A novel sulfur-nitrogen dual doped ordered mesoporous carbon electrocatalyst for efficient oxygen reduction reaction

电催化剂 聚吡咯 介孔材料 甲醇 杂原子 硫黄 化学工程 碳纤维 阴极 材料科学 介孔二氧化硅 无机化学 化学 氮气 催化作用 聚合物 聚合 电极 电化学 有机化学 物理化学 复合数 冶金 复合材料 工程类 戒指(化学)
作者
Tingting Jiang,Yi Wang,Kun Wang,Yeru Liang,Dehai Wu,Panagiotis Tsiakaras,Shuqin Song
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:189: 1-11 被引量:123
标识
DOI:10.1016/j.apcatb.2016.02.009
摘要

Despite nitrogen doped carbon (NC) materials as metal-free electrocatalysts for oxygen reduction reaction (ORR) have shown desirable performance, the state-of-the-art of NC materials is still far from satisfaction for practical fuel cell applications. In the present work, sulfur (S) and nitrogen (N) dual doped ordered mesoporous carbon (SN-OMC) materials are for the first time successfully obtained by the aid of a convenient method under the same conditions, using polythiophene (PTh) and polypyrrole (PPy) as the precursors, ordered mesoporous silica (SBA-15) as the hard template, and FeCl3 as the catalyst. The preparation conditions of the adopted method are gentle and easy to control and regulate. The experimental results have demonstrated that the obtained materials possess high ordering degree, large specific surface area and adjustable sulfur and nitrogen contents. It is found that the S1N5-OMC (the PTh/PPy feeding volume ratio is 0.5:2.5) exhibits excellent ORR electrocatalytic activity in alkaline media with desirable current density, methanol tolerance and long-term stability. Such excellent performance could be attributed to the synergistic effect between S and N, the high density of catalytic sites for ORR provided by high S-N heteroatoms loading, and the excellent mass transfer benefiting from ordered mesoporous pore structure. The present investigation provides a new approach to prepare S and N dual doped mesoporous carbons, which show great potential to be applied as fuel cell cathode electrocatalysts.
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
1秒前
洛莫完成签到,获得积分10
2秒前
yaxianzhi完成签到,获得积分10
4秒前
5秒前
水滴完成签到,获得积分10
6秒前
Lucas应助慈祥的世界采纳,获得10
6秒前
孤独聪健完成签到,获得积分10
7秒前
肖123发布了新的文献求助10
7秒前
张欢馨应助玲月采纳,获得30
7秒前
华仔应助玲月采纳,获得10
7秒前
ding应助玲月采纳,获得10
7秒前
打打应助温婉的以松采纳,获得10
8秒前
蓬蓬完成签到,获得积分10
10秒前
10秒前
可爱的函函应助黑胡椒采纳,获得10
10秒前
乌龟电车完成签到,获得积分10
12秒前
科研通AI6.1应助无情天川采纳,获得10
12秒前
13秒前
17秒前
Jasper应助甜甜飞阳采纳,获得10
18秒前
21秒前
21秒前
axiba应助科研通管家采纳,获得10
21秒前
AdamJie应助科研通管家采纳,获得10
22秒前
莫德里奇发布了新的文献求助10
22秒前
领导范儿应助科研通管家采纳,获得10
22秒前
liangc110完成签到,获得积分10
22秒前
shisong发布了新的文献求助50
22秒前
田様应助科研通管家采纳,获得10
22秒前
axiba应助科研通管家采纳,获得10
22秒前
无花果应助科研通管家采纳,获得10
22秒前
AdamJie应助科研通管家采纳,获得10
22秒前
小蘑菇应助科研通管家采纳,获得20
22秒前
完美世界应助科研通管家采纳,获得10
22秒前
隐形曼青应助科研通管家采纳,获得30
22秒前
彭于晏应助科研通管家采纳,获得10
22秒前
AdamJie应助科研通管家采纳,获得10
22秒前
22秒前
小马甲应助科研通管家采纳,获得10
22秒前
AdamJie应助科研通管家采纳,获得10
22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
Les Mantodea de Guyane Insecta, Polyneoptera 2000
Leading Academic-Practice Partnerships in Nursing and Healthcare: A Paradigm for Change 800
Signals, Systems, and Signal Processing 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Research Methods for Applied Linguistics 500
Picture Books with Same-sex Parented Families Unintentional Censorship 444
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 6412589
求助须知:如何正确求助?哪些是违规求助? 8231642
关于积分的说明 17471003
捐赠科研通 5465296
什么是DOI,文献DOI怎么找? 2887699
邀请新用户注册赠送积分活动 1864401
关于科研通互助平台的介绍 1702961