Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/137804
Title: Identifying the origin and contribution of surface storage in TiO2 (B) nanotube electrode by in situ dynamic valence state monitoring
Authors: Tang, Yuxin
Zhang, Yanyan
Malyi, Oleksandr I.
Bucher, Nicolas
Xia, Huarong
Xi, Shibo
Zhu, Zhiqiang
Lv, Zhisheng
Li, Wenlong
Wei, Jiaqi
Srinivasan, Madhavi
Borgna, Armando
Antonietti, Markus
Du, Yonghua
Chen, Xiaodong
Keywords: Engineering::Materials
Issue Date: 2018
Source: Tang, Y., Zhang, Y., Malyi, O. I., Bucher, N., Xia, H., Xi, S., . . ., Chen, X. (2018). Identifying the origin and contribution of surface storage in TiO2 (B) nanotube electrode by in situ dynamic valence state monitoring. Advanced materials, 30(33), 1802200-. doi:10.1002/adma.201802200
Journal: Advanced materials
Abstract: Fundamental insight into the surface charging mechanism of TiO2 (B) nanomaterials is limited due to the complicated nature of lithiation behavior, as well as the limitations of available characterization tools that can directly probe surface charging process. Here, an in situ approach is reported to monitor the dynamic valence state of TiO2 (B) nanotube electrodes, which utilizes in situ X-ray absorption spectroscopy (XAS) to identify the origin and contribution of surface storage. A real-time correlation is elucidated between the rate-dependent electrode performance and dynamic Ti valence-state change. A continuous Ti valence state change is directly observed through the whole charging/discharging process regardless of charging rates, which proves that along with the well-known non-faradaic reaction, the surface charging process also originates from a faradaic reaction. The quantification of these two surface storage contributions at different charging rates is further realized through in situ dynamic valence state monitoring combined with traditional cyclic voltammetry measurement. The methodology reported here can also be applied to other electrode materials for the real-time probing of valence state change during electrochemical reactions, the quantification of the faradaic and non-faradaic reactions, and the eventual elucidation of electrochemical surface charging mechanisms.
URI: https://hdl.handle.net/10356/137804
ISSN: 0935-9648
DOI: 10.1002/adma.201802200
Rights: © 2018 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved. This paper was published in Advanced materials and is made available with permission of WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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