English 
     
   科学研究
   热点信息
学生工作办公室简介
联系我们
语言中心主任致辞
培养方案
专业介绍
招生问答
请加QQ群312279505
李彦光教授课题组在Advanced Functional Materials上发表论文
发布时间:2017-09-27 点击:0

题目:

High-Performance Oxygen Reduction Electrocatalyst Derived from Polydopamine and Cobalt Supported on Carbon Nanotubes for Metal-Air Batteries

作者:

Yiling Liu, Fengjiao Chen, Wen Ye, Min Zeng, Na Han, Feipeng Zhao, Xinxia Wang, and Yanguang Li*

单位:

Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123, China.

摘要:

The development of nonprecious metal-based electrocatalysts for the oxygen reduction reaction holds the decisive key to many energy conversion devices. Among several potential candidates, transition metal and nitrogen co-doped carbonaceous materials are the most promising, yet their activity and stability are still insufficient to meet   the needs of practical applications. In this study, a core–shell hybrid electrocatalyst is developed via the self-polymerization of dopamine and cobalt on carbon nanotubes (CNTs), followed by high temperature pyrolysis. The polymer-derived carbonaceous shell contains abundant structural defects and facilitates the formation of Co–N/C active sites, whereas the graphitic carbon nanotube core provides high electrical conductivity and corrosion resistance. These two components separately fulfill different functionalities, and jointly afford the catalyst with excellent electrochemical   performance. In 1M KOH, Co–N/CNT exhibits a positive half-wave potential of ≈0.91 V, low peroxide yield of <7%, as well as great stability. When used as the air catalyst of primary Zn–air and Al–air   batteries, this hybrid electrocatalyst enables large discharge current   density, high peak power density, and prolonged operation stability.

影响因子:

12.124

分区情况:

一区

链接:

http://onlinelibrary.wiley.com/doi/10.1002/adfm.201606034/full



责任编辑:向丹婷


Copyright © 2012 苏州大学纳米科学技术学院 All Rights Reserved.
  地址:苏州工业园区仁爱路199号910楼  邮编:215123
您是第 位访问者