TY - JOUR
T1 - Fabrication of FeF3 nanocrystals dispersed into a porous carbon matrix as a high performance cathode material for lithium ion batteries
AU - Ma, Ruguang
AU - Wang, Man
AU - Tao, Pengpeng
AU - Wang, Yu
AU - Cao, Chenwei
AU - Shan, Guangcun
AU - Yang, Shiliu
AU - Xi, Liujiang
AU - Chung, Jonathan C. Y.
AU - Lu, Zhouguang
PY - 2013/12/21
Y1 - 2013/12/21
N2 - FeF3/C nanocomposites, where FeF3 nanocrystals had been dispersed into a porous carbon matrix, were successfully fabricated by a novel vapour-solid method in a tailored autoclave. Phase evolution of the reaction between the precursor and HF solution vapour under air and argon gas atmospheres were investigated. The results showed that the air in the autoclave played an important role in driving the reaction to form FeF3. The as-prepared FeF3/C delivered 134.3, 103.2 and 71.0 mA h g -1 of charge capacity at a current density of 104, 520, and 1040 mA g-1 in turn, exhibiting superior rate capability to the bare FeF 3. Moreover, it displayed stable cycling performance, with a charge capacity of 196.3 mA h g-1 at 20.8 mA g-1. EIS and BET investigations indicated that the good electrochemical performance can be attributed to the good electrical conductivity and high specific surface area that result from the porous carbon matrix. © 2013 The Royal Society of Chemistry.
AB - FeF3/C nanocomposites, where FeF3 nanocrystals had been dispersed into a porous carbon matrix, were successfully fabricated by a novel vapour-solid method in a tailored autoclave. Phase evolution of the reaction between the precursor and HF solution vapour under air and argon gas atmospheres were investigated. The results showed that the air in the autoclave played an important role in driving the reaction to form FeF3. The as-prepared FeF3/C delivered 134.3, 103.2 and 71.0 mA h g -1 of charge capacity at a current density of 104, 520, and 1040 mA g-1 in turn, exhibiting superior rate capability to the bare FeF 3. Moreover, it displayed stable cycling performance, with a charge capacity of 196.3 mA h g-1 at 20.8 mA g-1. EIS and BET investigations indicated that the good electrochemical performance can be attributed to the good electrical conductivity and high specific surface area that result from the porous carbon matrix. © 2013 The Royal Society of Chemistry.
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U2 - 10.1039/c3ta13086j
DO - 10.1039/c3ta13086j
M3 - RGC 21 - Publication in refereed journal
SN - 2050-7488
VL - 1
SP - 15060
EP - 15067
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 47
ER -