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具有分级纳米多孔结构的柔性Co-Mo-N/Au电极作为析氧反应的高效电催化剂

Flexible Co-Mo-N/Au Electrodes with a Hierarchical Nanoporous Architecture as Highly Efficient Electrocatalysts for Oxygen Evolution Reaction.

作者信息

Yao Rui-Qi, Shi Hang, Wan Wu-Bin, Wen Zi, Lang Xing-You, Jiang Qing

机构信息

Key Laboratory of Automobile Materials (Jilin University), Ministry of Education, and School of Materials Science and Engineering, Jilin University, Changchun, 130022, China.

出版信息

Adv Mater. 2020 Mar;32(10):e1907214. doi: 10.1002/adma.201907214. Epub 2020 Jan 30.

Abstract

Designing highly active and robust electrocatalysts for oxygen evolution reaction (OER) is crucial for many renewable energy storage and conversion devices. Here, self-supported monolithic hybrid electrodes that are composed of bimetallic cobalt-molybdenum nitride nanosheets vertically aligned on 3D and bicontinuous nanoporous gold (NP Au/CoMoN ) are reported as highly efficient electrocatalysts to boost the sluggish reaction kinetics of water oxidation in alkaline media. By virtue of the constituent CoMoN nanosheets having large accessible CoMoO surface with remarkably enhanced electrocatalytic activity and the nanoporous Au skeleton facilitating electron transfer and mass transport, the NP Au/CoMoN electrode exhibits superior OER electrocatalysis in 1 m KOH, with low onset overpotential (166 mV) and Tafel slope (46 mV dec ). It only takes a low overpotential of 370 mV to reach ultrahigh current density of 1156 mA cm , ≈140-fold higher than free CoMoN nanosheets. The electrocatalytic performance makes it an attractive candidate as the OER catalyst in the water electrolysis.

摘要

设计用于析氧反应(OER)的高活性和稳健的电催化剂对于许多可再生能源存储和转换装置至关重要。在此,报道了由垂直排列在三维双连续纳米多孔金(NP Au/CoMoN)上的双金属钴钼氮化物纳米片组成的自支撑整体式混合电极,作为高效电催化剂以加速碱性介质中缓慢的水氧化反应动力学。由于组成的CoMoN纳米片具有大的可及CoMoO表面且电催化活性显著增强,以及纳米多孔金骨架促进电子转移和质量传输,NP Au/CoMoN电极在1 m KOH中表现出优异的OER电催化性能,具有低起始过电位(166 mV)和塔菲尔斜率(46 mV dec⁻¹)。仅需370 mV的低过电位就能达到1156 mA cm⁻²的超高电流密度,比游离的CoMoN纳米片高约140倍。这种电催化性能使其成为水电解中OER催化剂的有吸引力的候选者。

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