Xu Zichen, Jiang Yuanjuan, Chen Jeng-Lung, Lin Ryan Yeh-Yung
State Key Laboratory of Fine Chemicals, Zhang Dayu School of Chemistry, Dalian University of Technology, Dalian, 116024 Liaoning, China.
National Synchrotron Radiation Research Center, Hsinchu 300092, Taiwan.
ACS Appl Mater Interfaces. 2023 Apr 5;15(13):16702-16713. doi: 10.1021/acsami.2c22632. Epub 2023 Mar 27.
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()F nanorods, denoted as Co-FeOOH@Ir-Co()F. The Ir-doping couples with the synergy between Co-FeOOH and Ir-Co()F effectively modulate the electronic structures and induce defect-enriched interfaces. This bestows Co-FeOOH@Ir-Co()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()F exhibits low overpotentials of 192/231/251 and 38/83/111 mV at current densities of 10/100/250 mA cm toward the OER and HER in a 1.0 M KOH electrolyte, respectively. When Co-FeOOH@Ir-Co()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. 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.
开发用于全水分解的高性能且稳健的电催化剂是非常有必要的,因为现有的电催化剂在相同电解质中对析氢反应和析氧反应(HER和OER)表现出较差的催化性能,导致成本高、能量转换效率低以及操作程序复杂。在此,通过在一维铱掺杂的氢氧化钴纳米棒上生长钴 - 沸石咪唑酯骨架材料衍生的二维钴掺杂氢氧化铁,实现了一种异质结构电催化剂,记为Co - FeOOH@Ir - Co(OH)F。铱掺杂与Co - FeOOH和Ir - Co(OH)F之间的协同作用有效地调节了电子结构并诱导了富含缺陷的界面。这赋予Co - FeOOH@Ir - Co(OH)F丰富的暴露活性位点、加速的反应动力学、改善的电荷转移能力以及优化的反应中间体吸附能,最终提高了双功能催化活性。因此,在1.0 M KOH电解质中,Co - FeOOH@Ir - Co(OH)F在电流密度为10/100/250 mA cm²时,对OER和HER的过电位分别低至192/231/251和38/83/111 mV。当Co - FeOOH@Ir - Co(OH)F用于全水分解时,在电流密度为10/100/250 mA cm²时需要的电池电压分别为1.48/1.60/1.67 V。此外,它在OER、HER和全水分解方面具有出色的长期稳定性。我们的研究为制备用于碱性全水分解的先进异质结构双功能电催化剂提供了一条有前景的途径。