Hydrogen spillover enhances alkaline hydrogen electrocatalysis on interface-rich metallic Pt-supported MoO3

Rajib Samanta; Biplab Kumar Manna; Ravi Trivedi; Brahmananda Chakraborty; Sudip Barman

doi:10.1039/d3sc04126c

Hydrogen spillover enhances alkaline hydrogen electrocatalysis on interface-rich metallic Pt-supported MoO₃

Chem Sci. 2023 Dec 8;15(1):364-378. doi: 10.1039/d3sc04126c. eCollection 2023 Dec 20.

Authors

Rajib Samanta^{1

2}, Biplab Kumar Manna^{1

2}, Ravi Trivedi^{3

4}, Brahmananda Chakraborty^{2

5}, Sudip Barman^{1

2}

Affiliations

¹ School of Chemical Sciences, National Institute of Science Education and Research (NISER), HBNI Bhubaneswar Orissa 752050 India sbarman@niser.ac.in +91 6742494183.
² Homi Bhabha National Institute, Training School Complex Anushakti Nagar Mumbai 400094 India.
³ Department of Physics, Karpagam Academy of Higher Education Coimbatore 641021 India.
⁴ Centre for High Energy Physics, Karpagam Academy of Higher Education Coimbatore 641021 India.
⁵ High Pressure & Synchroton Radiation Physics Division, Bhabha Atomic Research Centre Trombay Mumbai 400085 India.

Abstract

Efficient and cost-effective electrocatalysts for the hydrogen oxidation/evolution reaction (HOR/HER) are essential for commercializing alkaline fuel cells and electrolyzers. The sluggish HER/HOR reaction kinetics in base is the key issue that requires resolution so that commercialization may proceed. It is also quite challenging to decrease the noble metal loading without sacrificing performance. Herein, we report improved HER/HOR activity as a result of hydrogen spillover on platinum-supported MoO₃ (Pt/MoO₃-CN_x-400) with a Pt loading of 20%. The catalyst exhibited a decreased over-potential of 66.8 mV to reach 10 mA cm^-2 current density with a Tafel slope of 41.2 mV dec^-1 for the HER in base. The Pt/MoO₃-CN_x-400 also exhibited satisfactory HOR activity in base. The mass-specific exchange current density of Pt/MoO₃-CN_x-400 and commercial Pt/C are 505.7 and 245 mA mg_Pt^-1, respectively. The experimental results suggest that the hydrogen binding energy (HBE) is the key descriptor for the HER/HOR. We also demonstrated that the enhanced HER/HOR performance was due to the hydrogen spillover from Pt to MoO₃ sites that enhanced the Volmer/Heyrovsky process, which led to high HER/HOR activity and was supported by the experimental and theoretical investigations. The work function value of Pt [Φ = 5.39 eV) is less than that of β-MoO₃ (011) [Φ = 7.09 eV], which revealed the charge transfer from Pt to the β-MoO₃ (011) surface. This suggested the feasibility of hydrogen spillover, and was further confirmed by the relative hydrogen adsorption energy [ΔG_H] at different sites. Based on these findings, we propose that the H₂O or H₂ dissociation takes place on Pt and interfaces to form Pt-H_ad or (Pt/MoO₃)-H_ad, and some of the H_ad shifted to MoO₃ sites through hydrogen spillover. Then, H_ad at the Pt and interface, and MoO₃ sites reacted with H₂O and HO^- to form H₂ or H₂O molecules, thereby boosting the HER/HOR activity. This work may provide valuable information for the development of hydrogen-spillover-based electrocatalysts for use in various renewable energy devices.