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Issue 33, 2019
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Rate-independent and ultra-stable low-temperature sodium storage in pseudocapacitive TiO2 nanowires

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Abstract

Sodium-ion batteries (SIBs) are faced with several challenges, including low capacity, short cycle life, and poor low-temperature performance. In this work, TiO2-B/anatase dual-phase nanowires are synthesized and applied as SIB anodes to address the above challenges. For the first time, we find the excellent Na-storage performance of the nanowire anode like rate-independent capacities and ultra-stable cycling stability at low temperature. Operando Raman spectroscopy shows that the nanowires are completely amorphized after cycling at 303 K; however, the TiO2-B phase of the dual-phase nanowires remains crystalline after cycling at 273 K. The different sodiation mechanisms at different temperatures result in a lower capacity but a more stable structure during cycling at 273 K than at 303 K. Kinetic analysis shows that the nanowire anode possesses an ultralow charge-transfer energy barrier and resistance with a higher apparent Na diffusion coefficient at 273 K than at 303 K during desodiation, which significantly enhances the Na+ intercalation pseudocapacitive process at low temperature. The synergy between the structural transition and diffusion kinetics leads to rate-independent and ultra-stable Na-storage performance at low temperature. This work provides new perspectives for the understanding and design of low-temperature SIBs with high rate capability and long cycle life.

Graphical abstract: Rate-independent and ultra-stable low-temperature sodium storage in pseudocapacitive TiO2 nanowires

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Publication details

The article was received on 14 May 2019, accepted on 28 Jul 2019 and first published on 31 Jul 2019


Article type: Paper
DOI: 10.1039/C9TA05039F
J. Mater. Chem. A, 2019,7, 19297-19304

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    Rate-independent and ultra-stable low-temperature sodium storage in pseudocapacitive TiO2 nanowires

    D. Lin, K. Li, Q. Wang, L. Lyu, B. Li and L. Zhou, J. Mater. Chem. A, 2019, 7, 19297
    DOI: 10.1039/C9TA05039F

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