Recent Advances in Graphene-Based Single-Atom Photocatalysts for CO2 Reduction and H2 Production

Abstract

The extensive use of single-atom catalysts (SACs) has appeared as a significant area of investigation in contemporary study. The single-atom catalyst, characterized by its maximum atomic proficiency and great discernment of the transition-metal center, has a unique combination of benefits from both heterogeneous and homogeneous catalysts. Consequently, it effectively bridges the gap between these two types of catalysts, leveraging their distinctive features. The utilization of SACs immobilized on graphene substrates has garnered considerable interest, primarily because of their capacity to facilitate selective and efficient photocatalytic processes. This review aims to comprehensively summarize the progress and potential uses of SACs made from graphene in photocatalytic carbon dioxide (CO2) reduction and hydrogen (H2) generation. The focus is on their contribution to converting solar energy into chemical energy. The present study represents the various preparation methods and characterization approaches of graphene-based single-atom photocatalyst This review investigates the detailed mechanisms underlying these photocatalytic processes and discusses recent studies that have demonstrated remarkable H2 production rates through various graphene-based single-atom photocatalysts. Additionally, the pivotal roleof theoretical simulations, likedensity functional theory (DFT), to understand the structural functional relationships of these SACs are discussed. The potential of graphene-based SACs to revolutionize solar-to-chemical energy conversion through photocatalytic CO2 reduction and H2 production is underscored, along with addressing challenges and outlining future directions for this developing area of study. By shedding light on the progress and potential of these catalysts, this review contributes to the collective pursuit of sustainable and efficient energy conversion strategies to mitigate the global climate crisis.