Zhou Xin, Zhou Xiaoliang, Liu Limin, Chen Hanyu, Hu Xingguo, Qian Jiaqi, Huang Di, Zhang Bo, Tang Junlei
College of Chemistry and Chemical Engineering, Southwest Petroleum University Chengdu 610500 PR China
Hydrogen Energy Division, Dong Fang Boiler Group Co., Ltd. Chengdu 611731 PR China.
RSC Adv. 2021 Oct 21;11(54):34137-34143. doi: 10.1039/d1ra05526g. eCollection 2021 Oct 18.
Hydrogen is an ideal energy carrier due to its abundant reserves and high energy density. Electrolyzing water is one of the carbon free technologies for hydrogen production, which is limited by the sluggish kinetics of the half reaction of the anode - the oxygen evolution reaction (OER). In this study, a self-supported CuP nanowire (CuP NWs/CF) electrode is prepared by electrodeposition of a Cu(OH) nanowire precursor on conductive Cu foam (Cu(OH) NWs/CF) with a subsequent phosphating procedure under a N atmosphere. When used as an OER working electrode in 1.0 M KOH solution at room temperature, CuP NWs/CF exhibits excellent catalytic performance with an overpotential of 327 mV that delivers a current density of 20 mA cm. Notably, it can run stably for 22 h at a current density of 20 mA cm without obvious performance degradation. This highly efficient and stable OER catalytic performance is mainly attributed to the unique nanostructure and stable electrode construction. Interestingly, this synthesis strategy has been proved to be feasible to prepare large-area working electrodes ( 40 cm) with unique nanowire structure. Therefore, this work has provided a good paradigm for the mass fabrication of self-supporting non-noble metal OER catalysts and effectively promoted the reaction kinetics of the anode of the electrolyzing water reaction.
氢因其储量丰富和能量密度高而成为一种理想的能量载体。电解水是制氢的无碳技术之一,其受到阳极半反应——析氧反应(OER)缓慢动力学的限制。在本研究中,通过在导电泡沫铜(Cu(OH) NWs/CF)上电沉积Cu(OH)纳米线前驱体,随后在N气氛下进行磷化处理,制备了自支撑的CuP纳米线(CuP NWs/CF)电极。当在室温下于1.0 M KOH溶液中用作OER工作电极时,CuP NWs/CF表现出优异的催化性能,过电位为327 mV,可提供20 mA cm的电流密度。值得注意的是,它能在20 mA cm的电流密度下稳定运行22 h而无明显性能下降。这种高效且稳定的OER催化性能主要归因于独特的纳米结构和稳定的电极构造。有趣的是,已证明这种合成策略对于制备具有独特纳米线结构的大面积工作电极(40 cm)是可行的。因此,这项工作为自支撑非贵金属OER催化剂的大规模制备提供了一个良好的范例,并有效促进了电解水反应阳极的反应动力学。