Operando double-edge high-resolution X-ray absorption spectroscopy study of BiVO4 photoanodes.

High energy resolution fluorescence detected X-ray absorption spectroscopy is a powerful method for probing the electronic structure of functional materials. The X-ray penetration depth and photon-in/photon-out nature of the method allow operando experiments to be performed, in particular in electrochemical cells. Here, operando high-resolution X-ray absorption measurements of a BiVO4 photoanode are reported, simultaneously probing the local electronic states of both cations. Small but significant variations of the spectral lineshapes induced by the applied potential were observed and an explanation in terms of the occupation of electronic states at or near the band edges is proposed.

Artificial photosynthesis: photoanodes based on polyquinoid dyes onto mesoporous tin oxide surface.

Dye-sensitized photoelectrochemical cells represent an appealing solution for artificial photosynthesis, aimed at the conversion of solar light into fuels or commodity chemicals. Extensive efforts have been directed towards the development of photoelectrodes combining semiconductor materials and organic dyes; the use of molecular components allows to tune the absorption and redox properties of the material. Recently, we have reported the use of a class of pentacyclic quinoid organic dyes (KuQuinone) chemisorbed onto semiconducting tin oxide as photoanodes for water oxidation. In this work, we investigate the effect of the SnO2 semiconductor thickness and morphology and of the dye-anchoring group on the photoelectrochemical performance of the electrodes. The optimized materials are mesoporous SnO2 layers with 2.5 µm film thickness combined with a KuQuinone dye with a 3-carboxylpropyl-anchoring chain: these electrodes achieve light-harvesting efficiency of 93% at the maximum absorption wavelength of 533 nm, and photocurrent density J up to 350 µA/cm2 in the photoelectrochemical oxidation of ascorbate, although with a limited incident photon-to-current efficiency of 0.075%. Calculations based on the density functional theory (DFT) support the role of the reduced species of the KuQuinone dye via a proton-coupled electron transfer as the competent species involved in the electron transfer to the tin oxide semiconductor. Finally, a preliminary investigation of the photoelectrodes towards benzyl alcohol oxidation is presented, achieving photocurrent density up to 90 µA/cm2 in acetonitrile in the presence of N-hydroxysuccinimide and pyridine as redox mediator and base, respectively. These results support the possibility of using molecular-based materials in synthetic photoelectrochemistry.

Photoelectrocatalytic degradation of emerging contaminants at WO3/BiVO4 photoanodes in aqueous solution.

WO3/BiVO4 films obtained by electrochemical deposition of BiVO4 over mesoporous WO3 were applied to the photoelectrochemical degradation of selected emerging contaminants (ketoprofen and levofloxacine) in aqueous solutions. The WO3/BiVO4 films in this work are characterized by a mesoporous morphology with a maximum photoconversion efficiency >40% extending beyond 500 nm in Na2SO4 electrolytes. Oxygen was found to be the dominant water oxidation product (ca. 90% faradaic yield) and no evidence for the photogeneration of OH radicals was obtained. Nevertheless, both 10 ppm levofloxacine and ketoprofen could be degraded at WO3/BiVO4 junctions upon a few hours of illumination under visible light. However, while levofloxacine degradation intermediates were progressively consumed by further oxidation at the WO3/BiVO4 interface, ketoprofen oxidation byproducts, being stable aromatic species, were found to be persistent in aqueous solution even after 15 hours of solar simulated illumination. This indicates that, due to the lower oxidizing power of photogenerated holes in BiVO4 and a different water oxidation mechanism, the employment of WO3/BiVO4 in photoelectrochemical environmental remediation processes is much less universal than that possible with wider band gap semiconductors such as TiO2 and WO3.

Molecular artificial photosynthesis.

The replacement of fossil fuels by a clean and renewable energy source is one of the most urgent and challenging issues our society is facing today, which is why intense research has been devoted to this topic recently. Nature has been using sunlight as the primary energy input to oxidise water and generate carbohydrates (solar fuel) for over a billion years. Inspired, but not constrained, by nature, artificial systems can be designed to capture light and oxidise water and reduce protons or other organic compounds to generate useful chemical fuels. This tutorial review covers the primary topics that need to be understood and mastered in order to come up with practical solutions for the generation of solar fuels. These topics are: the fundamentals of light capturing and conversion, water oxidation catalysis, proton and CO2 reduction catalysis and the combination of all of these for the construction of complete cells for the generation of solar fuels.

Oxygenation by ruthenium monosubstituted polyoxotungstates in aqueous solution: experimental and computational dissection of a Ru(III)-Ru(V) catalytic cycle.

Molecular polyoxometalates with one embedded ruthenium center, with general formula [Ru(II/III)(DMSO)XW11O39](n-) (X = P, Si; n = 4-6), are readily synthesized in gram scale under microwave irradiation by a flash hydrothermal protocol. These nanodimensional and polyanionic complexes enable aerobic oxygenation in water. Catalytic oxygen transfer to dimethylsulfoxide (DMSO) yielding the corresponding sulfone (DMSO2 ) has been investigated with a combined kinetic, spectroscopic and computational approach addressing: (i ) the Ru(III) catalyst resting state; (ii ) the bimolecular event dictating its transformation in the rate-determining step; (iii ) its aerobic evolution to a high-valent ruthenium oxene species; (iv ) the terminal fate to diamagnetic dimers. This pathway is reminiscent of natural heme systems and of bioinspired artificial porphyrins. The in silico characterization of a key bis-Ru(IV)-µ-peroxo-POM dimeric intermediate has been accessed by density functional theory. This observation indicates a new landmark for tracing POM-based manifolds for multiredox oxygen reduction/activation, where metal-centered oxygenated species play a pivotal role.

Hematite photoanodes modified with an Fe(III) water oxidation catalyst.

Hematite photoelectrodes prepared via a hydrothermal route are functionalized with a water oxidation catalyst consisting of amorphous Fe(III) oxide, obtained by successive ionic layer adsorption and reaction. The performances of the catalyst-modified photoanodes are considerably higher than those of the parent electrodes, resulting in a nearly doubled photoanodic current in all the basic aqueous electrolytes explored in this study. The combination of electrochemical impedance spectroscopy and laser flash photolysis indicates that the presence of the catalyst results in enhanced hole trapping in surface reactive states exposed to the electrolyte, allowing for a more successful competition between charge transfer and recombination.

Photocatalytic water oxidation by a mixed-valent Mn(III)3Mn(IV)O3 manganese oxo core that mimics the natural oxygen-evolving center.

The functional core of oxygenic photosynthesis is in charge of catalytic water oxidation by a multi-redox Mn(III)/Mn(IV) manifold that evolves through five electronic states (S(i), where i=0-4). The synthetic model system of this catalytic cycle and of its S0→S4 intermediates is the expected turning point for artificial photosynthesis. The tetramanganese-substituted tungstosilicate [Mn(III)3Mn(IV)O3(CH3COO)3(A-α-SiW9O34)](6-)(Mn4POM) offers an unprecedented mimicry of the natural system in its reduced S0 state; it features a hybrid organic-inorganic coordination sphere and is anchored on a polyoxotungstate. Evidence for its photosynthetic properties when combined with [Ru(bpy)3](2+) and S2O8(2-) is obtained by nanosecond laser flash photolysis; its S0→S1 transition within milliseconds and multiple-hole-accumulating properties were studied. Photocatalytic oxygen evolution is achieved in a buffered medium (pH 5) with a quantum efficiency of 1.7%.

Role of Intragap States in Sensitized Sb-Doped Tin Oxide Photoanodes for Solar Fuels Production.

In view of developing photoelectrosynthetic cells which are able to store solar energy in chemical bonds, water splitting is usually the reaction of choice when targeting hydrogen production. However, alternative approaches can be considered, aimed at substituting the anodic reaction of water oxidation with more commercially capitalizable oxidations. Among them, the production of bromine from bromide ions was investigated long back in the 1980s by Texas Instruments. Herein we present optimized perylene-diimide (PDI)-sensitized antimony-doped tin oxide (ATO) photoanodes enabling the photoinduced HBr splitting with >4 mA/cm2 photocurrent densities under 0.1 W/cm2 AM1.5G illumination and 91 ± 3% faradaic efficiencies for bromine production. These remarkable results, among the best currently reported for the photoelectrochemical Br- oxidation by dye sensitized photoanodes, are strongly related to the occupancy extent of ATO's intragap (IG) states, generated upon Sb-doping, as demonstrated by comparing their performances with PDI-sensitized analogues on both undoped SnO2- and TiO2-passivated ATO scaffolds by means of (spectro)electrochemistry and electrochemical impedance spectroscopy. The architecture of the ATO-PDI photoanodic assembly was further modified via the introduction of a molecular iridium-based water oxidation catalyst, thus proving the versatility of the proposed hybrid interfaces as photoanodic platforms for photoinduced oxidations in PEC devices.

Efficient solar water oxidation using photovoltaic devices functionalized with earth-abundant oxygen evolving catalysts.

Indium tin oxide (ITO) surfaces of triple junction photovoltaic cells were functionalized with oxygen evolving catalysts (OECs) based on amorphous hydrous earth-abundant metal oxides (metal = Fe, Ni, Co), obtained by straightforward Successive Ionic Layer Adsorption and Reaction (SILAR) in an aqueous environment. Functionalization with Fe(iii) oxides gave the best results, leading to photoanodes capable of efficiently splitting water, with photocurrent densities up to 6 ± 1 mA cm(-2) at 0 V vs. the reversible hydrogen electrode (RHE) under AM 1.5 G simulated sunlight illumination. The resulting Solar To Hydrogen (STH) conversion efficiencies, measured in two electrodes configuration, were in the range 3.7-5%, depending on the counter electrode that was employed. Investigations on the stability showed that these photoanodes were able to sustain 120 minutes of continuous illumination with a < 10% photocurrent loss at 0 V vs. RHE. Pristine photoanodic response of the cells could be fully restored by an additional SILAR cycle, evidencing that the observed loss is due to the detachment of the more weakly surface bound catalyst.

Photoelectrochemical C-H Activation Through a Quinacridone Dye Enabling Proton-Coupled Electron Transfer.

Dye-sensitized photoanodes for C-H activation in organic substrates are assembled by vacuum sublimation of a commercially available quinacridone (QNC) dye in the form of nanosized rods onto fluorine-doped tin oxide (FTO), TiO2 , and SnO2 slides. The photoanodes display extended absorption in the visible range (450-600 nm) and ultrafast photoinduced electron injection (<1 ps, as revealed by transient absorption spectroscopy) of the QNC dye into the semiconductor. The proton-coupled electron-transfer reactivity of QNC is exploited for generating a nitrogen-based radical as its oxidized form, which is competent in C-H bond activation. The key reactivity parameter is the bond-dissociation free energy (BDFE) associated with the N⋅/N-H couple in QNC of 80.5±2.3 kcal mol-1 , which enables hydrogen atom abstraction from allylic or benzylic C-H moieties. A photoelectrochemical response is indeed observed for organic substrates characterized by C-H bonds with BDFE below the 80.5 kcal mol-1 threshold, such as γ-terpinene, xanthene, or dihydroanthracene. This work provides a rational, mechanistically oriented route to the design of dye-sensitized photoelectrodes for selective organic transformations.

Photocatalytic water oxidation: tuning light-induced electron transfer by molecular Co4O4 cores.

Isostructural cubane-shaped catalysts [Co(III)(4)(µ-O)(4)(µ-CH(3)COO)(4)(p-NC(5)H(4)X)(4)], 1-X (X = H, Me, t-Bu, OMe, Br, COOMe, CN), enable water oxidation under dark and illuminated conditions, where the primary step of photoinduced electron transfer obeys to Hammett linear free energy relationship behavior. Ligand design and catalyst optimization are instrumental for sustained O(2) productivity with quantum efficiency up to 80% at λ > 400 nm, thus opening a new perspective for in vitro molecular photosynthesis.

Photoinduced water oxidation by a tetraruthenium polyoxometalate catalyst: ion-pairing and primary processes with Ru(bpy)3(2+) photosensitizer.

The tetraruthenium polyoxometalate [Ru(4)(µ-O)(4)(µ-OH)(2)(H(2)O)(4)(γ-SiW(10)O(36))(2)](10-) (1) behaves as a very efficient water oxidation catalyst in photocatalytic cycles using Ru(bpy)(3)(2+) as sensitizer and persulfate as sacrificial oxidant. Two interrelated issues relevant to this behavior have been examined in detail: (i) the effects of ion pairing between the polyanionic catalyst and the cationic Ru(bpy)(3)(2+) sensitizer, and (ii) the kinetics of hole transfer from the oxidized sensitizer to the catalyst. Complementary charge interactions in aqueous solution leads to an efficient static quenching of the Ru(bpy)(3)(2+) excited state. The quenching takes place in ion-paired species with an average 1:Ru(bpy)(3)(2+) stoichiometry of 1:4. It occurs by very fast (ca. 2 ps) electron transfer from the excited photosensitizer to the catalyst followed by fast (15-150 ps) charge recombination (reversible oxidative quenching mechanism). This process competes appreciably with the primary photoreaction of the excited sensitizer with the sacrificial oxidant, even in high ionic strength media. The Ru(bpy)(3)(3+) generated by photoreaction of the excited sensitizer with the sacrificial oxidant undergoes primary bimolecular hole scavenging by 1 at a remarkably high rate (3.6 ± 0.1 × 10(9) M(-1) s(-1)), emphasizing the kinetic advantages of this molecular species over, e.g., colloidal oxide particles as water oxidation catalysts. The kinetics of the subsequent steps and final oxygen evolution process involved in the full photocatalytic cycle are not known in detail. An indirect indication that all these processes are relatively fast, however, is provided by the flash photolysis experiments, where a single molecule of 1 is shown to undergo, in 40 ms, ca. 45 turnovers in Ru(bpy)(3)(3+) reduction. With the assumption that one molecule of oxygen released after four hole-scavenging events, this translates into a very high average turnover frequency (280 s(-1)) for oxygen production.

Indium-modified copper nanocubes for syngas production by aqueous CO2 electroreduction.

Electroreduction of carbon dioxide represents an appealing strategy to rethink a waste product as a valuable feedstock for the formation of value-added compounds. Among the metal electrodes able to catalyze such processes, copper plays a central role due to its rich chemistry. Strategies aimed at tuning Cu selectivity comprise nanostructuring and alloying/post-functionalization with heterometals. In this contribution, we report on straightforward electrochemical methods for the formation of nanostructured Cu-In interfaces. The latter were fully characterized and then used as cathodes for CO2 electroreduction in aqueous environment, leading to the selective production of syngas, whose composition varies upon changing the applied bias and indium content. In particular, gaseous mixtures compatible with the synthesis of methanol or aldehydes (i.e. respectively with 1 : 2 and 1 : 1 CO/H2 ratios) are produced at low (i.e. -0.62 V vs. RHE) applied bias with >3.5 mA cm-2 current densities (in absolute value). Even if the proposed cathodes undergo structural modifications upon prolonged exposure to CO2 reduction conditions, their catalytic activity can be restored by introducing an additional In(III) precursor to the electrolytic solution.

Better Together: Ilmenite/Hematite Junctions for Photoelectrochemical Water Oxidation.

Hematite (α-Fe2O3) is an earth-abundant indirect n-type semiconductor displaying a band gap of about 2.2 eV, useful for collecting a large fraction of visible photons, with frontier energy levels suitably aligned for carrying out the photoelectrochemical water oxidation reaction under basic conditions. The modification of hematite mesoporous thin-film photoanodes with Ti(IV), as well as their functionalization with an oxygen-evolving catalyst, leads to a 6-fold increase in photocurrent density with respect to the unmodified electrode. In order to provide a detailed understanding of this behavior, we report a study of Ti-containing phases within the mesoporous film structure. Using X-ray absorption fine structure and high-resolution transmission electron microscopy coupled with electron energy loss spectroscopy, we find that Ti(IV) ions are incorporated within ilmenite (FeTiO3) near-surface layers, thus modifying the semiconductor-electrolyte interface. To the best of our knowledge, this is the first time that an FeTiO3/α-Fe2O3 composite is used in a photoelectrochemical setup for water oxidation. In fact, previous studies of Ti(IV)-modified hematite photoanodes reported the formation of pseudobrookite (Fe2TiO5) at the surface. By means of transient absorption spectroscopy, transient photocurrent experiments, and electrochemical impedance spectroscopy, we show that the formation of the Fe2O3/FeTiO3 interface passivates deep traps at the surface and induces a large density of donor levels, resulting in a strong depletion field that separates electron and holes, favoring hole injection in the electrolyte. Our results provide the identification of a phase coexistence with enhanced photoelectrochemical performance, allowing for the rational design of new photoanodes with improved kinetics.

Photoelectrochemical Properties of SnO2 Photoanodes Sensitized by Cationic Perylene-Di-Imide Aggregates for Aqueous HBr Splitting.

Perylene-sensitized mesoporous SnO2 films were used as electrodes for photoelectrochemical HBr splitting in aqueous solution. Upon AM 1.5 G illumination a 3-4 fold increase of the saturated photocurrent was observed when decreasing the pH of the aqueous solution from pH 3 to pH 0 (j max = 0.05 ± 0.01 mAcm-2 at pH 3 and 0.17 ± 0.02 mAcm-2 at pH 0, respectively). A detailed spectroscopic and electrochemical analysis of the hybrid material was carried out in order to address the impact of interfacial energetics on charge separation dynamics. UV/Vis spectroelectrochemical measurements showed that the energy of semiconductor states in such systems can be adjusted independently from the molecular levels by varying proton concentration. Photoelectrochemical measurements and ns-µs transient absorption spectroscopy reveal that pH-related changes of the interfacial energetics have only a minor impact on the charge injection rate. An increase of the proton concentration improves charge collection mainly by retarding recombination, which in the case of Br- oxidation is in critical competition with perylene regeneration. Control of the back recombination appears to be a key feature in heterogeneous molecular systems tasked to drive energetically demanding redox reactions.

Syngas Evolution from CO2 Electroreduction by Porous Au Nanostructures.

Electrocatalytic reduction of CO2 recently emerged as a viable solution in view of changing the common belief and considering carbon dioxide as a valuable reactant instead of a waste product. In this view, we herein propose the one-step synthesis of gold nanostructures of different morphologies grown on fluorine-doped tin oxide electrodes by means of pulsed-laser deposition. The resulting cathodes are able to produce syngas mixtures of different compositions at overpotentials as low as 0.31 V in CO2-presaturated aqueous media. Insights into the correlation between the structural features/morphology of the cathodes and their catalytic activity are also provided, confirming recent reports on the remarkable sensitivity toward CO production for gold electrodes exposing undercoordinated sites and facets.

Photoanodes for water oxidation with visible light based on a pentacyclic quinoid organic dye enabling proton-coupled electron transfer.

A pentacyclic quinoid dye, KuQ(O)3OH, combining (i) extended visible absorption up to 600 nm, (ii) excited state reduction potential >2 V vs. NHE, and (iii) a photoinduced proton-coupled electron transfer mechanism, has been used for the fabrication of dye-sensitized SnO2 photoanodes integrating a ruthenium polyoxometalate water oxidation catalyst. The resulting photoelectrode SnO2|KuQ(O)3OH|Ru4POM displays a light harvesting efficiency up to 90% in the range 500-600 nm, an onset potential as low as 0.2 V vs. NHE at pH 5.8, photoinduced oxygen evolution with a faradaic efficiency of 70 ± 15% and an absorbed-photon-to-current efficiency up to 0.12 ± 0.01%.

Rational Design Combining Morphology and Charge-Dynamic for Hematite/Nickel-Iron Oxide Thin-Layer Photoanodes: Insights into the Role of the Absorber/Catalyst Junction.

Water oxidation represents the anodic reaction in most of the photoelectrosynthetic setups for artificial photosynthesis developed so far. The efficiency of the overall process strongly depends on the joint exploitation of good absorber domains and interfaces with minimized recombination pathways. To this end, we report on the effective coupling of thin-layer hematite with amorphous porous nickel-iron oxide catalysts prepared via pulsed laser deposition. The rational design of such composite photoelectrodes leads to the formation of a functional adaptive junction, with enhanced photoanodic properties with respect to bare hematite. Electrochemical impedance spectroscopy has contributed to shed light on the mechanisms of photocurrent generation, confirming the reduction of recombination pathways as the main contributor to the improved performances of the functionalized photoelectrodes. Our results highlight the importance of the amorphous catalysts' morphology, as dense and electrolyte impermeable layers hinder the pivotal charge compensation processes at the interface. The direct comparison with all-iron and all-nickel catalytic counterparts further confirms that control over the kinetics of both hole transfer and charge recombination, enabled by the adaptive junction, is key for the optimal operation of this kind of semiconductor/catalyst interfaces.

Fluorinated ZnII Porphyrins for Dye-Sensitized Aqueous Photoelectrosynthetic Cells.

Three perfluorinated ZnII porphyrins were evaluated as n-type sensitizers in photoelectrosynthetic cells for HBr and water splitting. All the dyes are featured by the presence of pentafluorophenyl electron-withdrawing groups to increase the ground-state oxidation potential and differ for the nature and position of the π-conjugate linker between the core and anchoring group tasked to bind the metal oxide, in order to assess the best way of coupling with the semiconductor. A phenyl-triazole moiety was used to link the carboxylic anchoring group onto the meso position, while an ethynyl-phenyl linker was chosen to bridge carboxylic and cyanoacrylic groups onto the ß-pyrrolic position. A combination of electrochemical, computational, and spectroscopic investigations confirmed the strong electron-withdrawing effect of the perfluorinated porphyrin core, which assures all the investigated dyes of the high oxidation potential required to the coupling with water oxidation catalysts (WOC). Such an electron-poor core, however, affects the charge separation character of the dyes, as demonstrated by the spatial distribution of the excited states, leading to a nonquantitative charge injection, although tilting of the molecules on the semiconductor surface could bring the porphyrin ring closer to the semiconductor, offering additional charge-transfer pathways. Indeed, all the dyes demonstrated successful in the splitting of both aqueous HBr and water, with the best results found for the SnO2/TiO2 photoanode sensitized with the ß-substituted porphyrin equipped with a cyanoacrylic terminal group, achieving 0.4 and 0.1 mA/cm2 photoanodic currents in HBr and water under visible light, respectively. The faradaic yield for oxygen evolution in the presence of an IrIV catalyst was over 95%, and the photoanode operation was stable for more than 1000 s. Thus, the perfluorinated porphyrins with a cyanoacrylic anchoring group at the ß-position should be considered for further development to improve the charge-transfer character.

Publisher Correction: Hierarchical organization of perylene bisimides and polyoxometalates for photo-assisted water oxidation.

In the version of this Article originally published, in the graphical abstract the y-axis units of the plot read 'mA cm-2', but should have read 'µA cm-2'. Additionally, an erroneous gap appeared in the red trace. These errors have now been corrected.