Summary
Solar-driven CO hydrogenation to light olefins holds great potential as a petroleum-independent process. Herein, a series of Fe5C2 loading on tunable N-doped carbon as photothermal catalysts are developed to achieve an efficient Fischer-Tropsch synthesis to olefin (FTO) reaction. Under light irradiation, the optimized catalyst delivers a selectivity of 55.3% for light olefins (CO(2 )free) at a CO conversion of 22.3%, showing 3.5 times the activity of pristine Fe5C2 catalyst. Experimental characterizations reveal electron transfer from the N atoms in support to the active phase of Fe(5)C(2 )to construct electronrich active sites and therefore to boost the catalytic performance. N-concentrationdependent activity evaluation and density functional theory calculations ascertain that pyrrolic N plays a dominant role in promoting CO adsorption and activation. This study provides an alternative strategy of rational modulation of support to enhance solar-to-chemical conversion.
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Institution中国科学院研究生院