Efficient etching of oxygen-incorporated molybdenum disulfide nanosheet arrays for excellent electrocatalytic hydrogen evolution

纳米片 二硫化钼 蚀刻(微加工) 材料科学 催化作用 电催化剂 氟化铵 纳米技术 化学工程 无机化学 电化学 化学 电极 复合材料 有机化学 图层(电子) 工程类 物理化学
作者
Xiao‐Yu Yang,Xiaoyun Li,Yi Long Wang,Cuifang Ye,Zuokai Du,Huogen Yu,Jinping Liu,Lihua Chen,Bao‐Lian Su
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:491: 245-255 被引量:22
标识
DOI:10.1016/j.apsusc.2019.06.153
摘要

Molybdenum disulfide (MoS2) has attracted considerable attention in electrocatalysis for hydrogen evolution reaction (HER). Nevertheless, its HER activity is far from that of platinum-containing electrocatalysts. Therefore, it is urgent to develop a novel strategy to simultaneously increase the number of active sites (NAC) and decrease charge-transfer resistance (RCT) to favor HER. Herein, we have demonstrated an efficient approach to etching oxygen-incorporated MoS2 (O-MoS2) nanosheet arrays on carbon cloth for excellent electrocatalytic hydrogen evolution. The influence of temperature (T) at the etching stage and the concentration of ammonium fluoride ([NH4F]) on the micro-structure and HER activity of the as-obtained catalysts have been systematically investigated. The higher etching temperature or [NH4F] is achieved; the faster etching kinetics is obtained. At slow etching kinetics, the etching degree of O-MoS2 nanosheets is relatively low, which cannot supply sufficient unsaturated sulfur atoms for HER. At fast etching, the balance between active site and electron transfer for these etched nanosheets is achieved, which is available to efficient HER. However, excessive etching leads to inefficient HER because of the unsatisfactory RCT. The optimized elctrocatalysts exhibit the superior HER activity among all samples, accompanied by excellent catalytic stability. Therefore, this work promises important application in production of hydrogen.

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
共享精神应助大力的图图采纳,获得10
1秒前
李宗洋完成签到,获得积分10
2秒前
Ax发布了新的文献求助10
2秒前
六个核桃完成签到,获得积分10
2秒前
Albert_Z应助爱喝汤的番茄采纳,获得10
2秒前
4秒前
李健的小迷弟应助汪汪智采纳,获得10
4秒前
Lily完成签到,获得积分10
4秒前
4秒前
5秒前
zsj发布了新的文献求助10
5秒前
赘婿应助零食宝采纳,获得10
5秒前
小蘑菇应助lijun采纳,获得10
6秒前
7秒前
海峰荣完成签到,获得积分10
7秒前
wanci应助mary采纳,获得10
8秒前
8秒前
青青发布了新的文献求助10
9秒前
今后应助3152采纳,获得10
9秒前
11秒前
11秒前
xingzhutang完成签到,获得积分10
12秒前
彭于晏应助张安安采纳,获得10
14秒前
Aqian发布了新的文献求助10
15秒前
15秒前
16秒前
希望天下0贩的0应助HelenZ采纳,获得10
16秒前
xingzhutang发布了新的文献求助10
17秒前
传奇3应助Icelyn采纳,获得10
17秒前
gjt完成签到,获得积分10
17秒前
Owen应助qian采纳,获得10
17秒前
19秒前
20秒前
悦耳昊强发布了新的文献求助10
20秒前
keleboys完成签到 ,获得积分10
22秒前
cc2004bj完成签到,获得积分0
22秒前
22秒前
str发布了新的文献求助10
23秒前
小周完成签到,获得积分10
25秒前
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
The Graphene Handbook (2019 Edition) 800
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
IEST-RP-CC018: Cleanroom Cleaning and Sanitization: Operating and Monitoring Procedures 600
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
How to Design, Write and Publish Qualitative Research for Insight and Impact 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 6533971
求助须知:如何正确求助?哪些是违规求助? 8327376
关于积分的说明 17837353
捐赠科研通 5635636
什么是DOI,文献DOI怎么找? 2934162
邀请新用户注册赠送积分活动 1910456
关于科研通互助平台的介绍 1769037