Abstract

AbstractThe utilization of green hydrogen sources in H2O for alkynols electrocatalytic semihydrogenation reaction (ESHR) at ambient temperature provides a promising pathway toward the sustainable conversion of alkynols. However, it is still a great challenge to construct specific interfacial structure to adjust the electronic structure of Pd for the purpose of altering the strong adsorption of Pd with active hydrogen to enhance the production of alkenols. Here, the atomically dispersed GaOx‐PdMo bimetallene nanoribbons (GaOx‐PdMo BNRs) via oxygen bridging Ga atoms is designed to the surface of PdMo BNRs for 2‐methyl‐3‐butyn‐2‐ol (MBY) ESHR to the synthesis of 2‐methyl‐3‐buten‐2‐ol (MBE). The GaOx‐PdMo BNRs achieve the excellent MBE selectivity (≈97.4%), Faraday efficiency (≈96.1%), and maintain long‐term stability. Density functional theory demonstrates that the top electron‐enriched Ga atoms and the bottom electron‐deficient Pd atoms construct a “pyramidal” interface via the oxygen bridge. The unique surface can effectively activate H2O and weaken interaction between catalyst and MBE, thus promoting MBE generation. Moreover, the electron bridge effect between Ga‐O‐PdMo can induce p‐d orbital hybridization to achieve lower the d‐band center of surface Pd thus modulating the reactants adsorption. This work provides a strategy to improve ESHR performance by electron bridge effect to modulate interfacial electron distribution.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.