Nickel ferrocyanide as a high-performance urea oxidation electrocatalyst

过电位 催化作用 尿素 电催化剂 无机化学 化学 亚铁氰化物 分解 氧化还原 制氢 化学工程 电化学 电极 有机化学 物理化学 工程类
作者
Shi-Kui Geng,Yao Zheng,Shanqing Li,Hui Su,Xu Zhao,Jun Hu,Haibo Shu,Mietek Jaroniec,Ping Chen,Qinghua Liu,Shi‐Zhang Qiao
出处
期刊:Nature Energy [Nature Portfolio]
卷期号:6 (9): 904-912 被引量:688
标识
DOI:10.1038/s41560-021-00899-2
摘要

Urea is often present in waste water but can be used in powering fuel cells and as an alternative oxidation substrate to water in an electrolyser. However, an insufficient mechanistic understanding and the lack of efficient catalysts for the urea oxidation reaction have hampered the development of such applications. Here we demonstrate that a nickel ferrocyanide (Ni2Fe(CN)6) catalyst supported on Ni foam can drive the urea oxidation reaction with a higher activity and better stability than those of conventional Ni-based catalysts. Our experimental and computational data suggest a urea oxidation reaction pathway different from most other Ni-based catalysts that comprise NiOOH derivatives as the catalytically active compound. Ni2Fe(CN)6 appears to be able to directly facilitate a two-stage reaction pathway that involves an intermediate ammonia production (on the Ni site) and its decomposition to N2 (on the Fe site). Owing to the different rate-determining steps with more favourable thermal/kinetic energetics, Ni2Fe(CN)6 achieves a 100 mA cm−2 anodic current density at a potential of 1.35 V (equal to an overpotential of 0.98 V). Urea oxidation could be a lower-energy alternative to water oxidation in hydrogen-producing electrolysers, but improved catalysts are required to facilitate the reaction. Geng et al. report nickel ferrocyanide as a promising catalyst and suggest that it operates via a different pathway to that of previous materials.
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
1秒前
1秒前
大意的书兰完成签到 ,获得积分10
2秒前
3秒前
研友_VZG7GZ应助mosisa采纳,获得10
3秒前
顾矜应助rudjs采纳,获得10
4秒前
天天快乐应助林悦酥采纳,获得10
5秒前
cocodu应助sweet采纳,获得10
5秒前
7秒前
稳重的雪瑶完成签到,获得积分10
8秒前
lucky发布了新的文献求助30
9秒前
CC完成签到,获得积分10
9秒前
uu完成签到 ,获得积分10
10秒前
11秒前
进击的水稻完成签到 ,获得积分10
11秒前
12秒前
13秒前
叶子完成签到,获得积分10
13秒前
jack-hunt完成签到,获得积分10
14秒前
14秒前
666完成签到,获得积分10
15秒前
15秒前
17秒前
Sonnet发布了新的文献求助10
17秒前
xiezizai发布了新的文献求助10
18秒前
吴糖完成签到,获得积分10
18秒前
科研通AI6.2应助gerolng采纳,获得10
18秒前
lucky完成签到,获得积分10
19秒前
19秒前
就是现在发布了新的文献求助10
20秒前
20秒前
21秒前
21秒前
22秒前
22秒前
RJ完成签到,获得积分20
22秒前
田様应助苹果摇伽采纳,获得10
23秒前
23秒前
无敌咖啡豆完成签到,获得积分10
23秒前
Bugu发布了新的文献求助10
23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
Reducing Compassion Fatigue, Secondary Traumatic Stress and Burnout 600
Comparative Elite Sport Development Systems, Structures and Public Policy 600
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Auslegungsgeschichte 500
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
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 7636785
求助须知:如何正确求助?哪些是违规求助? 9210552
关于积分的说明 19756125
捐赠科研通 7204274
什么是DOI,文献DOI怎么找? 3275534
关于科研通互助平台的介绍 2437291
邀请新用户注册赠送积分活动 2272660