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:82
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

祝大家在新的一年里科研腾飞
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
马某发布了新的文献求助30
刚刚
义气的映萱完成签到 ,获得积分10
刚刚
Ternura发布了新的文献求助10
4秒前
4秒前
坦率的镜子完成签到,获得积分10
5秒前
vicin发布了新的文献求助10
6秒前
毛豆应助enchanted采纳,获得10
7秒前
8秒前
8秒前
宋小悦完成签到,获得积分20
8秒前
保温杯坏了应助Ternura采纳,获得10
9秒前
wanci应助迷路的煎蛋采纳,获得20
9秒前
tad81发布了新的文献求助10
9秒前
一追再追完成签到,获得积分10
11秒前
11秒前
汉堡包应助外向访卉采纳,获得10
11秒前
毛豆应助亲爱的安德烈采纳,获得10
11秒前
12秒前
12秒前
13秒前
14秒前
14秒前
16秒前
17秒前
漏晨发布了新的文献求助10
17秒前
18秒前
瘦瘦不乐发布了新的文献求助10
19秒前
20秒前
nana湘发布了新的文献求助10
20秒前
风趣灵槐完成签到,获得积分10
21秒前
jzx关注了科研通微信公众号
22秒前
毛豆应助烂漫的飞松采纳,获得10
22秒前
23秒前
外向访卉发布了新的文献求助10
24秒前
24秒前
咕咕咕咕咕完成签到,获得积分10
24秒前
漏晨完成签到,获得积分10
28秒前
28秒前
29秒前
Jasper应助要减肥的鹤采纳,获得10
30秒前
高分求助中
Востребованный временем 2500
The Three Stars Each: The Astrolabes and Related Texts 1500
Classics in Total Synthesis IV: New Targets, Strategies, Methods 1000
Les Mantodea de Guyane 800
Mantids of the euro-mediterranean area 700
The Oxford Handbook of Educational Psychology 600
有EBL数据库的大佬进 Matrix Mathematics 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 内科学 纳米技术 物理 计算机科学 化学工程 基因 复合材料 遗传学 物理化学 免疫学 细胞生物学 催化作用 病理
热门帖子
关注 科研通微信公众号,转发送积分 3416546
求助须知:如何正确求助?哪些是违规求助? 3018380
关于积分的说明 8884060
捐赠科研通 2705746
什么是DOI,文献DOI怎么找? 1483862
科研通“疑难数据库(出版商)”最低求助积分说明 685830
邀请新用户注册赠送积分活动 680985