TY - JOUR
T1 - Solution-Processable Microstructuring of 1T′-Phase Janus MoSSe Monolayers for Boosted Hydrogen Production
AU - Liu, Zhengqing
AU - Sun, Zhehao
AU - Qu, Xiaoyan
AU - Nie, Kunkun
AU - Yang, Yawei
AU - Li, Binjie
AU - Chong, Shaokun
AU - Yin, Zongyou
AU - Huang, Wei
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/8/21
Y1 - 2024/8/21
N2 - Janus monolayers of transition metal dichalcogenides (TMDs) offer versatile applications due to their tunable polymorphisms. While previous studies focused on conventional 2H-phase Janus monolayers, the scalable synthesis of an unconventional 1T′ phase remains challenging. We present a novel solution strategy for fabricating Janus 1T′-MoOSe and MoSSe monolayers by growing sandwiched Se-Mo-O/S shells onto Au nanocores. The Janus Au@1T′-MoSSe catalyst exhibits superior electrocatalytic hydrogen evolution reaction (HER) activity compared to 1T′-MoS2, -MoSe2, and -MoOSe, attributed to its unique electronic structure and intrinsic strain. Remarkably, photoexciting the nanoplasmonic Au cores further enhances the HER via a localized surface plasmon (LSP) effect that drives hot electron injection into surface sulfur vacancies of 1T′-MoSSe monolayer shells, accelerating proton reduction. This synergistic activation of anion vacancies by internal strain and external light-induced Au LSPs, coupled with our scalable synthesis, provides a pathway for developing tailorable polymorphic Janus TMDs for specific applications.
AB - Janus monolayers of transition metal dichalcogenides (TMDs) offer versatile applications due to their tunable polymorphisms. While previous studies focused on conventional 2H-phase Janus monolayers, the scalable synthesis of an unconventional 1T′ phase remains challenging. We present a novel solution strategy for fabricating Janus 1T′-MoOSe and MoSSe monolayers by growing sandwiched Se-Mo-O/S shells onto Au nanocores. The Janus Au@1T′-MoSSe catalyst exhibits superior electrocatalytic hydrogen evolution reaction (HER) activity compared to 1T′-MoS2, -MoSe2, and -MoOSe, attributed to its unique electronic structure and intrinsic strain. Remarkably, photoexciting the nanoplasmonic Au cores further enhances the HER via a localized surface plasmon (LSP) effect that drives hot electron injection into surface sulfur vacancies of 1T′-MoSSe monolayer shells, accelerating proton reduction. This synergistic activation of anion vacancies by internal strain and external light-induced Au LSPs, coupled with our scalable synthesis, provides a pathway for developing tailorable polymorphic Janus TMDs for specific applications.
UR - http://www.scopus.com/inward/record.url?scp=85200896884&partnerID=8YFLogxK
U2 - 10.1021/jacs.4c05692
DO - 10.1021/jacs.4c05692
M3 - 文章
C2 - 39120959
AN - SCOPUS:85200896884
SN - 0002-7863
VL - 146
SP - 23252
EP - 23264
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 33
ER -