Hubei Key Laboratory of Pollutant Analysis & Reuse Technology, College of Chemistry and Chemical Engineering, Hubei Normal University, Huangshi 435002, China.
Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices, Hubei University of Arts and Science, Xiangyang 441053, China.
J Colloid Interface Sci. 2023 Jun;639:416-423. doi: 10.1016/j.jcis.2023.02.071. Epub 2023 Feb 16.
The development of inexpensive, high efficiency electrocatalysts is a major challenge for electrolytic water to hydrogen production. Herein, an efficient porous nanoblock catalyst N-doped FeO/NiTe heterojunction for overall water splitting is reported. Notably, the obtained 3D self-supported catalysts exhibit good hydrogen evolution. reaction (HER) activity and oxygen evolution reaction (OER) properties in alkaline solution (only 70 mV and 253 mV of overpotential are needed to provide 10 mA cm current density, respectively). This is mainly due to the N-doped electronic structure optimized, the strong electronic interaction between FeO and NiTe that facilitates rapid electron transfer, the porous structure which allows the catalyst to have large surface area for effective gas release, and their synergistic effect. When used as a dual function catalyst with overall water splitting, it achieved a current density of 10 mA cm under 1.54 V with good durability (at least 42 h). The present work provides a new methodology for the study of high-performance, low-cost, and corrosion-resistant bifunctional electrocatalysts.
开发廉价、高效的电催化剂是电解水制氢的主要挑战。本文报道了一种用于全水解的高效多孔纳米块催化剂 N 掺杂 FeO/NiTe 异质结。值得注意的是,所获得的 3D 自支撑催化剂在碱性溶液中表现出良好的析氢反应 (HER) 活性和析氧反应 (OER) 性能(仅需 70 mV 和 253 mV 的过电势即可提供 10 mA cm 的电流密度)。这主要归因于 N 掺杂优化的电子结构、FeO 和 NiTe 之间的强电子相互作用,促进了快速电子转移、多孔结构使催化剂具有大的表面积,有利于有效释放气体,以及它们的协同效应。当用作具有全水解功能的双功能催化剂时,它在 1.54 V 下实现了 10 mA cm 的电流密度,具有良好的耐久性(至少 42 小时)。本工作为研究高性能、低成本、耐腐蚀的双功能电催化剂提供了一种新方法。