Cai Kunting, Chen Weibin, Wan Yinji, Chu Hsingkai, Hai Xiao, Zou Ruqiang
Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, School of Materials Science and Engineering, Peking University, No. 5 Yiheyuan Road, Haidian District, Beijing 100871, China.
State Key Laboratory of Heavy Oil Processing, China University of Petroleum, No. 18 Fuxue Road, Changping District, Beijing 102249, China.
Nanomaterials (Basel). 2024 Jul 9;14(14):1168. doi: 10.3390/nano14141168.
Refining synthesis strategies for metal-organic framework (MOF)-based catalysts to improve their performance and stability in an oxygen evolution reaction (OER) is a big challenge. In this study, a series of nanostructured electrocatalysts were synthesized through a solvothermal method by growing MOFs and metal-triazolates (METs) on nickel foam (NF) substrates (named MET-M/NF, M = Fe, Co, Cu), and these electrocatalysts could be used directly as OER self-supporting electrodes. Among these electrocatalysts, MET-Fe/NF exhibited the best OER performance, requiring only an overpotential of 122 mV at a current density of 10 mA cm and showing remarkable stability over 15 h. The experimental results uncovered that MET-Fe/NF underwent an in situ structural reconstruction, resulting in the formation of numerous iron/nickel (oxy)hydroxides with high OER activity. Furthermore, in a two-electrode water-splitting setup, MET-Fe/NF only required 1.463 V to achieve a current density of 10 mA cm. Highlighting its potential for practical applications. This work provides insight into the design and development of efficient MOF-based OER catalysts.
改进基于金属有机框架(MOF)的催化剂的合成策略,以提高其在析氧反应(OER)中的性能和稳定性是一项巨大挑战。在本研究中,通过溶剂热法在泡沫镍(NF)基底上生长MOF和金属三唑化物(METs)(命名为MET-M/NF,M = Fe、Co、Cu)合成了一系列纳米结构电催化剂,这些电催化剂可直接用作OER自支撑电极。在这些电催化剂中,MET-Fe/NF表现出最佳的OER性能,在电流密度为10 mA cm时仅需122 mV的过电位,并且在15小时内表现出显著的稳定性。实验结果表明,MET-Fe/NF经历了原位结构重构,形成了大量具有高OER活性的铁/镍(氧)氢氧化物。此外,在两电极水分解装置中,MET-Fe/NF仅需1.463 V即可达到10 mA cm的电流密度。突出了其实际应用潜力。这项工作为高效的基于MOF的OER催化剂的设计和开发提供了见解。