Abstract Abundant transition metal borides are emerging as substitute electrochemical hydrogen evolution reaction (HER) catalysts for noble metals. Herein, an unusual canonic‐like behavior of theclattice parameter in the AlB2‐type solid solution Cr1–xMoxB2(x= 0, 0.25, 0.4, 0.5, 0.6, 0.75, 1) and its direct correlation to the HER activity in 0.5 M H2SO4solution are reported. The activity increases with increasingx, reaching its maximum atx= 0.6 before decreasing again. At high current densities, Cr0.4Mo0.6B2outperforms Pt/C, as it needs 180 mV less overpotential to drive an 800 mA cm−2current density. Cr0.4Mo0.6B2has excellent long‐term stability and durability showing no significant activity loss after 5000 cycles and 25 h of operation in acid. First‐principles calculations have correctly reproduced the nonlinear dependence of theclattice parameter and have shown that the mixed metal/B layers, such as (110), promote hydrogen evolution more efficiently forx= 0.6, supporting the experimental results. 
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                            Construction of a Pt‐CeO x Interface for the Electrocatalytic Hydrogen Evolution Reaction
                        
                    
    
            Abstract The creation of metal‐metal oxide interfaces is an important approach to fine‐tuning catalyst properties through strong interfacial interactions. This article presents the work on developing interfaces between Pt and CeOxthat improve Pt surface energetics for the hydrogen evolution reaction (HER) within an alkaline electrolyte. The Pt‐CeOxinterfaces are formed by depositing size‐controlled Pt nanoparticles onto a carbon support already coated with ultrathin CeOxnanosheets. This interface structure facilitates substantial electron transfer from Pt to CeOx, resulting in decreased hydrogen binding energies on Pt surfaces, and water dissociation for the HER, as predicted by the density functional theory (DFT) calculations. Electrochemical testing indicates that both Pt specific activity and mass activity are improved by a factor of 2 to 3 following the formation of Pt‐CeOxinterfaces. This study underscores the significance and potential of harnessing robust interfacial effects to enhance electrocatalytic reactions. 
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                            - Award ID(s):
- 2011967
- PAR ID:
- 10590671
- Publisher / Repository:
- Wiley
- Date Published:
- Journal Name:
- Advanced Functional Materials
- Volume:
- 34
- Issue:
- 38
- ISSN:
- 1616-301X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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