lithium batteries.It is essential to design functional separat...The growing demands for energy storage systems,electric vehicles,and portable electronics have significantly pushed forward the need for safe and reliable lithium batteries.It is essential to design functional separators with improved mechanical and electrochemical characteristics.This review covers the improved mechanical and electrochemical performances as well as the advancements made in the design of separators utilizing a variety of techniques.In terms of electrolyte wettability and adhesion of the coating materials,we provide an overview of the current status of research on coated separators,in situ modified separators,and grafting modified separators,and elaborate additional performance parameters of interest.The characteristics of inorganics coated separators,organic framework coated separators and inorganic-organic coated separators from different fabrication methods are compared.Future directions regarding new modified materials,manufacturing process,quantitative analysis of adhesion and so on are proposed toward next-generation advanced lithium batteries.展开更多
Listeria monocytogenes(LM)is a dangerous foodborne pathogen for humans.One emerging and validated method of indirectly assessing LM in food is detecting 3-hydroxy-2-butanone(3H2B)gas.In this study,the synthesis of 3-(...Listeria monocytogenes(LM)is a dangerous foodborne pathogen for humans.One emerging and validated method of indirectly assessing LM in food is detecting 3-hydroxy-2-butanone(3H2B)gas.In this study,the synthesis of 3-(2-aminoethylamino)propyltrimethoxysilane(AAPTMS)functionalized hierarchical hollow TiO_(2)nanospheres was achieved via precise controlling of solvothermal reaction temperature and post-grafting route.The sensors based on as-prepared materials exhibited excellent sensitivity(480 Hz@50 ppm),low detection limit(100 ppb),and outstanding selectivity.Moreover,the evaluation of LM with high sensitivity and specificity was achieved using the sensors.Such stable three-dimensional spheres,whose distinctive hierarchical and hollow nanostructure simultaneously improved both sensitivity and response/recovery speed dramatically,were spontaneously assembled by nanosheets.Meanwhile,the moderate loadings of AAPTMS significantly improved the selectivity of sensors.Then,the gas-sensing mechanism was explored by utilizing thermodynamic investigation,Gaussian 16 software,and in situ diffuse reflectance infrared transform spectroscopy,illustrating the weak chemisorption between the-NHgroup and 3H2B molecules.These portable sensors are promising for real-time assessment of LM at room temperature,which will make a magnificent contribution to food safety.展开更多
Shuttle effect of polysulfides overshadows the superiorities of lithium-sulfur batteries.Size-sieving effect could address this thorny trouble rely on size differ in polysulfides and lithium ions.However,clogged polys...Shuttle effect of polysulfides overshadows the superiorities of lithium-sulfur batteries.Size-sieving effect could address this thorny trouble rely on size differ in polysulfides and lithium ions.However,clogged polysulfides pose some challenges for cathode and are rarely recycled during charging/discharging.Herein,an amino functionalized titanium-organic framework is designed for modifying lithium-sulfur batteries separator to address the aforementioned challenges.Wherein,the introduction of amino narrows titanium-organic framework pore size,enabling functional separator to selectively modulate lithium ions and polysulfides migration using size-sieving effect,thereby completely suppressing polysulfides shuttle.Furthermore,the blocked polysulfides will be adsorbed on the separator surface by positively charged amino leveraging electrostatic adsorption,ensuring polysulfides to redistribute and reuse,and boosting active materials utilization.Significantly,the migration of lithium ions is not hindered since there are lithium ions transfer channels formed via Lewis acid-base interaction with the help of amino.Combined with these virtues,the lithium-sulfur batteries with amino functionalized titanium-organic framework modified separator enjoy an ultralow attenuation rate of 0.045%per cycle over 1000 cycles at 1.0C.Electrostatic adsorption and Lewis acid-base interaction cover deficiencies existing in the inhibition of polysulfides shuttle by size-sieving effect,providing fresh insight into the advancement of lithium-sulfur batteries.展开更多
In order to further improve the transfection efficiency of hydroxyapatite nanoparticle （HAp）, arginine functionalized hydroxyapatite （HAp/Arg） was synthesized by hydrothermal synthesis. The morphology, crystallite...In order to further improve the transfection efficiency of hydroxyapatite nanoparticle （HAp）, arginine functionalized hydroxyapatite （HAp/Arg） was synthesized by hydrothermal synthesis. The morphology, crystallite size and zeta potential of the HAp/Arg were characterized by transmission electron microscopy （TEM）, atomic force microscopy （AFM） and zeta potential analyzer. The loading and protecting properties of HAp/Arg to DNA were tested by electrophoresis. Its cytotoxicity was also measured in Hela cells and HAEC cells by MTT and LDH, and its transfection efficiency was examined by fluorescence microscope and flow cytometry. The results reveal that HAp/Arg is short rod-like and nano single crystal, the mean diameter is 50-90 nm and zeta potential is 35.8 mV at pH 7.4. HAp/Arg to DNA can be condensed by electrostatic effect and protect DNA against degradation in DNase I, and shows high transfection efficiency without cytotoxicity. These results suggest that HAp/Arg can be a promising alternative as a novel gene delivery system.展开更多
Functionalized carbon dots(CDs)obtained from citric acid derivative were selected as intercalatorto modify graphene and then dispersed into epoxy matrix to prepare CDs modified graphene/epoxy(CDs-G/EP)coatings.Meanwhi...Functionalized carbon dots(CDs)obtained from citric acid derivative were selected as intercalatorto modify graphene and then dispersed into epoxy matrix to prepare CDs modified graphene/epoxy(CDs-G/EP)coatings.Meanwhile,their microstructure,self-healing and corro sion resistance behaviors were analyzed deeply.Structural characterizations indicated the formation of"π-π"interaction between functionalized carbon dots and graphene.By observation,the dispersion and interface compatibility of graphene were greatly enhanced by CDs.The change rules of electrochemistry results implied that the addition of 0.5 wt.%CDs-G in EP coating(CDs-G0.5%/EP)demonstrated a superior protective property on steel,which was attributed to the physical barrier of highly dispersed graphene and the self-healing ability of CDs.After 50 days immersion,the oxygen permeability coefficient and water absorption of CDs-G0.5%/EP coating were only 4.27×10^(-13)cm^(3)cm cm^(-2)s^(-1)Pa^(-1) and 4.4%,respectively.展开更多
A molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-dichlorophenoxyacetic acid （2,4-D） was prepared by a surface imprinting technique in combination with a sol-gel process. The 2,4-D-im...A molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-dichlorophenoxyacetic acid （2,4-D） was prepared by a surface imprinting technique in combination with a sol-gel process. The 2,4-D-imprinted amino-functionalized silica sorbent was characterized by FT-IR, nitrogen adsorption and static adsorption experiments. The selectivity of the sorbent was investigated by a batch competitive binding experiment using an aqueous 2,4-D and 2,4-dichlorophenol （2,4-DCP） mixture or using an aqueous 2,4-D and 2,4- dichlorophenylacetic acid （DPAC） mixture. The largest selectivity coefficient for 2,4-D in the presence of 2,4-DCP was found to be over 18, the largest relative selectivity coefficient between 2,4-D and 2,4-DCP over 9. The static uptake capacity and selectivity coefficient of the 2,4-D-imprinted functionalized sorbent are higher than those of the non-imprinted sorbent. The imprinted functionalized silica gel sorbent offered a fast kinetics for the extraction/stripping of 2,4-D, 73% of binding capacity （200 mg/L 2,4-D onto 20 mg of imprinted sorbent） was obtained within 5 min and the adsorbed 2,4-D can be easily stripped by the mixture solution of ethanol and 6 mol/L HC1 （V：V =1：1）. In a test of five extraction/stripping cycles, the adsorption capacity of the sorbent was all above 93% of that of the fresh sorbent. Experimental result showed the potential of molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-D.展开更多
Global warming and associated global climate change have led to serious efforts towards reducing CO_(2)emissions through the CO_(2)capture from the major emission sources.CO_(2)capture using the amine functionalized a...Global warming and associated global climate change have led to serious efforts towards reducing CO_(2)emissions through the CO_(2)capture from the major emission sources.CO_(2)capture using the amine functionalized adsorbents is regard as a direct and effective way to reducing CO_(2)emissions due to their large CO_(2)adsorption amount,excellent CO_(2)adsorption selectivity and lower energy requirements for adsorbent regeneration.Moreover,large number of achievements on the amine functionalized solid adsorbent have been recorded for the enhanced CO_(2)capture in the past few years.In view of this,we review and analyze the recent advances in amine functionalized solid adsorbents prepared with different supporting materials including mesoporous silica,zeolite,porous carbon materials,metal organic frameworks(MOF)and other composite porous materials.In addition,amine functionalized solid adsorbents derived from waste resources are also reviewed because of the large number demand for cost-effective carbon dioxide adsorbents and the processing needs of waste resources.Considering the importance of the stability of the adsorbent in practical applications,advanced research in the capture cycle stability has also been summarized and analyzed.Finally,we summarize the review and offer the recommendations for the development of amine-based solid adsorbents for carbon dioxide capture.展开更多
Articular cartilage(AC)is an avascular and flexible connective tissue located on the bone surface in the diarthrodial joints.AC defects are common in the knees of young and physically active individuals.Because of the...Articular cartilage(AC)is an avascular and flexible connective tissue located on the bone surface in the diarthrodial joints.AC defects are common in the knees of young and physically active individuals.Because of the lack of suitable tissue-engineered artificial matrices,current therapies for AC defects,espe-cially full-thickness AC defects and osteochondral interfaces,fail to replace or regenerate damaged carti-lage adequately.With rapid research and development advancements in AC tissue engineering(ACTE),functionalized hydrogels have emerged as promising cartilage matrix substitutes because of their favor-able biomechanical properties,water content,swelling ability,cytocompatibility,biodegradability,and lubricating behaviors.They can be rationally designed and conveniently tuned to simulate the extracel-lular matrix of cartilage.This article briefly introduces the composition,structure,and function of AC and its defects,followed by a comprehensive review of the exquisite(bio)design and(bio)fabrication of func-tionalized hydrogels for AC repair.Finally,we summarize the challenges encountered in functionalized hydrogel-based strategies for ACTE both in vivo and in vitro and the future directions for clinical translation.展开更多
A novel adsorbent （AMPS-silica） was synthesized by bounding AMPS （2-acrylamido-2-methylpropanesulfonic acid） onto silica surface, which functioned with γ-methacryloxypropyltrimethoxysilane reagent. The adsorbent ...A novel adsorbent （AMPS-silica） was synthesized by bounding AMPS （2-acrylamido-2-methylpropanesulfonic acid） onto silica surface, which functioned with γ-methacryloxypropyltrimethoxysilane reagent. The adsorbent was characterized by nitrogen adsorption/desorption measurement, thermogravimetric analysis （TGA） and potentiometric titration analysis. The TGA result indicated that the surface modification reactions introduced some organic functional groups onto the surface of silica. The surface area of AMPSsilica was 389.7 m2/g. The adsorbent was examined for copper ion removal in series of batch adsorption experiments. Results showed that the adsorption of Cu2＋ onto AMPS-silica was pH dependent, and the adsorption capacity increased with increasing pH from 2 to 6. The adsorption kinetics showed that Cu^2＋ adsorption was fast and the data fitted well with a pseudo secondorder kinetic model. The adsorption of Cu^2＋ onto AMPS-silica obeyed both Freundlich and Langmuir isotherms, with r^2 = 0.993 and r^2 = 0.984, respectively. The maximum Cu^2＋ adsorption capacity was 19.9 mg/g. The involved mechanism might be the adsorption through metal binding with organic functional groups such as carboxyl, amino and sulfonic groups. Cu^2＋ loaded on AMPS-silica could be desorbed in HNO3 solution, and the adsorption properties remain stable after three adsorption-desorption cycles.展开更多
The nanophotocatalysts were synthesized in four stages and evaluated by FTIR, FESEM and VSM analysis. The influence of nanofluids containing functionalized magnetic Ti O2 nanophotocatalyst and dipalmitoylphosphatidylc...The nanophotocatalysts were synthesized in four stages and evaluated by FTIR, FESEM and VSM analysis. The influence of nanofluids containing functionalized magnetic Ti O2 nanophotocatalyst and dipalmitoylphosphatidylcholine lecithin in drag reduction of turbulent flow in four horizontal pipelines was studied. The effective parameters on drag reduction(nanoparticle concentration, surfactant concentration, p H and Re number) were investigated and optimized in each pipeline using response surface method. The drag reduction in 1/2 " galvanized, 3/4" galvanized, 1/2 "five-layer and 1/2" cuprous pipelines was found 99.1%, 92.5%, 87.6% and 85.2%, respectively. The model adequacy was measured using ANOVA. Based on the high determination coefficient, more than 95% of variance of experimental data in all pipelines was described by quadratic model.展开更多
The use of biochars formed by hydrothermal carbonization for the treatment of contaminated water has been greatly limited, due to their poorly developed porosity and low content of surface functional groups. Also, the...The use of biochars formed by hydrothermal carbonization for the treatment of contaminated water has been greatly limited, due to their poorly developed porosity and low content of surface functional groups. Also, the most common modification routes inevitably require post-treatment processes, which are time-consuming and energy-wasting. Hence, the objective of this research was to produce a cost-effective biochar with improved performance for the treatment of heavy metal pollution through a facile one-step hydrothermal carbonization process coupled with ammonium phosphate, thiocarbamide, ammonium chloride or urea, without any posttreatment. The effects of various operational parameters, including type of modification reagent, time and temperature of hydrothermal treatment, and ratio of modification reagent to precursor during impregnation, on the copper ion adsorption were examined. The adsorption data fit the Langmuir adsorption isotherm model quite well. The maximum adsorption capacities （mg/g） of the biochars towards copper ions followed the order of 40-8h-1.0-APBC （95.24） 〉 140-Sh-O-BC （12.52） 〉 140-8h-1.0-TUBC （12.08） 〉 140-Sh-1.0-ACBC （7.440） 〉 140-Sh-1.0-URBC （5.277）. The results indicated that biochars modified with ammonium phosphate displayed excellent adsorption performance toward copper ions, which was 7.6-fold higher than that of the pristine biochar. EDX and FT-IR analyses before and after adsorption demonstrated that the main removal mechanism involved complexation between the phosphate groups on the surface of the modified biochars and copper ions.展开更多
Fischer indole cyclization of phenylhydrazine and various ketones using carboxyl-functionalized ionic liquid, 1-carboxymethyl- 3-methylimidazolium tetrafluoroborate （abbreviated as [crnmim] [BF4]） as catalyst was su...Fischer indole cyclization of phenylhydrazine and various ketones using carboxyl-functionalized ionic liquid, 1-carboxymethyl- 3-methylimidazolium tetrafluoroborate （abbreviated as [crnmim] [BF4]） as catalyst was successfully performed. The yields of the target compounds were 80-92%, the purities were 96-98%. The catalyst could be recovered and reused for at least six times without significant loss in activity.展开更多
Breathing is an inherent human activity;however,the composition of the air we inhale and gas exhale remains unknown to us.To address this,wearable vapor sensors can help people monitor air composition in real time to ...Breathing is an inherent human activity;however,the composition of the air we inhale and gas exhale remains unknown to us.To address this,wearable vapor sensors can help people monitor air composition in real time to avoid underlying risks,and for the early detection and treatment of diseases for home healthcare.Hydrogels with three-dimensional polymer networks and large amounts of water molecules are naturally flexible and stretchable.Functionalized hydrogels are intrinsically conductive,self-healing,self-adhesive,biocompatible,and room-temperature sensitive.Compared with traditional rigid vapor sensors,hydrogel-based gas and humidity sensors can directly fit human skin or clothing,and are more suitable for real-time monitoring of personal health and safety.In this review,current studies on hydrogel-based vapor sensors are investigated.The required properties and optimization methods of wearable hydrogel-based sensors are introduced.Subsequently,existing reports on the response mechanisms of hydrogel-based gas and humidity sensors are summarized.Related works on hydrogel-based vapor sensors for their application in personal health and safety monitoring are presented.Moreover,the potential of hydrogels in the field of vapor sensing is elucidated.Finally,the current research status,challenges,and future trends of hydrogel gas/humidity sensing are discussed.展开更多
Lithium metal batteries(LMBs)have attracted wide attentions because of their high theoretical specific capacity and low electrochemical potential.However,the growth of lithium dendrites seriously affects the practical...Lithium metal batteries(LMBs)have attracted wide attentions because of their high theoretical specific capacity and low electrochemical potential.However,the growth of lithium dendrites seriously affects the practical application of LMBs.Thus,the lithium-philic carbonyl and carboxy dualgroup-modified covalent organic framework(COF-COOH)is designed to coat the polypropylene(PP)separator(COF-COOH@PP separator),realizing the regulation of ion transport and uniform lithium deposition.The plentiful and negative charge sites in the COF-COOH can suppress the diffusion of the freely movable lithium salt anion by the electrostatic interaction.Density functional theory(DFT)calculations demonstrate that the COF-COOH possesses the function of anchoring anion and desolvation.Consequently,the Li^(+)transference number(0.7),ion conductivity(0.64 mS cm^(-1)),and desolvating of Li^(+)are obviously improved by using the COF-COOH@PP separator.The modified Li-Li symmetric battery delivers stable cycle for more than 1000 h and lower voltage hysteresis(0.02 V).This dendrite-free deposition strategy holds great promise for practical application of Li metal anodes.展开更多
Glycine functionalized activated carbon adsorption material(NOPAC-GLY-X)was successfully prepared by one-step thermal decomposition using agricultural waste navel orange peel as a precursor.Through batch adsorption ex...Glycine functionalized activated carbon adsorption material(NOPAC-GLY-X)was successfully prepared by one-step thermal decomposition using agricultural waste navel orange peel as a precursor.Through batch adsorption experiments,it is found that the adsorption performance of Gd(Ⅲ)on activated carbon can be significantly enhanced by glycine modification.The adsorption isotherms of the NOPACs conform to the Langmuir isotherm model,and the maximum adsorption capacity of the activated carbon sample NOPAC-Gly-60 is approximately 48.5 mg/g.The Gd(Ⅲ)adsorption capacity of navel orange peel activated carbon can be doubled after glycine modification,and the adsorption efficiency of gadolinium can reach99%at pH=7.The physicochemical properties of the prepared adsorbents were characterized by Brunauer-Emmett-Teller(BET),Fourier transform infrared spectroscopy(FTIR),elemental analysis(EA),and X-ray photoelectron spectroscopy(XPS).The characterization test shows that the specific surface area of the sample increases from 1121 to 1523 m^(2)/g,and the ratio of(N+O)/C increases from 10.8%to 30.0%by the glycine modification.After five cycles of adsorption-desorption,the adsorption capacity can still be maintained at 88%of the initial capacity.NOPAC-GLY-60 has excellent adsorption selectivity for Gd(Ⅲ).With the obvious advantages of simple synthesis steps and low cost,the activated carbon modification method adopted in this study has great application value in the field of rare earth adsorption and recovery.展开更多
We report a high performance supported Pt catalyst, in which a perfluorosulfonic acid （Nation） functionalized carbon black is used as support. The catalyst is characterized by infrared spectroscopy （IR）, transmiss...We report a high performance supported Pt catalyst, in which a perfluorosulfonic acid （Nation） functionalized carbon black is used as support. The catalyst is characterized by infrared spectroscopy （IR）, transmission electron microscopy （TEM） and X-ray diffraction （XRD）. The TEM image shows that the active Pt component is in nanoparticles and highly dispersed on the carbon black with an average particle size of 1.9 nm. The catalyst shows improved activity towards the methanol anodic oxidation and oxygen reduction reaction （ORR）, resulting from the high dispersion of active Pt component. It leads to increases in electrochemically accessible surface areas and ion channels, as well as easier charge- transfer at polymer/electrolyte interfaces. The high platinum utilization and high performance of Pt/Nafion-C catalyst make it a promising electrocatalyst for fuel cell application.展开更多
基金financially supported by the National Natural Science Foundation of China under Grant numbers 22379030,52001079 and 52261038the Guangxi Key Laboratory of Green Manufacturing for Ecological Aluminum Industry(GXGMEA2024)the Nanning Excellent Young Talents Cultivation Project for Scientific and Technological Innovation and Entrepreneurship(RC20220102).
文摘The deposition of ultrafine single-atom nickel particles on Nb_(2)C(MXene)was successfully achieved using a wet chemistry method to synthesize Ni@Nb_(2)C composite.This study explored the effect of Ni@Nb_(2)C on the hydrogen absorption and desorption properties of MgH_(2) through theoretical calculations and experimental investigations.Under the catalytic action of Ni@Nb2C,the initial dehydrogenation temperature of MgH_(2) was reduced by 121℃,with approximately 4.26 wt.% of H_(2) desorbed at 225℃ in 100 min.The dehydrogenation activation energy of the MgH_(2)+Ni@Nb_(2)C composite dropped to 86.7 kJ·mol^(-1),a reduction of 60.5 kJ·mol^(-1) compared to pure MgH_(2).Density functional theory calculations indicated that the incorporation of Ni@Nb_(2)C enhanced the performance of MgH_(2) performance by improving interactions among Nb_(2)C,Ni,Mg,and H atoms.In the Ni@Nb_(2)C+MgH_(2) system,the lengths of Mg-H bonds(1.91-1.99 A)were found to be longer than those observed in pure MgH_(2)(1.71 A).The dehydrogenation energy for this system(1.08 eV)was lower than that for Nb_(2)C(1.52 eV).These findings suggest that the synergistic effect of Ni and Nb2C significantly enhances the hydrogenation/dehydrogenation kinetics of MgH_(2),thereby introducing a novel approach for catalytic modification of solid hydrogen storage materials through synergistic actions.
基金Innovation Groups of Basic Research in Gansu Province(No.23JRRA570)。
文摘An ionic liquid assisted hydrogel modified silica was synthesized using a one-pot polymerization and physical coating technique and subsequently applied to mixed-mode liquid chromatography.Analytical techniques,including Fourier transform infrared spectroscopy(FT-IR),X-ray photoelectron spectroscopy(XPS),and elemental analysis,etc.,confirmed the successful prepared of this innovative stationary phase.The unique combination of amide,long alkyl chain,and imidazole ring in the hydrogel coating enables the stationary phase to function effectively in hydrophilic/reversed-phase/ion exchange liquid chromatography.Notably,the stationary phase exhibited superior separation performance owing to the synergistic effect of the ionic liquid and hydrogel.This was particularly evident when analyzing various analytes such as organic acids,nucleosides/bases,polycyclic aromatic hydrocarbons(PAHs)and anions.Furthermore,under our operating conditions,an excellent column efficiency of 53,642.9 plates/m was achieved for theobromine.In summary,we have proposed a straightforward strategy to enhance the separation performance of hydrogel coatings in liquid chromatography,thereby broadening the potential applications of hydrogels in the field of separation.
基金the Beijing Natural Science Foundation(Z240029)the National Natural Science Foundation of China(22472004)+2 种基金China National Petroleum Corporation-Peking University Strategic Cooperation Project of Fundamental Researchthe New Cornerstone Science Foundationsupport from the Tencent Foundation through the Xplorer Prize.
文摘Polyvinyl chloride(PVC)is one of the most widely used plastic materials worldwide,particularly in long-life applications such as construction materials.However,recycling options for PVC waste remain limited,as conventional methods often degrade material quality or generate environmentally hazardous byproducts.In this study,we demonstrate an efficient process to convert PVC into new polymers with variable aromatic groups,using triethylsilane as the reductant in different solvents.This approach enables the production of polymers analogous to functionalized polyethylene(PE),which are typically challenging to obtain through conventional copolymerization or direct post-modification of C-H bonds in PE.The resulting polymers exhibit tunable thermal and mechanical properties depending on the introduced aromatic groups,which not only enhance the sustainable valorization of PVC waste,but also provide an opportunity for the synthesis of new functionalized polymers.
基金financially supported by the Shanghai RisingStar Program(No.23QA1403700)the National Natural Science Foundation of China(NSFC,Grant No.U2230102)+1 种基金the sponsored by National Key Research and Development Program of China(No.2021YFB3502200)the Shanghai Technical Service Center of Science and Engineering Computing,Shanghai University.
文摘Platinum-based(Pt)catalysts are notoriously susceptible to deactivation in industrial chemical processes due to carbon monoxide(CO)poisoning.Overcoming this poisoning deactivation of Pt-based catalysts while enhancing their catalytic activity,selectivity,and durability remains a major challenge.Herein,we propose a strategy to enhance the CO tolerance of Pt clusters(Pt_n)by introducing neighboring functionalized vip single atoms(such as Fe,Co,Ni,Cu,Sb,and Bi).Among them,antimony(Sb)single atoms(SAs)exhibit significant performance enhancement,achieving 99%CO selectivity and 33.6%CO_(2)conversion at 450℃,Experimental results and density functional theory(DFT)calculations indicate the optimization arises from the electronic interaction between neighboring functionalized Sb SAs and Pt clusters,leading to optimal 5d electron redistribution in Pt clusters compared to other functionalized vip single atoms.The redistribution of 5d electrons weaken both theσdonation andπbackdonation interactions,resulting in a weakened bond strength with CO and enhancing catalyst activity and selectivity.In situ environmental transmission electron microscopy(ETEM)further demonstrates the exception thermal stability of the catalyst,even under H_(2)at 700℃.Notably,the functionalized Sb SAs also improve CO tolerance in various heterogenous catalysts,including Co/CeO_(2),Ni/CeO_(2),Pt/Al_(2)O_(3),and Pt/CeO_(2)-C.This finding provides an effective approach to overcome the primary challenge of CO poisoning in Pt-based catalysts,making their broader applications in various industrial catalysts.
基金the Center of Lithium Battery Membrane Materials jointly established by School of Chemistry and Chemical Engineering of Huazhong University of Science and Technology and Shenzhen Senior Technology Material Co.Ltd.,the National Natural Science Foundation of China(52020105012,52303084)the Young Scientists Fund of Natural Science Foundation of Hubei Province(2023AFB220)for the support of this work.
文摘The growing demands for energy storage systems,electric vehicles,and portable electronics have significantly pushed forward the need for safe and reliable lithium batteries.It is essential to design functional separators with improved mechanical and electrochemical characteristics.This review covers the improved mechanical and electrochemical performances as well as the advancements made in the design of separators utilizing a variety of techniques.In terms of electrolyte wettability and adhesion of the coating materials,we provide an overview of the current status of research on coated separators,in situ modified separators,and grafting modified separators,and elaborate additional performance parameters of interest.The characteristics of inorganics coated separators,organic framework coated separators and inorganic-organic coated separators from different fabrication methods are compared.Future directions regarding new modified materials,manufacturing process,quantitative analysis of adhesion and so on are proposed toward next-generation advanced lithium batteries.
基金supported by the National Natural Science Foundation of China(No.32272399)the Shanghai Natural Science Foundation(No.21ZR1427500).
文摘Listeria monocytogenes(LM)is a dangerous foodborne pathogen for humans.One emerging and validated method of indirectly assessing LM in food is detecting 3-hydroxy-2-butanone(3H2B)gas.In this study,the synthesis of 3-(2-aminoethylamino)propyltrimethoxysilane(AAPTMS)functionalized hierarchical hollow TiO_(2)nanospheres was achieved via precise controlling of solvothermal reaction temperature and post-grafting route.The sensors based on as-prepared materials exhibited excellent sensitivity(480 Hz@50 ppm),low detection limit(100 ppb),and outstanding selectivity.Moreover,the evaluation of LM with high sensitivity and specificity was achieved using the sensors.Such stable three-dimensional spheres,whose distinctive hierarchical and hollow nanostructure simultaneously improved both sensitivity and response/recovery speed dramatically,were spontaneously assembled by nanosheets.Meanwhile,the moderate loadings of AAPTMS significantly improved the selectivity of sensors.Then,the gas-sensing mechanism was explored by utilizing thermodynamic investigation,Gaussian 16 software,and in situ diffuse reflectance infrared transform spectroscopy,illustrating the weak chemisorption between the-NHgroup and 3H2B molecules.These portable sensors are promising for real-time assessment of LM at room temperature,which will make a magnificent contribution to food safety.
基金supported by the National Natural Science Foundation of China(52463013 and 52073133)Key Talent Project Foundation of Gansu Province+3 种基金Joint fund between Shenyang National Laboratory for Materials ScienceState Key Laboratory of Advanced Processing and Recycling of Nonferrous Metals(18LHPY002)the Program for Hongliu Distinguished Young Scholars in Lanzhou University of Technologythe Incubation Program of Excellent Doctoral Dissertation–Lanzhou University of Technology
文摘Shuttle effect of polysulfides overshadows the superiorities of lithium-sulfur batteries.Size-sieving effect could address this thorny trouble rely on size differ in polysulfides and lithium ions.However,clogged polysulfides pose some challenges for cathode and are rarely recycled during charging/discharging.Herein,an amino functionalized titanium-organic framework is designed for modifying lithium-sulfur batteries separator to address the aforementioned challenges.Wherein,the introduction of amino narrows titanium-organic framework pore size,enabling functional separator to selectively modulate lithium ions and polysulfides migration using size-sieving effect,thereby completely suppressing polysulfides shuttle.Furthermore,the blocked polysulfides will be adsorbed on the separator surface by positively charged amino leveraging electrostatic adsorption,ensuring polysulfides to redistribute and reuse,and boosting active materials utilization.Significantly,the migration of lithium ions is not hindered since there are lithium ions transfer channels formed via Lewis acid-base interaction with the help of amino.Combined with these virtues,the lithium-sulfur batteries with amino functionalized titanium-organic framework modified separator enjoy an ultralow attenuation rate of 0.045%per cycle over 1000 cycles at 1.0C.Electrostatic adsorption and Lewis acid-base interaction cover deficiencies existing in the inhibition of polysulfides shuttle by size-sieving effect,providing fresh insight into the advancement of lithium-sulfur batteries.
基金Project(2013SK2024)supported by the Key Projects in Social Development Pillar Program of Hunan Province,ChinaProject(20130162120094)supported by Specialized Research Fund for the Doctoral Program of Higher Education(SRFDP),Ministry of Education,ChinaProjects(81071869,51305464)supported by the National Natural Science Foundation of China
文摘In order to further improve the transfection efficiency of hydroxyapatite nanoparticle （HAp）, arginine functionalized hydroxyapatite （HAp/Arg） was synthesized by hydrothermal synthesis. The morphology, crystallite size and zeta potential of the HAp/Arg were characterized by transmission electron microscopy （TEM）, atomic force microscopy （AFM） and zeta potential analyzer. The loading and protecting properties of HAp/Arg to DNA were tested by electrophoresis. Its cytotoxicity was also measured in Hela cells and HAEC cells by MTT and LDH, and its transfection efficiency was examined by fluorescence microscope and flow cytometry. The results reveal that HAp/Arg is short rod-like and nano single crystal, the mean diameter is 50-90 nm and zeta potential is 35.8 mV at pH 7.4. HAp/Arg to DNA can be condensed by electrostatic effect and protect DNA against degradation in DNase I, and shows high transfection efficiency without cytotoxicity. These results suggest that HAp/Arg can be a promising alternative as a novel gene delivery system.
基金supported by the Scientific Research Foundation of Jiangxi University of Science and Technology(No.205200100421)the Jiangxi Provincial Department of Education(No.GJJ190469)+3 种基金Postdoctoral fund of Jiangxi Province(2019KY29)the Research and Development Project of Ganzhouthe Science and Technology Innovation Talents Program of Ganzhouthe Program of Qingjiang Excellent Young Talents(Jiangxi University of Science and Technology)。
文摘Functionalized carbon dots(CDs)obtained from citric acid derivative were selected as intercalatorto modify graphene and then dispersed into epoxy matrix to prepare CDs modified graphene/epoxy(CDs-G/EP)coatings.Meanwhile,their microstructure,self-healing and corro sion resistance behaviors were analyzed deeply.Structural characterizations indicated the formation of"π-π"interaction between functionalized carbon dots and graphene.By observation,the dispersion and interface compatibility of graphene were greatly enhanced by CDs.The change rules of electrochemistry results implied that the addition of 0.5 wt.%CDs-G in EP coating(CDs-G0.5%/EP)demonstrated a superior protective property on steel,which was attributed to the physical barrier of highly dispersed graphene and the self-healing ability of CDs.After 50 days immersion,the oxygen permeability coefficient and water absorption of CDs-G0.5%/EP coating were only 4.27×10^(-13)cm^(3)cm cm^(-2)s^(-1)Pa^(-1) and 4.4%,respectively.
基金supported by the Natural Science Foundation of Zhejiang Province (No.Y505073)the Scientific Project of Zhejiang Province (No.2008C22012)
文摘A molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-dichlorophenoxyacetic acid （2,4-D） was prepared by a surface imprinting technique in combination with a sol-gel process. The 2,4-D-imprinted amino-functionalized silica sorbent was characterized by FT-IR, nitrogen adsorption and static adsorption experiments. The selectivity of the sorbent was investigated by a batch competitive binding experiment using an aqueous 2,4-D and 2,4-dichlorophenol （2,4-DCP） mixture or using an aqueous 2,4-D and 2,4- dichlorophenylacetic acid （DPAC） mixture. The largest selectivity coefficient for 2,4-D in the presence of 2,4-DCP was found to be over 18, the largest relative selectivity coefficient between 2,4-D and 2,4-DCP over 9. The static uptake capacity and selectivity coefficient of the 2,4-D-imprinted functionalized sorbent are higher than those of the non-imprinted sorbent. The imprinted functionalized silica gel sorbent offered a fast kinetics for the extraction/stripping of 2,4-D, 73% of binding capacity （200 mg/L 2,4-D onto 20 mg of imprinted sorbent） was obtained within 5 min and the adsorbed 2,4-D can be easily stripped by the mixture solution of ethanol and 6 mol/L HC1 （V：V =1：1）. In a test of five extraction/stripping cycles, the adsorption capacity of the sorbent was all above 93% of that of the fresh sorbent. Experimental result showed the potential of molecularly-imprinted amino-functionalized sorbent for selective removal of 2,4-D.
基金supported by the National Natural Science Foundation of China(21878200 and 21676174)International S&T Cooperation Program of Shanxi province(201703D421038)+1 种基金Shanxi Scholarship Council of China(2017-036)Joint Fund of Shanxi Provincial Coal Seam Gas(2015012019)。
文摘Global warming and associated global climate change have led to serious efforts towards reducing CO_(2)emissions through the CO_(2)capture from the major emission sources.CO_(2)capture using the amine functionalized adsorbents is regard as a direct and effective way to reducing CO_(2)emissions due to their large CO_(2)adsorption amount,excellent CO_(2)adsorption selectivity and lower energy requirements for adsorbent regeneration.Moreover,large number of achievements on the amine functionalized solid adsorbent have been recorded for the enhanced CO_(2)capture in the past few years.In view of this,we review and analyze the recent advances in amine functionalized solid adsorbents prepared with different supporting materials including mesoporous silica,zeolite,porous carbon materials,metal organic frameworks(MOF)and other composite porous materials.In addition,amine functionalized solid adsorbents derived from waste resources are also reviewed because of the large number demand for cost-effective carbon dioxide adsorbents and the processing needs of waste resources.Considering the importance of the stability of the adsorbent in practical applications,advanced research in the capture cycle stability has also been summarized and analyzed.Finally,we summarize the review and offer the recommendations for the development of amine-based solid adsorbents for carbon dioxide capture.
基金supported by grants from the AO Foundation (AOOCD Consortium TA1711481)Areas of Excellence Scheme from the University Grant Council of Hong Kong (Ao E/M-402/20)+1 种基金Theme-based Research Scheme from the University Grant Council of Hong Kong (T13-402/17-N)Key-Area Research and Development Program of Guangdong Province (2019B010941001)
文摘Articular cartilage(AC)is an avascular and flexible connective tissue located on the bone surface in the diarthrodial joints.AC defects are common in the knees of young and physically active individuals.Because of the lack of suitable tissue-engineered artificial matrices,current therapies for AC defects,espe-cially full-thickness AC defects and osteochondral interfaces,fail to replace or regenerate damaged carti-lage adequately.With rapid research and development advancements in AC tissue engineering(ACTE),functionalized hydrogels have emerged as promising cartilage matrix substitutes because of their favor-able biomechanical properties,water content,swelling ability,cytocompatibility,biodegradability,and lubricating behaviors.They can be rationally designed and conveniently tuned to simulate the extracel-lular matrix of cartilage.This article briefly introduces the composition,structure,and function of AC and its defects,followed by a comprehensive review of the exquisite(bio)design and(bio)fabrication of func-tionalized hydrogels for AC repair.Finally,we summarize the challenges encountered in functionalized hydrogel-based strategies for ACTE both in vivo and in vitro and the future directions for clinical translation.
基金supported by the Fundation for Creative Research Groups of China (No. 50621804)
文摘A novel adsorbent （AMPS-silica） was synthesized by bounding AMPS （2-acrylamido-2-methylpropanesulfonic acid） onto silica surface, which functioned with γ-methacryloxypropyltrimethoxysilane reagent. The adsorbent was characterized by nitrogen adsorption/desorption measurement, thermogravimetric analysis （TGA） and potentiometric titration analysis. The TGA result indicated that the surface modification reactions introduced some organic functional groups onto the surface of silica. The surface area of AMPSsilica was 389.7 m2/g. The adsorbent was examined for copper ion removal in series of batch adsorption experiments. Results showed that the adsorption of Cu2＋ onto AMPS-silica was pH dependent, and the adsorption capacity increased with increasing pH from 2 to 6. The adsorption kinetics showed that Cu^2＋ adsorption was fast and the data fitted well with a pseudo secondorder kinetic model. The adsorption of Cu^2＋ onto AMPS-silica obeyed both Freundlich and Langmuir isotherms, with r^2 = 0.993 and r^2 = 0.984, respectively. The maximum Cu^2＋ adsorption capacity was 19.9 mg/g. The involved mechanism might be the adsorption through metal binding with organic functional groups such as carboxyl, amino and sulfonic groups. Cu^2＋ loaded on AMPS-silica could be desorbed in HNO3 solution, and the adsorption properties remain stable after three adsorption-desorption cycles.
文摘The nanophotocatalysts were synthesized in four stages and evaluated by FTIR, FESEM and VSM analysis. The influence of nanofluids containing functionalized magnetic Ti O2 nanophotocatalyst and dipalmitoylphosphatidylcholine lecithin in drag reduction of turbulent flow in four horizontal pipelines was studied. The effective parameters on drag reduction(nanoparticle concentration, surfactant concentration, p H and Re number) were investigated and optimized in each pipeline using response surface method. The drag reduction in 1/2 " galvanized, 3/4" galvanized, 1/2 "five-layer and 1/2" cuprous pipelines was found 99.1%, 92.5%, 87.6% and 85.2%, respectively. The model adequacy was measured using ANOVA. Based on the high determination coefficient, more than 95% of variance of experimental data in all pipelines was described by quadratic model.
基金supported by the Tai Shan Scholar Foundation(No.ts201511003)the Fundamental Research Funds for the Central Universities(No.DUT17RC(3)044)
文摘The use of biochars formed by hydrothermal carbonization for the treatment of contaminated water has been greatly limited, due to their poorly developed porosity and low content of surface functional groups. Also, the most common modification routes inevitably require post-treatment processes, which are time-consuming and energy-wasting. Hence, the objective of this research was to produce a cost-effective biochar with improved performance for the treatment of heavy metal pollution through a facile one-step hydrothermal carbonization process coupled with ammonium phosphate, thiocarbamide, ammonium chloride or urea, without any posttreatment. The effects of various operational parameters, including type of modification reagent, time and temperature of hydrothermal treatment, and ratio of modification reagent to precursor during impregnation, on the copper ion adsorption were examined. The adsorption data fit the Langmuir adsorption isotherm model quite well. The maximum adsorption capacities （mg/g） of the biochars towards copper ions followed the order of 40-8h-1.0-APBC （95.24） 〉 140-Sh-O-BC （12.52） 〉 140-8h-1.0-TUBC （12.08） 〉 140-Sh-1.0-ACBC （7.440） 〉 140-Sh-1.0-URBC （5.277）. The results indicated that biochars modified with ammonium phosphate displayed excellent adsorption performance toward copper ions, which was 7.6-fold higher than that of the pristine biochar. EDX and FT-IR analyses before and after adsorption demonstrated that the main removal mechanism involved complexation between the phosphate groups on the surface of the modified biochars and copper ions.
基金the Key Project of Shanghai Educational Committee(No.06ZZ82)
文摘Fischer indole cyclization of phenylhydrazine and various ketones using carboxyl-functionalized ionic liquid, 1-carboxymethyl- 3-methylimidazolium tetrafluoroborate （abbreviated as [crnmim] [BF4]） as catalyst was successfully performed. The yields of the target compounds were 80-92%, the purities were 96-98%. The catalyst could be recovered and reused for at least six times without significant loss in activity.
基金Jin Wu acknowledges financial support from the National Natural Science Foundation of China(No.61801525)the Guangdong Basic and Applied Basic Research Foundation(No.2020A1515010693)+1 种基金the Fundamental Research Funds for the Central Universities,Sun Yat-sen University(No.22lgqb17)the Independent Fund of the State Key Laboratory of Optoelectronic Materials and Technologies(Sun Yat-sen University)under grant No.OEMT-2022-ZRC-05.
文摘Breathing is an inherent human activity;however,the composition of the air we inhale and gas exhale remains unknown to us.To address this,wearable vapor sensors can help people monitor air composition in real time to avoid underlying risks,and for the early detection and treatment of diseases for home healthcare.Hydrogels with three-dimensional polymer networks and large amounts of water molecules are naturally flexible and stretchable.Functionalized hydrogels are intrinsically conductive,self-healing,self-adhesive,biocompatible,and room-temperature sensitive.Compared with traditional rigid vapor sensors,hydrogel-based gas and humidity sensors can directly fit human skin or clothing,and are more suitable for real-time monitoring of personal health and safety.In this review,current studies on hydrogel-based vapor sensors are investigated.The required properties and optimization methods of wearable hydrogel-based sensors are introduced.Subsequently,existing reports on the response mechanisms of hydrogel-based gas and humidity sensors are summarized.Related works on hydrogel-based vapor sensors for their application in personal health and safety monitoring are presented.Moreover,the potential of hydrogels in the field of vapor sensing is elucidated.Finally,the current research status,challenges,and future trends of hydrogel gas/humidity sensing are discussed.
基金financial support provided by the National Natural Science Foundation of China(52064049)the Key National Natural Science Foundation of Yunnan Province(2018FA028 and 2019FY003023)+2 种基金International Joint Research Center for Advanced Energy Materials of Yunnan Province(202003AE140001)Key Laboratory of Solid State Ions for Green Energy of Yunnan University(2019)the Analysis and Measurements Center of Yunnan University for the sample testing service.
文摘Lithium metal batteries(LMBs)have attracted wide attentions because of their high theoretical specific capacity and low electrochemical potential.However,the growth of lithium dendrites seriously affects the practical application of LMBs.Thus,the lithium-philic carbonyl and carboxy dualgroup-modified covalent organic framework(COF-COOH)is designed to coat the polypropylene(PP)separator(COF-COOH@PP separator),realizing the regulation of ion transport and uniform lithium deposition.The plentiful and negative charge sites in the COF-COOH can suppress the diffusion of the freely movable lithium salt anion by the electrostatic interaction.Density functional theory(DFT)calculations demonstrate that the COF-COOH possesses the function of anchoring anion and desolvation.Consequently,the Li^(+)transference number(0.7),ion conductivity(0.64 mS cm^(-1)),and desolvating of Li^(+)are obviously improved by using the COF-COOH@PP separator.The modified Li-Li symmetric battery delivers stable cycle for more than 1000 h and lower voltage hysteresis(0.02 V).This dendrite-free deposition strategy holds great promise for practical application of Li metal anodes.
基金Project supported by the National Natural Science Foundation of China(41662004)。
文摘Glycine functionalized activated carbon adsorption material(NOPAC-GLY-X)was successfully prepared by one-step thermal decomposition using agricultural waste navel orange peel as a precursor.Through batch adsorption experiments,it is found that the adsorption performance of Gd(Ⅲ)on activated carbon can be significantly enhanced by glycine modification.The adsorption isotherms of the NOPACs conform to the Langmuir isotherm model,and the maximum adsorption capacity of the activated carbon sample NOPAC-Gly-60 is approximately 48.5 mg/g.The Gd(Ⅲ)adsorption capacity of navel orange peel activated carbon can be doubled after glycine modification,and the adsorption efficiency of gadolinium can reach99%at pH=7.The physicochemical properties of the prepared adsorbents were characterized by Brunauer-Emmett-Teller(BET),Fourier transform infrared spectroscopy(FTIR),elemental analysis(EA),and X-ray photoelectron spectroscopy(XPS).The characterization test shows that the specific surface area of the sample increases from 1121 to 1523 m^(2)/g,and the ratio of(N+O)/C increases from 10.8%to 30.0%by the glycine modification.After five cycles of adsorption-desorption,the adsorption capacity can still be maintained at 88%of the initial capacity.NOPAC-GLY-60 has excellent adsorption selectivity for Gd(Ⅲ).With the obvious advantages of simple synthesis steps and low cost,the activated carbon modification method adopted in this study has great application value in the field of rare earth adsorption and recovery.
文摘We report a high performance supported Pt catalyst, in which a perfluorosulfonic acid （Nation） functionalized carbon black is used as support. The catalyst is characterized by infrared spectroscopy （IR）, transmission electron microscopy （TEM） and X-ray diffraction （XRD）. The TEM image shows that the active Pt component is in nanoparticles and highly dispersed on the carbon black with an average particle size of 1.9 nm. The catalyst shows improved activity towards the methanol anodic oxidation and oxygen reduction reaction （ORR）, resulting from the high dispersion of active Pt component. It leads to increases in electrochemically accessible surface areas and ion channels, as well as easier charge- transfer at polymer/electrolyte interfaces. The high platinum utilization and high performance of Pt/Nafion-C catalyst make it a promising electrocatalyst for fuel cell application.
