期刊
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
卷 162, 期 5, 页码 A5083-A5090出版社
ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.0141505jes
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资金
- Center for Molecularly Engineered Energy Materials, an Energy Frontier Research Center - US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC001342]
- NSF [0840531]
- Direct For Mathematical & Physical Scien [0840531] Funding Source: National Science Foundation
- Division Of Chemistry [0840531] Funding Source: National Science Foundation
Pseudocapacitive charge storage materials offer the opportunity to bridge the gap between high energy density battery materials and high power density electrical double layer capacitor materials through the rational design of transition metal oxide nanoscale architectures. The research reported in this paper describes the origins and development of pseudocapacitance in MoO2. Micron-size particles of MoO2 exhibit a reversible monoclinic to orthorhombic phase transition upon lithium insertion/deinsertion, however, this phase transformation is suppressed when using 15 nm nanocrystals of MoO2. The nanoscale MoO2 exhibits pseudocapacitive behavior and achieves substantially better energy storage kinetics than the corresponding bulk material. Such size-dependent electrochemical behavior is an essential feature of an extrinsic pseudocapacitor material. The high power capability of nanoscale MoO2 is improved further by synthesizing hybrid materials in which MoO2 nanoparticles are grown on reduced graphene oxide (RGO) scaffolds. Electrode architectures containing MoO2-RGO hybrid materials preserve the pseudocapacitance of MoO2 as lithium capacities of nearly 150 mAh g(-1) are obtained at a rate of 50 C. (C) The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives 4.0 License (CC BY-NC-ND, http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is not changed in any way and is properly cited. For permission for commercial reuse, please email: oa@electrochem.org. All rights reserved.
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