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Transition metals of Pt and Pd on the surface of topological insulator Bi2Se3.
- Source :
- Journal of Chemical Physics; 4/14/2024, Vol. 160 Issue 14, p1-5, 5p
- Publication Year :
- 2024
-
Abstract
- Transition metal catalysts supported on topological insulators are predicted to show improved catalytic properties due to the presence of topological surface states, which may float up to the catalysts and provide robust electron transfer. However, experimental studies of surface structures and corresponding catalytic properties of transition metal/topological insulator heterostructures have not been demonstrated so far. Here, we report the structures, chemical states, and adsorption behaviors of two conventional transition metal catalysts, Pt and Pd, on the surface of Bi<subscript>2</subscript>Se<subscript>3</subscript>, a common topological insulator material. We reveal that Pt forms nanoparticles on the Bi<subscript>2</subscript>Se<subscript>3</subscript> surface. Moreover, the interaction between Pt and surface Se is observed. Furthermore, thermal dosing of O<subscript>2</subscript> onto the Pt/Bi<subscript>2</subscript>Se<subscript>3</subscript> heterostructure leads to no oxygen adsorption. Detailed scanning tunneling microscopy study indicates that Pt transforms into PtSe<subscript>2</subscript> after the thermal process, thus preventing O<subscript>2</subscript> from adsorption. For another transition metal Pd, it exhibits approximate layer-island growth on Bi<subscript>2</subscript>Se<subscript>3</subscript>, and Pd–Se interaction is also observed. Our work provides significant insights into the behaviors of transition metals on top of a common topological insulator material and will assist in the future design of catalysts built with topological materials. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00219606
- Volume :
- 160
- Issue :
- 14
- Database :
- Complementary Index
- Journal :
- Journal of Chemical Physics
- Publication Type :
- Academic Journal
- Accession number :
- 176628323
- Full Text :
- https://doi.org/10.1063/5.0191941