In natural photosynthesis, light is used for the production of chemical energy carriers to fuel biological activity. The re-engineering of natural photosynthetic pathways can provide inspiration for sustainable fuel production and insights for understanding the process itself. Here, we employ a semiartificial approach to study photobiological water splitting via a pathway unavailable to nature: the direct coupling of the water oxidation enzyme, photosystem II, to the H2 evolving enzyme, hydrogenase. Essential to this approach is the integration of the isolated enzymes into the artificial circuit of a photoelectrochemical cell. We therefore developed a tailor-made hierarchically structured indium-tin oxide electrode that gives rise to the excellent integration of both photosystem II and hydrogenase for performing the anodic and cathodic half-reactions, respectively. When connected together with the aid of an applied bias, the semiartificial cell demonstrated quantitative electron flow from photosystem II to the hydrogenase with the production of H2 and O2 being in the expected two-to-one ratio and a light-to-hydrogen conversion efficiency of 5.4% under low-intensity red-light irradiation. We thereby demonstrate efficient light-driven water splitting using a pathway inaccessible to biology and report on a widely applicable in vitro platform for the controlled coupling of enzymatic redox processes to meaningfully study photocatalytic reactions.

A rational approach for a photosystem II-based electrode assembly is described, integrating redox polymers with high surface area hierarchically structured electrodes.

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Take a breath: An oxygen‐tolerant hydrogenase can be employed with a dye in a photocatalytic scheme for the generation of H2. The homogeneous system does not require a redox mediator and visible‐light irradiation yields high amounts of H2 even in the presence of air.

Ein optisch transparenter mesoporöser ITO‐Film wurde mit dem neuartigen Cobaltkatalysator [Co] für die Elektroreduktion wässriger Protonen derivatisiert. An der Hybridelektrode wurde in wässriger Elektrolytlösung bei pH 7 mit hoher Stromdichte elektrochemisch H2 entwickelt. Nach spektroelektrochemischen Untersuchungen bleibt der immobilisierte molekulare Katalysator beim Anlegen eines niedrigen Potentials an der Elektrode intakt.

We report on a cobalt sulphide (CoS) electrode prepared by simple and scalable chemical bath deposition (CBD), which performs as a highly efficient and robust electrocatalyst for the H 2 evolution reaction (HER) in both neutral and pH 13 electrolyte solution at a small overpotential (η < 90 mV). At η = 390 mV, turnover frequencies of 38.8 ± 1.9 and 52.1 ± 2.0 mol H 2 (mol Co) -1 h -1 were achieved with high stability (Faradaic efficiency > 95% for at least 72 h) and turnover numbers of approximately 2,600 and 3,400 in neutral and basic electrolyte solution, respectively. The rate of 10 HER per geometric area is further enhanced by employing a CoS microtube array (microCoS), which is prepared by sulfurisation of a cobalt hydroxide carbonate nanorod array template using CBD. MicroCoS shows excellent HER activity when it is coupled with a nanostructured hematite (α-Fe 2 O 3 ) photoanode for H 2 generation from photoelectrochemical water splitting in basic electrolyte solution. 15 80 deposition (CBD) in an aqueous solution (10 mL) containing urea (50 mM), CoCl 2 ·6H 2 O (50 mM), and thioacetamide (0.1 M) at 90

This discussion describes a direct comparison of photoelectrochemical (PEC) water oxidation activity between a photosystem II (PSII)-functionalised photoanode and a synthetic nanocomposite photoanode. The semi-biological photoanode is composed of PSII from the thermophilic cyanobacterium Thermosynechococcus elongatus on a mesoporous indium tin oxide electrode (mesoITO|PSII). PSII embeds all of the required functionalities for light absorption, charge separation and water oxidation and ITO serves solely as the electron collector. The synthetic photoanode consists of a TiO(2) and NiO(x) coated nanosheet-structured WO(3) electrode (nanoWO(3)|TiO(2)|NiO(x)). The composite structure of the synthetic electrode allows mimicry of the functional key features in PSII: visible light is absorbed by WO(3), TiO(2) serves as a protection and charge separation layer and NiO(x) serves as the water oxidation electrocatalyst. MesoITO|PSII uses low energy red light, whereas nanoWO(3)|TiO(2)|NiO(x) requires high energy photons of blue-end visible and UV regions to oxidise water. The electrodes have a comparable onset potential at approximately 0.6 V vs. reversible hydrogen electrode (RHE). MesoITO|PSII reaches its saturation photocurrent at 0.84 V vs. RHE, whereas nanoWO(3)|TiO(2)NiO(x) requires more than 1.34 V vs. RHE. This suggests that mesoITO|PSII suffers from fewer limitations from charge recombination and slow water oxidation catalysis than the synthetic electrode. MesoITO|PSII displays a higher 'per active' site activity, but is less photostable and displays a much lower photocurrent per geometrical surface area and incident photon to current conversion efficiency (IPCE) than nanoWO(3)|TiO(2)|NiO(x_.