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Curved Fragmented Graphenic Hierarchical Architectures for Extraordinary Charging Capacities
Author(s) -
Lian HongYuan,
Dutta Saikat,
Tominaka Satoshi,
Lee YuAn,
Huang ShuYun,
Sakamoto Yasuhiro,
Hou ChiaHung,
Liu WeiRen,
Henzie Joel,
Yamauchi Yusuke,
Wu Kevin C.W.
Publication year - 2018
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.201702054
Subject(s) - materials science , capacitive deionization , anode , microporous material , nanotechnology , mesoporous material , carbon fibers , electrode , lithium (medication) , porosity , diffusion , nanometre , battery (electricity) , micrometer , electrochemistry , composite material , chemistry , medicine , biochemistry , physics , power (physics) , quantum mechanics , composite number , optics , thermodynamics , endocrinology , catalysis
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 × 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.