TY - JOUR
T1 - Aluminum Interdiffusion into LiCoO2 Using Atomic Layer Deposition for High Rate Lithium Ion Batteries
AU - Teranishi, Takashi
AU - Yoshikawa, Yumi
AU - Yoneda, Mika
AU - Kishimoto, Akira
AU - Halpin, Jennifer
AU - O'Brien, Shane
AU - Modreanu, Mircea
AU - Povey, Ian M.
N1 - Funding Information:
This work was supported by a Grant-in-Aid for Scientific Research (B) (No. 15H04126) and Challenging Exploratory Research (Grant No. 16K14094) from the Japan Society for the Promotion of Science.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/7/23
Y1 - 2018/7/23
N2 - Here, as with previous work, atomic layer deposition (ALD) has been used to deposit Al2O3 on positive electrode active materials, LiCoO2, to create a protective barrier layer, suppress the high potential phase transition, and thus reduce the subsequent Co dissolution. However, in this study it was found that it also resulted in the reduction of the charge transfer resistance at the positive electrode-electrolyte interface, thus enhancing the performance of the battery. Energy-dispersive X-ray spectroscopy, in conjunction with transmission electron microscopy, shows that a discrete Al2O3 shell was not formed under the selected growth conditions and that the Al diffused into the bulk LiCoO2. The resulting active oxide material, which was significantly thicker than the nominally ALD growth rate would predict, is proposed to be of the form LiCoO2:Al with amorphous and crystalline regions depending on the Al content. The cells consisting of the modified electrodes were found to have good cycling stability and discharge capacities of ∼110 mA h g-1 (0.12 mA h cm-2) and ∼35 mA h g-1 (0.04 mA h cm-2) at 50 and 100 C, respectively.
AB - Here, as with previous work, atomic layer deposition (ALD) has been used to deposit Al2O3 on positive electrode active materials, LiCoO2, to create a protective barrier layer, suppress the high potential phase transition, and thus reduce the subsequent Co dissolution. However, in this study it was found that it also resulted in the reduction of the charge transfer resistance at the positive electrode-electrolyte interface, thus enhancing the performance of the battery. Energy-dispersive X-ray spectroscopy, in conjunction with transmission electron microscopy, shows that a discrete Al2O3 shell was not formed under the selected growth conditions and that the Al diffused into the bulk LiCoO2. The resulting active oxide material, which was significantly thicker than the nominally ALD growth rate would predict, is proposed to be of the form LiCoO2:Al with amorphous and crystalline regions depending on the Al content. The cells consisting of the modified electrodes were found to have good cycling stability and discharge capacities of ∼110 mA h g-1 (0.12 mA h cm-2) and ∼35 mA h g-1 (0.04 mA h cm-2) at 50 and 100 C, respectively.
KW - AlO
KW - atomic layer deposition
KW - charge transfer
KW - high charge-discharge rate
KW - lithium ion batteries
KW - solid electrolyte interface
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U2 - 10.1021/acsaem.8b00496
DO - 10.1021/acsaem.8b00496
M3 - Article
AN - SCOPUS:85064599473
SN - 2574-0962
VL - 1
SP - 3277
EP - 3282
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 7
ER -