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:27
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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
许十五完成签到,获得积分10
刚刚
调皮小蘑菇完成签到,获得积分10
刚刚
拉布拉卡发布了新的文献求助10
刚刚
爆米花应助难过的谷芹采纳,获得10
刚刚
一期一会发布了新的文献求助10
刚刚
小二郎应助忧郁凌波采纳,获得10
1秒前
1秒前
wang完成签到,获得积分10
2秒前
所所应助LLL采纳,获得10
2秒前
2秒前
开心的又夏完成签到,获得积分10
2秒前
欣喜冷卉完成签到,获得积分10
2秒前
青雪完成签到 ,获得积分10
2秒前
2秒前
今后应助loopy采纳,获得10
2秒前
今后应助loopy采纳,获得10
2秒前
木槐草发布了新的文献求助30
2秒前
CUI发布了新的文献求助10
2秒前
2秒前
小蘑菇应助团子采纳,获得10
4秒前
塞班发布了新的文献求助10
4秒前
浅浅的发布了新的文献求助10
4秒前
5秒前
5秒前
小狮子发布了新的文献求助30
5秒前
无极微光应助Lloyd_Lee采纳,获得20
5秒前
6秒前
keke发布了新的文献求助30
7秒前
7秒前
7秒前
WF完成签到,获得积分10
8秒前
8秒前
一灯大师发布了新的文献求助30
8秒前
冯斌发布了新的文献求助10
8秒前
8秒前
8秒前
9秒前
量子星尘发布了新的文献求助10
9秒前
帕丁顿发布了新的文献求助10
10秒前
10秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Introduction to strong mixing conditions volume 1-3 5000
Clinical Microbiology Procedures Handbook, Multi-Volume, 5th Edition 2000
从k到英国情人 1500
The Cambridge History of China: Volume 4, Sui and T'ang China, 589–906 AD, Part Two 1000
The Composition and Relative Chronology of Dynasties 16 and 17 in Egypt 1000
Russian Foreign Policy: Change and Continuity 800
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5727863
求助须知:如何正确求助?哪些是违规求助? 5310392
关于积分的说明 15312447
捐赠科研通 4875237
什么是DOI,文献DOI怎么找? 2618649
邀请新用户注册赠送积分活动 1568278
关于科研通互助平台的介绍 1524932