Heterostructured Ultrathin Two-Dimensional Co-FeOOH Nanosheets@1D Ir-Co(OH)F Nanorods for Efficient Electrocatalytic Water Splitting

分解水 双功能 析氧 电催化剂 材料科学 纳米棒 催化作用 电解质 化学工程 电化学 纳米技术 无机化学 电极 化学 物理化学 生物化学 光催化 工程类
作者
Zichen Xu,Yuanjuan Jiang,Jeng‐Lung Chen,Ryan Yeh‐Yung Lin
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (13): 16702-16713 被引量:36
标识
DOI:10.1021/acsami.2c22632
摘要

It is highly desirable to develop high-performance and robust electrocatalysts for overall water splitting, as the existing electrocatalysts exhibit poor catalytic performance toward hydrogen and oxygen evolution reactions (HER and OER) in the same electrolytes, resulting in high cost, low energy conversion efficiency, and complicated operating procedures. Herein, a heterostructured electrocatalyst is realized by growing Co-ZIF-67-derived 2D Co-doped FeOOH on 1D Ir-doped Co(OH)F nanorods, denoted as Co-FeOOH@Ir-Co(OH)F. The Ir-doping couples with the synergy between Co-FeOOH and Ir-Co(OH)F effectively modulate the electronic structures and induce defect-enriched interfaces. This bestows Co-FeOOH@Ir-Co(OH)F with abundant exposed active sites, accelerated reaction kinetics, improved charge transfer abilities, and optimized adsorption energies of reaction intermediates, which ultimately boost the bifunctional catalytic activity. Consequently, Co-FeOOH@Ir-Co(OH)F exhibits low overpotentials of 192/231/251 and 38/83/111 mV at current densities of 10/100/250 mA cm-2 toward the OER and HER in a 1.0 M KOH electrolyte, respectively. When Co-FeOOH@Ir-Co(OH)F is used for overall water splitting, cell voltages of 1.48/1.60/1.67 V are required at current densities of 10/100/250 mA cm-2. Furthermore, it possesses outstanding long-term stability for OER, HER, and overall water splitting. Our study provides a promising way to prepare advanced heterostructured bifunctional electrocatalysts for overall alkaline water splitting.
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