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Strain-Engineered Oxygen-Modified Nickel Telluride/Nickel Oxide Heterostructures for Bifunctional Alkaline Water Electrocatalysis

Sang-Cheol Shin, Iaan Cho, Sun Kyung Han, Jaewon Heo, Junhwi Han, Hotae Jeon, Jaehyun Lee, Min Kyung Cho, Daniel J. Preston, In Soo Kim, Bonggeun Shong, Won‐Kyu Lee

2025ACS Nano5 citationsDOI

Abstract

We present a strain-engineering strategy for oxygen-modified nickel telluride/nickel oxide heterostructures capable of enabling bifunctional alkaline water electrolysis with performance surpassing Pt and IrO x benchmarks. The heterostructures are synthesized via electrochemical Te dissolution and mild oxidation of mechanically exfoliated NiTe 2, followed by controlled strain induction through substrate buckling. Atomic-scale simulations and spectroscopic analyses indicate that Te-vacancy/O-substituted NiTe 2 domains promote oxygen-intermediate spillover between adjacent active sites, reducing OER overpotentials. In parallel, strained NiTe 2 domains facilitate hydrogen-intermediate transfer to NiO containing Ni vacancies, leading to accelerated HER kinetics and near-thermoneutral hydrogen adsorption. Strain modulation adjusts the electronic structure and increases active-site density, enabling stable operation at industrial-level current densities (>1 A cm –2 ). These findings illustrate how defect chemistry coupled with strain engineering can be utilized to develop high-performance, earth-abundant bifunctional electrocatalysts.

Topics & Concepts

BifunctionalElectrocatalystMaterials scienceAlkaline water electrolysisWater splittingOxideHeterojunctionElectrochemistryNickelNickel oxideChemical engineeringElectrolysisStrain engineeringNon-blocking I/OElectrolysis of waterOxygen evolutionInorganic chemistryDissolutionSubstrate (aquarium)Hydrogen productionElectrodeImidazolateNanotechnologyElectron transferCatalysisReversible hydrogen electrodeHydrogenHydrogen spilloverPalladiumElectrocatalysts for Energy ConversionAmmonia Synthesis and Nitrogen ReductionTiO2 Photocatalysis and Solar Cells
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