Multivalent Sulfur Vacancy‐Rich NiCo2S4@MnO2 Urchin‐Like Heterostructures for Ambient Electrochemical N2 Reduction to NH3

Abstract

AbstractInnovative advances in the exploitation of effective electrocatalytic materials for the reduction of nitrogen (N2) to ammonia (NH3) are highly required for the sustainable production of fertilizers and zero‐carbon emission fuel. In order to achieve zero‐carbon footprints and renewable NH3 production, electrochemical N2 reduction reaction (NRR) provides a favorable energy‐saving alternative but it requires more active, efficient, and selective catalysts. In current work, sulfur vacancy (Sv)‐rich NiCo2S4@MnO2 heterostructures are efficaciously fabricated via a facile hydrothermal approach followed by heat treatment. The urchin‐like Sv‐NiCo2S4@MnO2 heterostructures serve as cathodes, which demonstrate an optimal NH3 yield of 57.31 µg h−1 mgcat−1 and Faradaic efficiency of 20.55% at −0.2 V versus reversible hydrogen electrode (RHE) in basic electrolyte owing to the synergistic interactions between Sv‐NiCo2S4 and MnO2. Density functional theory (DFT) simulation further verifies that Co‐sites of urchin‐like Sv‐NiCo2S4@MnO2 heterostructures are beneficial to lowering the energy threshold for N2 adsorption and successive protonation. Distinctive micro/nano‐architectures exhibit high NRR electrocatalytic activities that might motivate researchers to explore and concentrate on the development of heterostructures for ambient electrocatalytic NH3 generation.