Electrocatalysis with molecules and molecular assemblies within gas diffusion electrodes.

Molecular catalysts and their assemblies are important model systems in electrocatalysis. This is largely because their active sites, secondary coordination spheres, and reaction environments can be rationally modulated. Such experiments yield important insights into the structure-activity relationships that can be used to design improved catalysts or translated to more technologically mature systems. However, in the context of electrocatalysis, molecular catalysts are often dissolved in an electrolyte or heterogenized on an electrode that is completely submersed in an electrolyte (e.g. H-cell) or reaction setups that are not used in practical systems and use poorly soluble gaseous reactants like CO2, CO, or O2. This is beginning to change, with a growing emphasis being placed on investigating molecular catalysts and catalytic assemblies (e.g. metal/covalent organic frameworks and polymers with molecular active sites) in gas-diffusion electrodes (GDEs) that feed the reactant directly from the gas phase to the catalytic sites and enable industrially viable current densities. Against this backdrop, this perspective first details the emerging set of molecular catalyst-embedded GDE-based systems and what the community has learned thus far from these efforts. We next identify the gaps in knowledge and performance that are yet to be closed and offer strategies for exploring in this direction. Finally, we conclude with a forward-looking discussion that highlights several new avenues to be pursued with molecule-based GDE platforms and how this can accelerate progress in the electrocatalysis field as a whole.

Visible-light photoredox catalysis: selective reduction of carbon dioxide to carbon monoxide by a nickel N-heterocyclic carbene-isoquinoline complex.

The solar-driven reduction of carbon dioxide to value-added chemical fuels is a longstanding challenge in the fields of catalysis, energy science, and green chemistry. In order to develop effective CO2 fixation, several key considerations must be balanced, including (1) catalyst selectivity for promoting CO2 reduction over competing hydrogen generation from proton reduction, (2) visible-light harvesting that matches the solar spectrum, and (3) the use of cheap and earth-abundant catalytic components. In this report, we present the synthesis and characterization of a new family of earth-abundant nickel complexes supported by N-heterocyclic carbene-amine ligands that exhibit high selectivity and activity for the electrocatalytic and photocatalytic conversion of CO2 to CO. Systematic changes in the carbene and amine donors of the ligand have been surveyed, and [Ni((Pr)bimiq1)](2+) (1c, where (Pr)bimiq1 = bis(3-(imidazolyl)isoquinolinyl)propane) emerges as a catalyst for electrochemical reduction of CO2 with the lowest cathodic onset potential (E(cat) = -1.2 V vs SCE). Using this earth-abundant catalyst with Ir(ppy)3 (where ppy = 2-phenylpyridine) and an electron donor, we have developed a visible-light photoredox system for the catalytic conversion of CO2 to CO that proceeds with high selectivity and activity and achieves turnover numbers and turnover frequencies reaching 98,000 and 3.9 s(-1), respectively. Further studies reveal that the overall efficiency of this solar-to-fuel cycle may be limited by the formation of the active Ni catalyst and/or the chemical reduction of CO2 to CO at the reduced nickel center and provide a starting point for improved photoredox systems for sustainable carbon-neutral energy conversion.