检索结果-南通市图书馆

Surface reconstruction of Se-doped NiS_(2) enables high-efficiency oxygen evolution reaction

Journal of Energy Chemistry 2023年第9期84卷 173-180页

作者： Mengxin Chen Yuanyuan Zhang Ran Wang Bin Zhang Bo Song Yanchao Guan Siwei Li Ping Xu MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage School of Chemistry and Chemical EngineeringHarbin Institute of TechnologyHarbin 150001HeilongjiangChina National Key Laboratory of Science and Technology on Advanced Composites in Special Environments Harbin Institute of TechnologyHarbin 150001HeilongjiangChina Key Laboratory of Micro-systems and Micro-structures Manufacturing Ministry of EducationHarbin Institute of TechnologyHarbin 150001HeilongjiangChina Institute of Industrial Catalysis School of Chemical Engineering and TechnologyXi’an Jiaotong UniversityXi’an 710049ShaanxiChina

Surface reconstruction of electrocatalysts has been widely witnessed during the electrochemical processes.Here,NiS_(2),NiSe_(2), and Se doped NiS_(2)(Se-NiS_(2)) are fabricated for oxygen evolution reaction(OER) through a mild sulfuration and/or selenylation process of Ni(OH)_(2) supported on carbon cloth(CC).Through careful in-situ Raman spectroscopy and ex-situ X-ray photoelectron spectroscopy,surface reconstruction of NiS_(2),NiSe_(2),and Se-NiS_(2) during the OER process has been revealed.A potentialdependent study shows that Se-NiS_(2) undergoes surface evolution at lower potentials and requires the lowest potential for conversion to NiOOH as a highly OER-active species,accompanied by the leaching of SO_(4)^(2-) and SeO_(4)^(2-) that can again be adsorbed on the catalyst surface to enhance the catalytic activity.Density functional theory(DFT) calculations confirm that Se-NiS_(2) is more susceptible to surface oxidation through the OER process.Therefore,Se-NiS_(2) exhibits outstanding OER activity and stability in alkaline conditions,requiring an overpotential of 343 mV at a current density of 50 mA cm^(-2).A novel insight is provided by our work in understanding the surface reconstruction and electrocatalytic mechanism of Ni-based chalcogenides.

关键词： oxygen evolution reaction Se-NiS_(2) In-situ Raman spectroscopy Anion leaching Surface reconstruction

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Mixed iridium-nickel oxides supported on antimony-doped tin oxide as highly efficient and stable acidic oxygen evolution catalysts

Materials Futures

引用

Materials Futures 2024年第1期3卷 165-180页

作者： Jonathan Ruiz Esquius Alec P LaGrow Haiyan Jin Zhipeng Yu Ana Araujo Rita Marques Adélio Mendes Lifeng Liu Clean Energy Cluster International Iberian Nanotechnology LaboratoryAv.Mestre JoséVeigaBraga 4715-330Portugal Carbon Science and Technology Institute INCAR-CSICFrancisco Pintado Fe 26Oviedo 33011Spain Scientific Imaging Section Okinawa Institute of Science and Technology Graduate UniversityKunigami-gunOkinawa 904-0412Japan Songshan Lake Materials Laboratory Dongguan 523808People’s Republic of China Laboratory for Process Engineering EnvironmentBiotechnology and EnergyFaculty of EngineeringUniversity of PortoRua Dr Roberto FriasPorto 4200-465Portugal Associate Laboratory in Chemical Engineering Faculty of EngineeringUniversity of PortoRua Dr Roberto FriasPorto 4200-465Portugal.

Proton exchange membrane(PEM)water electrolysis represents a promising technology for green hydrogen production,but its widespread deployment is greatly hindered by the indispensable usage of platinum group metal catalysts,especially iridium(Ir)based materials for the energy-demanding oxygen evolution reaction(OER).Herein,we report a new sequential precipitation approach to the synthesis of mixed Ir-nickel(Ni)oxy-hydroxide supported on antimony-doped tin oxide(ATO)nanoparticles(IrNiyO_(x)/ATO,20 wt.%(Ir+Ni),y=0,1,2,and 3),aiming to reduce the utilisation of scarce and precious Ir while maintaining its good acidic OER performance.When tested in strongly acidic electrolyte(0.1 M HClO_(4)),the optimised IrNi1Ox/ATO shows a mass activity of 1.0 mAµgIr^(−1) and a large turnover frequency of 123 s^(−1) at an overpotential of 350 mV,as well as a comparatively small Tafel slope of 50 mV dec^(−1),better than the IrOx/ATO control,particularly with a markedly reduced Ir loading of only 19.7µgIr cm^(−2).Importantly,IrNi1O_(x)/ATO also exhibits substantially better catalytic stability than other reference catalysts,able to continuously catalyse acidic OER at 10 mA cm^(−2) for 15 h without obvious degradation.Our in-situ synchrotron-based x-ray absorption spectroscopy confirmed that the Ir^(3+)/Ir^(4+)species are the active sites for the acidic OER.Furthermore,the performance of IrNi1Ox/ATO was also preliminarily evaluated in a membrane electrode assembly,which shows better activity and stability than other reference catalysts.The IrNi1Ox/ATO reported in this work is a promising alternative to commercial IrO_(2) based catalysts for PEM electrolysis.

关键词： mixed oxides oxygen evolution reaction polymer electrolyte membrane antimony doped tin oxide membrane electrode assembly

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Light Inducing the Geometric Conversion of NiO_(6) to Trigger a Faster oxygen evolution reaction Pathway:The Coupled oxygen evolution Mechanism

引用

Energy & Environmental Materials 2023年第2期6卷 408-410页

作者： Hao Wang Siyu Lu Green Catalysis Center College of ChemistryZhengzhou UniversityZhengzhou 450001China

Developing highly active and robust oxygen evolution reaction(OER)electrocatalysts is still a critical challenge for water electrolyzers and metal-air batteries.Realizing the dynamic evolution of the intermediate and charge transfer during OER and developing a clear OER mechanism is crucial to design high-performance OER catalysts.Recently in Nature,Xue and colleagues revealed a new OER mechanism,coupled oxygen evolution mechanism(COM),which involves a switchable metal and oxygen redox under light irradiation in nickel oxyhydroxide-based materials.This newly developed mechanism requires a reversible geometric conversion between octahedron(NiO_(6))and square planar(NiO_(4))to achieve electronic states with both“metal redox”and“oxygen redox”during OER.The asymmetric structure endows NR-NiOOH with a nonoverlapping region between the dz^(2) orbitals and a_(1g)^(*)bands,which facilitate the geometric conversion and enact the COM pathway.As a result,NR-NiOOH exhibited better OER activity and stability than the traditional NiOOH.

关键词： coupled oxygen evolution mechanism geometric conversion light-induced oxygen evolution reaction

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Nano-Au-decorated hierarchical porous cobalt sulfide derived from ZIF-67 toward optimized oxygen evolution catalysis:Important roles of microstructures and electronic modulation

引用

Carbon Energy 2024年第5期6卷 1-14页

作者： Hongyu Gong Guanliang Sun Wenhua Shi Dongwei Li Xiangjun Zheng Huan Shi Xiu Liang Ruizhi Yang Changzhou Yuan Department of New Energy Materials School of Environmental and Chemical EngineeringJiangsu University of Science and TechnologyZhenjiangJiangsuChina Advanced Materials Institute Qilu University of Technology(Shandong Academy of Sciences)JinanShandongChina Shandong Saikesaisi Hydrogen Energy Co. Ltd.JinanShandongChina Department of Materials Science and Engineering School of Materials Science&EngineeringUniversity of JinanJinanShandongChina Department of New Energy Science and Engineering College of EnergySoochow Institute for Energy and Materials InnovationsSoochow UniversitySuzhouJiangsuChina

Enhancing both the number of active sites available and the intrinsic activity of Co-based electrocatalysts simultaneously is a desirable goal.Herein,a ZIF-67-derived hierarchical porous cobalt sulfide decorated by Au nanoparticles(NPs)(denoted as HP-Au@CoxSy@ZIF-67)hybrid is synthesized by low-temperature sulfuration treatment.The well-defined macroporous-mesoporous-microporous structure is obtained based on the combination of polystyrene spheres,as-formed CoxSy nanosheets,and ZIF-67 frameworks.This novel three-dimensional hierarchical structure significantly enlarges the three-phase interfaces,accelerating the mass transfer and exposing the active centers for oxygen evolution reaction.The electronic structure of Co is modulated by Au through charge transfer,and a series of experiments,together with theoretical analysis,is performed to ascertain the electronic modulation of Co by Au.Meanwhile,HP-Au@CoxSy@ZIF-67 catalysts with different amounts of Au were synthesized,wherein Au and NaBH4 reductant result in an interesting“competition effect”to regulate the relative ratio of Co^(2+)/Co^(3+),and moderate Au assists the electrochemical performance to reach the highest value.Consequently,the optimized HP-Au@CoxSy@ZIF-67 exhibits a low overpotential of 340 mV at 10 mA cm^(-2)and a Tafel slope of 42 mV dec-1 for OER in 0.1 M aqueous KOH,enabling efficient water splitting and Zn-air battery performance.The work here highlights the pivotal roles of both microstructural and electronic modulation in enhancing electrocatalytic activity and presents a feasible strategy for designing and optimizing advanced electrocatalysts.

关键词： Au nanoparticles cobalt sulfide electronic modulation hierarchical porous structure oxygen evolution reaction

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Electrochemical oxygen evolution Performance of Nitrogen-Doped Ultra-Thin Carbon Nanosheets Composite Ru1Co Single Atom Alloy Catalysts

引用

Chinese Journal of Chemistry 2024年第9期42卷 973-979页

作者： Ziwei Deng Zhiyi Sun Yaqiong Li Jiajing Pei Wenxing Chen Energy&Catalysis Center Schoolof Materials Science and EngineeringBeijing Institute of TechnologyBeijing 100081China Beijing Synchrotron Radiation Facility Institute of High Energy PhysicsChinese Academy of SciencesBeijing 00049China

Energy transformation is imminent,and hydrogen energy is one of the important new energy sources.One of the keys to increasing the rate of hydrogen evolution during electrolysis is the use of high-performance catalysts for oxygen evolution reactions(OER).Single-atom alloys(SAAs)have garnered significant attention because they partially reduce costs and combine the advantages of both single-atom catalysts(SACs)and alloy catalysts.Herein,an efficient pyrolysis strategy based on a mixing and drying process is designed to anchor ultra-small Co cluster particles,combined with Ru single atoms dispersed on nitrogen-doped ultra-thin carbon nanosheets(Ru_(1)Co SAA/NC).The prepared electrocatalyst exhibits superior OER activity and superb stability,demonstrating an overpotential of 238 mV for OER with a current density of 10 mA·cm^(-2) in 0.5 mol/L H_(2)SO_(4).And we also utilized in-situ XAS to detect the oxidation state of Ru sites during OER.All in all,this method achieves cost reductions and efficiency improvements through the design of SAAs,offering new prospects for the structural transformation of clean energy.

关键词： oxygen evolution reaction Single alloy catalyst Ultra-thin carbon nanosheets Electrocatalyst Pyrolysis RuiCo SAA/NC

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Hierarchical FeO_(χ)H_(y)@Ni_(3)B hybrid for efficient alkaline oxygen evolution at high current density

引用

Journal of Energy Chemistry 2024年第7期94卷 599-607页

作者： Fuxi Liu Qing Liang Zhenyu Li Meiqi Liu Nailin Yue Zizhun Wang Xu Zou Wei Zhang Key Laboratory of Automobile Materials Ministry of Education School of Materials Science&EngineeringElectron Microscopy CenterInternational Center of Future ScienceJilin Provincial International Cooperation Key Laboratory of High-Efficiency Clean Energy MaterialsJilin UniversityChangchun 130012JilinChina

Electrocatalysts with high activity and long-term durability are vital toward large-scale hydrogen pro-duction from electrocatalytic water splitting.Here,the self-supported electrode(FeO_(χ)H_(y)@Ni_(3)B/NF)with hierarchical heterostructure was simply prepared by using Ni_(3)B chunks grown on nickel foam as sub-strate to in situ form vertical FeO_(χ)H_(y)nanosheets.Such hybrid shows efficient oxygen evolution reaction activity with overpotentials as low as 267 and 249 mV at 100 mA cm^(-2)in 1 M KOH solution and 30 wt%KOH solution,respectively.Meanwhile,it also exhibits excellent catalytic stability,sustaining catalysis at 500 mA cm^(-2)in 1 M KOH solution for 200 h,and even for 200 h at 1000 mA cm^(-2)in 30 wt%KOH solution.Further experimental results reveal that the FeO_(χ)H_(y)@Ni_(3)B/NF is endowed with superhydrophilic and superaerophobic surface properties,which not only provide more mass transport channels,as well as facilitated the diffusion of reaction intermediates and gas bubbles.Also,it holds faster reaction kinetics,more accessible active sites and accelerated electron transfer rates due to strong synergistic interactions attheheterogeneous interface.

关键词： FeO_(χ)H_(y)@Ni_(3)B/NF hybrid Heterostructure oxygen evolution reaction Electrocatalytic

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Phase transition of SrCo_(0.9)Fe_(0.1)O_(3) electrocatalysts and their effects on oxygen evolution reaction

引用

SusMat 2022年第4期2卷 445-455页

作者： Cheng Zhang Fangfang Wang Mariam Batool Beichen Xiong Hong Yang Department of Chemical and Biomolecular Engineering University of Illinois at Urbana-ChampaignUrbanaIllinoisUSA School of Mechanical and Power Engineering Zhengzhou UniversityZhengzhouHenan ProvinceChina

Complex metal oxide has emerged as an important class of electrocatalyst for oxygen evolution reaction(OER)because of its flexibility in the crystal phase and relative ease in the control of defect structures.While different crystalline phases and solid structures may be produced from the same reactant precursors,their phase transitions and OER performances are not well understood.In this work,we present the preparation of different phases of SrCo_(0.9)Fe_(0.1)O_(3-δ)(nominal ratio)solids using a sol-gel method and the structure-catalytic property relationship of both crystalline and amorphous structures formed at different temperatures.We observed as synthetic temperature increased,phase and composition transitions occurred from the amorphous phase to strontium carbonate and cobalt oxide,to oxygen-deficient perovskite,and finally to perovskite.The OER activity depended highly on crystal structures.The oxygen-deficient perovskite prepared at 750℃ exhibited the highest catalytic activity,while the perovskite showed the lowest activity.X-ray photoelectron spectroscopy analysis reveals the change of oxidation state occurred during the phase transition.This work provides a useful guideline for the design of OER electrocatalysts through controlling the crystal structures and defects in complex metal oxides,such as perovskite.

关键词： metal substitution oxygen evolution reaction oxygen vacancy perovskite phase transition

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Ni(OH)_(2) Derived from NiS_(2) Induced by Reflux Playing Three Roles for Hydrogen/oxygen evolution reaction

引用

Chinese Journal of Structural Chemistry 2022年第8期41卷 52-57页

作者： Sheng-Jun Xu Ya-Nan Zhou Guo-Ping Shen Bin Dong Dongying Haike Ruilin Chemical Co. LTD.Dongying 257000China State Key Laboratory of Heavy Oil Processing College of Chemistry and Chemical EngineeringChina University of Petroleum(East China)Qingdao 266580China

Developing efficient and promising non-noble catalysts for oxygen evolution reaction(OER) and hydrogen evolution reaction(HER) is vital but still a huge challenge for the clean energy system. Herein, we have integrated the active components for OER(Ni(OH)_(2)) and HER(Ni S_(2) and Ni(OH)_(2)) into Ni(OH)_(2)@NiS_(2) heterostructures by a facile reflux method. The in-situ formed Ni(OH)_(2) thin layer is coated on the surface of hollow Ni S2 nanosphere. The uniform Ni(OH)_(2)@NiS_(2) hollow sphere processes enlarge the electrochemically active specific surface area and enhance the intrinsic activity compared to NiS_(2) precursor, which affords a current density of 10 m A cm^(-2) at the overpotential of 309 m V and 100 m Acm^(-2) at 359 m V for OER. Meanwhile, Ni(OH)_(2)@NiS_(2) can reach 10 m A cm^(-2) at 233 m V for HER, superior to pure NiS_(2). The enhanced performance can be attributed to the synergy between Ni(OH)_(2) and NiS_(2). Specifically, Ni(OH)_(2) has three functions for water splitting: providing active sites for hydrogen adsorption and hydroxyl group desorption and working as real OER active sites. Moreover, Ni(OH)_(2)@NiS_(2) displays great stability for OER(50 h) and HER(30 h).

关键词： Ni(OH)_(2) NiS_(2) heterostructures oxygen evolution reaction hydrogen evolution reaction

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

Interface engineering of Fe-Co_(3)N/CoP composite with N-doped C by using soybean:Fabrication of efficient electrocatalysts for oxygen evolution reaction

引用

Carbon Resources Conversion 2023年第2期6卷 98-105页

作者： Longqing Gao Xiumin Li Chao Tang Tianshuo Xie Zhengkun Xie Haimei Li Guoqing Guan Jie Liu Keyong Tang School of Materials Science and Engineering Zhengzhou UniversityZhengzhou 450001PR China College of Chemistry Zhengzhou UniversityZhengzhou 450001PR China Energy Conversion Engineering Laboratory Institute of Regional InnovationHirosaki University3-BunkyochoHirosaki 036-8561Japan

Soybean can serve as an efficient carbon and nitrogen source for in-situ fabrication of efficient composite electrocatalysts with conductive nitrogen-doped carbon(N-C)material.In this study,the iron-doped cobalt nitride/phosphide(Fe-Co_(3)N/CoP)nanosheet was composited with a conductive N-C material by using soybean as C and N source,as well as NH3 as additional nitrogen source.During the nitridation process of Fe-Co_(3)N,N-C bond was formed as a newly generated Co(Fe)-N-C active sites.Therefore,it fabricates a good microscopic contact interface between the catalyst and carbon material for charge transfer.Besides,the introduction of Fe-CoP by partially phosphating Fe-Co_(3)N further improved the OER activity due to the high catalytic activity of Co sites with high valence state.As a result,the obtained electrocatalyst exhibited overpotentials as low as 285 and 390 mV for supporting 10 and 100 mA/cm􀀀2 current densities.This work indicates that the design of materials with good interfaces could be an effective approach for the preparation of electrocatalysts for water electrolysis.

关键词： Water electrolysis oxygen evolution reaction Co_(3)N CoP Co-N-C Soybean template

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Iridium-Doped 10H-Phase Perovskite BaCo_(0.8)Fe_(0.15)Ir_(0.05)O_(3-δ)as an Efficient oxygen evolution reaction Catalyst

引用

Chinese Journal of Chemistry 2022年第19期40卷 2276-2284页

作者： Huimin Liu Qinxin Luo Jiaping Hu Lianwei Wei Wanqun Zhang Hui Zheng Shusheng Wu Kaibin Tang Hefei National Research Center for Physical Sciences at the Microscale University of Science and Technology of ChinaHefeiAnhui230026 China Department of Chemistry University of Science and Technology of ChinaHefeiAnhui230026 China Department of Chemistry City University of Hong KongHong KongChina Chemistry Experiment Teaching Center University of Science and Technology of ChinaHefeiAnhui230026 China

Designing low-cost and high-performance catalysts of electrocatalytic oxygen evolution reaction(OER)has always been one of the hot topics in current research.Hexagonal perovskite materials show great application potential in this field.Here,we synthesized 5%Iridium(Ir)-doped hexagonal phase perovskite BaCo_(0.8)Fe_(0.15)Ir_(0.05)O_(3–δ)(BCFI).Using the Rietveld method to refine the structure,combining with the spherical aberration corrected high-angle annular dark-field scanning transmission electron microscopy(HAADF-STEM)atomic imaging,we found that BCFI is a ten-layer hexagonal(10H)structure,which belongs to the Purn:x-wiley:1001604X:media:cjoc202200200:cjoc202200200-math-0001m2 space group.In addition,BCFI shows excellent OER catalytic effect and good stability in 1 mol/L KOH solution,and the overpotential reaches 294 mV at a current density of 10 mA cm^(–2).The reduction of Cobalt(Co)valence state induced by Ir doping significantly enhances the OER activity of BCFI.Meanwhile,density functional theory(DFT)calculations show that the 2p-band center of oxygen(O)in BCFI is closer to the Fermi level than that in undoped BaCo_(0.8)Fe_(0.15)Ir_(0.05)O_(3–δ)(BCF),which is beneficial to the OER.This work reveals a novel 10H-BCFI material with excellent OER performance,and provides a basis for the design of hexagonal perovskite materials in OER and other energy conversion fields.

关键词： Electrochemistry Perovskite phases oxygen evolution reaction Cobalt Iridium

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：