孙家祺, 马自在, 周兵, 杨杰, 王孝广. 高效草酸镍钴双金属电催化剂的制备及析氧性能研究[J]. 燃料化学学报(中英文), 2022, 50(10): 1278-1287. DOI: 10.19906/j.cnki.JFCT.2022032
引用本文: 孙家祺, 马自在, 周兵, 杨杰, 王孝广. 高效草酸镍钴双金属电催化剂的制备及析氧性能研究[J]. 燃料化学学报(中英文), 2022, 50(10): 1278-1287. DOI: 10.19906/j.cnki.JFCT.2022032
SUN Jia-qi, MA Zi-zai, ZHOU Bing, YANG Jie, WANG Xiao-guang. Bimetallic nickel-cobalt oxalate as highly efficient electrocatalyst for oxygen evolution reaction[J]. Journal of Fuel Chemistry and Technology, 2022, 50(10): 1278-1287. DOI: 10.19906/j.cnki.JFCT.2022032
Citation: SUN Jia-qi, MA Zi-zai, ZHOU Bing, YANG Jie, WANG Xiao-guang. Bimetallic nickel-cobalt oxalate as highly efficient electrocatalyst for oxygen evolution reaction[J]. Journal of Fuel Chemistry and Technology, 2022, 50(10): 1278-1287. DOI: 10.19906/j.cnki.JFCT.2022032

高效草酸镍钴双金属电催化剂的制备及析氧性能研究

Bimetallic nickel-cobalt oxalate as highly efficient electrocatalyst for oxygen evolution reaction

  • 摘要: 开发用于析氧反应(OER)的高性能非贵金属催化剂有望提高电解水制氢的效率,促进氢能的开发利用。本研究采用简便的一步溶剂热法在泡沫镍(NF)上原位生长NiC2O4-Co(草酸镍钴)双金属电催化剂,可应用于高效的析氧反应。在1 mol/L KOH溶液中,自支撑NiC2O4-Co1双金属催化剂在10 mA/cm2下的析氧过电位仅为278 mV,塔菲尔斜率为65 mV/dec,并显现出优异稳定的OER性能。NiC2O4-Co双金属催化剂优异的性能归因于优化的电子结构,增大的比表面积,快速的界面电荷转移能力,以及OER过程中Ni位点和Co位点之间的协同效应。

     

    Abstract: Developing highly active and non-noble-metal electrocatalyst for oxygen evolution reaction (OER) is expected to accomplish efficient water splitting hydrogen production and promote the commercial utilization of hydrogen energy. We in-situ fabricated bimetallic NiC2O4-Co electrocatalyst on nickel foam (NF) by a facile one-step solvothermal method in this work. NiC2O4-Co1 self-supported electrocatalyst presents superb OER performance with a low overpotential of 278 mV at 10 mA/cm2 and a Tafel slope of 65 mV/dec, accompanied by excellent stability in 1 mol/L KOH electrolyte. The superior catalytic activity of bimetallic NiC2O4-Co electrocatalyst is attributed to optimized electronic structure, high specific surface area, rapid interfacial charge transfer and the synergistic effect between Ni sites and Co sites during OER process.

     

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