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Carbon-Free TiO2 Microspheres as Anode Materials for Sodium Ion Batteries AITranslate

Hanyang University; Korea Institute of Science and Technology; Korea Institute of Science and Technology; Hanyang University; Korea Institute of Science and Technology; Korea Institute of Science and Technology; Korea University of Science and Technology; Hanyang University
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Publisher: ACS
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Abstract AITranslate

In this study, we synthesize a carbon-free anatase/bronze TiO2 microsphere (TiO2(A/B)-MS) via the solvothermal method and demonstrate its potential for use as a high-performance anode material for sodium-ion batteries. The highly compact structure of the microsphere constructed from nanoprimary particles not only enhances the structural stability and subsequently leads to good cycling performance but also enables the transport pathways for Na+ ions and electrons to be shortened, ensuring fast Na-storage performance. In addition, an anatase/bronze interfacial structure of the material further improves fast Na+-ion diffusion kinetics. Benefiting from these merits, the proposed TiO2(A/B)-MS demonstrates a high specific capacity of 221 mAh g–1 at 0.1 C, fast charge–discharge capability up to 50 C, and long-term cycling stability over 1000 cycles at 1 and 10 C without using a conductive carbon matrix. A combination of various experiments and theoretical studies is used to verify the outstanding Na-storage performance of TiO2(A/B)-MS.

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DOI:https://doi.org/10.1021/acsenergylett.8b02510

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Citation Information:

In this study, we synthesize a carbon-free anatase/bronze TiO2 microsphere (TiO2(A/B)-MS) via the solvothermal method and demonstrate its potential for use as a high-performance anode material for sodium-ion batteries. The highly compact structure of the microsphere constructed from nanoprimary particles not only enhances the structural stability and subsequently leads to good cycling performance but also enables the transport pathways for Na+ ions and electrons to be shortened, ensuring fast Na-storage performance. In addition, an anatase/bronze interfacial structure of the material further improves fast Na+-ion diffusion kinetics. Benefiting from these merits, the proposed TiO2(A/B)-MS demonstrates a high specific capacity of 221 mAh g–1 at 0.1 C, fast charge–discharge capability up to 50 C, and long-term cycling stability over 1000 cycles at 1 and 10 C without using a conductive carbon matrix. A combination of various experiments and theoretical studies is used to verify the outstanding Na-storage performance of TiO2(A/B)-MS.

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GB/T 7714-2015 [1] JangYeon Hwang, HoangLong Du, BinNa Yun, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.8b02510.
MLA [1] JangYeon Hwang, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.8b02510.
APA [1] JangYeon Hwang, HoangLong Du, BinNa Yun, MinGi Jeong, JiSu Kim, Hyoungchul Kim, HunGi Jung, & YangKook Sun. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.8b02510
IEEE [1] JangYeon Hwang, HoangLong Du, BinNa Yun, MinGi Jeong, JiSu Kim, Hyoungchul Kim, HunGi Jung, and YangKook Sun, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.8b02510.