Yuan Qunyao, Yu Youxing, Sherrell Peter C, Chen Jun, Bi Xiaofang
School of Materials Science and Engineering, Beihang University, Beijing, 100191, China.
Department of Chemical Engineering, The University of Melbourne, Parkville, VIC 3010, Australia.
Chem Asian J. 2020 Jun 2;15(11):1728-1735. doi: 10.1002/asia.202000321. Epub 2020 Apr 29.
Electrocatalytic water splitting to produce hydrogen and oxygen is regarded as one of the most promising methods to generate clean and sustainable energy for replacing fossil fuels. However, the design and development of an efficient bifunctional catalyst for simultaneous generation of hydrogen and oxygen remains extremely challenging yet is critical for the practical implementation of water electrolysis. Here, we report a facile method to fabricate novel N-doped carbon nanotube frameworks (NCNTFs) by the pyrolysis of a bimetallic metal organic framework (MIL-88-Fe/Co). The resultant electrocatalyst, Co Fe @NCNTFs, exhibits excellent oxygen evolution reaction (OER) activity, achieving 10 mA/cm at a low overpotential of just 264 mV in 1 M KOH solution, and 197 mV for the hydrogen evolution reaction. The high electrocatalytic activity arises from the synergistic effect between the chemistry of the Co Fe and the NCNTs coupled to the novel framework structure. The remarkable electrocatalytic performance of our bifunctional electrocatalyst provides a promising pathway to high-performance overall water splitting and electrochemical energy devices.
电催化水分解制氢和氧被认为是生成清洁可持续能源以替代化石燃料的最具前景的方法之一。然而,设计和开发一种高效的双功能催化剂以同时产生氢气和氧气仍然极具挑战性,但对于水电解的实际应用至关重要。在此,我们报道了一种通过双金属金属有机框架(MIL-88-Fe/Co)热解制备新型氮掺杂碳纳米管框架(NCNTFs)的简便方法。所得的电催化剂Co Fe@NCNTFs表现出优异的析氧反应(OER)活性,在1 M KOH溶液中,仅在264 mV的低过电位下即可达到10 mA/cm²,析氢反应的过电位为197 mV。高电催化活性源于Co Fe的化学性质与NCNTs之间的协同效应以及新颖的框架结构。我们的双功能电催化剂卓越的电催化性能为高性能全水分解和电化学能量装置提供了一条有前景的途径。