Back to Search Start Over

Heterointerface and crystallinity engineering of Ru/RuS2 dual co-catalysts for enhanced photocatalytic hydrogen evolution.

Authors :
Wang, Xinyu
You, Junhua
Ren, Jiali
Xue, Yanjun
Tian, Jian
Zhang, Hangzhou
Source :
Applied Catalysis B: Environmental. May2024, Vol. 345, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

In this paper, the Ru/RuS 2 nanoparticles as dual co-catalysts were self-assembled on the surface of g-C 3 N 4 nanotubes (Ru/RuS 2 /g-C 3 N 4 NTs) for photocatalytic H 2 production. The Ru/RuS 2 /g-C 3 N 4 NTs showed greatly enhanced photocatalytic H 2 production activity (1409 μmol·g−1·h−1), 1.16 times of RuS 2 /g-C 3 N 4 NTs (1212 μmol·h−1·g−1), 10.51 times of Ru/g-C 3 N 4 NTs (134 μmol·g−1·h−1), and 82.88 times of the pure g-C 3 N 4 NTs (17 μmol·g−1·h−1). Besides, the apparent quantum yield value (AQE) of Ru/RuS 2 /g-C 3 N 4 NTs is 3.92% at 370 nm. Ru/RuS 2 as dual co-catalysts are self-assembled on the surface of g-C 3 N 4 NTs and show strong electronic synergistic interaction between the interfaces, reduce Δ G H* of RuS 2 and desorption energy of Ru, and promote the selectivity and activity of HER kinetically and thermodynamically respectively, which exhibits higher photogenerated carrier concentration and lower charge migration resistance than RuS 2 and Ru, showing the synergistic effect to facilitate the generation and migration of carriers and provides active sites for photocatalysis. [Display omitted] • Ru/RuS 2 nanoparticles as dual co-catalysts are self-assembled on the surface of g-C 3 N 4 nanotubes. • Ru/RuS 2 /g-C 3 N 4 NTs show greatly enhanced photocatalytic H 2 production activity (1409 μmol·g−1·h−1). • Ru/RuS 2 show strong electronic synergistic interaction between the interfaces. • Ru/RuS 2 promote the selectivity and activity of HER kinetically and thermodynamically respectively. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09263373
Volume :
345
Database :
Academic Search Index
Journal :
Applied Catalysis B: Environmental
Publication Type :
Academic Journal
Accession number :
175026483
Full Text :
https://doi.org/10.1016/j.apcatb.2024.123722