Continuous Network of Phase-Tuned Nickel Sulfide Nanostructures for Electrocatalytic Water Splitting

硫化镍 分解水 过电位 材料科学 硫化物 电解质 贵金属 电化学 化学工程 无机化学 析氧 电催化剂 纳米结构 催化作用 纳米技术 金属 化学 电极 冶金 物理化学 光催化 有机化学 工程类
作者
Anand P. Tiwari,Yeoheung Yoon,Travis G. Novak,Ki‐Seok An,Seungwon Jeon
出处
期刊:ACS applied nano materials [American Chemical Society]
卷期号:2 (8): 5061-5070 被引量:50
标识
DOI:10.1021/acsanm.9b00985
摘要

To date, nanostructures of 3d-group transition metal (i.e., Fe, Co, Ni, etc.) derivatives show the highest electrocatalytic performance among non-noble-metal electrocatalysts for water splitting in acidic electrolyte. However, the poor electrochemical conductivity (∼10–4 S/cm) of nanostructures restricts practical application for overall electrocatalytic activity. Herein, continuously networked nanostructures of phase-tuned nickel sulfide foams for efficient water splitting electrocatalysts in both acidic and alkaline electrolytes are reported. Because continuously networked nanostructures of nickel sulfide foams possess an integral structure, they exhibit high electrochemical conductivity (∼1 S/cm), which eases adsorption/desorption of H+ and OH– ions for efficient overall water splitting. By tuning the stoichiometry of sulfur, four different phases of continuously networked nanostructures of nickel sulfides (αNiS, βNiS, Ni3S2, and Ni7S6) foams are formed by facile phase transformation of nickel. Among them, the Ni7S6 foam (Ni7S6-F) possesses superior electrocatalytic activity with extremely low overpotential of 70 mV (for hydrogen evolution reaction) and 1.37 V (for oxygen evolution reaction) at 10 mA/cm2 in acidic and alkaline medium, respectively, which is close to noble-metal-based electrocatalysts. As a result, this work demonstrates a facile synthesis route to optimize nickel sulfide electrocatalysts through phase-tuning and continuous networking for overall water splitting and would be applicable on other nanostructured electrocatalysts to improve their electrocatalytic activity for practical applications in future energy devices.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
乐风完成签到,获得积分10
1秒前
sandy完成签到 ,获得积分20
1秒前
gdh发布了新的文献求助10
2秒前
科研通AI5应助小白采纳,获得10
2秒前
脑洞疼应助舒心书南采纳,获得10
4秒前
Hello应助coco采纳,获得10
4秒前
奶盖呀完成签到 ,获得积分10
4秒前
天天快乐应助小C采纳,获得10
5秒前
Rainnnn完成签到,获得积分20
7秒前
感动水杯发布了新的文献求助10
7秒前
迪迦完成签到,获得积分10
8秒前
Estella发布了新的文献求助10
9秒前
倔驴发布了新的文献求助10
9秒前
10秒前
11秒前
倷倷完成签到 ,获得积分10
11秒前
SciGPT应助McGrady采纳,获得10
14秒前
15秒前
个性凡儿完成签到,获得积分10
16秒前
wang97发布了新的文献求助10
17秒前
lzq完成签到,获得积分10
17秒前
522完成签到,获得积分10
19秒前
jxm完成签到 ,获得积分10
19秒前
Zoe_Zhang发布了新的文献求助10
20秒前
langchaozhong发布了新的文献求助10
20秒前
21秒前
彭于晏应助wangli采纳,获得10
21秒前
22秒前
22秒前
Joanna完成签到,获得积分10
24秒前
南瓜豆腐完成签到 ,获得积分10
25秒前
东莱牧鲲完成签到,获得积分10
25秒前
McGrady发布了新的文献求助10
26秒前
wwj完成签到,获得积分10
26秒前
小马甲应助852采纳,获得10
26秒前
mrt发布了新的文献求助30
26秒前
27秒前
28秒前
Cosmicspirit完成签到,获得积分10
31秒前
kokjh发布了新的文献求助10
32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
Manipulating the Mouse Embryo: A Laboratory Manual, Fourth Edition 1000
Determination of the boron concentration in diamond using optical spectroscopy 600
The Netter Collection of Medical Illustrations: Digestive System, Volume 9, Part III - Liver, Biliary Tract, and Pancreas (3rd Edition) 600
Founding Fathers The Shaping of America 500
A new house rat (Mammalia: Rodentia: Muridae) from the Andaman and Nicobar Islands 500
Writing to the Rhythm of Labor Cultural Politics of the Chinese Revolution, 1942–1976 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 催化作用 遗传学 冶金 电极 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 4545841
求助须知:如何正确求助?哪些是违规求助? 3977345
关于积分的说明 12316080
捐赠科研通 3645565
什么是DOI,文献DOI怎么找? 2007662
邀请新用户注册赠送积分活动 1043268
科研通“疑难数据库(出版商)”最低求助积分说明 932088