Towards a new avenue for rapid synthesis of electrocatalytic electrodes via laser-induced hydrothermal reaction for water splitting

过电位 分解水 材料科学 电极 制氢 热液循环 化学工程 煅烧 电化学 电流密度 析氧 氢氧化物 催化作用 化学 光催化 生物化学 物理 物理化学 量子力学 工程类
作者
Sha Yang,Menghui Zhu,Kun Huang,Yang Zhang,Francis Peter Moissinac,Zhizhou Zhang,Dongxu Cheng,Paul Mativenga,Zhu Liu
出处
期刊:International journal of extreme manufacturing [IOP Publishing]
卷期号:6 (1): 015502-015502 被引量:1
标识
DOI:10.1088/2631-7990/ad038f
摘要

Abstract Electrochemical production of hydrogen from water requires the development of electrocatalysts that are active, stable, and low-cost for water splitting. To address these challenges, researchers are increasingly exploring binder-free electrocatalytic integrated electrodes (IEs) as an alternative to conventional powder-based electrode preparation methods, for the former is highly desirable to improve the catalytic activity and long-term stability for large-scale applications of electrocatalysts. Herein, we demonstrate a laser-induced hydrothermal reaction (LIHR) technique to grow NiMoO 4 nanosheets on nickel foam, which is then calcined under H 2 /Ar mixed gases to prepare the IE IE-NiMo-LR. This electrode exhibits superior hydrogen evolution reaction performance, requiring overpotentials of 59, 116 and 143 mV to achieve current densities of 100, 500 and 1000 mA·cm −2 . During the 350 h chronopotentiometry test at current densities of 100 and 500 mA·cm −2 , the overpotential remains essentially unchanged. In addition, NiFe-layered double hydroxide grown on Ni foam is also fabricated with the same LIHR method and coupled with IE-NiMo-IR to achieve water splitting. This combination exhibits excellent durability under industrial current density. The energy consumption and production efficiency of the LIHR method are systematically compared with the conventional hydrothermal method. The LIHR method significantly improves the production rate by over 19 times, while consuming only 27.78% of the total energy required by conventional hydrothermal methods to achieve the same production.

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
肉鸡完成签到,获得积分10
刚刚
迷路的迎南完成签到,获得积分10
1秒前
轻抚女高脸颊完成签到,获得积分10
1秒前
哈哈哈发布了新的文献求助20
2秒前
3秒前
yyc发布了新的文献求助10
3秒前
4秒前
袁睿韬发布了新的文献求助10
4秒前
ding应助爱学习的慕采纳,获得10
5秒前
泥丸不丸发布了新的文献求助10
5秒前
5秒前
芸芸发布了新的文献求助10
7秒前
我是老大应助djbj2022采纳,获得20
8秒前
Bellamie发布了新的文献求助30
8秒前
科目三应助TATA采纳,获得10
9秒前
9秒前
慕青应助康康采纳,获得10
9秒前
小马甲应助无情白羊采纳,获得10
10秒前
10秒前
123完成签到,获得积分10
10秒前
11秒前
12秒前
xiaxia发布了新的文献求助10
12秒前
杨华启应助慕沐采纳,获得10
13秒前
感性的梦露完成签到,获得积分10
13秒前
狮子沟核聚变骡子完成签到 ,获得积分10
15秒前
15秒前
解寄灵发布了新的文献求助10
15秒前
深情安青应助ZZY采纳,获得10
15秒前
ccnss完成签到,获得积分10
18秒前
快快快快快快快快快完成签到 ,获得积分10
19秒前
yazhong发布了新的文献求助10
19秒前
核桃发布了新的文献求助10
20秒前
李健的小迷弟应助sci大户采纳,获得10
22秒前
22秒前
22秒前
mt完成签到 ,获得积分10
22秒前
23秒前
爱学习的慕完成签到,获得积分10
24秒前
量子星尘发布了新的文献求助10
25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
Handbook of pharmaceutical excipients, Ninth edition 5000
Aerospace Standards Index - 2026 ASIN2026 3000
Terrorism and Power in Russia: The Empire of (In)security and the Remaking of Politics 1000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6044918
求助须知:如何正确求助?哪些是违规求助? 7814182
关于积分的说明 16246605
捐赠科研通 5190603
什么是DOI,文献DOI怎么找? 2777460
邀请新用户注册赠送积分活动 1760669
关于科研通互助平台的介绍 1643815