Application of synthesized porous graphitic carbon nitride and it's composite as excellent electrocatalysts in microbial fuel cell

被引:25
|
作者
Chakraborty, Indrajit [1 ]
Ghosh, Neel [1 ]
Ghosh, Debanjali [2 ]
Dubey, B. K. [1 ]
Pradhan, D. [2 ]
Ghangrekar, M. M. [1 ]
机构
[1] Indian Inst Technol Kharagpur, Dept Civil Engn, Kharagpur 721302, W Bengal, India
[2] Indian Inst Technol Kharagpur, Mat Sci Ctr, Kharagpur 721302, W Bengal, India
关键词
Carbon nitride; Cathode catalyst; Microbial fuel cell; Oxygen reduction reaction; Wastewater treatment; OXYGEN REDUCTION REACTION; NITROGEN-DOPED GRAPHENE; WASTE-WATER TREATMENT; EFFICIENT HYDROGEN EVOLUTION; METAL-FREE ELECTROCATALYST; AIR-CATHODE; G-C3N4; NANOSHEETS; BIOELECTRICITY GENERATION; MESOPOROUS CARBON; POWER-GENERATION;
D O I
10.1016/j.ijhydene.2020.08.118
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
The performance of microbial fuel cells (MFCs) consisting of exfoliated porous graphitic carbon nitride (ep-GCN) and its composite with acetylene black (AB) as cathode catalyst is evaluated. The cyclic voltammetry and electrochemical impedance spectroscopy of composite ep-GCN-AB indicated excellent oxygen reduction reaction activity and comparable charge transfer resistance with respect to Pt-C. The absence of X-ray diffraction peak at 2 theta = 13 degrees (corresponding to stacked structure of bulk GCN) indicated reduction in thickness. Four MFCs were operated with simulated wastewater with chemical oxygen demand (COD) of 3000 mg L-1. The maximum power densities of MFC-GAB (14.74 +/- 0.17 W m(-3)), MFC-PAB (15.68 +/- 0.58 W m(-3)) and MFC-G (12.47 +/- 0.30 W m(-3)) using ep-GCN-AB, Pt-C and ep-GCN electrocatalyst, respectively, were 2.6, 2.7 and 2.2 times higher than MFC-AB operated with only acetylene black coated cathode. The investigation demonstrates that ep-GCN and its composites can be utilized as excellent cathode catalysts in MFCs at 20 folds lesser cost than Pt-C. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:31056 / 31069
页数:14
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