Cao Hongshuai, Li Zhibin, Xie Ying, Xiao Fang, Wang Honglei, Wang Xiaoyan, Pan Kai, Cabot Andreu
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, Harbin, 150080, P. R. China.
Catalonia Institute for Energy Research (IREC), 08930, Sant Adrià de Besòs, Barcelona, Spain.
ChemSusChem. 2021 Feb 18;14(4):1094-1102. doi: 10.1002/cssc.202002624. Epub 2021 Jan 7.
A highly active and cheap catalyst is also key to hydrogen production by water splitting. However, most of the high-efficiency catalysts reported to date only are catalytically active for either the hydrogen evolution reaction (HER) or the oxygen evolution reaction (OER), which makes the development of multifunctional catalysts more meaningful. Here, for the first time, Co(CO ) OH 0.11 H O (CHCH) as precursor with different microstructures on the surface of nickel foam (NF) was obtained using a facile hydrothermal method. The CoP/NF catalyst was obtained after thermal phosphating that retained the microhierarchical structure of the precursor and greatly improved the catalytic performance, with a highly efficiency performance as HER and OER dual-functional catalyst. Density functional theory (DFT) calculations showed that the possible reason for the excellent performance of the CoP/NF layered structure is an increase in the number of of surface defects and an increased active surface area. The results reported in this paper show that CoP/NF, a layered bifunctional electrocatalyst, is a cost-effective and efficient water-splitting electrode. This finding can offer the opportunity for the commercial use of excess electric energy for large-scale water splitting hydrogen production.
高活性且廉价的催化剂也是通过水分解制氢的关键。然而,迄今为止报道的大多数高效催化剂仅对析氢反应(HER)或析氧反应(OER)具有催化活性,这使得多功能催化剂的开发更具意义。在此,首次使用简便的水热法在泡沫镍(NF)表面获得了具有不同微观结构的Co(CO₃)₀.₁₁(OH)₀.₈₉·H₂O(CH₃CH₂OH)作为前驱体。经过热磷化后得到CoP/NF催化剂,其保留了前驱体的微纳结构并大大提高了催化性能,作为HER和OER双功能催化剂具有高效性能。密度泛函理论(DFT)计算表明,CoP/NF层状结构优异性能的可能原因是表面缺陷数量增加和活性表面积增大。本文报道的结果表明,CoP/NF这种层状双功能电催化剂是一种经济高效的水分解电极。这一发现可为将多余电能用于大规模水分解制氢的商业应用提供契机。