Zheng Tingting, Shi JunYu, Wang Dandan, Min Yulin, Xu Qunjie, Li Qiaoxia
Shanghai Key Laboratory of Materials Protection and Advanced Materials in Electric Power, College of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai, 200090, China.
Shanghai Institute of Pollution Control and Ecological Security, Shanghai, 200090, China.
Chemistry. 2025 Jan 22;31(5):e202403628. doi: 10.1002/chem.202403628. Epub 2024 Nov 26.
Green hydrogen production can be achieved through electrolysis of fresh water or the use of renewable energy to electrolyze seawater. However, due to the low activity and poor stability of oxygen evolution reaction catalysts, direct electrolysis of alkaline seawater faces significant challenges. Herein, The catalyst F-CoFe(OH)-CO/NF with three-dimensional nanosphere structure was prepared, The introduction of CO into the intermediate layer of CoFe hydroxide improves the corrosion resistance of alkaline electrolyte and the doping of F is to design three-dimensional layered nanostructures, increase the active site, and accelerate the diffusion of the electrolyte. By in situ Raman analysis, partial oxidation of CoFe hydroxide to CoFe (oxy)hydroxide as the active center can accelerating the adsorption of oxygen-related intermediates. In 1 M KOH, it requires overpotentials of 210 mV and 251 mV to drive current densities of 10 and 100 mA cm, respectively. And it remained stable at the current density of 100 mA cm for 120 h in 1 M KOH. F-CoFe(OH)-CO/NF can also catalyzes the decomposition of electrolytic seawater. Compared with hydroxide, anion-doped carbonate hydroxide is more efficient and stable in electrolyte solution, which is of great importance for the development of a new stable electrocatalyst for water decomposition.
绿色氢气的生产可以通过电解淡水或利用可再生能源电解海水来实现。然而,由于析氧反应催化剂的活性低和稳定性差,碱性海水的直接电解面临重大挑战。在此,制备了具有三维纳米球结构的催化剂F-CoFe(OH)-CO/NF,将CO引入氢氧化钴铁的中间层提高了碱性电解质的耐腐蚀性,F的掺杂则是为了设计三维层状纳米结构、增加活性位点并加速电解质的扩散。通过原位拉曼分析,氢氧化钴铁部分氧化为羟基氧化钴铁作为活性中心可加速氧相关中间体的吸附。在1 M KOH中,驱动电流密度分别为10和100 mA cm−2时所需的过电位分别为210 mV和251 mV。并且在1 M KOH中,在100 mA cm−2的电流密度下保持稳定120小时。F-CoFe(OH)-CO/NF还可以催化电解海水的分解。与氢氧化物相比,阴离子掺杂的碳酸羟基化物在电解质溶液中更高效、更稳定,这对于开发用于水分解的新型稳定电催化剂具有重要意义。