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镍铁水滑石/还原氧化石墨烯的制备及电催化水氧化性能 被引量:9
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作者 杜世超 任志宇 +1 位作者 吴君 付宏刚 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2016年第8期1415-1420,共6页
首先制备了不同镍/铁比的镍铁水滑石,并通过液相剥离法得到水滑石纳米薄片溶胶,随后将其与还原氧化石墨烯复合,并对其进行了电催化水氧化的性能测试.结果表明,镍铁水滑石的剥离可以大幅度提高其电催化性能,起峰电位为1.47V,电流密度为10... 首先制备了不同镍/铁比的镍铁水滑石,并通过液相剥离法得到水滑石纳米薄片溶胶,随后将其与还原氧化石墨烯复合,并对其进行了电催化水氧化的性能测试.结果表明,镍铁水滑石的剥离可以大幅度提高其电催化性能,起峰电位为1.47V,电流密度为10mA/cm^2时,电位仅为1.53V;与还原氧化石墨烯复合后,其催化活性得到了进一步提高,在10mA/cm^2时电位降为1.515V. 展开更多
关键词 镍铁滑石 电催化水制氧 分解 还原化石墨
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3D ordered mesoporous cobalt ferrite phosphides for overall water splitting 被引量:10
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作者 Yarong Huang Menggang Li +2 位作者 Weiwei Yang Yongsheng Yu Sue Hao 《Science China Materials》 SCIE EI CSCD 2020年第2期240-248,共9页
Developing low-cost and earth-abundant electrocatalysts with high performance for electrochemical water splitting is a challenging issue. Herein, we report a facile and effective way to fabricate three-dimension(3D) o... Developing low-cost and earth-abundant electrocatalysts with high performance for electrochemical water splitting is a challenging issue. Herein, we report a facile and effective way to fabricate three-dimension(3D) ordered mesoporous Co1-xFexP(x=0, 0.25, 0.5, 0.75) electrocatalyst.Benefiting from 3D ordered mesoporous pore channels and composition optimization, the Co0.75Fe0.25 P exhibits excellent electrocatalytic activities with low overpotentials of 270 and 209 mV at 10 mA cm^-2 for oxygen evolution reaction(OER)and hydrogen evolution reaction(HER), respectively, in the alkaline electrolyte along with a durable electrochemical stability. In addition, as both the cathode and anode, the Co0.75Fe0.25P also exhibits superior electrolysis water splitting performance with only an applied voltage of 1.63 V to attain a current density of 10 m A cm^-2 without obvious decay for 18 h,indicating that the Co0.75Fe0.25P is an efficient electrocatalyst for overall water splitting. 展开更多
关键词 cobalt ferrite phosphides 3D ordered mesoporous structure highly efficient electrocatalysts water splitting
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Decoupling hydrogen production from water oxidation by integrating a triphase interfacial bioelectrochemical cascade reaction
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作者 Jun Zhang Xia Sheng +6 位作者 Zhenyao Ding Haili Wang Lai Feng Xiqi Zhang Liping Wen Lei Jiang Xinjian Feng 《Science Bulletin》 SCIE EI CSCD 2021年第2期164-169,M0004,共7页
Water electrolysis to produce H2 is a promising strategy for generating a renewable fuel.However,the sluggish-kinetics and low value-added anodic oxygen evolution reaction(OER)restricts the overall energy conversion e... Water electrolysis to produce H2 is a promising strategy for generating a renewable fuel.However,the sluggish-kinetics and low value-added anodic oxygen evolution reaction(OER)restricts the overall energy conversion efficiency.Herein we report a strategy of boosting H_(2)production at low voltages by replacing OER with a bioelectrochemical cascade reaction at a triphase bioanode.In the presence of oxygen,oxidase enzymes can convert biomass into valuable products,and concurrently generate H_(2)O_(2) that can be further electrooxidized at the bioanode.Benefiting from the efficient oxidase kinetics at an oxygen-rich triphase bioanode and the more favorable thermodynamics of H_(2)O_(2)oxidation than that of OER,the cell voltage and energy consumption are reduced by~0.70 V and~36%,respectively,relative to regular water electrolysis.This leads to an efficient H_(2)production at the cathode and valuable product generation at the bioanode.Integration of a bioelectrochemical cascade into the water splitting process provides an energy-efficient and promising pathway for achieving a renewable fuel. 展开更多
关键词 Hydrogen production Water electrolysis OXIDASE Bioelectrochemical cascade reaction
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