Lattice -Mismatch-Induced Ultrastable 1T-Phase MoS2–Pd/Au for Plasmon-Enhanced Hydrogen Evolution

Metallic 1T-phase transition metal dichalcogenides (TMDs) are of considerable interest in enhancing catalytic applications due to their abundant active sites and good conductivity. However, the unstable nature of 1T-phase TMDs greatly impedes their practical applications. Herein, we developed a new...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nano letters 2019-05, Vol.19 (5), p.2758-2764
Hauptverfasser: Shang, Bo, Cui, Xiaoqiang, Jiao, Lin, Qi, Kun, Wang, Yingwei, Fan, Jinchang, Yue, Yuanyuan, Wang, Haiyu, Bao, Qiaoliang, Fan, Xiaofeng, Wei, Shuting, Song, Wei, Cheng, Zhiliang, Guo, Shaojun, Zheng, Weitao
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Metallic 1T-phase transition metal dichalcogenides (TMDs) are of considerable interest in enhancing catalytic applications due to their abundant active sites and good conductivity. However, the unstable nature of 1T-phase TMDs greatly impedes their practical applications. Herein, we developed a new approach for the synthesis of highly stable 1T-phase Au/Pd-MoS2 nanosheets (NSs) through a metal assembly induced ultrastable phase transition for achieving a very high electrocatalytic activity in the hydrogen evolution reaction. The phase transition was evoked by a novel mechanism of lattice-mismatch-induced strain based on density functional theory (DFT) calculations. Raman spectroscopy and transmission electron microscopy (TEM) were used to confirm the phase transition on experimental grounds. A novel heterostructured 1T MoS2–Au/Pd catalyst was designed and synthesized using this mechanism, and the catalyst exhibited a 0 mV onset potential in the hydrogen evolution reaction under light illumination. Therefore, this method can potentially be used to fabricate 1T-phase TMDs with remarkably enhanced activities for different applications.
ISSN:1530-6984
1530-6992
DOI:10.1021/acs.nanolett.8b04104