Ligand-engineered Cu-based halide perovskite for highly efficient near-infrared photocatalytic CO2 reduction

Abstract

A key challenge in harvesting solar energy for efficient chemical conversion is the lack of photocatalysts with wide activation wavelengths. Herein, we propose for the first time to utilize halide perovskite to absorb the full spectrum (200–2500 nm), including ultraviolet (UV), visible (Vis), and near-infrared (NIR) light, to directly power photocatalytic CO2 reduction. This full-spectrum light-responsive occurs on metal halide perovskite Cs2CuCl4 microcrystals (MCs), and the ligand soybean lecithin is applied to optimize the active phase of Cs2CuCl4 photocatalyst, such as morphology, particle size, crystal face and electronic structure. As revealed by optical absorption analysis, the Cs2CuCl4 and ligand soybean lecithin modified Cs2CuCl4 (SL-Cs2CuCl4) MCs exhibit significant optical absorption in the UV, Vis light and NIR light regions. The photocatalytic CO2 reduction performance was assessed under simulated sunlight (200–2500 nm), and the SL-Cs2CuCl4 MCs achieved a CO fuel yield of 254.46 µmol g−1, which increased the yield by 5 times relative to the initial sample. Based on in-situ Fourier transform infrared, electron spin resonance and X-ray photoelectron spectroscopy, the active substances and reaction intermediates at the active site of SL-Cs2CuCl4 MCs were dynamically monitored, and the photocatalytic mechanism was revealed together with density functional theory (DFT) calculations. The DFT calculation shows that the photocatalytic reduction of CO2 to CO by Cs2CuCl4 is proposed to involve the concerted action of both Cs and Cu sites.