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Doping of Cr to Regulate the Valence State of Cu and Co Contributes to Efficient Water Splitting

Xiaoming Mu, Kai Wang, Keyi Lv, Bo Feng, Xiaofei Yu, Lanlan Li, Xinghua Zhang, Xiaojing Yang, Zunming Lu

2023ACS Applied Materials & Interfaces52 citationsDOI

Abstract

Water electrolysis in alkaline media is the most promising technology for hydrogen production, but efficient electrocatalysts are required to reduce the overpotential in HER and OER processes. In this work, the multicomponent transition metal catalyst Cr–Cu/CoO x was loaded on copper foam by electrodeposition and annealing, and the catalyst exhibited excellent electrochemical activity. The HER overpotential is 21 mV and the OER overpotential is 252 mV at a current density of 10 mA cm –2 . The overall water splitting voltage is 1.51 V, even better than the Pt/C//RuO 2 two-electrode system (1.61 V). The excellent performance of this catalyst is mainly derived from the close synergistic interaction among Cu, Co, and Cr. The doping of Cr modulates the valence states of Cu and Co at the active sites and improves the adsorption of various reaction intermediates. Density functional theory (DFT) calculations show that the doping of Cr can optimize the adsorption of the reaction intermediate H*. Meanwhile, the high-valent Cr and Co promote hydrolysis through strong adsorption with OH – . The present work provides a reasonable strategy for designing low-cost transition metals as efficient catalysts for water electrolysis.

Topics & Concepts

OverpotentialWater splittingMaterials scienceElectrolysis of waterCatalysisElectrolysisElectrochemistryAdsorptionInorganic chemistryTransition metalValence (chemistry)Hydrogen productionCopperDensity functional theoryChemical engineeringOxygen evolutionAlkaline water electrolysisElectrodePhysical chemistryChemistryMetallurgyElectrolyteComputational chemistryPhotocatalysisEngineeringBiochemistryOrganic chemistryElectrocatalysts for Energy ConversionAdvanced battery technologies researchCO2 Reduction Techniques and Catalysts
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