Quench‐Induced Surface Engineering Boosts Alkaline Freshwater and Seawater Oxygen Evolution Reaction of Porous NiCo<sub>2</sub>O<sub>4</sub> Nanowires
Jin Yang, Yanan Wang, Jie Yang, Yajun Pang, Xinqiang Zhu, Yinzhuo Lu, Yitian Wu, Jiajie Wang, Jiajie Wang, Hao Chen, Zongkui Kou, Zhehong Shen, Zhenghui Pan, John Wang, John Wang
Abstract
Abstract The electrochemical oxygen evolution reaction (OER) by efficient catalysts is a crucial step for the conversion of renewable energy into hydrogen fuel, in which surface/near‐surface engineering has been recognized as an effective strategy for enhancing the intrinsic activities of the OER electrocatalysts. Herein, a facile quenching approach is demonstrated that can simultaneously enable the required surface metal doping and vacancy generation in reconfiguring the desired surface of the NiCo 2 O 4 catalyst, giving rise to greatly enhanced OER activities in both alkaline freshwater and seawater electrolytes. As a result, the quenched‐engineered NiCo 2 O 4 nanowire electrode achieves a current density of 10 mA cm −2 at a low overpotential of 258 mV in 1 m KOH electrolyte, showing the remarkable catalytic performance towards OER. More impressively, the same electrode also displays extraordinary activity in an alkaline seawater environment and only needs 293 mV to reach 10 mA cm −2 . Density functional theory (DFT) calculations reveal the strong electronic synergies among the metal cations in the quench‐derived catalyst, where the metal doping regulates the electronic structure, thereby yielding near‐optimal adsorption energies for OER intermediates and giving rise to superior activity. This study provides a new quenching method to obtain high‐performance transition metal oxide catalysts for freshwater/seawater electrocatalysis.