State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, Wuhan 430070, PR China.
Nanoscale. 2018 Jul 5;10(25):11997-12002. doi: 10.1039/c8nr02198h.
Rational design and understanding of the intrinsic mechanism are critical to develop highly active and durable electrocatalysts. In this study, a series of bi-metallic boride catalysts based on Ni and Co were prepared, and their activities were evaluated. The synthesised Co-10Ni-B catalyst exhibited excellent activity for water splitting in a 1 M KOH electrolyte. The overpotential was 330 mV at a current density of 10 mA cm-2, better than previously reported mono-metallic borides and even IrO2. The synergistic effect of Co and Ni was proved by X-ray photoelectron spectroscopy and electrochemical impedance spectroscopy. The facile formation of critical intermediates CoOOH and NiOOH during the catalytic processes and a significant increase in surface area owing to the introduction of a second metal into mono-metallic boride were attributed to the superior catalytic performance of catalysts for the oxygen evolution reaction. A Co-10Ni-B-sp catalyst with a higher surface area than the Co-10Ni-B catalyst was also synthesised to evaluate the effect of a high surface area on the catalytic activity. A lower overpotential of 310 mV at a current density of 10 mA cm-2 was achieved.
合理的设计和对内在机制的理解对于开发高活性和耐用的电催化剂至关重要。在本研究中,制备了一系列基于 Ni 和 Co 的双金属硼化物催化剂,并对其活性进行了评估。合成的 Co-10Ni-B 催化剂在 1 M KOH 电解质中对水分解表现出优异的活性。在 10 mA cm-2 的电流密度下,过电位为 330 mV,优于先前报道的单金属硼化物,甚至优于 IrO2。X 射线光电子能谱和电化学阻抗谱证明了 Co 和 Ni 的协同作用。在催化过程中,关键中间体 CoOOH 和 NiOOH 的形成容易,并且由于第二种金属引入单金属硼化物,表面积显著增加,这归因于催化剂对析氧反应的优异催化性能。还合成了具有比 Co-10Ni-B 催化剂更高表面积的 Co-10Ni-B-sp 催化剂,以评估高表面积对催化活性的影响。在 10 mA cm-2 的电流密度下,实现了更低的过电位 310 mV。