The
photoreduction of CO<sub>2</sub> into renewable fuels is a
promising approach to solve the global energy and environmental crisis.
All-inorganic bismuth (Bi) halide perovskite nanocrystals (NCs) have
emerged as an appealing photocatalyst for visible-light-driven CO<sub>2</sub> reduction, but they still have low photocatalytic activity.
Herein, a set of lead-free and stable Cs<sub>3</sub>Bi<sub>2</sub>X<sub>9</sub> (X = Cl, Cl<sub>0.5</sub>Br<sub>0.5</sub>, Br, Br<sub>0.5</sub>I<sub>0.5</sub>, I) perovskite NCs were explored for the
photocatalytic reduction of CO<sub>2</sub> to CO at the gas–solid
interface. In all of the recorded perovskite NCs, the as-synthesized
Cs<sub>3</sub>Bi<sub>2</sub>(Br<sub>0.5</sub>I<sub>0.5</sub>)<sub>9</sub> showed the highest efficiency of CO<sub>2</sub>-to-CO conversion
producing 54 μmol g<sup>–1</sup> of CO yield under visible-light
irradiation for 3 h. The strategy we proposed may bring up new opportunities
for an efficient photocatalytic CO<sub>2</sub> reduction of lead-free
perovskite NCs.