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| 1 | 析氢反应中电催化剂设计与构效关系:从纳米结构到单原子显示文摘随着全球能源需求的增加和环境污染的加剧,氢能作为一种新型的能源越来越受到广泛的关注.高效催化剂的设计和开发是制氢研究中极具挑战性的难题.催化剂的表界面组成与结构对其性能具有极其重要的影响,如何科学地设计调控催化材料表界面结构来提高电催化析氢反应的活性和稳定性一直是催化领域研究的重点.本综述针对电催化析氢体系中的多尺度催化剂设计合成为研究对象,以纳米结构催化剂的设计及构效关系为出发点,总结了目前针对电催化析氢反应的纳米催化剂的合成及构效关系的研究进展,从原子尺度提出纳米催化剂高活性的起源.结合目前报道的各种单原子催化剂的设计合成、在析氢反应中的应用及构效关系的研究,讨论了设计定向单原子位点析氢催化剂的方向,同时对电解水制氢催化剂的发展趋势和挑战进行了展望. | 潘原 张超 林燕 刘智 王敏敏 陈晨 | 2020 | Science China Materials2020，63，6： | 17 |
| 2 | Metal-organic framework derived CoSe2 nanoparticles anchored on carbon fibers as bifunctional electrocatalysts for efficient overall water splitting显示文摘发展有效,便宜,稳定,为切开的水的 non-noble-metal electrocatalysts,特别地能两个都催化氢进化反应的那些(她的) 在在阳极的阴极和氧进化反应(OER ) ,是挑战。我们开发了一个灵巧的方法因为综合从从容容宽敞 2 nanoparticles 一致地在碳纤维纸上抛锚了(经由热分解和 selenization 的从从容容宽敞 2/CF) 在 situ 成年 zeolitic imidazolate framework-67 (ZIF-67 ) 。从从容容宽敞 2/CF 在碱的答案在 HER 和 OER 显示出高、稳定的催化活动。在一个低房间潜力,即, 1.63 V,与二个从从容容宽敞 2/CF 电极装备的水 electrolyzer 给了 10 mAen 的切开水的水流 2007 并且 2014 年 10 月 21 日。我们然后与一个低级术语并且通过临床的描述的一篇详细摘要识别了 PAOD 的盒子。结果我们识别了 POAD 的 25 个盒子。大多数病人比 60 老 ? 年(84 ?%) 或有象血胆脂醇过多那样的另一个心血管的风险因素,钰 ? 钰吗?? | Chencheng Sun Qiuchun Dong Jun Yang Ziyang Dai Jianjian Lin Peng Chen Wei Huang Xiaochen Dong | 2016 | Nano Research2016，9，8： | 16 |
| 3 | Nickel cobalt phosphide with three-dimensional nanostructure as al highly efficient electrocatalyst for hydrogen evolution reaction in both I acidic and alkaline electrolytes显示文摘Transition metal phosphides (TMPs) are promising candidates for noble metal free electrocatalysts in water splitting applicati ons. In this work, we prese nt the facile syn thesis of nickel cobalt phosphide electrocatalyst with three-dime nsional nano structure (3D-NiCoP) on the nickel foam, via hydrothermal reaction and phosphorization. The as-prepared electrocatalyst exhibits an excellent activity for hydrogen evolution reaction (HER) in both acidic and alkaline electrolytes, with small overpotentials to drive 10 mA/cm^2 (80 mV for 0.5 M H2SO4, 105 mV for 1 M KOH), small Tafel slopes (37 mV/dec for 0.5 M H2SO4, 79 mV/dec for 1 M KOH), and satisfying durability in long-term electrolysis. 3D-NiCoP also shows a superior HER activity compared to single metal phosphide, such as cobalt phosphide and nickel phosphide. The outstanding performa nee for HER suggests the great pote ntial of 3D-NiCoP as a highly efficient electrocatalyst for water splitting technology. | Bo Ma Zhengchun Yang Yantao Chen Zhihao Yuan | 2019 | Nano Research2019，12，2： | 14 |
| 4 | Recent progress on earth abundant electrocatalysts for hydrogen evolution reaction(HER) in alkaline medium to achieve efficient water splitting–A review显示文摘Developing earth-abundant-electrocatalysts for hydrogen evolution reaction is one of the promising ways to achieve efficient water-splitting for hydrogen production(a clean chemical fuel).This paper reviews the activity,stability and durability for hydrogen evolution reaction in alkaline medium of different types of recently reported potential electrocatalysts such as Ni,Co,NiCo,Fe,Cu,W,Mo,Se,Mn.Zn,V,and metal free based earth-abundant-electrocatalysts.Further,this paper reviews the strategies used to achieve the remarkably low overpotential(including r/i0:<35mV),high long term stability(including^:100 h)and high durability(including>5000 cycles)of potential earth-abundant-electrocatalysts for hydrogen evolution reaction in alkaline medium and those are better or well comparable with the state-of-the-art,noble,Pt/C electrocatalyst.Finally,this paper summarizes the efficient strategies such as preparing porous structured materials,preparing nanostructured materials with superaerophobic surface,preparing nanostructured materials,preparing carbon composites/integrating electrocatalysts with carbon,preparing amorphous materials,preparing materials w让h oxygen vacancies/defects,preparing metal chalcogenides,preparing bimetallic/multi-metallic materials,doping metals or heteroatoms,preparing electrocatalysts with core-shell structure,decorating electrocatalysts with amines,preparing homojunction/heterojunction structured materials,preparing hollow structured materials,and preparing boronrich surface to enhance the activity,stability,and durability for HER. | Jamesh Mohammed-Ibrahim xiaoming Sun | 2019 | Journal of Energy Chemistry2019，28，7： | 14 |
| 5 | Synthesis and application of transition metal phosphides as electrocatalyst for water splitting显示文摘With continuous research on photocatalytic water splitting, searching for efficient catalyst for hydrogen evolution reaction(HER) becomes popular topic in addition to main catalyst research. Transition metal phosphides are receiving intense attention due to its abundance in the Earth's crust and comparable catalytic properties to noble metals. In this review, the synthesis approaches, HER reaction mechanism,photocatalytic activity, approaches to improve the activity of transition metal phosphides were reviewed and discussed. It was showed that the transition metal phosphides have great potential to reduce the cost of photocatalyst and promising application on water splitting. The stability problem and participation of poisonous reactant and product in its synthesis reaction limit its application and developing in a certain extent, but with the continuous efforts on the development and improvement of the synthesis methods,transition metal phosphides will find wide application in water splitting. | Jinzhan Su Jinglan Zhou Lu Wang Cong Liu Yubin Chen | 2017 | Science Bulletin2017，62，9： | 13 |
| 6 | Enhanced N-doping in mesoporous carbon for efficient electrocatalytic CO2 conversion显示文摘The capability of electrocatalytic reducti on of carbon dioxide(CO2)using nitrogen(N)-doped carb on strongly depe nds on the N-dopi ng level and their types.In this work,we developed a strategy to generate mesoporous N-doped carb on frameworks with tun able configurati ons and contents of N dopants,by using a secondary doping process via the treatment of N,N-dimethylformamide(DMF)solvent.The obtained mesoporous N-doped carbon(denoted as MNC-D)served as an efficient electrocatalyst for electroreduction of CO2 to CO.A high Faradaic efficiency of^92%and a partial current density for CO of-6.8 mA·cm^-2 were achieved at a potential of-0.58 V vs.RHE.Electrochemical analyses further revealed that the active sites within the N-doped carb on catalysts were the pyridinic N and defects gen erated by the DMF treatme nt,which enhan ced the activati on and adsorpti on CO2 molecules.Our study suggests a new approach to develop efficie nt carb on-based catalysts for potential scalable CO2 reduction reaction(CO2RR)to fuels and chemicals. | Min Kuang Anxiang Guan Zhengxiang Gu Peng Han Linping Qian Gengfeng Zheng | 2019 | Nano Research2019，12，9： | 11 |
| 7 | Few-layered ReS_2 nanosheets grown on graphene as electrocatalyst for hydrogen evolution reaction显示文摘Few-layered ReS_2 two-dimensional(2 D) semiconductor nanosheets directly nucleated and grown on reduced graphene oxide(RGO) were synthesized through a facile hydrothermal method. Compared with bare ReS_2, the ReS2/RGO hybrid delivers much better electrocatalytic activity for hydrogen evolution reaction(HER) in acidic media. It exhibits a lower Tafel slope of 107.4 mV dec^(-1)and a larger current density of-5.2 mA·cm^(-2) at-250 mV(vs. RHE),compared with ReS_2(152.7 mV·dec^(-1),-3.1 mA·cm^(-2)). The ReS_2/RGO hybrid has a unique architecture constructed by highly conductive and porous RGO internetworks, which guarantees easy electrolyte infiltration and efficient charge transfer and provides sufficient active edge sites, resulting in enhanced HER performance. The present synthesis approach can be extended to synthesize other 2 D-semiconductor-based composites for energy storage and catalytic devices. | Han Gao Hu-Hu Yue Fei Qi Bo Yu Wan-Li Zhang Yuan-Fu Chen | 2018 | Rare Metals2018，37，12： | 10 |
| 8 | Single-Atom Catalysts for Electrochemical Hydrogen Evolution Reaction: Recent Advances and Future Perspectives显示文摘Hydrogen,a renewable and outstanding energy carrier with zero carbon dioxide emission,is regarded as the best alternative to fossil fuels.The most preferred route to large-scale production of hydrogen is by water electrolysis from the intermittent sources(e.g.,wind,solar,hydro,and tidal energy).However,the efficiency of water electrolysis is very much dependent on the activity of electrocatalysts.Thus,designing high-effective,stable,and cheap materials for hydrogen evolution reaction(HER)could have a substantial impact on renewable energy technologies.Recently,single-atom catalysts(SACs)have emerged as a new frontier in catalysis science,because SACs have maximum atom-utilization efficiency and excellent catalytic reaction activity.Various synthesis methods and analytical techniques have been adopted to prepare and characterize these SACs.In this review,we discuss recent progress on SACs synthesis,characterization methods,and their catalytic applications.Particularly,we highlight their unique electrochemical characteristics toward HER.Finally,the current key challenges in SACs for HER are pointed out and some potential directions are proposed as well. | Zonghua Pu Ibrahim Saana Amiinu Ruilin Cheng Pengyan Wang Chengtian Zhang Shichun Mu Weiyue Zhao Fengmei Su Gaixia Zhang Shijun Liao Shuhui Sun | 2020 | Nano-Micro Letters2020，12，2： | 10 |
| 9 | PtAu Bimetallic Heteronanostructures Made by Post-Synthesis Modification of Pt-on-Au Nanoparticles显示文摘Bimetallic PtAu heteronanostructures have been synthesized from Pt-on-Au nanoparticles,which were made from platinum acetylacetonate and gold nanoparticles.Using the Pt-on-Au nanoparticles as precursors,Pt-surface rich PtAu bimetallic heteronanostructures can be produced through controlled thermal treatments,as confirmed by field emission high-resolution transmission electron microscopy(HR-TEM)and elemental mapping using a high-angle annular dark-field scanning transmission electron microscope(HAADF-STEM).Oxidation of formic acid was used as a model reaction to demonstrate the effects of varying composition and surface structure on the catalytic performance of PtAu bimetallic nanostructures.Cyclic voltammetry(CV)showed that these carbon-supported PtAu heteronanostructures were much more active than platinum in catalyzing the oxidation of formic acid,judging by the mass current density.The results showed that post-synthesis modification can be a very useful approach to the control of composition distributions in alloy nanostructures. | Zhenmeng Peng Hong Yang | 2009 | Nano Research2009，2，5： | 9 |
| 10 | Recent advances in nanostructured heterogeneous catalysts for N-cycle electrocatalysis显示文摘To restore the natural nitrogen cycle(N-cycle),artificial N-cycle electrocatalysis with flexibility,sustainability,and compatibility can convert intermittent renewable energy(e.g.,wind)to harmful or value-added chemicals with minimal carbon emissions.The background of such N-cycles,such as nitrogen fixation,ammonia oxidation,and nitrate reduction,is briefly introduced here.The discussion of emerging nanostructures in various conversion reactions is focused on the architecture/compositional design,electrochemical performances,reaction mechanisms,and instructive tests.Energy device advancements for achieving more functions as well as in situ/operando characterizations toward understanding key steps are also highlighted.Furthermore,some recently proposed reactions as well as less discussed C-N coupling reactions are also summarized.We classify inorganic nitrogen sources that convert to each other under an applied voltage into three types,namely,abundant nitrogen,toxic nitrate(nitrite),and nitrogen oxides,and useful compounds such as ammonia,hydrazine,and hydroxylamine,with the goal of providing more critical insights into strategies to facilitate the development of our circular nitrogen economy. | Jie Liang Qian Liu Abdulmohsen Ali Alshehri Xuping Sun | 2022 | Nano Research Energy2022，1，2： | 8 |
| 11 | Effect of plating bath composition on chemical composition and oxygen reduction reaction activity of electrodeposited Pt–Co catalysts显示文摘Platinum–cobalt(Pt–Co) alloy electrocatalysts were prepared on pretreated carbon cloth by electrodeposition from different plating baths with the aim of finding suitable plating bath conditions that could control the chemical composition of the Pt–Co alloy electrodeposits over a wide range(from 0 to 100 at% Pt) and then to study the relationship of the deposit composition on the oxygen reduction reaction(ORR) electroactivity. The type of supporting electrolyte, the solution pH, Pt and Co concentrations of the plating bath and the current density used for electrodeposition all play a crucial role in the composition of the electrodeposited Pt–Co alloy. Pt contents in all the Pt–Co alloys deposited in H_2SO_4 are at a relatively high and narrow level(83 at%–97 at% Pt), regardless of the electrodeposition conditions used. While the Pt contents in the Pt–Co alloys deposited in Na_2SO_4 could reach a very low and broad level(5 at%–97 at% Pt), evidence of Co oxide formation is observed. Of the three supporting electrolytes studied, only NaCl effectively produces Pt–Co deposits over a wide range of compositions(8–90 at% Pt)by controlling the Pt and Co concentrations of the plating bath and using the high enough current density. The results show a qualitative correlation between Pt–Co deposit composition and ORR activity, where Pt–Co alloy catalysts with ≥ 45 at% Pt tend to yield higher ORR activities than the pure Pt catalyst, with the best ORR performance obtained from the Pt–Co alloy catalyst with 78 at% Pt. | Pranee Puangsombut Nisit Tantavichet | 2019 | Rare Metals2019，38，2： | 8 |
| 12 | Mn3O4 nanoparticles@reduced graphene oxide composite:An efficient electrocatalyst for artificial N2 fixation to NH3 at ambient conditions显示文摘Currently,industrial-scale NH3 production almost relies on energy-intensive Haber-Bosch process from atmospheric N2 with large amount of CO2 emission,while low-cost and high-efficient catalysts are demanded for the N2 reduction reaction (NRR).In this study,Mn3O4 nanoparticles@reduced graphene oxide (Mn3O4@rGO) composite is reported as an efficient NRR electrocatalyst with excellent selectivity for NH3 formation.In 0.1 M Na2SO4 solution,such catalyst obtains a NH3 yield of 17.4 μg·h^-1·mg^-1cat.and a Faradaic efficiency of 3.52% at-0.85 V vs.reversible hydrogen electrode.Notably,it also shows high electrochemical stability during electrolysis process.Density functional theory (DFT) calculations also demonstrate that the (112) planes of Mn3O4 possess superior NRR activity. | Hong Huang Feng Gong Yuan Wang Huanbo Wang Xiufeng Wu Wenbo Lu Runbo Zhao Hongyu Chen Xifeng Shi Abdullah M.Asiri Tingshuai Li Qian Liu Xuping Sun | 2019 | Nano Research2019，12，5： | 8 |
| 13 | Defect and Doping Co‑Engineered Non‑Metal Nanocarbon ORR Electrocatalyst显示文摘Exploring low-cost and earth-abundant oxygen reduction reaction(ORR)electrocatalyst is essential for fuel cells and metal–air batteries.Among them,non-metal nanocarbon with multiple advantages of low cost,abundance,high conductivity,good durability,and competitive activity has attracted intense interest in recent years.The enhanced ORR activities of the nanocarbons are normally thought to originate from heteroatom(e.g.,N,B,P,or S)doping or various induced defects.However,in practice,carbon-based materials usually contain both dopants and defects.In this regard,in terms of the co-engineering of heteroatom doping and defect inducing,we present an overview of recent advances in developing non-metal carbon-based electrocatalysts for the ORR.The characteristics,ORR performance,and the related mechanism of these functionalized nanocarbons by heteroatom doping,defect inducing,and in particular their synergistic promotion effect are emphatically analyzed and discussed.Finally,the current issues and perspectives in developing carbon-based electrocatalysts from both of heteroatom doping and defect engineering are proposed.This review will be beneficial for the rational design and manufacturing of highly efficient carbon-based materials for electrocatalysis. | Jian Zhang Jingjing Zhang Feng He Yijun Chen Jiawei Zhu Deli Wang Shichun Mu Hui Ying Yang | 2021 | Nano-Micro Letters2021，13，4： | 8 |
| 14 | In Situ Coupling Strategy for Anchoring Monodisperse Co_9S_8 Nanoparticles on S and N Dual?Doped Graphene as a Bifunctional Electrocatalyst for Rechargeable Zn–Air Battery显示文摘An in situ coupling strategy to prepare Co_9S_8/S and N dual?doped graphene composite(Co_9S_8/NSG) has been proposed. The key point of this strategy is the function?oriented design of organic compounds. Herein, cobalt porphyrin derivatives with sulfo groups are employed as not only the coupling agents to form and anchor Co_9S_8 on the graphene in situ, but also the heteroatom?doped agent to generate S and N dual?doped graphene. The tight coupling of multiple active sites endows the composite materials with fast electrochemical kinetics and excellent stability for both oxygen reduction reaction(ORR) and oxygen evolution reaction(OER). The obtained electrocatalyst exhibits better activity parameter(ΔE = 0.82 V) and smaller Tafel slope(47.7 mV dec^(-1) for ORR and 69.2 mV dec^(-1) for OER) than commercially available Pt/C and RuO_2. Most importantly, as electrocatalyst for rechargeable Zn–air battery, Co_9S_8/NSG displays low charge–discharge voltage gap and outstanding long?term cycle stability over 138 h compared to Pt/C–RuO_2. To further broaden its application scope, a homemade all?solid?state Zn–air battery is also prepared, which displays good charge–discharge performance and cycle performance. The function?oriented design of N_4?metallomacrocycle derivatives might open new avenues to strategic construction of high?performance and long?life multifunctional electrocatalysts for wider electro?chemical energy applications. | Qi Shao Jiaqi Liu Qiong Wu Qiang Li Heng?guo Wang Yanhui Li Qian Duan | 2019 | Nano-Micro Letters2019，11，1： | 8 |
| 15 | Sponge-like nickel phosphide-carbon nanotube hybrid electrodes for efficient hydrogen evolution over a wide pH range显示文摘经由水的电解的划算的氢生产为氢进化反应要求有效、持久的地球丰富的催化剂(她的) 在一个宽 pH 范围上。此处,我们报导像海绵的镍磷化物碳 nanotube (Ni x P/CNT ) 被非结晶的 Ni x P 催化剂到 threedimensional (3D ) 上多孔的 CNT 支持。这些混合物在酸、中立、基本的媒介为持续的氢进化展出优异催化活动。特别地, Ni x P/CNT 电极产生 10 和 100 mAapy 的 cathodic 水流,但是总是 regressed onanticoagulation。传单限制和最大的厚度的功课在二个组之间是显著地不同的( P ? P ?=? 0.005 )并且传单限制分数由一中部 1 [ quartiles 0 ; 2 ]( P ?=? 0.013 ),而在 anticoagulation 组,在 2.57 的最大的厚度 regressed ?甘油的 n 作为副产品。最后的紧张生产了 9.8 ? l 33 ?%( 从 205 ~ 272 ? mg/L ) 。直角的策略 inte?? | Shuying Wang Li Zhang Xiao Li Changli Li Rujing Zhang Yingjiu Zhang Hongwei Zhu | 2017 | Nano Research2017，10，2： | 8 |
| 16 | Boosting electrocatalytic water splitting via metal-metalloid combined modulation in quaternary Ni-Fe-P-B amorphous compound显示文摘Design and synthesis of highly efficient and cost-effective bifunctional catalysts for hydrogen evolution reaction(HER)and oxygen evolution reaction(OER)remain a big challenge.Herein,a quaternary amorphous nanocompound Ni-Fe-P-B has been synthesized by a facile,scalable co-reduction method.The Ni-Fe-P-B exhibits high electrocatalytic activity and outstanding durability for both HER and OER,delivering a current density of 10 mA·cm^-2 at overpotentials of 220 and 269 mV,respectively.When loaded on carbon fiber paper(CFP)as a bifunctional catalyst,the Ni-Fe-P-B@CFP electrode requires a low cell voltage of 1.58 V to obtain 10 mA·cm^-2 for overall water splitting with negligible recession over 60 h.The excellent catalytic performances of Ni-Fe-P-B mainly benefit from the metal-metalloid combined composition modulation and the unique amorphous structure.This work provides new insights into the design of robust bifunctional catalysts for water splitting,and may promote the development of multicomponent amorphous catalysts. | Wukui Tang Xiaofang Liu Ya Li Yanhui Pu Yao Lu Zhiming Song Qiang Wang Ronghai Yu Jianglan Shui | 2020 | Nano Research2020，13，2： | 8 |
| 17 | In Situ X-ray Absorption Spectroscopy Studies of Nanoscale Electrocatalysts显示文摘Nanoscale electrocatalysts have exhibited promising activity and stability,improving the kinetics of numerous electrochemical reactions in renewable energy systems such as electrolyzers,fuel cells,and metal-air batteries.Due to the size effect,nano particles with extreme small size have high surface areas,complicated morphology,and various surface terminations,which make them different from their bulk phases and often undergo restructuring during the reactions.These restructured materials are hard to probe by conventional ex-situ characterizations,thus leaving the true reaction centers and/or active sites difficult to determine.Nowadays,in situ techniques,particularly X-ray absorption spectroscopy(XAS),have become an important tool to obtain oxidation states,electronic structure,and local bonding environments,which are critical to investigate the electrocatalysts under real reaction conditions.In this review,we go over the basic principles of XAS and highlight recent applications of in situ XAS in studies of nanoscale electrocatalysts. | Maoyu Wang Líneyárnadóttir Zhichuan JXu Zhenxing Feng | 2019 | Nano-Micro Letters2019，11，3： | 8 |
| 18 | 3D nickel-cobalt diselenide nanonetwork for highly efficient oxygen evolution显示文摘Active, stable and low-cost oxygen evolution reaction(OER) catalyst for electrochemical water splitting is key to efficient energy conversion and storage. Here, we report a three-dimensional(3D) nanonetwork as noble-metal-free electrode consisting of nickel cobalt diselenide(NiCoSe_2) nanobrush arrays on Ni foam(NF) through the initial hydrothermal reaction and subsequent thermal selenization process. Introducing ammonium fluoride as surface controller, different NiCoSe_2 hierarchical architecture can be modulated from nanorods, nanobrush to nanosheets. The unique brush-like NiCoSe_2 possesses high surface area for mass transfer, rough surface with rich active sites, 3D nanostructure preventing the accumulation of O2 bubbles. Compared to NiCoSe_2 nanorods/NF, NiCoSe_2 nanosheets/NF and commercial Ru O2,NiCoSe_2 nanobrush/NF exhibits an enhanced OER performance in alkaline media to reach a low overpotential of 274 m V at the current density of 10 m A/cm2, small Tafel slope and a long-term stability. The developed 3D nanonetwork highlights the nanoscale engineering and offers a promising alternative to noble metal catalysts for electrochemical water oxidation. | Hengli Zhu Rui Jiang Xiaoqing Chen Yueguang Chen Leyu Wang | 2017 | Science Bulletin2017，62，20： | 7 |
| 19 | Continuous nitrogen-doped carbon nanotube matrix for boosting oxygen electrocatalysis in rechargeable Zn-air batteries显示文摘Developing robust oxygen electrocatalyst with high-performance is very significant for practical rechargeable Zn-air battery.We report herein the preparation of three-dimensional continuous nanocarbon network composed of interconnected nitrogen-doped carbon nanotubes and its application as oxygen electrocatalysis in rechargeable Zn-air battery.Except the excellent electrochemical bifunctionality,this carbon nanotube matrix also delivers an impressive battery performance.Specifically,an opencircuit voltage of 1.50 V as well as a high power density of 220 m W cm^(-2) with remarkable cycling stability for 1600 h is achieved in the rechargeable Zn-air battery.The study not only provides an efficient bifunctional oxygen electrocatalyst but more importantly may pave significant concepts in designing robust electrode for long-life rechargeable Zn-air battery and other energy technologies. | Guangda Chen Yangyang Xu Lei Huang Aboulkader Ibro Douka Bao Yu Xia | 2021 | Journal of Energy Chemistry2021，30，4： | 7 |
| 20 | Chromium-ruthenium oxide solid solution electrocatalyst for highly efficient oxygen evolution reaction in acidic media显示文摘With the support of the National Natural Science Foundation of China and the aided program for Science and Technology Innovative Research Team of Ningbo Municipality,the research team led by Prof.ChenLiang(陈亮)at Ningbo Institute of Materials Technology and Engineering,Chinese Academy of Sciences,reported a chromium-ruthenium oxide solid solution electrocatalyst for the highly efficient oxygen evolution reaction(OER)in acidic media. | | 2019 | Science Foundation in China2019，27，1： | 7 |
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