Substantial Impact of Built-in Electric Field and Electrode Potential on the Alkaline Hydrogen Evolution Reaction of Ru-CoP Urchin Arrays

被引:58
作者
Liu, Shangguo [1 ]
Li, Zijian [2 ]
Chang, Yaxiang [1 ]
Kim, Min Gyu [3 ]
Jang, Haeseong [4 ]
Cho, Jaephil [5 ]
Hou, Liqiang [1 ]
Liu, Xien [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem Engn, Qingdao 266042, Peoples R China
[2] City Univ Hong Kong, Dept Chem, Hong Kong 999077, Peoples R China
[3] Pohang Accelerator Lab PAL, Beamline Res Div, Pohang 37673, South Korea
[4] Chung Ang Univ, Dept Adv Mat Engn, Anseong 17546, Gyeonggi Do, South Korea
[5] Ulsan Natl Inst Sci & Technol UNIST, Sch Energy & Chem Engn, Dept Energy Engn, Ulsan 689798, South Korea
基金
中国国家自然科学基金;
关键词
built-in electric field; interfacial hydrogen spillover; electrode potential; alkaline HER; ELECTROCHEMICAL REDUCTION; OXYGEN; WATER;
D O I
10.1002/anie.202400069
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Although great efforts on the delicate construction of a built-in electric field (BIEF) to modify the electronic properties of active sites have been conducted, the substantial impact of BIEF coupled with electrode potential on the electrochemical reactions has not been clearly investigated. Herein, we designed an alkaline hydrogen evolution reaction (HER) catalyst composed of heterogeneous Ru-CoP urchin arrays on carbon cloth (Ru-CoP/CC) with a strong BIEF with the guidance of density functional theory (DFT) calculations. Impressively, despite its unsatisfactory activity at 10 mA cm-2 (overpotential of 44 mV), Ru-CoP/CC exhibited better activity (357 mV) than the benchmark Pt/C catalyst (505 mV) at 1 A cm-2. Experimental and theoretical studies revealed that strong hydrogen adsorption on the interfacial Ru atoms created a high energy barrier for hydrogen desorption and spillover, resulting in unsatisfactory activity at low current densities. However, as the electrode potential became more negative (i.e., the current density increased), the barrier for hydrogen spillover from the interfacial Ru to the Co site, which had near-zero hydrogen adsorption energy, significantly decreased, thus greatly accelerating the whole alkaline HER process. This explains why the activity of Ru-CoP is relatively susceptible to the electrode potential compared to Pt/C. A strong built-in electric field (BIEF) resulted in a strong asymmetrical charge distribution on the Ru cluster, which accelerated water dissociation. However, strong hydrogen adsorption on the interfacial Ru atoms created a high energy barrier for hydrogen desorption and spillover, resulting in unsatisfactory activity at low potentials. As the potential became more negative, the barrier for hydrogen spillover from the interfacial Ru to the Co site, which had a near-zero hydrogen adsorption energy, significantly decreased, thus accelerating the entire alkaline hydrogen evolution reaction (HER) process.+ image
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页数:8
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