Charge transfer of carbon nanomaterials for efficient metal-free electrocatalysis

被引:107
|
作者
Paul, Rajib [1 ]
Zhai, Qingfeng [2 ]
Roy, Ajit K. [3 ]
Dai, Liming [2 ]
机构
[1] Case Western Reserve Univ, Case Sch Engn, Dept Macromol Sci & Engn, Cleveland, OH USA
[2] Univ New South Wales, Australian Carbon Mat Ctr A CMC, Sch Chem Engn, Sydney, NSW 2052, Australia
[3] Air Force Res Lab, Mat & Mfg Directorate, Dayton, OH USA
来源
INTERDISCIPLINARY MATERIALS | 2022年 / 1卷 / 01期
基金
澳大利亚研究理事会;
关键词
carbon; catalyst; charge transfer; defect; doping; OXYGEN REDUCTION REACTION; NITROGEN-DOPED GRAPHENE; ENERGY-CONVERSION; MICROWAVE PLASMA; ORGANIC POLYMERS; CO2; ADSORPTION; ACTIVE-SITES; NANOTUBES; CATALYSTS; FUNCTIONALIZATION;
D O I
10.1002/idm2.12010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Recently, carbon-based metal-free electrocatalysts (C-MFECs) have drawn considerable research attention because of their attractive physicochemical characteristics, cost-effectiveness, and ability to convert and store energy efficiently. Efficient intramolecular charge transfer among different parts of the carbon electrocatalyst and/or intermolecular charge transfer between electrocatalyst and electrolyte dictate the ultimate energy conversion performance. Experimental results and theoretical analyses have demonstrated that rational design of metal-free carbon nanomaterials, coupled with proper intramolecular charge transfer through heteroatom doping, incorporation of Stone-Wales defects, and/or intermolecular charge transfer through adsorption of appropriate molecules/moieties, can promote efficient electrocatalysis. In this article, we will first provide the related theoretical principles and then present an overview on the rational design and development of C-MFECs for efficient charge transfer, followed by elucidating charge-transfer processes for different electrocatalytic reactions related to renewable energy conversion and environmental remediation technologies. Finally, the current challenges and future perspectives in this exciting field will be discussed.
引用
收藏
页码:28 / 50
页数:23
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