Issue 43, 2018

Mesoporous carbon matrix confinement synthesis of ultrasmall WO3 nanocrystals for lithium ion batteries

Abstract

Transition metal oxides (TMOs)/carbon nanocomposites are promising for high capacity long life lithium ion batteries (LIBs). Herein, we report a mesoporous carbon matrix confinement growth strategy to synthesize ultrasmall WO3 nanocrystals for lithium storage. In this strategy, WCl6 and phenolic resins (resol) are co-assembled with amphiphilic diblock copolymer PEO-b-PS into ordered mesostructures through an evaporation induced self-assembly (EISA) process. During the pyrolysis process, the resol molecules can be polymerized and carbonized into amorphous mesoporous carbon matrices, which lock the amorphous W species well. Then, WO3 nanocrystals are formed and are uniformly distributed in the ordered mesoporous carbon matrix with the increased pyrolysis temperature; moreover, the particle size is well controlled to ∼3 nm under the confinement effect of the carbon matrices. The resultant ordered mesoporous carbon/WO3 composites show very large pore size (∼11.3 nm), high surface area (∼157 m2 g−1), high pore volume (∼0.25 cm3 g−1), and WO3 content of 84%. As an anode material for LIBs, the obtained composites show excellent cycling stability and rate performance. A high specific capacity of 440 mA h g−1 can be achieved after 100 cycles at a current density of 0.1 A g−1. We believe that such a confinement synthesis strategy is versatile to create TMO-based nanocomposites for outstanding LIBs.

Graphical abstract: Mesoporous carbon matrix confinement synthesis of ultrasmall WO3 nanocrystals for lithium ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
24 Jul 2018
Accepted
24 Sep 2018
First published
24 Sep 2018

J. Mater. Chem. A, 2018,6, 21550-21557

Mesoporous carbon matrix confinement synthesis of ultrasmall WO3 nanocrystals for lithium ion batteries

C. Wang, Y. Zhao, L. Zhou, Y. Liu, W. Zhang, Z. Zhao, W. N. Hozzein, H. M. S. Alharbi, W. Li and D. Zhao, J. Mater. Chem. A, 2018, 6, 21550 DOI: 10.1039/C8TA07145D

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