Efficient photoreduction of CO2 to CO by Co-ZIL-L derived NiCo–OH with ultrathin nanosheet assembled 2D leaf superstructure†
Abstract
The photocatalytic reduction of CO2 into valuable chemicals and fuels is considered a promising solution to address the energy crisis and environmental challenges. In this work, we introduce a Co-ZIL-L mediated in situ etching and integration process to prepare NiCo–OH with an ultrathin nanosheet-assembled 2D leaf-like superstructure (NiCo–OH UNLS). The resulting catalyst demonstrates excellent photocatalytic performance for CO2 reduction, achieving a CO evolution rate as high as 309.5 mmol g−1 h−1 with a selectivity of 91.0%. Systematic studies reveal that the ultrathin nanosheet structure and 2D leaf-like architecture not only enhance the transfer efficiency of photoexcited electrons but also improve the accessibility of active reaction sites. Additionally, the Ni–Co dual sites in NiCo–OH UNLS accelerate CO2 conversion kinetics by stabilizing the *COOH intermediate, significantly contributing to its high activity. This work offers valuable insights for designing advanced photocatalysts for CO2 conversion.