Standalone macroporous graphitic nanowebs for vanadium redox flow batteries
- Authors
- Lee, Min Eui; Lee, Sungho; Jin, Hyoung-Joon; Yun, Young Soo
- Issue Date
- 2018-04
- Publisher
- 한국공업화학회
- Citation
- Journal of Industrial and Engineering Chemistry, v.60, pp.85 - 90
- Abstract
- Vanadium redox flow batteries (VRFBs) have attracted much attention as next-generation large-scale energy storage devices. However, they suffer from a drop in the energy efficiency induced by the large activation polarization during vanadium redox reactions. In this study, we designed electrode materials with a high energy efficiency that are a macroporous monolith composed of three-dimensionally entangled graphitic nanoribbons. These materials were denoted as macroporous graphitic nanowebs (M-GNWs), possessing a high specific surface area of 213 m(2) g(-1) and a large pore volume of 0.82 cm(3) g(-1). A large number of oxygen functional groups (C/O ratio of 4.4) were introduced after immersing the M-GNWs in the acidic electrolyte used in VRFBs. These properties of M-GNWs led to beneficial electrochemical catalytic effects such as low anodic and cathodic peak potential separation (Delta E-p) values of similar to 73.4 mV (catholyte) in a cyclic voltammetry test conducted at a sweep rate of 2 mV s(-1). Furthermore, the VRFBs based on an M-GNW anode and cathode pair exhibited a significantly improved energy efficiency of 85.8%, which is 12.4% higher than that (73.4%) of the commercial carbon felt-based VRFBs. (C) 2017 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
- Keywords
- CARBON-FELT ELECTRODE; OXYGEN FUNCTIONAL-GROUPS; SODIUM-ION STORAGE; SIZE L-A; ELECTROCHEMICAL PERFORMANCE; RAMAN-SPECTROSCOPY; GRAPHENE OXIDE; ENERGY-STORAGE; ELECTROCATALYST; FABRICATION; Macroporous carbon; Nanoweb; Nanoribbon; Electrode; Redox flow batteries
- ISSN
- 1226-086X
- URI
- https://pubs.kist.re.kr/handle/201004/121551
- DOI
- 10.1016/j.jiec.2017.09.043
- Appears in Collections:
- KIST Article > 2018
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