Direct solution-phase synthesis of 1T′ WSe2 nanosheets

被引:181
|
作者
Sokolikova, Maria S. [1 ]
Sherrell, Peter C. [1 ]
Palczynski, Pawel [1 ]
Bemmer, Victoria L. [1 ]
Mattevi, Cecilia [1 ]
机构
[1] Imperial Coll London, Dept Mat, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
TRANSITION-METAL DICHALCOGENIDES; EFFICIENT HYDROGEN EVOLUTION; COLLOIDAL SYNTHESIS; CATALYTIC-ACTIVITY; WS2; NANOSHEETS; MOS2; ELECTROCHEMISTRY; NANOFLOWERS; PARTICLES; STORAGE;
D O I
10.1038/s41467-019-08594-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Crystal phase control in layered transition metal dichalcogenides is central for exploiting their different electronic properties. Access to metastable crystal phases is limited as their direct synthesis is challenging, restricting the spectrum of reachable materials. Here, we demonstrate the solution phase synthesis of the metastable distorted octahedrally coordinated structure (1T' phase) of WSe2 nanosheets. We design a kinetically-controlled regime of colloidal synthesis to enable the formation of the metastable phase. 1T' WSe2 branched few-layered nanosheets are produced in high yield and in a reproducible and controlled manner. The 1T' phase is fully convertible into the semiconducting 2H phase upon thermal annealing at 400 degrees C. The 1T' WSe2 nanosheets demonstrate a metallic nature exhibited by an enhanced electrocatalytic activity for hydrogen evolution reaction as compared to the 2H WSe2 nanosheets and comparable to other 1T' phases. This synthesis design can potentially be extended to different materials providing direct access of metastable phases.
引用
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页数:8
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