Spin Manipulation of Co sites in Co9S8/Nb2CTx Mott–Schottky Heterojunction for Boosting the Electrocatalytic Nitrogen Reduction Reaction

Abstract

Abstract Regulating the adsorption of an intermediate on an electrocatalyst by manipulating the electron spin state of the transition metal is of great significance for promoting the activation of inert nitrogen molecules (N2) during the electrocatalytic nitrogen reduction reaction (eNRR). However, achieving this remains challenging. Herein, a novel 2D/2D Mott–Schottky heterojunction, Co9S8/Nb2CTx‐P, is developed as an eNRR catalyst. This is achieved through the in situ growth of cobalt sulfide (Co9S8) nanosheets over a Nb2CTx MXene using a solution plasma modification method. Transformation of the Co spin state from low (t2g6eg1) to high (t2g5eg2) is achieved by adjusting the interface electronic structure and sulfur vacancy of Co9S8/Nb2CTx‐P. The adsorption ability of N2 is optimized through high spin Co(II) with more unpaired electrons, significantly accelerating the *N2→*NNH kinetic process. The Co9S8/Nb2CTx‐P exhibits a high NH3 yield of 62.62 µg h−1 mgcat.−1 and a Faradaic efficiency (FE) of 30.33% at −0.40 V versus the reversible hydrogen electrode (RHE) in 0.1 m HCl. Additionally, it achieves an NH3 yield of 41.47 µg h−1 mgcat.−1 and FE of 23.19% at −0.60 V versus RHE in 0.1 m Na2SO4. This work demonstrates a promising strategy for constructing heterojunction electrocatalysts for efficient eNRR.

Keywords

• ammonia synthesis
• cobalt sulfide
• Nb2CTx MXene
• nitrogen reduction reaction
• spin manipulation