Related Experiment Video
Updated: Oct 25, 2025

Hydrogen Production and Utilization in a Membrane Reactor
Published on: March 10, 2023
PtSe2 /Pt Heterointerface with Reduced Coordination for Boosted Hydrogen Evolution Reaction.
Zongpeng Wang1, Beibei Xiao2, Zhiping Lin1
1School of Advanced study, Taizhou University, Taizhou, China.
Platinum diselenide (PtSe2) shows sluggish hydrogen evolution reaction (HER) kinetics. Constructing a PtSe2/Pt heterointerface with Se vacancies significantly enhances HER activity, outperforming commercial Pt/C catalysts.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Noble metal dichalcogenides (NMDs) like PtSe2 are promising for electronics and photonics.
- PtSe2 exhibits insufficient active species absorption, limiting its efficiency in hydrogen evolution reactions (HER).
Purpose of the Study:
- To enhance the HER kinetics of PtSe2 by constructing a PtSe2/Pt heterointerface.
- To investigate the role of Se vacancies and Pt atom activation in improving catalytic performance.
Main Methods:
- In situ electrochemical method to create PtSe2/Pt heterointerfaces.
- Characterization of Se vacancies and electronic structure changes.
- Electrochemical testing for HER activity (overpotential, Tafel slope).
Main Results:
- Se vacancies were induced at the PtSe2/Pt heterointerface, reducing coordination and activating adjacent Pt atoms.
- Enhanced overlap between activated Pt atoms and H 1s orbitals strengthened H* adsorption.
- The PtSe2/Pt catalyst achieved an overpotential of 42 mV at 10 mA/cm² and a Tafel slope of 53 mV/dec, surpassing Pt/C.
Conclusions:
- The constructed PtSe2/Pt heterointerface effectively boosts HER activity.
- Se vacancies play a crucial role in activating Pt sites for efficient hydrogen evolution.
- This study offers insights into designing advanced NMD-based electrocatalysts for HER.
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Hybridization of Atomic Orbitals II
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Insensitive Nuclei Enhanced by Polarization Transfer (INEPT)

