Nitrogen and oxygen dual-doped porous carbons prepared from pea protein as electrode materials for high performance supercapacitors

被引:71
作者
Demir, Muslum [1 ,2 ]
Ashourirad, Babak [3 ]
Mugumya, Jethrine H. [1 ]
Saraswat, Sushi K. [1 ]
El-Kaderi, Hani M. [3 ]
Gupta, Ram B. [1 ]
机构
[1] Virginia Commonwealth Univ, Dept Chem & Life Sci Engn, Med Coll Virginia Campus, Richmond, VA 23284 USA
[2] Osmaniye Korkut Ata Univ, Dept Chem Engn, Fakiusagi, Osmaniye, Turkey
[3] Virginia Commonwealth Univ, Dept Chem, Box 2006, Richmond, VA 23284 USA
关键词
Porous carbons; Biochar; Electrode; Supercapacitor; Nitrogen and oxygen co-doping; TRANSITION-METAL OXIDES; CAPACITY BATTERY ANODES; ACTIVATED CARBONS; HYDROTHERMAL CARBONIZATION; ELECTROCHEMICAL STORAGE; KOH ACTIVATION; ENERGY; BIOMASS; GRAPHENE; MICRO;
D O I
10.1016/j.ijhydene.2018.03.220
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
Porous carbons as electrode materials are highly desired for use in energy storage/conversion devices. Herein, the development of a series of highly porous nitrogen and oxygen co-doped carbons by using pea protein (PP) as a cost-effective, sustainable and nitrogen rich precursor is reported. Pea protein derived carbons (PPDCs) have been prepared by applying a straightforward two-step synthetic route including pyrolysis and KOH-chemical activation. Potassium hydroxide has been employed to generate porosity and introduce oxygen functionalities into the framework of carbon. The heteroatoms doping content and porosity parameters have been tuned by varying the synthesis temperature and activator to precursor ratio. The carbon obtained with optimal synthetic parameters (T = 800 degrees C and KOH/Precursor = 4) featured the highest surface area, the maximal pore volume and N-/O doping level of 3500 m(2) g(-1), 1.76 cm(3) g(-1), and 2.5-/17.9 at%, respectively. PPDC-4-800 as supercapacitor presented a very high specific capacitance (413 F g(-1) at 1.0 A g(-1) in 1 M KOH), remarkable cycling stability (92% retention after 20000 cycles) and outstanding rate capability (210 F g(-1) at 30 A g(-1)). The cooperative effects of the well-developed porous architecture and surface modification of PPDCs resulted in enhanced electrochemical performances, suggesting their potential application for energy storage devices. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:18549 / 18558
页数:10
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