TY - JOUR
T1 - Mechano-thermal nanoparticulate coatings for enhancing the cycle stability of LiCoO2
AU - Fey, George Ting Kuo
AU - Lu, Cheng Zhang
AU - Prem Kumar, T.
AU - Muralidharan, P.
AU - Chiang, Anthony S.T.
N1 - Funding Information:
Financial support for this work from the Industrial Technology Research Institute is gratefully acknowledged. TPK and PMD thank the National Research Council of the Republic of China for the award of post-doctoral fellowships.
PY - 2006/11
Y1 - 2006/11
N2 - A mechano-thermal coating method was adopted for obtaining LiCoO2 coated particles with pre-formed pseudo-boehmite nanoparticulate, followed by calcination at 723 K for 10 h. From X-ray diffraction (XRD) analysis it was seen that the coated cathode materials did not show any extraneous phase peaks corresponding to the pseudo-boehmite and the crystal structure, α-NaFeO2, remained the same as pristine LiCoO2. Scanning electron micrograph (SEM) of the coated samples showed that above the 1.0 wt.% coating level, the excess pseudo-boehmite got glued to the coated cathode particles as spherules. TEM images showed that the Al2O3 particles derived from pseudo-boehmite formed ∼20 nm thickness coating layer on the LiCoO2 particles. The XPS/ESCA results revealed that the presence of two different O 1s corresponds to the surface coated Al2O3 and the core material. The electrochemical performance of the coated materials by a cycling study suggest that 1.0 wt.% coated Al2O3 derived from pseudo-boehmite on the two commercial LiCoO2 samples improved cycle stability by a factor of five and 11 times over the pristine LiCoO2 cathode material. Cyclic voltammetry revealed that the hexagonal-monoclinic-hexagonal phase transformations were retained for the coated cathode materials upon continuous cycling.
AB - A mechano-thermal coating method was adopted for obtaining LiCoO2 coated particles with pre-formed pseudo-boehmite nanoparticulate, followed by calcination at 723 K for 10 h. From X-ray diffraction (XRD) analysis it was seen that the coated cathode materials did not show any extraneous phase peaks corresponding to the pseudo-boehmite and the crystal structure, α-NaFeO2, remained the same as pristine LiCoO2. Scanning electron micrograph (SEM) of the coated samples showed that above the 1.0 wt.% coating level, the excess pseudo-boehmite got glued to the coated cathode particles as spherules. TEM images showed that the Al2O3 particles derived from pseudo-boehmite formed ∼20 nm thickness coating layer on the LiCoO2 particles. The XPS/ESCA results revealed that the presence of two different O 1s corresponds to the surface coated Al2O3 and the core material. The electrochemical performance of the coated materials by a cycling study suggest that 1.0 wt.% coated Al2O3 derived from pseudo-boehmite on the two commercial LiCoO2 samples improved cycle stability by a factor of five and 11 times over the pristine LiCoO2 cathode material. Cyclic voltammetry revealed that the hexagonal-monoclinic-hexagonal phase transformations were retained for the coated cathode materials upon continuous cycling.
UR - http://www.scopus.com/inward/record.url?scp=33749262011&partnerID=8YFLogxK
U2 - 10.1016/j.jpcs.2006.05.023
DO - 10.1016/j.jpcs.2006.05.023
M3 - 期刊論文
AN - SCOPUS:33749262011
SN - 0022-3697
VL - 67
SP - 2337
EP - 2344
JO - Journal of Physics and Chemistry of Solids
JF - Journal of Physics and Chemistry of Solids
IS - 11
ER -