Dual Doping of N and F on Co 3 O 4 to Activate the Lattice Oxygen for Efficient and Robust Oxygen Evolution Reaction

析氧 材料科学 兴奋剂 氧气 格子(音乐) 物理化学 光电子学 化学 电化学 物理 电极 声学 有机化学
作者
Chen Li,Beirong Ye,Bo Ouyang,Tengfei Zhang,Tao Tang,Zhong Qiu,Sipu Li,Yongqi Li,Renhong Chen,Wei Wen,Ming Song,Bingbao Mei,Xinhui Xia,Yongqi Zhang
出处
期刊:Advanced Materials [Wiley]
卷期号:37 (28): e2501381-e2501381 被引量:73
标识
DOI:10.1002/adma.202501381
摘要

Abstract The oxygen evolution reaction (OER) is a pivotal process in numerous renewable energy conversion technologies. However, its sluggish intrinsic kinetics and intricate transfer process impede the efficient conversion of energy. Activating the lattice oxygen mechanism (LOM) is of paramount importance to break through the theoretical scaling relationship and boost the oxygen evolution catalytic activity. In this contribution, N and F are successfully introduced into Co 3 O 4 simultaneously as heteroatoms via a controllable plasma strategy to modulate the covalency property of metal‐oxygen. Theoretical simulations and experiment results demonstrated that the covalency of the cobalt‐oxygen bond is significantly enhanced under the synergistic effect of N and F, successfully triggering the LOM pathway and facilitating the OER process. The N, F‐Co 3 O 4 composite displays an impressive OER performance, exhibiting a low overpotential of 254 mV at 10 mA cm −2 and remarkable stability at 20, 150, and 400 mA cm −2 . In addition, The N, F‐Co 3 O 4 also exhibits a low overpotential of 285 mV at 20 mA cm −2 in 1 m KOH + 0.5 m NaCl solution, and remarkable performance on overall water splitting. This work offers profound insights into the OER mechanism and a crucial strategy for enhancing the electrocatalytic activity of spinel oxides.
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
2秒前
仙人掌完成签到 ,获得积分10
2秒前
lilli完成签到,获得积分10
2秒前
呵呵应助安和桥采纳,获得30
2秒前
桐桐应助lzh1353730567采纳,获得10
2秒前
小小的飞机完成签到,获得积分10
2秒前
七七不爱喝水完成签到,获得积分10
2秒前
HH完成签到,获得积分10
3秒前
11111完成签到 ,获得积分10
3秒前
Altain发布了新的文献求助10
3秒前
3秒前
NexusExplorer应助123采纳,获得10
4秒前
5秒前
我是老大应助乱飞的令牌采纳,获得10
6秒前
竹子发布了新的文献求助10
6秒前
8秒前
Jasper应助song采纳,获得10
9秒前
lhy12345完成签到,获得积分0
9秒前
9秒前
10秒前
追寻完成签到,获得积分10
11秒前
跳跃的语柔完成签到,获得积分10
11秒前
吃吃吃完成签到,获得积分10
12秒前
12秒前
12秒前
13秒前
研友_VZG7GZ应助哈哈哈采纳,获得10
14秒前
Hhh完成签到,获得积分20
14秒前
小巧天亦完成签到,获得积分10
15秒前
15秒前
lipeng完成签到,获得积分10
15秒前
Gilhog应助HHMTT采纳,获得10
16秒前
干净的天与完成签到,获得积分10
16秒前
17秒前
ricardo完成签到,获得积分10
17秒前
荷呵呵完成签到,获得积分10
17秒前
i3utter完成签到,获得积分10
17秒前
18秒前
18秒前
Sxq完成签到,获得积分10
18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
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 500
What is the Future of Psychotherapy in Digital Age? Technology, AI Bots, and Psychotherapy after Covid 444
Management and the Arts 310
Teaching Social and Emotional Learning in Physical Education 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7634923
求助须知:如何正确求助?哪些是违规求助? 9208939
关于积分的说明 19750352
捐赠科研通 7202899
什么是DOI,文献DOI怎么找? 3275133
关于科研通互助平台的介绍 2436999
邀请新用户注册赠送积分活动 2272066