Heterostructured Ni3S2–Ni3P/NF as a Bifunctional Catalyst for Overall Urea–Water Electrolysis for Hydrogen Generation

制氢 催化作用 材料科学 电解 分解水 阳极 电解水 化学工程 双功能 析氧 无机化学 电化学 化学 电极 物理化学 有机化学 光催化 工程类 电解质
作者
Jinchao Liu,Yao Wang,Yifei Liao,Chaoling Wu,Yigang Yan,Haijiao Xie,Yungui Chen
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (23): 26948-26959 被引量:100
标识
DOI:10.1021/acsami.1c04325
摘要

Urea oxidation reaction (UOR) has been proposed to replace the formidable oxygen evolution reaction (OER) to reduce the energy consumption for producing hydrogen from electrolysis of water owing to its much lower thermodynamic oxidation potential compared to that of the OER. Therefore, exploring a highly efficient and stable hydrogen evolution and urea electrooxidation bifunctional catalyst is the key to achieve economical and efficient hydrogen production. In this paper, we report a heterostructured sulfide/phosphide catalyst (Ni3S2–Ni3P/NF) synthesized via one-step thermal treatment of Ni(OH)2/NF, which allows the simultaneous occurrence of phosphorization and sulfuration. The obtained Ni3S2–Ni3P/NF catalyst shows a sheet structure with an average sheet thickness of ∼100 nm, and this sheet is composed of interconnected Ni3S2 and Ni3P nanoparticles (∼20 nm), between which there are a large number of accessible interfaces of Ni3S2–Ni3P. Thus, the Ni3S2–Ni3P/NF exhibits superior performance for both UOR and hydrogen evolution reaction (HER). For the overall urea–water electrolysis, to achieve current densities of 10 and 100 mA cm–2, cell voltage of only 1.43 and 1.65 V is required using this catalyst as both the anode and the cathode. Moreover, this catalyst also maintains fairly excellent stability after a long-term testing, indicating its potential for efficient and energy-saving hydrogen production. The theoretical calculation results show that the Ni atoms at the interface are the most efficient catalytically active site for the HER, and the free energy of hydrogen adsorption is closest to thermal neutrality, which is only 0.16 eV. A self-driven electron transfer at the interface, making the Ni3S2 sides become electron donating while Ni3P sides become electron withdrawing, may be the reason for the enhancement of the UOR activity. Therefore, this work shows an easy treatment for enhancing the catalytic activity of Ni-based materials to achieve high-efficiency urea–water electrolysis.
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
wuzhei完成签到,获得积分10
刚刚
打打应助调皮的小甜瓜采纳,获得10
刚刚
123发布了新的文献求助10
1秒前
上官若男应助青松果采纳,获得10
1秒前
爆米花应助123采纳,获得10
1秒前
czy完成签到,获得积分10
2秒前
淡然新蕾完成签到,获得积分10
2秒前
Zz发布了新的文献求助10
2秒前
俏皮短靴完成签到,获得积分10
3秒前
3秒前
4秒前
11234发布了新的文献求助10
6秒前
7秒前
小雪完成签到 ,获得积分10
7秒前
joe完成签到,获得积分10
7秒前
深情安青应助华华采纳,获得20
8秒前
9秒前
眯眯眼完成签到,获得积分10
9秒前
耘清完成签到,获得积分10
9秒前
活泼孤风完成签到,获得积分10
10秒前
12秒前
zxz193发布了新的文献求助10
13秒前
科目三应助hhh采纳,获得10
13秒前
眯眯眼发布了新的文献求助10
14秒前
一袋干脆面完成签到,获得积分10
15秒前
shuyingRen完成签到,获得积分10
16秒前
希望天下0贩的0应助hhhyd采纳,获得10
17秒前
Abstract完成签到,获得积分10
17秒前
田様应助玛卡巴卡小心点采纳,获得10
18秒前
慕青应助LYC采纳,获得10
18秒前
18秒前
huhuhuhu发布了新的文献求助10
19秒前
20秒前
21秒前
头头发布了新的文献求助10
21秒前
万能图书馆应助sqw采纳,获得10
21秒前
李晨旭完成签到,获得积分10
22秒前
随机昵称完成签到,获得积分10
22秒前
22秒前
YYY完成签到 ,获得积分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
晶种分解过程与铝酸钠溶液混合强度关系的探讨 8888
Les Mantodea de Guyane Insecta, Polyneoptera 2000
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
Signals, Systems, and Signal Processing 610
The Sage Handbook of Digital Labour 600
汪玉姣:《金钱与血脉:泰国侨批商业帝国的百年激荡(1850年代-1990年代)》(2025) 500
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6415336
求助须知:如何正确求助?哪些是违规求助? 8234308
关于积分的说明 17486200
捐赠科研通 5468303
什么是DOI,文献DOI怎么找? 2889047
邀请新用户注册赠送积分活动 1865926
关于科研通互助平台的介绍 1703553