Modulating the Oxidation State of Titanium via Dual Anions Substitution for Efficient N2 Electroreduction

Abstract

The electrocatalytic nitrogen reduction reaction (NRR) is a promising approach for renewable ammonia synthesis but remains significantly challenging due to the low yield and poor selectivity. Herein, a facile N and S dual anions substitution strategy is developed to tune the Ti oxidation states of TiO₂ nanohybrid catalyst (NS-TiO₂ /C), in which anatase TiO₂ nanoplates with dense Ti³⁺ active sites are uniformly dispersed on porous carbon derived from 2D Ti₃ C₂ T_x nanosheets. The catalyst NS-TiO₂ /C exhibits a superior ambient NRR efficiency with an NH₃ yield rate of 19.97 µg h^-1 mg^-1_cat and Faradaic efficiency of 25.49% and is coupled with a remarkable 50 h long-term stability at -0.25 V versus RHE. Both experimental and theoretical results reveal that the N and S dual-substitution effectively regulate the Ti oxidation state and electronical properties of the NS-TiO₂ /C via simultaneously forming interstitial and substitutional TiS and TiN bonds in the anatase TiO₂ lattice, inducing oxygen vacancies and dense Ti³⁺ active species as well as better electronic conductivity, which substantially facilitates N₂ chemisorption and activation, and reduces the energy barrier of the rate-determining step, thereby essentially boosting NRR efficiency. This work provides a valuable approach to the rational design of advanced materials by modulating oxidation states for efficient electrocatalysis.

Keywords: MXene-derived materials; Ti 3+; dual anion substitution; electrochemical nitrogen reduction; oxidation state modulation.