Unique-Structure MoS2 Grow on Nickel Foam As Highly Efficient Self-Supported Electrode for Oxygen Evolution Reaction

过电位 材料科学 析氧 线性扫描伏安法 介电谱 化学工程 电催化剂 电化学 催化作用 电解质 电极 循环伏安法 冶金 化学 有机化学 物理化学 工程类
作者
Zizhou He,Hui Guo,Sydney Ardoin,Jed D. Lacoste,Ling Fei
出处
期刊:Meeting abstracts 卷期号:MA2019-01 (29): 1419-1419
标识
DOI:10.1149/ma2019-01/29/1419
摘要

Growing demand for sustainable, clean, efficient energy conversion system has derived tremendous interest to develop cost-effective and highly efficient electrocatalysts for oxygen evolution reaction (OER). Sulfides have recently attracted great attention due to their highly efficient electrocatalytic activity. MoS 2 has been verified as an efficient catalyst toward OER because of its durability, cost-efficiency and high activity. However, binder and extra conductive materials are required to attach electrocatalyst on a conductive substrate which will result in restricted active surface areas, undesirable interfaces and lots of dead volumes. Binder-free self-supported material can eliminate these problems. Herein, we synthesize self-supported binder-free MoS 2 on 3D porous nickel foam (NF) with excellent activity and stability via a facile hydrothermal method. The MoS 2 @NF electrode is tested in 0.1mol KOH by linear sweep voltammetry (LSV), electrochemical surface area (ECSA) and electrochemical impedance spectroscopy (EIS). Compared with different substrates (Cu foam, NF, Cu paper and carbon paper), MoS 2 @NF electrode where NF as substrate shows the lowest overpotential at 10mA cm -2 of 359mV for OER. Furthermore, the overpotential at 10mA cm -2 after 10hr is 419mV, which demonstrates high stability and activity. Such high electrochemical performance may attribute to the following reasons: 1) the large ECSA and good conductivity, that improves utilization of electroactive sites and electron transfer; 2) the unique 3D porous structure, that facilitates electrolyte penetration and reactant/product diffusion; and 3) the sulfur vacancy in MoS 2 , that accelerates the O-H bond breaking.

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
麦乐提完成签到,获得积分10
1秒前
姜懿发布了新的文献求助10
1秒前
整齐冬瓜发布了新的文献求助10
2秒前
2秒前
3秒前
3秒前
3秒前
Jamie2完成签到,获得积分10
3秒前
4秒前
康康发布了新的文献求助20
4秒前
5秒前
5秒前
WFZ发布了新的文献求助10
5秒前
高贵的不凡完成签到,获得积分10
6秒前
科研通AI2S应助省委一把手采纳,获得10
6秒前
6秒前
8秒前
所所应助外向从灵采纳,获得10
8秒前
ff999完成签到,获得积分10
8秒前
努力学习发布了新的文献求助10
9秒前
bwl发布了新的文献求助10
9秒前
10秒前
ll发布了新的文献求助10
10秒前
11秒前
12秒前
康康完成签到,获得积分20
13秒前
善学以致用应助bwl采纳,获得10
13秒前
14秒前
爱学习的好孩子完成签到,获得积分10
15秒前
SDNUDRUG发布了新的文献求助10
15秒前
16秒前
16秒前
academic_rookie完成签到,获得积分10
17秒前
努力学习完成签到,获得积分10
17秒前
22完成签到,获得积分20
18秒前
xiaowang完成签到,获得积分10
18秒前
香蕉觅云应助水博士采纳,获得10
18秒前
19秒前
qqdm完成签到 ,获得积分10
19秒前
澍澍完成签到,获得积分10
19秒前
高分求助中
Ophthalmic Equipment Market by Devices(surgical: vitreorentinal,IOLs,OVDs,contact lens,RGP lens,backflush,diagnostic&monitoring:OCT,actorefractor,keratometer,tonometer,ophthalmoscpe,OVD), End User,Buying Criteria-Global Forecast to2029 2000
A new approach to the extrapolation of accelerated life test data 1000
Cognitive Neuroscience: The Biology of the Mind 1000
Cognitive Neuroscience: The Biology of the Mind (Sixth Edition) 1000
ACSM’s Guidelines for Exercise Testing and Prescription, 12th edition 588
Christian Women in Chinese Society: The Anglican Story 500
A Preliminary Study on Correlation Between Independent Components of Facial Thermal Images and Subjective Assessment of Chronic Stress 500
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 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3961170
求助须知:如何正确求助?哪些是违规求助? 3507441
关于积分的说明 11136135
捐赠科研通 3239926
什么是DOI,文献DOI怎么找? 1790456
邀请新用户注册赠送积分活动 872439
科研通“疑难数据库(出版商)”最低求助积分说明 803152