LiMn0.8Fe0.2PO4/Carbon Nanospheres@Graphene Nanoribbons
Prepared by the Biomineralization Process as the Cathode for Lithium-Ion
Batteries
Hou, YK (Hou, Yu-Kun)[ 1 ] ; Pan, GL (Pan, Gui-Ling)[ 2 ] ; Sun, YY (Sun, Yan-Yun)[ 1 ] ; Gao, XP (Gao, Xue-Ping)[ 1 ]
ACS APPLIED
MATERIALS & INTERFACES, 2018, 10(19):
16500-16510
DOI: 10.1021/acsami.8b02736
WOS:000432753800031
Abstract
Biomineralization
technology is a feasible and promising route to fabricate phosphate cathode
materials with hierarchical nanostructure for high-performance lithium-ion
batteries (LIBs). In this work, to improve the electrochemical performance of
LiMn0.8Fe0.2PO4 (LMFP), hierarchical LMFP/carbon nanospheres are wrapped in
situ with N-doped graphene nanoribbons (GNRs) via biomineralization by using
yeast cells as the nucleating agent, self-assembly template, and carbon source.
Such LMFP nanospheres are assembled by more fine nanocrystals with an average
size of 18.3 nm. Moreover, the preferential crystal orientation along the [010]
direction and certain antisite lattice defects can be identified in LMFP
nanocrystals, which promote rapid diffusion of Li ions and generate more active
sites for the electrochemical reaction. Moreover, such N-doped GNR networks,
wrapped between LMFP/carbon nanospheres, are beneficial to the fast mobility of
electrons and good penetration of the electrolyte. As expected, the as-prepared
LMFP/carbon multicomposite presents the outstanding electrochemical
performance, including the large initial discharge capacity of 168.8 mA h
g(-1), good rate capability, and excellent long-term cycling stability over
2000 cycles. Therefore, the biomineralization method is demonstrated here to be
effective to manipulate the microstructure of multicomponent phosphate cathode
materials based on the requirement of capacity, rate capability, and cycle
stability for LIBs.