Interfacial Electronic Modulation of Mo 5 N 6 /Ni 3 S 2 Heterojunction Array Boosts Electrocatalytic Alkaline Overall Water Splitting.
Bin FangJutao JinYanqin LiHaifeng DangMengmeng ShaoLiyuan ZhaoNianliang YinWenlong WangPublished in: Small (Weinheim an der Bergstrasse, Germany) (2024)
Bifunctional electrocatalysts with excellent activity and durability are highly desirable for alkaline overall water splitting, yet remain a significant challenge. In this contribution, palm-like Mo 5 N 6 /Ni 3 S 2 heterojunction arrays anchored in conductive Ni foam (denoted as Mo 5 N 6 -Ni 3 S 2 HNPs/NF) are developed. Benefiting from the optimized electronic structure configuration, hierarchical branched structure and abundant heterogeneous interfaces, the as-synthesized Mo 5 N 6 -Ni 3 S 2 HNPs/NF electrode exhibits remarkably stable bifunctional electrocatalytic activity in 1 m KOH solution. It only requires ultralow overpotentials of 59 and 190 mV to deliver a current density of 10 mA cm -2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in 1 m KOH solution, respectively. Importantly, the overall water splitting electrolyzer assembled by Mo 5 N 6 -Ni 3 S 2 HNPs/NF exhibits an exceptionally low cell voltage (1.48 V@10 mA cm -2 ) and outstanding durability, surpassing most of the reported Ni-based bifunctional materials. Density functional theory (DFT) further confirms the heterostructure can optimize the Gibbs free energies of H and O-containing intermediates (OH, O, OOH) during HER and OER processes, thereby accelerating the catalytic kinetics of electrochemical water splitting. The findings provide a new design strategy toward low-cost and excellent catalysts for overall water splitting.
Keyphrases
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- molecular dynamics
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