期刊
SMALL
卷 14, 期 27, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201702054
关键词
capacitive deionization; charging capacity; curved graphene; porous carbon; X-ray pair distribution
类别
资金
- Ministry of Science and Technology of Taiwan [101-2628-E-002-015-MY3, 104-2628-E-002-004-MY3]
- National Taiwan University [102R7842, 102R7740]
- Center of Strategic Materials Alliance for Research and Technology (SMART Center), National Taiwan University from the Featured Areas Research Center Program by the Ministry of Education (MOE) in Taiwan [NTU 105R7706, 106R890702, 107L7828, 107L9008]
- Center of Atomic Initiative for New Materials, National Taiwan University from the Featured Areas Research Center Program by the Ministry of Education (MOE) in Taiwan [NTU 105R7706, 106R890702, 107L7828, 107L9008]
- World Premier International Research Center (WPI) Initiative on Materials Nanoarchitectonics from the MEXT, Japan
An approach to assemble hierarchically ordered 3D arrangements of curved graphenic nanofragments for energy storage devices is described. Assembling them into well-defined interconnected macroporous networks, followed by removal of the template, results in spherical macroporous, mesoporous, and microporous carbon microball (3MCM) architectures with controllable features spanning nanometer to micrometer length scales. These structures are ideal porous electrodes and can serve as lithium-ion battery (LIB) anodes as well as capacitive deionization (CDI) devices. The LIBs exhibit high reversible capacity (up to 1335 mAh g(-1)), with great rate capability (248 mAh g(-1) at 20 C) and a long cycle life (60 cycles). For CDI, the curved graphenic networks have superior electrosorption capacity (i.e., 5.17 mg g(-1) in 0.5 x 10(-3)m NaCl) over conventional carbon materials. The performance of these materials is attributed to the hierarchical structure of the graphenic electrode, which enables faster ion diffusion and low transport resistance.
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