Wang Hao, Wang Haoji, Wan Hao, Wu Dan, Chen Gen, Zhang Ning, Cao Yijun, Liu Xiaohe, Ma Renzhi
School of Chemical Engineering, Zhengzhou University, Zhengzhou, Henan 450001, P. R. China.
School of Materials Science and Engineering, Central South University, Changsha, Hunan 410083, China.
ACS Appl Mater Interfaces. 2020 Oct 14;12(41):46578-46587. doi: 10.1021/acsami.0c15253. Epub 2020 Sep 30.
Hydrogen as a reliable, sustainable, and efficient energy carrier can effectively alleviate global environmental issues and energy crisis. However, the electrochemical splitting of water for large-scale hydrogen generation is still impeded by the sluggish kinetics of the oxygen evolution reaction (OER) at the anode. Considering the synergistic effect of Co and Fe on the improvement of OER catalytic activity, we prepared Co-Fe hydroxide nanotubes through a facile sacrificial template route. The resultant CoFe hydroxide nanotubes exhibited remarkable electrocatalytic performance for OER in 1.0 M KOH, with a small overpotential of about 246 mV at 10 mA cm and a Tafel slope of 53 mV dec. The CoFeP nanotubes were further prepared by a phosphidation treatment, exhibiting excellent OER catalytic performance with an overpotential as low as 240 mV at 10 mA cm. Besides, the CoFeP nanotubes supported on a Ni foam (CoFeP/NF) used as both positive and negative poles in a two-electrode system achieved a cell voltage of about 1.67 V at 10 mA cm and exhibited outstanding stability. A water splitting system was constructed by CoFeP/NF electrodes connected with a crystalline silicon solar cell, demonstrating the application as an electrocatalyst.
氢作为一种可靠、可持续且高效的能量载体,能够有效缓解全球环境问题和能源危机。然而,阳极析氧反应(OER)缓慢的动力学过程仍然阻碍着通过电化学水分解进行大规模制氢。考虑到钴和铁在提高OER催化活性方面的协同效应,我们通过一种简便的牺牲模板法制备了氢氧化钴铁纳米管。所得的氢氧化钴铁纳米管在1.0 M氢氧化钾溶液中对OER表现出卓越的电催化性能,在10 mA cm时过电位约为246 mV,塔菲尔斜率为53 mV dec。通过磷化处理进一步制备了钴铁磷纳米管,其在10 mA cm时过电位低至240 mV,展现出优异的OER催化性能。此外,负载在泡沫镍上的钴铁磷纳米管(CoFeP/NF)在两电极体系中用作正极和负极时,在10 mA cm时电池电压约为1.67 V,并表现出出色的稳定性。通过将CoFeP/NF电极与晶体硅太阳能电池相连构建了一个水分解系统,证明了其作为电催化剂的应用。