posted on 2021-10-19, 14:11authored byFrancesca Arcudi, Luka Đorđević, Benjamin Nagasing, Samuel I. Stupp, Emily A. Weiss
Climate change and global energy
demands motivate the search for
sustainable transformations of carbon dioxide (CO2) to
storable liquid fuels. Photocatalysis is a pathway for direct conversion
of CO2 to CO, one step within light-powered reaction networks
that could, if efficient enough, transform the solar energy conversion
landscape. To date, the best performing photocatalytic CO2 reduction systems operate in nonaqueous solvents, but technologically
viable solar fuels networks will likely operate in water. Here we
demonstrate catalytic photoreduction of CO2 to CO in pure
water at pH 6–7 with an unprecedented combination of performance
parameters: turnover number (TON(CO)) = 72,484–84,101, quantum
yield (QY) = 0.96–3.39%, and selectivity (SCO) > 99%, using CuInS2 colloidal quantum
dots
(QDs) as photosensitizers and a Co-porphyrin catalyst. At higher catalyst
concentration, the system reaches QY = 3.53–5.23%. The performance
of the QD-driven system greatly exceeds that of the benchmark aqueous
system (926 turnovers with a quantum yield of 0.81% and selectivity
of 82%), due primarily to (i) electrostatic attraction of the QD to
the catalyst, which promotes fast multielectron delivery and colocalization
of protons, CO2, and catalyst at the source of photoelectrons,
and (ii) termination of the QD’s ligand shell with free amines,
which capture CO2 as carbamic acid that serves as a reservoir
for CO2, effectively increasing its solubility in water,
and lowers the onset potential for catalytic CO2 reduction
by the Co-porphyrin. The breakthrough efficiency achieved in this
work represents a nonincremental step in the realization of reaction
networks for direct solar-to-fuel conversion.