Integrating the active OER and HER components as the heterostructures for the efficient overall water splitting

过电位 分解水 材料科学 析氧 煅烧 催化作用 阳极 电解质 电流密度 阴极 化学工程 异质结 光电子学 纳米技术 电极 光催化 电化学 化学 物理化学 物理 工程类 量子力学 生物化学
作者
Aiping Wu,Ying Xie,Hui Ma,Chungui Tian,Ying Gu,Haijing Yan,Xiaomeng Zhang,Guo‐Yu Yang,Honggang Fu
出处
期刊:Nano Energy [Elsevier BV]
卷期号:44: 353-363 被引量:688
标识
DOI:10.1016/j.nanoen.2017.11.045
摘要

Developing the efficient and low-cost electrocatalysts for overall water splitting is of the great importance for the production of H2. The popular bi-functional catalysts usually shown good activity for one half reaction at expense of the activity for another half-reaction, thus given a moderate performance for overall water splitting. In this paper, we have reported on integrating the active OER (Ni3N) and HER (NiMoN) components as Ni3N-NiMoN heterostructures for the effective overall water splitting. The heterostructures were constructed by the controllable nitridation of the Ni-Mo-O precursor anchored on carbon cloth (CC) under NH3 atmosphere. The micro-structures of the catalyst could be tuned by regulating the surface properties of CC and the calcination temperature. Under optimized condition, the Ni3N-NiMoN catalysts exhibited good catalytic activity for both OER and HER in alkaline electrolyte. The catalysts can achieve a current density of 10 mA cm−2 at an overpotential of 31 mV for HER, being close to Pt catalyst. Also, it only requiring an overpotential of 277 mV to reach current density of 10 mA cm−2 for OER. Moreover, the cell assembled by the identical Ni3N-NiMoN as both the cathode and anode needs only a cell voltage of 1.54 V to achieve current density of 10 mA cm−2. The superior performance of Ni3N-NiMoN heterostructures can be ascribed to the following points: 1) the simultaneous presence of active OER and HER components and the promoted action each other in the heterostructures, and 2) the exposure of the abundant active sites in the sheet-like structure assembled by the nanoparticles.
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
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
wanci的应助被不知道叫啥采纳,获得10
1秒前
小蘑菇的应助被虚心逆蝶采纳,获得10
3秒前
五条悟完成签到,获得积分10
3秒前
XXZ发布了新的文献求助10
3秒前
ding的应助被wuyongxiang采纳,获得10
6秒前
王阳洋的应助被科研通管家采纳,获得10
8秒前
上官若男的应助被科研通管家采纳,获得10
8秒前
丘比特的应助被Faye采纳,获得10
8秒前
搜集达人的应助被科研通管家采纳,获得10
8秒前
8秒前
FashionBoy的应助被科研通管家采纳,获得10
8秒前
bkagyin的应助被科研通管家采纳,获得10
9秒前
上官若男的应助被科研通管家采纳,获得10
9秒前
11秒前
12秒前
13秒前
14秒前
Ming的应助被Ssyong采纳,获得10
15秒前
16秒前
16秒前
曲123发布了新的文献求助10
17秒前
Reedy完成签到,获得积分10
17秒前
17秒前
Faye发布了新的文献求助10
19秒前
吕慧玲发布了新的文献求助10
20秒前
23秒前
英姑的应助被许易安采纳,获得10
25秒前
25秒前
29秒前
HORIS的应助被活泼飞飞采纳,获得20
29秒前
图图发布了新的文献求助30
29秒前
xing_xing的应助被安详香旋采纳,获得20
30秒前
31秒前
31秒前
fufu完成签到,获得积分10
33秒前
37秒前
踏实的蜜蜂完成签到 ,获得积分10
39秒前
汉堡包的应助被xttju2014采纳,获得10
39秒前
不知道叫啥完成签到,获得积分10
39秒前
xing_xing的应助被安详香旋采纳,获得20
42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
Rosenblum, Global Change Biology 800
自動車の空力技術 800
Organizational Behavior 510
Management and the Arts 510
Issues in Task-Based Language Teaching 500
Wafer Surface Defect 420
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7784172
求助须知:如何正确求助?哪些是违规求助? 9323459
关于积分的说明 20394518
捐赠科研通 7372907
什么是DOI,文献DOI怎么找? 3320957
关于科研通互助平台的介绍 2468887
邀请新用户注册赠送积分活动 2337167