There has been a rapid rise in interest regarding the advantages of support materials to protect and immobilise molecular catalysts for the carbon dioxide reduction reaction (CO2RR) in order to overcome the weaknesses of many well‐known catalysts in terms of their stability and selectivity. In this Review, the state of the art of different catalyst‐support systems for the CO2RR is discussed with the intention of leading towards standard benchmarking for comparison of such systems across the most relevant supports and immobilisation strategies, taking into account these multiple pertinent metrics, and also enabling clearer consideration of the necessary steps for further progress. The most promising support systems are described, along with a final note on the need for developing more advanced experimental and computational techniques to aid the rational design principles that are prerequisite to prospective industrial upscaling.

The mechanism of H2 evolution catalyzed by the [Co(N4H)Cl2]+ complex is elucidated with quantitative determination of the rate-constants for the various protonation steps, and the identification of the aliphatic amine to act as a proton relay.

This study presents a new design of light-harvesting antenna materials using two dyes organised into mesoporous silica: an iridium(III) complex and a BODIPY-derived surfactant that undergo Förster resonance energy transfer (FRET), acting, respectively, as donor and acceptor. The chemical structure of each dye determines the position taken within the micellar templates used for the synthesis of the silica host, which maintains mesopore order as shown by TEM imaging. Steady-state and time-resolved UV-visible spectroscopy revealed that incorporation of the iridium complex into the silica shields it from oxygen-induced quenching and allows a degree of control over the donor-acceptor distance, yielding FRET efficiencies from 24 to 76 % and tuneable emission ranges. Such silica-based antennae show promising properties for the realisation of polychromatic sensitisers for photovoltaics and photocatalysis.

There has been a rapid rise in interest regarding the advantages of support materials to protect and immobilise molecular catalysts for the carbon dioxide reduction reaction (CO2RR) in order to overcome the weaknesses of many well‐known catalysts in terms of their stability and selectivity. In this Review, the state of the art of different catalyst‐support systems for the CO2RR is discussed with the intention of leading towards standard benchmarking for comparison of such systems across the most relevant supports and immobilisation strategies, taking into account these multiple pertinent metrics, and also enabling clearer consideration of the necessary steps for further progress. The most promising support systems are described, along with a final note on the need for developing more advanced experimental and computational techniques to aid the rational design principles that are prerequisite to prospective industrial upscaling.