Mesoporous Electrocatalysts with p-n Heterojunctions for Efficient Electroreduction of CO2 and N2 to Urea

The electrocatalytic synthesis of high-value-added urea by activating N-2 and CO2 is a green synthesis technology that has achieved carbon neutrality. However, the chemical adsorption and C-N coupling ability of N-2 and CO2 on the surface of the catalyst are generally poor, greatly limiting the improvement of electrocatalytic activity and selectivity in electrocatalytic urea synthesis. Herein, novel hierarchical mesoporous CeO2/Co3O4 heterostructures are fabricated, and at an ultralow applied voltage of -0.2 V, the urea yield rate reaches 5.81 mmol g(-1) h(-1), with a corresponding Faraday efficiency of 30.05%. The hierarchical mesoporous material effectively reduces the mass transfer resistance of reactants and intermediates, making it easier for them to access active centers. The emerging space-charge regions at the heterointerface generate local electrophilic and nucleophilic regions, facilitating CO2 targeted adsorption in the electrophilic region and activation to produce *CO intermediates and N-2 targeted adsorption in the nucleophilic region and activation to generate *N & boxH; N* intermediates. Then, the electrons in the sigma orbitals of *N & boxH; N* intermediates can be easily accepted by the empty e(g) orbitals of Co3+ in CeO2/Co3O4, which presents a low-spin state (LS: t(2g)(6)e(g)(0)). Subsequently, *CO couples with *N & boxH; N* to produce the key intermediate *NCON*. Interestingly, it was discovered through in situ Raman spectroscopy that the CeO2/Co3O4 catalyst has a reversible spinel structure before and after the electrocatalytic reaction, which is due to the surface reconstruction of the catalyst during the electrocatalytic reaction process, producing amorphous active cobalt oxides, which is beneficial for improving electrocatalytic activity.