Search

Developing low‐cost and efficient photocatalysts to convert CO2 into valuable fuels is desirable to realize a carbon‐neutral society. In this work, we report that polymer dots (Pdots) of poly[(9,9′‐dioctylfluorenyl‐2,7‐diyl)‐co‐(1,4‐benzo‐thiadiazole)] (PFBT), without adding any extra co‐catalyst, can photocatalyze reduction of CO2 into CO in aqueous solution, rendering a CO production rate of 57 μmol g−1 h−1 with a detectable selectivity of up to 100 %. After 5 cycles of CO2 re‐purging experiments, no distinct decline in CO amount and reaction rate was observed, indicating the promising photocatalytic stability of PFBT Pdots in the photocatalytic CO2 reduction reaction. A mechanistic study reveals that photoexcited PFBT Pdots are reduced by sacrificial donor first, then the reduced PFBT Pdots can bind CO2 and reduce it into CO via their intrinsic active sites. This work highlights the application of organic Pdots for CO2 reduction in aqueous solution, which therefore provides a strategy to develop highly efficient and environmentally friendly nanoparticulate photocatalysts for CO2 reduction. [ABSTRACT FROM AUTHOR]

A photocatalyst comprising binary organic polymer dots (Pdots) was prepared. The Pdots were constructed from poly(9,9‐dioctylfluorene‐alt‐benzothiadiazole), as an electron donor, and 1‐[3‐(methoxycarbonyl)propyl]‐1‐phenyl‐[6.6]C61, as an electron acceptor. The photocatalyst produces H2O2 in alkaline conditions (1 M KOH) with a production rate of up to 188 mmol h−1 g−1. The external quantum efficiencies were 30 % (5 min) and 14 % (75 min) at 450 nm. Furthermore, photo‐oxidation of methanol by Pdots, followed by a disproportionation reaction and an oxidation reaction, produced the high‐value chemical formate. On the basis of various spectroscopic and electrochemical measurements, the photophysical processes of the system were studied in detail and a reaction mechanism was proposed. [ABSTRACT FROM AUTHOR]