4.8 Article

Structural evolution of Ru/Te interaction for hydrogen generation engineered by proof of concept via carbon doping

Journal

MATERIALS TODAY PHYSICS
Volume 38, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.mtphys.2023.101262

Keywords

Carbon doping; Carbonization; Structural evolution; Metal-support interaction; Hydrogen evolution reaction

Ask authors/readers for more resources

In this study, carbon doping was used to engineer the Ru/Te interaction in Ru nanoparticles supported on semiconductor Te nanorods, resulting in efficient hydrogen evolution reaction. Carbon doping improved the conductivity and charge transfer ability, leading to catalytic performance comparable to commercial Pt/C catalyst with high stability.
Catalyst support with low conductivity and weak metal-support interaction is a tricky issue in advanced catalyst development. Herein, taking the semi-conductive Te nanorods supported Ru nanoparticles as an example, we proposed a proof of concept for carbon doping to engineer the Ru/Te interaction for efficient hydrogen evolution reaction (HER). It was found that the conventional approach for carbon layer formation over Te nanorods via glucose by hydrothermal approach (Te-C-1) was insufficient to boost the catalytic performance, but the deep carbonization via further thermal annealing of Te-C-1 can enhance the conductivity and metal-support inter-action when supporting Ru nanoparticles (Ru/Te-C-2). The important conductivity and charge transfer ability improvement and strong electronic interaction were found by the electrochemical measurements and the spectroscopic analysis, probably resulting from the deep carbonization induced Te nanorods structure destruction and in-depth carbon doping. As a result, Ru/Te-C-2 showed a catalytic performance as good as the commercial Pt/C catalyst for HER, which required ultralow overpotentials of 39 and 34 mV to achieve 10 mA cm-2 in 0.5 M H2SO4 and 1.0 M KOH, respectively, when loaded on the glass carbon electrode; Besides, the catalytic kinetics, charge transfer ability, and catalytic efficiency were also improved due to the carbon doping effect; high catalytic stability was also indicated by the dynamic stability running for 2000 cycles and steady-state operation for 20 h in both acidic and alkaline media. Density-functional theory calculations show that carbon doping effectively promotes the electron transfer from Te to Ru, thus changing the electronic structure and the adsorption energy for H* adsorption, which facilitates the HER process. The current study showed the validation of carbon doping for enhanced metal-supporting interaction that will be instructive for conductivity improvement of the relevant catalyst in electrocatalysis reaction.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available