TY - JOUR
T1 - Ultrahigh capacity and cyclability of dual-phase TiO2 nanowires with low working potential at room and subzero temperatures
AU - Lin, Dongmei
AU - Lyu, Linlong
AU - Li, Kaikai
AU - Chen, Guohua
AU - Yao, Haimin
AU - Kang, Feiyu
AU - Li, Baohua
AU - ZHOU Limin,
N1 - Funding Information:
This work was supported by General Research Fund (Grant No. 15210718, and Grant No. 16213315) from Hong Kong Research Grants Council and Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (Grant No. 2017BT01N111). D. Lin acknowledged the support by the Hong Kong Polytechnic University.
Publisher Copyright:
© The Royal Society of Chemistry 2021.
PY - 2021/4/14
Y1 - 2021/4/14
N2 - The commercialization of TiO2 materials for lithium-ion battery (LIB) anodes has been seriously limited due to unsatisfactory capacities and high voltage plateaus vs. Li/Li+ (∼1.75 V). In this work, we synthesized unique dual-phase TiO2 nanowires composed of anatase and TiO2–B phases with tunable phase ratios and studied their electrochemical performance in the extended potential range of 0.01–3.0 V. It was found that the dual-phase nanowire with a phase ratio of ∼1.0, named TiO2-350, possesses the best rate and cyclic performance. More importantly, lowering the discharge cut-off voltage from 1.0 V to 0.01 V significantly increases the capacities, and moreover results in a decreased average discharge voltage of ∼0.58 V vs. Li/Li+. At the rates of 0.5C and 1C, TiO2-350 delivers the ultrahigh capacities of 518.0 and 444.5 mA h g−1 and remarkable long-term cyclic stability, which are strikingly higher than those reported in the literature and the theoretical capacity of TiO2. Cyclic voltammetry results indicated that the ultrahigh capacity of the TiO2 nanowire is the main reason that the capacitive contribution is below 1.0 V. Structural analyses indicated the solid solution reaction of TiO2-350 nanowires with Li+ and the excellent structure stability during cycling, which contributes to the excellent cyclic performance of nanowires. Furthermore, the TiO2-350 anode exhibits superb low-temperature performance between 0.01 V and 3.0 V at 273 K and 248 K. This work demonstrates a TiO2-based anode with ultrahigh capacity and low working potential, and will promote the practical application of TiO2-based materials for all-climate LIB anodes.
AB - The commercialization of TiO2 materials for lithium-ion battery (LIB) anodes has been seriously limited due to unsatisfactory capacities and high voltage plateaus vs. Li/Li+ (∼1.75 V). In this work, we synthesized unique dual-phase TiO2 nanowires composed of anatase and TiO2–B phases with tunable phase ratios and studied their electrochemical performance in the extended potential range of 0.01–3.0 V. It was found that the dual-phase nanowire with a phase ratio of ∼1.0, named TiO2-350, possesses the best rate and cyclic performance. More importantly, lowering the discharge cut-off voltage from 1.0 V to 0.01 V significantly increases the capacities, and moreover results in a decreased average discharge voltage of ∼0.58 V vs. Li/Li+. At the rates of 0.5C and 1C, TiO2-350 delivers the ultrahigh capacities of 518.0 and 444.5 mA h g−1 and remarkable long-term cyclic stability, which are strikingly higher than those reported in the literature and the theoretical capacity of TiO2. Cyclic voltammetry results indicated that the ultrahigh capacity of the TiO2 nanowire is the main reason that the capacitive contribution is below 1.0 V. Structural analyses indicated the solid solution reaction of TiO2-350 nanowires with Li+ and the excellent structure stability during cycling, which contributes to the excellent cyclic performance of nanowires. Furthermore, the TiO2-350 anode exhibits superb low-temperature performance between 0.01 V and 3.0 V at 273 K and 248 K. This work demonstrates a TiO2-based anode with ultrahigh capacity and low working potential, and will promote the practical application of TiO2-based materials for all-climate LIB anodes.
UR - http://www.scopus.com/inward/record.url?scp=85104003698&partnerID=8YFLogxK
U2 - 10.1039/D0TA12112F
DO - 10.1039/D0TA12112F
M3 - Journal article
SN - 2050-7488
VL - 9
SP - 9256
EP - 9265
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 14
ER -