CoO/NiFe LDH heterojunction as a photo-assisted electrocatalyst for efficient oxygen evolution reaction

分解水 析氧 电催化剂 异质结 过电位 材料科学 化学工程 催化作用 光催化 纳米技术 光电子学 化学 电化学 电极 物理化学 生物化学 工程类
作者
Tingting Du,Yidan Gao,Ziyi Liu,Tianxiao Chen,Xin Zhang,Fengchun Yang
出处
期刊:International Journal of Hydrogen Energy [Elsevier]
卷期号:51: 907-915 被引量:14
标识
DOI:10.1016/j.ijhydene.2023.09.040
摘要

Photo-assisted electrocatalysis is a frontier direction of electrocatalysis in recent years, which is based on the synergistic effects of electrical and optical energy, providing a new strategy to improve the oxygen evolution reaction (OER) performance. The development of photo-assisted electrocatalysts for OER with high activity and long-term stability is of great significance for hydrogen production through water splitting. In this work, the CoO/NiFe LDH heterojunction are prepared as a photo-assisted electrocatalysts for the first time to enhance OER performance. The strong electron coupling between CoO and NiFe LDH is beneficial to change the electronic structure of catalyst and promote OER. Meanwhile, under illumination, NiFe LDH suppresses the photogenerated charge recombination of CoO and accelerates the charge transfer to promote the accumulation of holes in the CoO valence band, which can be used to further improve its OER performance. The CoO/NiFe LDH requires only an overpotential of 230 mV to achieve 10 mA cm−2 under illumination, which is 60 mV lower than that without irradiation. For water splitting, CoO/NiFe LDH heterojunction only requires 1.57 V (without light) and 1.52 V (with light) to achieve 10 mA cm−2, which is superiors to RuO2 and most NiFe LDH based materials. Even under the irradiation of low-power LED strip, the CoO/NiFe LDH can still exhibit excellent water splitting performance and long-term stability. This work adopts a promising photo-assisted electrocatalytic strategy to promote the efficiency of water splitting, and boosts the development of LDH-based two-dimensional materials in the field of photo-assisted electrocatalysis.
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