Alumina-Supported CoFe Alloy Catalysts Derived from Layered-Double-Hydroxide Nanosheets for Efficient Photothermal CO2 Hydrogenation to Hydrocarbons

Abstract

A series of novel CoFe-based catalysts are successfully fabricated by hydrogen reduction of CoFeAl layered-double-hydroxide (LDH) nanosheets at 300-700 °C. The chemical composition and morphology of the reaction products (denoted herein as CoFe-x) are highly dependent on the reduction temperature (x). CO₂ hydrogenation experiments are conducted on the CoFe-x catalysts under UV-vis excitation. With increasing LDH-nanosheet reduction temperature, the CoFe-x catalysts show a progressive selectivity shift from CO to CH₄ , and eventually to high-value hydrocarbons (C₂₊ ). CoFe-650 shows remarkable selectivity toward hydrocarbons (60% CH₄ , 35% C₂₊ ). X-ray absorption fine structure, high-resolution transmission electron microscopy, Mössbauer spectroscopy, and density functional theory calculations demonstrate that alumina-supported CoFe-alloy nanoparticles are responsible for the high selectivity of CoFe-650 for C₂₊ hydrocarbons, also allowing exploitation of photothermal effects. This study demonstrates a vibrant new catalyst platform for harnessing clean, abundant solar-energy to produce valuable chemicals and fuels from CO₂ .

Keywords: CoFe alloy; layered double hydroxides; photothermal CO2 hydrogenation; solar-to-fuel conversion; value-added compounds.