The need for bi-functional catalysts that facilit-ate both the oxygen reduction(ORR)and carbon dioxide re-duction(CO_(2)RR)reactions arises from their potential to help solve the critical problems of carbon neutrality...The need for bi-functional catalysts that facilit-ate both the oxygen reduction(ORR)and carbon dioxide re-duction(CO_(2)RR)reactions arises from their potential to help solve the critical problems of carbon neutrality and renew-able energy conversion.However,there are few reports on the development of bi-functional catalysts for zinc-air bat-tery-driven CO_(2)RR devices.We introduce a novel approach for synthesizing Fe_(2)N/Fe_(3)C species embedded in nitrogen-doped carbon nanofibers by electrospinning a solution of Hemin and polyacrylonitrile in N,N-dimethylformamide.The material has an exceptional catalytic performance,with a half-wave potential of 0.91 V versus RHE for the ORR and values of over 90%for both the selectivity and Faradaic efficiency for the CO_(2)RR.The high catalytic performances are attrib-uted to the strong coupling between the Fe_(3)C/Fe_(2)N heterostructure and the Fe-N-C sites in the nitrogen-doped carbon nan-ofibers.Notably,both Fe_(3)C and Fe_(2)N play distinct roles in both the ORR and CO_(2)RR.This investigation indicates a way for designing advanced carbon-based bi-functional catalysts for use in this field.展开更多
Sodium-ion batteries(SIBs)show promising potential in the field of electrochemical energy storage due to their cost-effectiveness and similar operational mechanisms to lithium-ion batteries(LIBs).However,the dramatic ...Sodium-ion batteries(SIBs)show promising potential in the field of electrochemical energy storage due to their cost-effectiveness and similar operational mechanisms to lithium-ion batteries(LIBs).However,the dramatic volume expansion of electrode materials and the slow reaction kinetics caused by the large sodium ion(Na^(+))radius hinder the practical application of SIBs,Here,we successfully prepared SnS_(2-x)Se_(x)nanodots embedded within N-doped carbon nanofibers(CNF)for use as electrode materials of SIBs,The introduction Se provided abundant anionic defect sites for Na+storage and enlarged the interlayer spacing of SnS_(2).In addition,the ultraifne nanodot structure reduces the volume expansion of SnS_(2-x)Se_(x)and shortens the ion transport path.As an anode of SIBs,SnS_(2-x)Se_(x)/CNF demonstrates remarkable reversible capacity(719 mAh g^(-1)at 0.5 A g^(-1)),along with rapid charging ability(completing a charge in just 127 s).Meanwhile,the assembled full-cell battery manifested exceptional energy density of 165.8 Wh kg^(-1)at a high-power output of 5526 W kg^(-1).This study presents an effective strategy for fabricating highperformance sulphide-based anode materials for SIBs,offering broad prospects for application.展开更多
Based on the unique catalytic properties of precious metals,the introduction of precious metals into metal oxide semiconductors will greatly improve the gas-sensitive properties of materials.As a new type of porous ma...Based on the unique catalytic properties of precious metals,the introduction of precious metals into metal oxide semiconductors will greatly improve the gas-sensitive properties of materials.As a new type of porous material,metal–organic frameworks(MOF)can be used for gas separation and adsorption due to their adjustable pore size and acceptable thermal stability.In this work,the ZIF-71 MOF was synthesized on CuO nanofibers doped with different concentrations of Ru to form a Ru–CuO@ZIF-71 nanocomposite sensor,which was then used for H_(2)S detection.The sensor shows sensitivity to trace amounts of H_(2)S gas(100 ppb),and the response is greatly enhanced at the optimal Ru doping ratio and operating temperature.The introduction of the ZIF-71 membrane can significantly increase the selectivity of the sensor while further improving the sensitivity.Finally,the possible sensing mechanism of the Ru–CuO@ZIF-71 sensor was explored.The enhancement of the H_(2)S gas sensing properties may be attributed to the catalysis of Ru and the formation of the Schottky junction at the Ru–CuO interface.Besides,the calculation based on density functional theory reveals enhanced adsorption capacities of CuO for H_(2)S after Ru doping.Therefore,the Ru–CuO@ZIF-71 sensor has strong application potential in exhaled gas detection and portable detection of H_(2)S gas in industrial environments.展开更多
The Cu^(+)/Cu^(0)sites of copper-based catalysts are crucial for enhancing the production of multicarbon(C_(2+))products from electrochemical CO_(2)reduction reaction(eCO_(2)RR).However,the unstable Cu^(+)and insuffic...The Cu^(+)/Cu^(0)sites of copper-based catalysts are crucial for enhancing the production of multicarbon(C_(2+))products from electrochemical CO_(2)reduction reaction(eCO_(2)RR).However,the unstable Cu^(+)and insufficient Cu^(+)/Cu^(0)active sites lead to their limited selectivity and stability for C_(2+)production.Herein,we embedded copper oxide(CuO_(x))particles into porous nitrogen-doped carbon nanofibers(CuO_(x)@PCNF)by pyrolysis of the electrospun fiber film containing ZIF-8 and Cu_(2)O particles.The porous nitrogendoped carbon nanofibers protected and dispersed Cu^(+)species,and its micro porous structure enhanced the interaction between CuO_(x)and reactants during eCO_(2)RR.The obtained CuO_(x)@PCNF created more effective and stable Cu^(+)/Cu^(0)active sites.It showed a high Faradaic efficiency of 62.5%for C_(2+)products in Hcell,which was 2 times higher than that of bare CuO_(x)(~31.1%).Furthermore,it achieved a maximum Faradaic efficiency of 80.7%for C_(2+)products in flow cell.In situ characterization and density functional theory(DFT)calculation confirmed that the N-doped carbon layer protected Cu^(+)from electrochemical reduction and lowered the energy barrier for the dimerization of^(*)CO.Stable and exposed Cu^(+)/Cu^(0)active sites enhanced the enrichment of^(*)CO and promoted the C-C coupling reaction on the catalyst surface,which facilitated the formation of C_(2+)products.展开更多
Piezocatalytic hydrogen peroxide(H_(2)O_(2))generation is a promising synthesis method that has received increasing attention;however,the reaction pathway requires further investigation.Here,Bi_(5)Ti_(3)FeO_(15)nanofi...Piezocatalytic hydrogen peroxide(H_(2)O_(2))generation is a promising synthesis method that has received increasing attention;however,the reaction pathway requires further investigation.Here,Bi_(5)Ti_(3)FeO_(15)nanofibers are used to generate H_(2)O_(2)by harvesting mechanical energy,and the reaction pathways are investigated.The H_(2)O_(2)yield over Bi_(5)Ti_(3)FeO_(15)nanofibers steadily increases from 331μmol g1 h1 in the first cycle to 746μmol g1 h1 in the tenth cycle in pure water without a sacrificial agent.Reliable reaction pathways are revealed by monitoring the pH value changes in the reaction solution during the H_(2)O_(2)generation process.In the H_(2)O_(2)generation process,the water oxidation reaction(WOR)provides a large amount of H+in the reaction solution,which promotes the oxygen reduction reaction(ORR)for H_(2)O_(2)generation.Therefore,an efficient synergistic effect between ORR and WOR achieves dual-pathway H_(2)O_(2)generation,contributing to the excellent piezocatalytic performance of Bi_(5)Ti_(3)FeO_(15)nanofibers.Furthermore,mechanistic studies indicate that the piezocatalytic H_(2)O_(2)generation follows the energy band theory.This work not only demonstrates Bi_(5)Ti_(3)FeO_(15)nanofibers as efficient piezocatalysts for H_(2)O_(2)generation but also provides a simple and effective approach to elucidate reaction pathways.This approach can be applied in photocatalytic,tribocatalytic,and electrocatalytic H_(2)O_(2)generation.展开更多
Lithium-sulfur battery is one of the most promising battery systems for industrialization due to its high theoretical specific capacity and high energy density.Nonetheless,the"shuttle effect"has restrained t...Lithium-sulfur battery is one of the most promising battery systems for industrialization due to its high theoretical specific capacity and high energy density.Nonetheless,the"shuttle effect"has restrained the advancement of lithium-sulfur batteries.In this work,a gradient-structured nanofiber membrane with pure gelatin on one side and Super P-MoO_(2)/MoS_(2)-gelatin on the other side was created using a multi-step electrostatic spinning technique,which was applied for multi-functional separator for lithium-sulfur batteries.The pure gelatin layer facing the anode side primarily homogenizes the lithium flux,whereas the Super P-MoO_(2)/MoS_(2)-gelatin layer facing the cathode side primarily adsorbs polysulfides by physical and chemical adsorption and enhancing polysulfide conversion efficiency.The findings demonstrate that even after 150 cycles at 0.2C,the lithium-sulfur battery can still sustain a discharge-specific capacity of 572.3 mAh·g^(-1).When used with Li||Li symmetric batteries,it has a cycle life of more than 1200 h.The commercialization of lithium-sulfur batteries is given a fresh idea by this straightforward preparation technique.展开更多
Considering the intrinsic advantages of natural copiousness and cost-effectiveness of potassium resource,potassium-ion batteries(KIBs) are booming as prospective alternatives to lithium-ion batteries(LIBs) in large-sc...Considering the intrinsic advantages of natural copiousness and cost-effectiveness of potassium resource,potassium-ion batteries(KIBs) are booming as prospective alternatives to lithium-ion batteries(LIBs) in large-scale energy storage scenarios. Nevertheless, lacking desirable electrodes for reversibly hosting the bulky K+hinders the widespread application of KIBs, and it needs to be urgently solved. Hereon, the porous S-doped Sb_(2)O_(3)-graphene-carbon(SAGC) nanofibers are manufactured through an adjustable and facile approach, which involves electrospinning, in situ etching and sulfuration. The synthesized SAGC is featured by the ultra-small amorphous Sb_(2)O_(3) homogeneously wrapped inside the carbon matrix, as well as the co-incorporation of graphene and sulfur. Tentatively,the SAGC nanofiber sheets are applied as binder-free anodes for KIBs, exhibiting a prominent cycling life(256.72 m Ah·g^(-1) over 150 cycles at 100 m A·g^(-1)) and rate·g^(-1) over 100 cycles at 1 A·g^(-1)). The positive synergy among all the active components accounts for the distinguished performances of the SAGC. By reinforcing the tolerability to the swelling stress, producing the valid electrochemical active sites, and promoting the charge transferring for reversible K+uptake, the SAGC finally renders the excellent cyclability, capacity, and rate capability. Moreover, the extrinsic electrochemical pseudocapacitance characteristics induced by the porous carbon substrate elevate the K-storage capacity of the SAGC as well. It is hoped that the conclusions drawn may offer new insights into a direction for the high-performance binderfree KIB anodes.展开更多
The unique characteristics of nanofibers in rational electrode design enable effec-tive utilization and maximizing material properties for achieving highly efficient and sustainable CO_(2) reduction reactions( CO_(2)R...The unique characteristics of nanofibers in rational electrode design enable effec-tive utilization and maximizing material properties for achieving highly efficient and sustainable CO_(2) reduction reactions( CO_(2)RRs)in solid oxide elec-trolysis cells(SOECs).However,practical appli-cation of nanofiber-based electrodes faces chal-lenges in establishing sufficient interfacial contact and adhesion with the dense electrolyte.To tackle this challenge,a novel hybrid nanofiber electrode,La_(0.6)Sr_(0.4)Co_(0.15)Fe_(0.8)Pd_(0.05)O_(3-δ)(H-LSCFP),is developed by strategically incorporating low aspect ratio crushed LSCFP nanofibers into the excess porous interspace of a high aspect ratio LSCFP nanofiber framework synthesized via electrospinning technique.After consecutive treatment in 100% H_(2) and CO_(2) at 700°C,LSCFP nanofibers form a perovskite phase with in situ exsolved Co metal nanocatalysts and a high concentration of oxygen species on the surface,enhancing CO_(2) adsorption.The SOEC with the H-LSCFP electrode yielded an outstanding current density of 2.2 A cm^(-2) in CO_(2) at 800°C and 1.5 V,setting a new benchmark among reported nanofiber-based electrodes.Digital twinning of the H-LSCFP reveals improved contact adhesion and increased reaction sites for CO_(2)RR.The present work demonstrates a highly catalytically active and robust nanofiber-based fuel electrode with a hybrid structure,paving the way for further advancements and nanofiber applications in CO_(2)-SOECs.展开更多
SnO2 nanofibers were synthesized by electrospinning and modified with Co3O4 via impregnation in this work. Chemical composition and morphology of the nanofibers were system- atically characterized, and their gas sensi...SnO2 nanofibers were synthesized by electrospinning and modified with Co3O4 via impregnation in this work. Chemical composition and morphology of the nanofibers were system- atically characterized, and their gas sensing properties were investigated. Results showed that Co3O4 modification significantly enhanced the sensing performance of SnO2 nanofibers to ethanol gas. For a sample with 1.2 mol% Co3O4, the response to 100 ppm ethanol was 38.0 at 300 ℃, about 6.7 times larger than that of SnO2 nanofibers. In addition, the response/recovery time was also greatly reduced. A power-law dependence of the sensor response on the ethanol concentration as well as excellent ethanol selectivity was observed for the Co3O4/SnO2 sensor. The enhanced ethanol sensing performance may be attributed to the formation of p-n heterojunctions between the two oxides.展开更多
A lightweight flexible thermally stable composite is fabricated by com-bining silica nanofiber membranes(SNM)with MXene@c-MWCNT hybrid film.The flexible SNM with outstanding thermal insulation are prepared from tetrae...A lightweight flexible thermally stable composite is fabricated by com-bining silica nanofiber membranes(SNM)with MXene@c-MWCNT hybrid film.The flexible SNM with outstanding thermal insulation are prepared from tetraethyl orthosilicate hydrolysis and condensation by electrospinning and high-temperature calcination;the MXene@c-MWCNT_(x:y)films are prepared by vacuum filtration tech-nology.In particular,the SNM and MXene@c-MWCNT_(6:4)as one unit layer(SMC_(1))are bonded together with 5 wt%polyvinyl alcohol(PVA)solution,which exhibits low thermal conductivity(0.066 W m^(-1)K^(-1))and good electromagnetic interference(EMI)shielding performance(average EMI SE_(T),37.8 dB).With the increase in func-tional unit layer,the overall thermal insulation performance of the whole composite film(SMC_(x))remains stable,and EMI shielding performance is greatly improved,especially for SMC_(3)with three unit layers,the average EMI SET is as high as 55.4 dB.In addition,the organic combination of rigid SNM and tough MXene@c-MWCNT_(6:4)makes SMC_(x)exhibit good mechanical tensile strength.Importantly,SMC_(x)exhibit stable EMI shielding and excellent thermal insulation even in extreme heat and cold environment.Therefore,this work provides a novel design idea and important reference value for EMI shielding and thermal insulation components used in extreme environmental protection equipment in the future.展开更多
Traditional ceramic materials are generally brittle and not flexible with high production costs,which seriously hinders their practical applications.Multifunctional nanofiber ceramic aerogels are highly desirable for ...Traditional ceramic materials are generally brittle and not flexible with high production costs,which seriously hinders their practical applications.Multifunctional nanofiber ceramic aerogels are highly desirable for applications in extreme environments,however,the integration of multiple functions in their preparation is extremely challenging.To tackle these challenges,we fabricated a multifunctional SiC@SiO_(2) nanofiber aerogel(SiC@SiO_(2) NFA)with a threedimensional(3D)porous cross-linked structure through a simple chemical vapor deposition method and subsequent heat-treatment process.The as-prepared SiC@SiO_(2) NFA exhibits an ultralow density(~11 mg cm^(-3)),ultra-elastic,fatigue-resistant and refractory performance,high temperature thermal stability,thermal insulation properties,and significant strain-dependent piezoresistive sensing behavior.Furthermore,the SiC@SiO_(2) NFA shows a superior electromagnetic wave absorption performance with a minimum refection loss(RL_(min))value of-50.36 d B and a maximum effective absorption bandwidth(EAB_(max))of 8.6 GHz.The successful preparation of this multifunctional aerogel material provides a promising prospect for the design and fabrication of the cutting-edge ceramic materials.展开更多
The development of well-defined TiO2 nanoarchitectures is a versatile strategy to achieve high-efficiency photocatalytic performance.In this study,mesoporous TiO2 nanofibers consisting of oriented nanocrystals were fa...The development of well-defined TiO2 nanoarchitectures is a versatile strategy to achieve high-efficiency photocatalytic performance.In this study,mesoporous TiO2 nanofibers consisting of oriented nanocrystals were fabricated by a facile vapothermal-assisted topochemical transformation of preformed H-titanate nanobelts.The vapothermal temperature is crucial in tuning the microstructures and photocatalytic redox properties of the resulting mesoporous TiO2 nanofibers.The microstructures were characterized with XRD,TEM,XPS and nitrogen adsorption-desorption isotherms,etc.The photocatalytic activities were evaluated by photocatalytic oxidation of organic pollutant(Rhodamine B as an example)as well as photocatalytic reduction of water to generate hydrogen(H2).The nanofibers vapothermally treated at 150°C showed the highest photocatalytic activity in both oxidation and reduction reactions,2 times higher than that of P25.The oriented alignment and suitable mesoporosity in the resulting nanofiber architecture were crucial for enhancing photocatalytic performances.The oriented alignment of anisotropic anatase nanocrystals shall facilitate faster vectorial charge transportation along the nanofibers architecture.And,the suitable mesoporosity and high surface area would also effectively enhance the mass exchange during photocatalytic reactions.We also demonstrate that efficient energy-recovering photocatalytic water treatments could be accomplished by a cascading oxic-anoxic process where the dye is degraded in the oxic phase and hydrogen is generated in the successive anoxic phase.This study showcases a novel and facile method to fabricate mesoporous TiO2 nanofibers with high photocatalytic activity for both clean energy production and environmental purification.展开更多
Antimony-based materials have become promising anodes within lithium-ion batteries(LIBs)due to their low cost and the high theoretical capacity.However,there is a potential to further enhance the electrochemical perfo...Antimony-based materials have become promising anodes within lithium-ion batteries(LIBs)due to their low cost and the high theoretical capacity.However,there is a potential to further enhance the electrochemical performance of such antimony-based materials.Herein,Sb2Se3@C nanofibers(Sb2Se3@CNFs)are designed and obtained via a novel electrospinning method.Upon electrochemically testing as an anode within LIBs,the Sb2Se3@CNFs(annealed at 600℃)delivers a remarkably good cycling performance of 625 mAh/g at 100 mA/g after 100 cycles.Moreover,it still remains at 490 mAh/g after 500 cycles with an applied current density of 1.0 A/g.The excellent performance of the Sb2 Se3@CNFs can be attributed to the fact that the N-doped C matrices not only remit the volume expansion of materials,but also enhance the electrical and ionic conductivity thusly increasing the lithium-ion diffusion.The obtained Sb2Se3@CNFs are promising anode for LIBs in the future.展开更多
Hierarchically structured nanomaterials have attracted much attention owing to their unique properties.In this study,TiO2 nanofibers assembled from nanosheets(TiO2-NFs-NSs)were fabricated through electrospinning techn...Hierarchically structured nanomaterials have attracted much attention owing to their unique properties.In this study,TiO2 nanofibers assembled from nanosheets(TiO2-NFs-NSs)were fabricated through electrospinning technique,which was followed by hydrothermal treatment in NaOH solution.The effect of hydrothermal reaction time(0-3 h)on the structure and properties of TiO2 nanofibers(TiO2-NFs)was systematically studied,and TiO2-NFs was evaluated in terms of the photocatalytic activity toward photocatalytic oxidation of acetone and the photoelectric conversion efficiency of dye-sensitized solar cells.It was found that(1)hydrothermal treatment of TiO2-NFs in NaOH solution followed by acid washing and calcination results in the formation of TiO2-NFs-NSs;(2)upon extending the hydrothermal reaction time from 0 h to 3 h,the BET surface area of TiO2-NFs-NSs(T3.0 sample)increases 3.8 times(from 28 to 106 m2 g^-1),while the pore volume increases 6.0 times(from 0.09 to 0.54 cm3 g^-1);(3)when compared with those of pristine TiO2-NFs(T0 sample),the photoreactivity of the optimized TiO2-NFs-NSs toward acetone oxidation increases 3.1 times and the photoelectric conversion efficiency increases 2.3 times.The enhanced photoreactivity of TiO2-NFs-NSs is attributed to the enlarged BET surface area and increased pore volume,which facilitate the adsorption of substrate and penetration of gas,and the unique hollow structure of TiO2-NFs-NSs,which facilitates light harvesting through multiple optical reflections between the TiO2 nanosheets.展开更多
In this work,nickel/T-Nb_(2)O_(5)nanoparticles encapsulated in mesoporous carbon nanofibers(denoted as Ni/T-Nb_(2)O_(5)@CNFs)are successfully prepared through a simple electrospinning route and succedent heating treat...In this work,nickel/T-Nb_(2)O_(5)nanoparticles encapsulated in mesoporous carbon nanofibers(denoted as Ni/T-Nb_(2)O_(5)@CNFs)are successfully prepared through a simple electrospinning route and succedent heating treatment.The presence of Ni in carbon nanofibers is beneficial for enhancing the electronic conductivity and the initial Coulombic efficiency.Ni/T-Nb_(2)O_(5)nanoparticles are homogeneously incorporated in carbon nanofibers to form a nanocomposite system,which provides effective buffering during the lithiation/delithiation process for cycling stability.The Ni/TNb_(2)O_(5)@CNFs show high surface area(26.321 m^(2)·g^(-1))and mesoporous microstructure,resulting in higher capacity and excellent rate performance.The Ni/T-Nb_(2)O_(5)@CNFs exhibit a remarkable capacity of 437 mAh·g^(-1)at a current density of0.5 A·g^(-1)after 230 cycles and a capacity of 173 mAh·g^(-1)at a current density up to 10.0 A·g^(-1)after 1400 cycles.This work indicates that nickel/T-Nb_(2)O_(5)nanoparticles encapsulated in carbon nanofibers can be a promising candidate for anode material in high-power LIBs.展开更多
Porous TiO2/ZnO composite nanofibers have been successfully prepared by electrospinning technique for the first time.It was generated by calcining TiO2/ZnCl2/PVP[PVP：polyvinyl pyrrolidone）]nanofibers,which were elec...Porous TiO2/ZnO composite nanofibers have been successfully prepared by electrospinning technique for the first time.It was generated by calcining TiO2/ZnCl2/PVP[PVP：polyvinyl pyrrolidone）]nanofibers,which were electrospun from a mixture solution of TiO2,ZnCl2 and PVP.Transmission electron microscopy（TEM） and X-ray diffraction（XRD） analyses were used to identify the morphology of the TiO2/ZnO nanofibers and a formation of inorganic TiO2/ZnO fibers.The porous structure of the TiO2/ZnO fibers was characterized by N2 adsoption/desorption isotherm.Surface photovoltage spectroscopy（SPS） and photocatalytic activity measurements revealed advance properties of the porous TiO2/ZnO composite nanofibers and the results were compared with pure TiO2 nanofibers,pure ZnO nanofibers and TiO2/ZnO nanoparticles.展开更多
Pseudo-capacitive mechanisms can provide higher energy densities than electrical double-layer capacitors while being faster than bulk storage mechanisms.Usually,they suffer from low intrinsic electronic and ion conduc...Pseudo-capacitive mechanisms can provide higher energy densities than electrical double-layer capacitors while being faster than bulk storage mechanisms.Usually,they suffer from low intrinsic electronic and ion conductivities of the active materials.Here,taking advantage of the combination of TiS2 decoration,sulfur doping,and a nanometer-sized structure,as-spun TiO2/C nanofiber composites are developed that enable rapid transport of sodium ions and electrons,and exhibit enhanced pseudo-capacitively dominated capacities.At a scan rate of 0.5 mV s−1,a high pseudo-capacitive contribution(76%of the total storage)is obtained for the S-doped TiS2/TiO2/C electrode(termed as TiS2/S-TiO2/C).Such enhanced pseudocapacitive activity allows rapid chemical kinetics and significantly improves the high-rate sodium storage performance of TiO2.The TiS2/S-TiO2/C composite electrode delivers a high capacity of 114 mAh g−1 at a current density of 5000 mA g−1.The capacity maintains at high level(161 mAh g−1)even after 1500 cycles and is still characterized by 58 mAh g−1 at the extreme condition of 10,000 mA g−1 after 10,000 cycles.展开更多
Electrocatalytic N2 reduction to NH3 under ambient conditions is an eco-friendly and sustainable alternative to the traditional Haber-Bosch process. However, inhibited by the high activation barrier of N2, this proces...Electrocatalytic N2 reduction to NH3 under ambient conditions is an eco-friendly and sustainable alternative to the traditional Haber-Bosch process. However, inhibited by the high activation barrier of N2, this process needs efficient electrocatalysts to adsorb and activate the N2, enabling the N2 reduction reaction(NRR). Herein, we report that porous LaFeO3 nanofiber with oxygen vacancies acts as an efficient NRR electrocatalyst with abundant active sites to enhance the adsorption and activation of N2. When tested in 0.1 M HCl, such electrocatalyst achieves a high Faradaic efficiency of 8.77% and a large NH3 yield rate of 18.59 μg h–1 mgcat–1.at-0.55 V versus reversible hydrogen electrode. This catalyst also shows high long-term electrochemical stability and excellent selectivity for NH3 formation. Density functional theory calculations reveal that, by introducing oxygen vacancy on LaFeO3, the subsurface metallic ions are exposed with newly localized electronic states near the Fermi level, which facilitates the adsorption and activation of N2 molecules as well as the subsequent hydrogenation reactions.展开更多
文摘The need for bi-functional catalysts that facilit-ate both the oxygen reduction(ORR)and carbon dioxide re-duction(CO_(2)RR)reactions arises from their potential to help solve the critical problems of carbon neutrality and renew-able energy conversion.However,there are few reports on the development of bi-functional catalysts for zinc-air bat-tery-driven CO_(2)RR devices.We introduce a novel approach for synthesizing Fe_(2)N/Fe_(3)C species embedded in nitrogen-doped carbon nanofibers by electrospinning a solution of Hemin and polyacrylonitrile in N,N-dimethylformamide.The material has an exceptional catalytic performance,with a half-wave potential of 0.91 V versus RHE for the ORR and values of over 90%for both the selectivity and Faradaic efficiency for the CO_(2)RR.The high catalytic performances are attrib-uted to the strong coupling between the Fe_(3)C/Fe_(2)N heterostructure and the Fe-N-C sites in the nitrogen-doped carbon nan-ofibers.Notably,both Fe_(3)C and Fe_(2)N play distinct roles in both the ORR and CO_(2)RR.This investigation indicates a way for designing advanced carbon-based bi-functional catalysts for use in this field.
基金financially supported by the National Natural Science Foundation of China(22278348)Natural Science Foundation of Xinjiang Autonomous Region(2022D01D05)+1 种基金National guidance for local projects of Xinjiang Autonomous Region(ZYYD2025JD09)Tianshan Leading technology talents Program of Xinjiang Autonomous Region。
文摘Sodium-ion batteries(SIBs)show promising potential in the field of electrochemical energy storage due to their cost-effectiveness and similar operational mechanisms to lithium-ion batteries(LIBs).However,the dramatic volume expansion of electrode materials and the slow reaction kinetics caused by the large sodium ion(Na^(+))radius hinder the practical application of SIBs,Here,we successfully prepared SnS_(2-x)Se_(x)nanodots embedded within N-doped carbon nanofibers(CNF)for use as electrode materials of SIBs,The introduction Se provided abundant anionic defect sites for Na+storage and enlarged the interlayer spacing of SnS_(2).In addition,the ultraifne nanodot structure reduces the volume expansion of SnS_(2-x)Se_(x)and shortens the ion transport path.As an anode of SIBs,SnS_(2-x)Se_(x)/CNF demonstrates remarkable reversible capacity(719 mAh g^(-1)at 0.5 A g^(-1)),along with rapid charging ability(completing a charge in just 127 s).Meanwhile,the assembled full-cell battery manifested exceptional energy density of 165.8 Wh kg^(-1)at a high-power output of 5526 W kg^(-1).This study presents an effective strategy for fabricating highperformance sulphide-based anode materials for SIBs,offering broad prospects for application.
基金supported by the National Natural Science Foundation of China(Nos.52003297 and 22302233)the Open Project of State Key Laboratory of Chemical Safety(No.SKLCS-2024020)+2 种基金the National Key R&D Program of China(Nos.2022YFB3205501 and 2022YFB3205504)and the Fundamental Research Funds for the Central Universities(No.24CX02014A)the Fund of State Key Laboratory of Deep Oil and Gas,China University of Petroleum(East China).
文摘Based on the unique catalytic properties of precious metals,the introduction of precious metals into metal oxide semiconductors will greatly improve the gas-sensitive properties of materials.As a new type of porous material,metal–organic frameworks(MOF)can be used for gas separation and adsorption due to their adjustable pore size and acceptable thermal stability.In this work,the ZIF-71 MOF was synthesized on CuO nanofibers doped with different concentrations of Ru to form a Ru–CuO@ZIF-71 nanocomposite sensor,which was then used for H_(2)S detection.The sensor shows sensitivity to trace amounts of H_(2)S gas(100 ppb),and the response is greatly enhanced at the optimal Ru doping ratio and operating temperature.The introduction of the ZIF-71 membrane can significantly increase the selectivity of the sensor while further improving the sensitivity.Finally,the possible sensing mechanism of the Ru–CuO@ZIF-71 sensor was explored.The enhancement of the H_(2)S gas sensing properties may be attributed to the catalysis of Ru and the formation of the Schottky junction at the Ru–CuO interface.Besides,the calculation based on density functional theory reveals enhanced adsorption capacities of CuO for H_(2)S after Ru doping.Therefore,the Ru–CuO@ZIF-71 sensor has strong application potential in exhaled gas detection and portable detection of H_(2)S gas in industrial environments.
基金supported by the National Natural Science Foundation of China(22222601 and 22076019)the Fundamental Research Funds for the Central Universities(DUT23LAB611).
文摘The Cu^(+)/Cu^(0)sites of copper-based catalysts are crucial for enhancing the production of multicarbon(C_(2+))products from electrochemical CO_(2)reduction reaction(eCO_(2)RR).However,the unstable Cu^(+)and insufficient Cu^(+)/Cu^(0)active sites lead to their limited selectivity and stability for C_(2+)production.Herein,we embedded copper oxide(CuO_(x))particles into porous nitrogen-doped carbon nanofibers(CuO_(x)@PCNF)by pyrolysis of the electrospun fiber film containing ZIF-8 and Cu_(2)O particles.The porous nitrogendoped carbon nanofibers protected and dispersed Cu^(+)species,and its micro porous structure enhanced the interaction between CuO_(x)and reactants during eCO_(2)RR.The obtained CuO_(x)@PCNF created more effective and stable Cu^(+)/Cu^(0)active sites.It showed a high Faradaic efficiency of 62.5%for C_(2+)products in Hcell,which was 2 times higher than that of bare CuO_(x)(~31.1%).Furthermore,it achieved a maximum Faradaic efficiency of 80.7%for C_(2+)products in flow cell.In situ characterization and density functional theory(DFT)calculation confirmed that the N-doped carbon layer protected Cu^(+)from electrochemical reduction and lowered the energy barrier for the dimerization of^(*)CO.Stable and exposed Cu^(+)/Cu^(0)active sites enhanced the enrichment of^(*)CO and promoted the C-C coupling reaction on the catalyst surface,which facilitated the formation of C_(2+)products.
文摘Piezocatalytic hydrogen peroxide(H_(2)O_(2))generation is a promising synthesis method that has received increasing attention;however,the reaction pathway requires further investigation.Here,Bi_(5)Ti_(3)FeO_(15)nanofibers are used to generate H_(2)O_(2)by harvesting mechanical energy,and the reaction pathways are investigated.The H_(2)O_(2)yield over Bi_(5)Ti_(3)FeO_(15)nanofibers steadily increases from 331μmol g1 h1 in the first cycle to 746μmol g1 h1 in the tenth cycle in pure water without a sacrificial agent.Reliable reaction pathways are revealed by monitoring the pH value changes in the reaction solution during the H_(2)O_(2)generation process.In the H_(2)O_(2)generation process,the water oxidation reaction(WOR)provides a large amount of H+in the reaction solution,which promotes the oxygen reduction reaction(ORR)for H_(2)O_(2)generation.Therefore,an efficient synergistic effect between ORR and WOR achieves dual-pathway H_(2)O_(2)generation,contributing to the excellent piezocatalytic performance of Bi_(5)Ti_(3)FeO_(15)nanofibers.Furthermore,mechanistic studies indicate that the piezocatalytic H_(2)O_(2)generation follows the energy band theory.This work not only demonstrates Bi_(5)Ti_(3)FeO_(15)nanofibers as efficient piezocatalysts for H_(2)O_(2)generation but also provides a simple and effective approach to elucidate reaction pathways.This approach can be applied in photocatalytic,tribocatalytic,and electrocatalytic H_(2)O_(2)generation.
基金financially supported by the Anhui Provincial Natural Science Foundation(Nos.2208085ME108,1708085QE98 and 2008085QE27)University Synergy Innovation Program of Anhui Province(No.GXXT-2023-024)+7 种基金Project for Cultivating Academic(or Disciplinary)Leaders(No.DTR2023043)Talent Scientific Research Foundation of Hefei University(No.23RC29)National Natural Science Foundation of China(Nos.21606065 and 51902079)University Natural Science Research Project of Anhui Province(Nos.KJ2021A1016,2022AH051788 and2022AH051792)the Natural Science Research Project of Education Department of Anhui Province(No.2022AH010096)University excellent talent program of Anhui Province(Nos.gxyqZD2021136and qxyq2021228)the Top Discipline Talents Foundation of Anhui Province Educational Committee(No.gxbjZD2021085)the Key Projects of Research and Development Program of Anhui Provence(No.201904b11020040)。
文摘Lithium-sulfur battery is one of the most promising battery systems for industrialization due to its high theoretical specific capacity and high energy density.Nonetheless,the"shuttle effect"has restrained the advancement of lithium-sulfur batteries.In this work,a gradient-structured nanofiber membrane with pure gelatin on one side and Super P-MoO_(2)/MoS_(2)-gelatin on the other side was created using a multi-step electrostatic spinning technique,which was applied for multi-functional separator for lithium-sulfur batteries.The pure gelatin layer facing the anode side primarily homogenizes the lithium flux,whereas the Super P-MoO_(2)/MoS_(2)-gelatin layer facing the cathode side primarily adsorbs polysulfides by physical and chemical adsorption and enhancing polysulfide conversion efficiency.The findings demonstrate that even after 150 cycles at 0.2C,the lithium-sulfur battery can still sustain a discharge-specific capacity of 572.3 mAh·g^(-1).When used with Li||Li symmetric batteries,it has a cycle life of more than 1200 h.The commercialization of lithium-sulfur batteries is given a fresh idea by this straightforward preparation technique.
基金financially supported by the National Natural Science Foundation of China (Nos.51404103,51574117 and 61376073)Hunan Provincial Education Department(No.20C0613)the College Student Innovation and Entrepreneurship Training Program of Hunan Province (No.S2022115350874)。
文摘Considering the intrinsic advantages of natural copiousness and cost-effectiveness of potassium resource,potassium-ion batteries(KIBs) are booming as prospective alternatives to lithium-ion batteries(LIBs) in large-scale energy storage scenarios. Nevertheless, lacking desirable electrodes for reversibly hosting the bulky K+hinders the widespread application of KIBs, and it needs to be urgently solved. Hereon, the porous S-doped Sb_(2)O_(3)-graphene-carbon(SAGC) nanofibers are manufactured through an adjustable and facile approach, which involves electrospinning, in situ etching and sulfuration. The synthesized SAGC is featured by the ultra-small amorphous Sb_(2)O_(3) homogeneously wrapped inside the carbon matrix, as well as the co-incorporation of graphene and sulfur. Tentatively,the SAGC nanofiber sheets are applied as binder-free anodes for KIBs, exhibiting a prominent cycling life(256.72 m Ah·g^(-1) over 150 cycles at 100 m A·g^(-1)) and rate·g^(-1) over 100 cycles at 1 A·g^(-1)). The positive synergy among all the active components accounts for the distinguished performances of the SAGC. By reinforcing the tolerability to the swelling stress, producing the valid electrochemical active sites, and promoting the charge transferring for reversible K+uptake, the SAGC finally renders the excellent cyclability, capacity, and rate capability. Moreover, the extrinsic electrochemical pseudocapacitance characteristics induced by the porous carbon substrate elevate the K-storage capacity of the SAGC as well. It is hoped that the conclusions drawn may offer new insights into a direction for the high-performance binderfree KIB anodes.
基金This work was supported by the National Research Foundation of Korea(NRF)grant funded by the Korean Government(MSIT)(2019M3E6A1103944,2020R1A2C2010690).
文摘The unique characteristics of nanofibers in rational electrode design enable effec-tive utilization and maximizing material properties for achieving highly efficient and sustainable CO_(2) reduction reactions( CO_(2)RRs)in solid oxide elec-trolysis cells(SOECs).However,practical appli-cation of nanofiber-based electrodes faces chal-lenges in establishing sufficient interfacial contact and adhesion with the dense electrolyte.To tackle this challenge,a novel hybrid nanofiber electrode,La_(0.6)Sr_(0.4)Co_(0.15)Fe_(0.8)Pd_(0.05)O_(3-δ)(H-LSCFP),is developed by strategically incorporating low aspect ratio crushed LSCFP nanofibers into the excess porous interspace of a high aspect ratio LSCFP nanofiber framework synthesized via electrospinning technique.After consecutive treatment in 100% H_(2) and CO_(2) at 700°C,LSCFP nanofibers form a perovskite phase with in situ exsolved Co metal nanocatalysts and a high concentration of oxygen species on the surface,enhancing CO_(2) adsorption.The SOEC with the H-LSCFP electrode yielded an outstanding current density of 2.2 A cm^(-2) in CO_(2) at 800°C and 1.5 V,setting a new benchmark among reported nanofiber-based electrodes.Digital twinning of the H-LSCFP reveals improved contact adhesion and increased reaction sites for CO_(2)RR.The present work demonstrates a highly catalytically active and robust nanofiber-based fuel electrode with a hybrid structure,paving the way for further advancements and nanofiber applications in CO_(2)-SOECs.
基金This work was supported by the National Natural Science Foundation of China （No.U1432108） and the Fundamental Research Funds for the Central Universities （No.WK2320000034）.
文摘SnO2 nanofibers were synthesized by electrospinning and modified with Co3O4 via impregnation in this work. Chemical composition and morphology of the nanofibers were system- atically characterized, and their gas sensing properties were investigated. Results showed that Co3O4 modification significantly enhanced the sensing performance of SnO2 nanofibers to ethanol gas. For a sample with 1.2 mol% Co3O4, the response to 100 ppm ethanol was 38.0 at 300 ℃, about 6.7 times larger than that of SnO2 nanofibers. In addition, the response/recovery time was also greatly reduced. A power-law dependence of the sensor response on the ethanol concentration as well as excellent ethanol selectivity was observed for the Co3O4/SnO2 sensor. The enhanced ethanol sensing performance may be attributed to the formation of p-n heterojunctions between the two oxides.
基金the China Scholarship Council(2021)the Deanship of Scientific Research at Northern Border University,Arar,KSA for funding this research work through the project number“NBU-FPEJ-2024-249-03”.
文摘A lightweight flexible thermally stable composite is fabricated by com-bining silica nanofiber membranes(SNM)with MXene@c-MWCNT hybrid film.The flexible SNM with outstanding thermal insulation are prepared from tetraethyl orthosilicate hydrolysis and condensation by electrospinning and high-temperature calcination;the MXene@c-MWCNT_(x:y)films are prepared by vacuum filtration tech-nology.In particular,the SNM and MXene@c-MWCNT_(6:4)as one unit layer(SMC_(1))are bonded together with 5 wt%polyvinyl alcohol(PVA)solution,which exhibits low thermal conductivity(0.066 W m^(-1)K^(-1))and good electromagnetic interference(EMI)shielding performance(average EMI SE_(T),37.8 dB).With the increase in func-tional unit layer,the overall thermal insulation performance of the whole composite film(SMC_(x))remains stable,and EMI shielding performance is greatly improved,especially for SMC_(3)with three unit layers,the average EMI SET is as high as 55.4 dB.In addition,the organic combination of rigid SNM and tough MXene@c-MWCNT_(6:4)makes SMC_(x)exhibit good mechanical tensile strength.Importantly,SMC_(x)exhibit stable EMI shielding and excellent thermal insulation even in extreme heat and cold environment.Therefore,this work provides a novel design idea and important reference value for EMI shielding and thermal insulation components used in extreme environmental protection equipment in the future.
基金financially supported by the National Natural Science Foundation of China(No.U2004177 and U21A2064)Outstanding Youth Fund of Henan Province(No.212300410081)+1 种基金Scientific and Technological Innovation Talents in Colleges and Universities in Henan Province(22HASTIT001)The Research and Entrepreneurship Start-up Projects for Overseas Returned Talents。
文摘Traditional ceramic materials are generally brittle and not flexible with high production costs,which seriously hinders their practical applications.Multifunctional nanofiber ceramic aerogels are highly desirable for applications in extreme environments,however,the integration of multiple functions in their preparation is extremely challenging.To tackle these challenges,we fabricated a multifunctional SiC@SiO_(2) nanofiber aerogel(SiC@SiO_(2) NFA)with a threedimensional(3D)porous cross-linked structure through a simple chemical vapor deposition method and subsequent heat-treatment process.The as-prepared SiC@SiO_(2) NFA exhibits an ultralow density(~11 mg cm^(-3)),ultra-elastic,fatigue-resistant and refractory performance,high temperature thermal stability,thermal insulation properties,and significant strain-dependent piezoresistive sensing behavior.Furthermore,the SiC@SiO_(2) NFA shows a superior electromagnetic wave absorption performance with a minimum refection loss(RL_(min))value of-50.36 d B and a maximum effective absorption bandwidth(EAB_(max))of 8.6 GHz.The successful preparation of this multifunctional aerogel material provides a promising prospect for the design and fabrication of the cutting-edge ceramic materials.
基金supported by the National Natural Science Foundation of China(21707173,51872341,51572209)the Science and Technology Program of Guangzhou(201707010095)+2 种基金the Start-up Funds for High-Level Talents of Sun Yat-sen University(38000-31131103)the Fundamental Research Funds for the Central Universities(19lgzd29)the China Postdoctoral Science Foundation(2017M622869)~~
文摘The development of well-defined TiO2 nanoarchitectures is a versatile strategy to achieve high-efficiency photocatalytic performance.In this study,mesoporous TiO2 nanofibers consisting of oriented nanocrystals were fabricated by a facile vapothermal-assisted topochemical transformation of preformed H-titanate nanobelts.The vapothermal temperature is crucial in tuning the microstructures and photocatalytic redox properties of the resulting mesoporous TiO2 nanofibers.The microstructures were characterized with XRD,TEM,XPS and nitrogen adsorption-desorption isotherms,etc.The photocatalytic activities were evaluated by photocatalytic oxidation of organic pollutant(Rhodamine B as an example)as well as photocatalytic reduction of water to generate hydrogen(H2).The nanofibers vapothermally treated at 150°C showed the highest photocatalytic activity in both oxidation and reduction reactions,2 times higher than that of P25.The oriented alignment and suitable mesoporosity in the resulting nanofiber architecture were crucial for enhancing photocatalytic performances.The oriented alignment of anisotropic anatase nanocrystals shall facilitate faster vectorial charge transportation along the nanofibers architecture.And,the suitable mesoporosity and high surface area would also effectively enhance the mass exchange during photocatalytic reactions.We also demonstrate that efficient energy-recovering photocatalytic water treatments could be accomplished by a cascading oxic-anoxic process where the dye is degraded in the oxic phase and hydrogen is generated in the successive anoxic phase.This study showcases a novel and facile method to fabricate mesoporous TiO2 nanofibers with high photocatalytic activity for both clean energy production and environmental purification.
基金supported by the National Natural Science Foundation of China(No.51302079)the Natural Science Foundation of Hunan Province(No.2017JJ1008)。
文摘Antimony-based materials have become promising anodes within lithium-ion batteries(LIBs)due to their low cost and the high theoretical capacity.However,there is a potential to further enhance the electrochemical performance of such antimony-based materials.Herein,Sb2Se3@C nanofibers(Sb2Se3@CNFs)are designed and obtained via a novel electrospinning method.Upon electrochemically testing as an anode within LIBs,the Sb2Se3@CNFs(annealed at 600℃)delivers a remarkably good cycling performance of 625 mAh/g at 100 mA/g after 100 cycles.Moreover,it still remains at 490 mAh/g after 500 cycles with an applied current density of 1.0 A/g.The excellent performance of the Sb2 Se3@CNFs can be attributed to the fact that the N-doped C matrices not only remit the volume expansion of materials,but also enhance the electrical and ionic conductivity thusly increasing the lithium-ion diffusion.The obtained Sb2Se3@CNFs are promising anode for LIBs in the future.
基金supported by the National Natural Science Foundation of China(51672312,21373275)the Fundamental Research Funds for the Central Universities,South-Central University for Nationalities(CZT19006)~~
文摘Hierarchically structured nanomaterials have attracted much attention owing to their unique properties.In this study,TiO2 nanofibers assembled from nanosheets(TiO2-NFs-NSs)were fabricated through electrospinning technique,which was followed by hydrothermal treatment in NaOH solution.The effect of hydrothermal reaction time(0-3 h)on the structure and properties of TiO2 nanofibers(TiO2-NFs)was systematically studied,and TiO2-NFs was evaluated in terms of the photocatalytic activity toward photocatalytic oxidation of acetone and the photoelectric conversion efficiency of dye-sensitized solar cells.It was found that(1)hydrothermal treatment of TiO2-NFs in NaOH solution followed by acid washing and calcination results in the formation of TiO2-NFs-NSs;(2)upon extending the hydrothermal reaction time from 0 h to 3 h,the BET surface area of TiO2-NFs-NSs(T3.0 sample)increases 3.8 times(from 28 to 106 m2 g^-1),while the pore volume increases 6.0 times(from 0.09 to 0.54 cm3 g^-1);(3)when compared with those of pristine TiO2-NFs(T0 sample),the photoreactivity of the optimized TiO2-NFs-NSs toward acetone oxidation increases 3.1 times and the photoelectric conversion efficiency increases 2.3 times.The enhanced photoreactivity of TiO2-NFs-NSs is attributed to the enlarged BET surface area and increased pore volume,which facilitate the adsorption of substrate and penetration of gas,and the unique hollow structure of TiO2-NFs-NSs,which facilitates light harvesting through multiple optical reflections between the TiO2 nanosheets.
基金the National Natural Science Foundation of China(Nos.51771236,51901249,U1904216)the Science Fund for Distinguished Young Scholars of Hunan Province(No.2018JJ1038)。
文摘In this work,nickel/T-Nb_(2)O_(5)nanoparticles encapsulated in mesoporous carbon nanofibers(denoted as Ni/T-Nb_(2)O_(5)@CNFs)are successfully prepared through a simple electrospinning route and succedent heating treatment.The presence of Ni in carbon nanofibers is beneficial for enhancing the electronic conductivity and the initial Coulombic efficiency.Ni/T-Nb_(2)O_(5)nanoparticles are homogeneously incorporated in carbon nanofibers to form a nanocomposite system,which provides effective buffering during the lithiation/delithiation process for cycling stability.The Ni/TNb_(2)O_(5)@CNFs show high surface area(26.321 m^(2)·g^(-1))and mesoporous microstructure,resulting in higher capacity and excellent rate performance.The Ni/T-Nb_(2)O_(5)@CNFs exhibit a remarkable capacity of 437 mAh·g^(-1)at a current density of0.5 A·g^(-1)after 230 cycles and a capacity of 173 mAh·g^(-1)at a current density up to 10.0 A·g^(-1)after 1400 cycles.This work indicates that nickel/T-Nb_(2)O_(5)nanoparticles encapsulated in carbon nanofibers can be a promising candidate for anode material in high-power LIBs.
基金supported in part by the National Natural Science Foundation of China(Nos.50473008 and 50673034)by Natural Science Foundation of the Jiangsu Higher Education Institutions of China(No.09KJD 150001)by DuPont Company through a Young Faculty Grant Award to Prof.C.Wang,and by Headwater Nanokinetix,Inc
文摘Porous TiO2/ZnO composite nanofibers have been successfully prepared by electrospinning technique for the first time.It was generated by calcining TiO2/ZnCl2/PVP[PVP：polyvinyl pyrrolidone）]nanofibers,which were electrospun from a mixture solution of TiO2,ZnCl2 and PVP.Transmission electron microscopy（TEM） and X-ray diffraction（XRD） analyses were used to identify the morphology of the TiO2/ZnO nanofibers and a formation of inorganic TiO2/ZnO fibers.The porous structure of the TiO2/ZnO fibers was characterized by N2 adsoption/desorption isotherm.Surface photovoltage spectroscopy（SPS） and photocatalytic activity measurements revealed advance properties of the porous TiO2/ZnO composite nanofibers and the results were compared with pure TiO2 nanofibers,pure ZnO nanofibers and TiO2/ZnO nanoparticles.
基金This work was financially supported by National Key R&D Program of China(No.2018YFB0905400)the National Natural Science Foundation of China(Nos.51925207,51872277,and U1910210)+2 种基金Dalian National Laboratory For Clean Energy(DNL)Cooperation Fund,the CAS(DNL180310)the Fundamental Research Funds for the Central Universities(Wk2060140026)Sofja Kovalevskaja award of the Humboldt Society.This project has received funding from the European Union’s Horizon 2020 research and innovation programme under Grant Agreement No.823717-ESTEEM3.
文摘Pseudo-capacitive mechanisms can provide higher energy densities than electrical double-layer capacitors while being faster than bulk storage mechanisms.Usually,they suffer from low intrinsic electronic and ion conductivities of the active materials.Here,taking advantage of the combination of TiS2 decoration,sulfur doping,and a nanometer-sized structure,as-spun TiO2/C nanofiber composites are developed that enable rapid transport of sodium ions and electrons,and exhibit enhanced pseudo-capacitively dominated capacities.At a scan rate of 0.5 mV s−1,a high pseudo-capacitive contribution(76%of the total storage)is obtained for the S-doped TiS2/TiO2/C electrode(termed as TiS2/S-TiO2/C).Such enhanced pseudocapacitive activity allows rapid chemical kinetics and significantly improves the high-rate sodium storage performance of TiO2.The TiS2/S-TiO2/C composite electrode delivers a high capacity of 114 mAh g−1 at a current density of 5000 mA g−1.The capacity maintains at high level(161 mAh g−1)even after 1500 cycles and is still characterized by 58 mAh g−1 at the extreme condition of 10,000 mA g−1 after 10,000 cycles.
基金the National Natural Science Foundation of China(Nos.21575137 and 11704005)。
文摘Electrocatalytic N2 reduction to NH3 under ambient conditions is an eco-friendly and sustainable alternative to the traditional Haber-Bosch process. However, inhibited by the high activation barrier of N2, this process needs efficient electrocatalysts to adsorb and activate the N2, enabling the N2 reduction reaction(NRR). Herein, we report that porous LaFeO3 nanofiber with oxygen vacancies acts as an efficient NRR electrocatalyst with abundant active sites to enhance the adsorption and activation of N2. When tested in 0.1 M HCl, such electrocatalyst achieves a high Faradaic efficiency of 8.77% and a large NH3 yield rate of 18.59 μg h–1 mgcat–1.at-0.55 V versus reversible hydrogen electrode. This catalyst also shows high long-term electrochemical stability and excellent selectivity for NH3 formation. Density functional theory calculations reveal that, by introducing oxygen vacancy on LaFeO3, the subsurface metallic ions are exposed with newly localized electronic states near the Fermi level, which facilitates the adsorption and activation of N2 molecules as well as the subsequent hydrogenation reactions.
