Using Exciton/Trion Dynamics to Spatially Monitor the Catalytic Activities of MoS 2 during the Hydrogen Evolution Reaction

The adsorption and desorption of electrolyte ions strongly modulates the carrier density or carrier type on the surface of monolayer-MoS catalyst during the hydrogen evolution reaction (HER). The buildup of electrolyte ions onto the surface of monolayer MoS during the HER may also result in the form...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ACS nano 2022-03, Vol.16 (3), p.4298-4307
Hauptverfasser: Hsiao, Fu-He, Chung, Cheng-Chu, Chiang, Chun-Hao, Feng, Wei-Neng, Tzeng, Wen-Yen, Lin, Hung-Min, Tu, Chien-Ming, Wu, Heng-Liang, Wang, Yu-Han, Woon, Wei-Yen, Chen, Hsiao-Chien, Chen, Ching-Hsiang, Lo, Chao-Yuan, Lai, Man-Hong, Chang, Yu-Ming, Lu, Li-Syuan, Chang, Wen-Hao, Chen, Chun-Wei, Luo, Chih-Wei
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The adsorption and desorption of electrolyte ions strongly modulates the carrier density or carrier type on the surface of monolayer-MoS catalyst during the hydrogen evolution reaction (HER). The buildup of electrolyte ions onto the surface of monolayer MoS during the HER may also result in the formation of excitons and trions, similar to those observed in gate-controlled field-effect transistor devices. Using the distinct carrier relaxation dynamics of excitons and trions of monolayer MoS as sensitive descriptors, an in situ microcell-based scanning time-resolved liquid cell microscope is set up to simultaneously measure the bias-dependent exciton/trion dynamics and spatially map the catalytic activity of monolayer MoS during the HER. This operando probing technique used to monitor the interplay between exciton/trion dynamics and electrocatalytic activity for two-dimensional transition metal dichalcogenides provides an excellent platform to investigate the local carrier behaviors at the atomic layer/liquid electrolyte interfaces during electrocatalytic reaction.
ISSN:1936-0851
1936-086X
DOI:10.1021/acsnano.1c10380