Department of Materials Science and Engineering, Liaoning Technical University, Fuxin 123000, China.
Department of Materials Science and Engineering, Liaoning Technical University, Fuxin 123000, China.
J Colloid Interface Sci. 2023 Aug;643:350-359. doi: 10.1016/j.jcis.2023.04.043. Epub 2023 Apr 15.
Rational design of low-cost and high-efficiency electrocatalysts for hydrogen evolution reaction (HER) is critical for scalable and sustainable hydrogen production from economical water-alkali splitting. Herein, density functional theory (DFT) calculations reveal that coupling NiO and CoP could effectively boost overall HER kinetics through lowing the HO dissociation barrier, accelerating the OH* transfer process, and providing the rapid H* migration kinetics as well as the appropriate H* energetics. Based on these findings, we successfully prepared a three-dimensional (3D) self-supported electrode of ultrathin CoP nanosheets directly grown on the surface-oxidized Ni nanotube arrays via a simple and scalable electrochemical synthesis method. As expected, such a heterostructure electrode exhibits superior alkaline HER performance with low overpotentials of 51 and 164 mV to drive the current densities of 10 and 500 mA cm, respectively, outperforming most of the efficient alkaline HER electrocatalysts.
理性设计低成本、高效率的析氢反应(HER)电催化剂对于从经济的水电解规模化、可持续制氢至关重要。在此,通过密度泛函理论(DFT)计算揭示,耦合 NiO 和 CoP 可以通过降低 HO 离解势垒、加速 OH转移过程、提供快速 H迁移动力学以及合适的 H*能量学,有效提升整体 HER 动力学。基于这些发现,我们成功地通过一种简单且可扩展的电化学合成方法,在表面氧化的 Ni 纳米管阵列上直接生长超薄 CoP 纳米片,制备了三维(3D)自支撑电极。不出所料,这种异质结构电极在碱性 HER 中表现出优异的性能,其电流密度为 10 和 500 mA cm 时,仅需 51 和 164 mV 的过电势,优于大多数高效碱性 HER 电催化剂。