journal article·2022

Controllable synthesis of few-layer ammoniated 1T′-phase WS 2 as an anode material for lithium-ion batteries

Xiang Li, Zhenzhen Liu, Ding Zhu, Yigang Yan, Yungui Chen

Nanoscale· Volume 14· Issue 15
Publisher page

Abstract

Two-dimensional transition metal dichalcogenide (TMDC) nanosheets have received significant attention as anode materials for lithium-ion batteries, especially in their metallic 1T/1T' phase. However, controllable synthesis of few-layer 1T/1T' phase is still a challenge. In the present study, we report a facile two-step hydrothermal method to controllably synthesize few-layer 1T'-phase WS2. By tuning the redox-temperature of (NH4)2WS4 from 160 to 200 °C, the thickness of 1T'-phase WS2 can be adjusted from 4-6 to 20 layers. A higher reversible capacity is achieved in 1T'-phase WS2 with a smaller thickness, but the cycling stability decreases due to the lower crystallinity. The 1T'-phase WS2 synthesized by reduction of (NH4)2WS4 at 180 °C shows a moderate thickness of 10 layers and crystallinity, exhibiting the optimal Li-ion storage properties, i.e. a reversible capacity of 855.9 mA h g-1 at 100 mA g-1 and a good rate performance of 354.4 mA h g-1 at 5000 mA g-1. These results provide new insights into understanding the impacts of layer number on the Li-ion storage properties of 1T'-phase WS2.
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Research context

OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Advancements in Battery Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Institute of New Energy and Low-Carbon Technology, Sichuan University, Chengdu 610065, China

College of Materials Science and Engineering, Sichuan University, Chengdu 610065, China

Engineering Research Center of Alternative Energy Materials and Devices, Ministry of Education, China

Funding

National Natural Science Foundation of China · Sichuan Province Science and Technology Support Program · Central University Basic Research Fund of China

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