Liu Shu, Jiang Yimin, Yang Miao, Zhang Mengjie, Guo Qifei, Shen Wei, He Rongxing, Li Ming
Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
Nanoscale. 2019 Apr 23;11(16):7959-7966. doi: 10.1039/c8nr10545f.
Water splitting has long been considered as a promising chemical reaction that can produce clean hydrogen fuel to relieve the energy crisis and environmental pollution. Herein, we report that Co0.75Ni0.25Se/NF formed by two-step growth of metallic cobalt-nickel selenide nanorods on porous nickel foam was used as a bifunctional electrocatalyst. Ni foam serves as a slow-releasing nickel source together with a Co source to form a special proportional cobalt-nickel selenide. Due to its unique rough nanostructure, bimetallic cooperative effects and intrinsic metallic character, the obtained Co0.75Ni0.25Se/NF electrode exhibits a low overpotential of 269 mV (50 mA cm-2) for the oxygen evolution reaction and an overpotential of 106 mV (10 mA cm-2) for the hydrogen evolution reaction. Furthermore, this bifunctional electrocatalyst requires a cell voltage of 1.60 V to achieve a current density of 10 mA cm-2. Besides, based on theoretical calculation, it is further shown that the synergy between Co and Ni elements is beneficial for improving the internal structure of the catalyst, resulting in a high electrical conductivity, and low HER Gibbs free-energy and water adsorption energy. The present results indicate that Co0.75Ni0.25Se/NF exhibits advanced electrocatalytic activity for overall water splitting. This work offers an appropriate methodology and theoretical guidance to synthesize a bimetal-selenide electrocatalyst for water splitting.
水分解长期以来一直被视为一种有前景的化学反应,它可以生产清洁的氢燃料,以缓解能源危机和环境污染。在此,我们报道了通过在多孔泡沫镍上两步生长金属钴镍硒纳米棒形成的Co0.75Ni0.25Se/NF用作双功能电催化剂。泡沫镍与钴源一起作为缓慢释放的镍源,形成特殊比例的钴镍硒化物。由于其独特的粗糙纳米结构、双金属协同效应和本征金属特性,所制备的Co0.75Ni0.25Se/NF电极在析氧反应中表现出269 mV(50 mA cm-2)的低过电位,在析氢反应中表现出106 mV(10 mA cm-2)的过电位。此外, 这种双功能电催化剂需要1.�0 V的电池电压才能实现10 mA cm-2的电流密度。此外,基于理论计算,进一步表明Co和Ni元素之间的协同作用有利于改善催化剂的内部结构,从而导致高电导率、低析氢吉布斯自由能和水吸附能。目前的结果表明,Co0.75Ni?5Se/NF对全水分解表现出先进的电催化活性。这项工作为合成用于水分解的双金属硒化物电催化剂提供了合适的方法和理论指导。