Multifunctional Coatings from Scalable Single Source Precursor Chemistry in Tandem Photoelectrochemical Water Splitting

The straightforward and inexpensive fabrication of stabilized and activated photoelectrodes for application to tandem photoelectrochemical (PEC) water splitting is reported. Semiconductors such as Si, WO₃, and BiVO₄ can be coated with a composite layer formed upon hydrolytic decomposition of hetero­bimetallic single source precursors (SSPs) based on Ti and Ni, or Ti and Co in a simple single‐step process under ambient conditions. The resulting 3d‐transition metal oxide composite films are multifunctional, as they protect the semiconductor electrode from corrosion with an amorphous TiO₂ coating and act as bifunctional electrocatalysts for H₂ and O₂ evolution based on catalytic Ni or Co species. Thus, this approach enables the use of the same precursors for both photoelectrodes in tandem PEC water splitting, and SSP chemistry is thereby established as a highly versatile low‐cost approach to protect and activate photoelectrodes. In an optimized system, SSP coating of a Si photocathode and a BiVO₄ photoanode resulted in a benchmark noble metal‐free dual‐photoelectrode tandem PEC cell for overall solar water splitting with an applied bias solar‐to‐hydrogen conversion efficiency of 0.59% and a half‐life photostability of 5 h.     

Recent Advancement of p‐ and d‐Block Elements,Single Atoms,and Graphene‐Based Photoelectrochemical Electrodes for Water Splitting

Solar‐assisted photoelectrochemical (PEC) water splitting to produce hydrogen energy is considered the most promising solution for clean, green, and renewable sources of energy. For scaled production of hydrogen and oxygen, highly active, robust, and cost‐effective PEC electrodes are required. However, most of the available semiconductors as a PEC electrodes have poor light absorption, material degradation, charge separation, and transportability, which result in very low efficiency for photo‐water splitting. Generally, a promising photoelectrode is obtained when the surface of the semiconductor is modified/decorated with a suitable co‐catalyst because it increases the light absorbance spectrum and prevents electron–hole recombination during photoelectrode reactions. In this regard, numerous p‐ and d‐block elements, single atoms, and graphene‐based PEC electrodes have been widely used as semiconductor/co‐catalyst junctions to boost the performances of PEC overall water splitting. This review enumerates the recent progress and applications of p‐ and d‐block elements, single atoms, and graphene‐based PEC electrodes for water splitting. The focus is placed on fundamental mechanism, efficiency, cells design, and various aspects that contribute to the large‐scale prototype device. Finally, future perspectives, summary, challenges, and outlook for improving the activity of PEC photoelectrodes toward whole‐cell water splitting are addressed.     

Recent Development of Ni/Fe‐Based Micro/Nanostructures toward Photo/Electrochemical Water Oxidation

The oxygen evolution reaction (OER), as an important process involved in water splitting and rechargeable metal–air batteries, has drawn increasing attention in the context of clean energy generation and efficient energy storage. This review concerns the progress and new discoveries in the field of Ni/Fe‐based micro/nanostructures toward electrochemical and photo‐electrochemical (PEC) water oxidation during last few years. First, toward the design and construction of new electrocatalysis, different types of current Ni/Fe‐based compounds for OER are summarized. The mechanism studies of the active phases and positions of Ni/Fe‐based micro/nanostructures are further introduced to understand the properties of catalytic active sites, which could facilitate further improving the performance of Ni/Fe‐based OER electrocatalysts. Second, splitting water using sunlight with low overpotential is another important target in making solar‐to‐hydrogen micro/nanodevices, and thus attention is then focused on the development of several important Ni/Fe‐based PEC catalysts. Third, the recent theoretical calculations on the OER mechanism during water splitting and insights into electronic structures are analyzed; finally, the future trends and perspectives are also discussed briefly.     

Interfacial Scaffolding Preparation of Hierarchical PBA‐Based Derivative Electrocatalysts for Efficient Water Splitting

The development of highly efficient and durable electrocatalysts is crucial for overall water splitting. Herein, the in situ scaffolding formation of 3D Prussian blue analogues (PBAs) on a variety of 2D or 1D metal hydroxides/oxides to fabricate hierarchical nanostructures is first demonstrated. Typically, cobalt hydroxide or oxide nanoarrays are used as the precursor and structural oriented template for the subsequent growth of 3D PBA nanocubes. The mechanism study reveals that the interfacial scaffolding process can be reversibly controlled via the in situ ion exchange process with adjusting coordination ions. Thus, the facile, versatile strategy can extend to successfully fabricate a variety of hierarchical PBA‐based nanostructures including on cobalt fluoride hydroxide, copper hydroxide, monometal or bimetal nickel–cobalt hydroxides, cobalt oxide, and manganese oxide nanosheets with structural tailor‐ability and chemical diversity. More interestingly, the metal nitride derivatives obtained via controlled calcination process exhibit good electrocatalytic activity for water splitting with low overpotentials, and remarkable durability for 1200 h, thanks to the superior intrinsic activity of bimetal nature and the scrupulous hierarchical structure. This versatile strategy provides a paradigm for rational design of PBA‐based functional nanomaterials, which is highly promising in energy conversion, storage, and electrocatalytic fields.     

Enhancing Mo:BiVO4 Solar Water Splitting with Patterned Au Nanospheres by Plasmon‐Induced Energy Transfer

Plasmonic metal nanostructures have been extensively investigated to improve the performance of metal oxide photoanodes for photoelectrochemical (PEC) solar water splitting cells. Most of these studies have focused on the effects of those metal nanostructures on enhancing light absorption and enabling direct energy transfer via hot electrons. However, several recent studies have shown that plasmonic metal nanostructures can improve the PEC performance of metal oxide photoanodes via another mechanism known as plasmon‐induced resonant energy transfer (PIRET). However, this PIRET effect has not yet been tested for the molybdenum‐doped bismuth vanadium oxide (Mo:BiVO₄), regarded as one of the best metal oxide photoanode candidates. Here, this study constructs a hybrid Au nanosphere/Mo:BiVO₄ photoanode interwoven in a hexagonal pattern to investigate the PIRET effect on the PEC performance of Mo:BiVO₄. This study finds that the Au nanosphere array not only increases light absorption of the photoanode as expected, but also improves both its charge transport and charge transfer efficiencies via PIRET, as confirmed by time‐correlated single photon counting and transient absorption studies. As a result, incorporating the Au nanosphere array increases the photocurrent density of Mo:BiVO₄ at 1.23 V versus RHE by ≈2.2‐fold (2.83 mA cm^?2).     

Over 17% Efficiency Stand‐Alone Solar Water Splitting Enabled by Perovskite‐Silicon Tandem Absorbers

Realizing solar‐to‐hydrogen (STH) efficiencies close to 20% using low‐cost semiconductors remains a major step toward accomplishing the practical viability of photoelectrochemical (PEC) hydrogen generation technologies. Dual‐absorber tandem cells combining inexpensive semiconductors are a promising strategy to achieve high STH efficiencies at a reasonable cost. Here, a perovskite photovoltaic biased silicon (Si) photoelectrode is demonstrated for highly efficient stand‐alone solar water splitting. A p⁺nn⁺ ‐Si/Ti/Pt photocathode is shown to present a remarkable photon‐to‐current efficiency of 14.1% under biased condition and stability over three days under continuous illumination. Upon pairing with a semitransparent mixed perovskite solar cell of an appropriate bandgap with state‐of‐the‐art performance, an unprecedented 17.6% STH efficiency is achieved for self‐driven solar water splitting. Modeling and analysis of the dual‐absorber PEC system reveal that further work into replacing the noble‐metal catalyst materials with earth‐abundant elements and improvement of perovskite fill factor will pave the way for the realization of a low‐cost high‐efficiency PEC system.     

Scalable Triple Cation Mixed Halide Perovskite–BiVO4 Tandems for Bias‐Free Water Splitting

Strong interest exists in the development of organic–inorganic lead halide perovskite photovoltaics and of photoelectrochemical (PEC) tandem absorber systems for solar fuel production. However, their scalability and durability have long been limiting factors. In this work, it is revealed how both fields can be seamlessly merged together, to obtain scalable, bias‐free solar water splitting tandem devices. For this purpose, state‐of‐the‐art cesium formamidinium methylammonium (CsFAMA) triple cation mixed halide perovskite photovoltaic cells with a nickel oxide (NiO_x) hole transport layer are employed to produce Field's metal‐epoxy encapsulated photocathodes. Their stability (up to 7 h), photocurrent density (–12.1 ± 0.3 mA cm^?2 at 0 V versus reversible hydrogen electrode, RHE), and reproducibility enable a matching combination with robust BiVO₄ photoanodes, resulting in 0.25 cm² PEC tandems with an excellent stability of up to 20 h and a bias‐free solar‐to‐hydrogen efficiency of 0.35 ± 0.14%. The high reliability of the fabrication procedures allows scaling of the devices up to 10 cm², with a slight decrease in bias‐free photocurrent density from 0.39 ± 0.15 to 0.23 ± 0.10 mA cm^?2 due to an increasing series resistance. To characterize these devices, a versatile 3D‐printed PEC cell is also developed.     

Recent Advances and Emerging Trends in Photo‐Electrochemical Solar Energy Conversion

Photo‐electrochemical (PEC) solar energy conversion offers the promise of low‐cost renewable fuel generation from abundant sunlight and water. In this Review, recent developments in photo‐electrochemical water splitting are discussed with respect to this promise. State‐of‐the‐art photo‐electrochemical device performance is put in context with the current understanding of the necessary requirements for cost‐effective solar hydrogen generation (in terms of solar‐to‐hydrogen conversion efficiency and system durability, in particular). Several important studies of photo‐electrochemical hydrogen generation at p‐type photocathodes are highlighted, mostly with protection layers (for enhanced durability), but also a few recent examples where protective layers are not needed. Recent work with the widely studied n‐type BiVO₄ photoanode is detailed, which highlights the needs and necessities for the next big photoanode material yet to be discovered. The emerging new research direction of photo‐electrocatalytic upgrading of biomass substrates toward value‐added chemicals is then discussed, before closing with a commentary on how research on PEC materials remains a worthwhile endeavor.     

Water Splitting Progress in Tandem Devices: Moving Photolysis beyond Electrolysis

Water photolysis is a sustainable technology to convert natural solar energy and water into chemical fuels and is thus considered a thorough solution to the forthcoming energy crises. Unassisted water splitting that could directly harvest solar light and subsequently split water in a single device has become an important research theme. Three types of tandem devices including photoelectrochemical (PEC), photovoltaic (PV) cell/PEC and PV/electrolyser tandem cells are proposed to realize water photolysis at different levels of integration and component. Recent progress in tandem water splitting devices is summarized, and crucial issues on device optimization from the perspective of each photo‐absorber functionalities in band edge potential, light absorptivity and transmittance are discussed. By increasing the performances of stand‐alone PEC or PV devices, a 20% solar to hydrogen efficiency is predicted that is a significant value towards further application in practice. Accordingly, the challenges for materials development and configuration optimization are further outlined.     

Hybrid Photoelectrochemical Water Splitting Systems: From Interface Design to System Assembly

Photoelectrochemical (PEC) water splitting has attracted increasing attention due to its potential to mitigate energy and environmental issues. Hybrid PEC systems containing semiconductor photosensitizers and molecular catalysts are reported to be highly active and stable for water splitting with great potential for facilitating clean fuels production. In this review, following a showcasing of the fundamental details of hybrid PEC systems for water splitting, semiconductor/molecular catalyst interface designs are highlighted, with a focus on interfacial physicochemical interactions and binding, and interfacial energetics and dynamics for efficient charge transfer. Recent advances in hybrid system assemblies for PEC water splitting are also briefly introduced. Finally, future challenges and directions in the field of hybrid PEC water splitting for solar energy conversion are reviewed. The current review provides state‐of‐the‐art strategies for optimized interface design for creating highly active and stable PEC water splitting assemblies.     

Boosting the Performance of WO3/n‐Si Heterostructures for Photoelectrochemical Water Splitting: from the Role of Si to Interface Engineering

Metal oxide/Si heterostructures make up an exciting design route to high‐performance electrodes for photoelectrochemical (PEC) water splitting. By monochromatic light sources, contributions of the individual layers in WO₃/n‐Si heterostructures are untangled. It shows that band bending near the WO₃/n‐Si interface is instrumental in charge separation and transport, and in generating a photovoltage that drives the PEC process. A thin metal layer inserted at the WO₃/n‐Si interface helps in establishing the relation among the band bending depth, the photovoltage, and the PEC activity. This discovery breaks with the dominant Z‐scheme design idea, which focuses on increasing the conductivity of an interface layer to facilitate charge transport, but ignores the potential profile around the interface. Based on the analysis, a high‐work‐function metal is predicted to provide the best interface layer in WO₃/n‐Si heterojunctions. Indeed, the fabricated WO₃/Pt/n‐Si photoelectrodes exhibit a 2 times higher photocurrent density at 1.23 V versus reversible hydrogen electrode (RHE) and a 10 times enhancement at 1.6 V versus RHE compared to WO₃/n‐Si. Here, it is essential that the native SiO₂ layer at the interface between Si and the metal is kept in order to prevent Fermi level pinning in the Schottky contact between the Si and the metal.     

Band Edge Engineering of Oxide Photoanodes for Photoelectrochemical Water Splitting: Integration of Subsurface Dipoles with Atomic‐Scale Control

One of the crucial parameters dictating the efficiency of photoelectrochemical water‐splitting is the semiconductor band edge alignment with respect to hydrogen and oxygen redox potentials. Despite the importance of metal oxides in their use as photoelectrodes, studies to control the band edge alignment in aqueous solution have been limited predominantly to compound semiconductors with modulation ranges limited to a few hundred mV. The ability to modulate the flat band potential of oxide photoanodes by as much as 1.3 V, using the insertion of subsurface electrostatic dipoles near a Nb‐doped SrTiO₃/aqueous electrolyte interface is reported. The tunable range achieved far exceeds previous reports in any semiconductor/aqueous electrolyte system and suggests a general design strategy for highly efficient oxide photoelectrodes.     

3D Porous Pyramid Heterostructure Array Realizing Efficient Photo‐Electrochemical Performance

Direct photo‐electrochemical (PEC) water splitting is of great practical interest for developing a sustainable energy systems, but remains a big challenge owing to sluggish charge separation, low efficiency, and poor stability. Herein, a 3D porous In₂O₃/In₂S₃ pyramid heterostructure array on a fluorine‐doped tin oxide substrate is fabricated by an ion exchange–induced synthesis strategy. Based on the synergistic structural and electronic modulations from density functional theory calculations and experimental observations, 3D porous In₂O₃/In₂S₃ photoanode by the protective layer delivers a low onset potential of ≈0.02 V versus reversible hydrogen electrode (RHE), the highest photocurrent density of 8.2 mA cm^?2 at 1.23 V versus RHE among all the In₂S₃ photoanodes reported to date, an incident photon‐to‐current efficiency of 76% at 400 nm, and high stability over 20 h for PEC water splitting are reported. This work provides an alternative promising prototype for the design and construction of novel heterostructures in robust PEC water splitting applications.     

Enhancing Charge Carrier Lifetime in Metal Oxide Photoelectrodes through Mild Hydrogen Treatment

Widespread application of solar water splitting for energy conversion is largely dependent on the progress in developing not only efficient but also cheap and scalable photoelectrodes. Metal oxides, which can be deposited with scalable techniques and are relatively cheap, are particularly interesting, but high efficiency is still hindered by the poor carrier transport properties (i.e., carrier mobility and lifetime). Here, a mild hydrogen treatment is introduced to bismuth vanadate (BiVO₄), which is one of the most promising metal oxide photoelectrodes, as a method to overcome the carrier transport limitations. Time‐resolved microwave and terahertz conductivity measurements reveal more than twofold enhancement of the carrier lifetime for the hydrogen‐treated BiVO₄, without significantly affecting the carrier mobility. This is in contrast to the case of tungsten‐doped BiVO₄, although hydrogen is also a donor type dopant in BiVO₄. The enhancement in carrier lifetime is found to be caused by significant reduction of trap‐assisted recombination, either via passivation or reduction of deep trap states related to vanadium antisite on bismuth or vanadium interstitials according to density functional theory calculations. Overall, these findings provide further insights on the interplay between defect modulation and carrier transport in metal oxides, which benefit the development of low‐cost, highly‐efficient solar energy conversion devices.     

Developments and Perspectives in 3d Transition‐Metal‐Based Electrocatalysts for Neutral and Near‐Neutral Water Electrolysis

Technology for producing highly pure hydrogen (99.999%) by water electrolysis is a field of importance in terms of the planets' current energy scenario. A much needed transition from a carbon economy to a hydrogen economy further adds importance to the field of hydrogen generation from water for a sustainable future. To avoid energy losses in the production process, the use of highly acidic (Proton Exchange Membrane (PEM) water electrolyzer) and alkaline (alkaline water electrolyzer) electrolytes is conventional practice in this field. Unfortunately, there are several other issues associated with the use of acidic and alkaline electrolytes such as the requirement of specific ion exchanging membranes with good stability, acid or alkali stable catalysts and corrosive environment withstanding cell stacks, etc. To overcome these issues, researchers have shown interest in the field of electrochemical water splitting in neutral and near‐neutral conditions. In this review, the chronological development of 3d transition‐metal‐based electrocatalysts for neutral and near‐neutral water splitting is extensively discussed with emphases on screening methodologies, mechanisms, structure‐activity correlations, and detailed catalyst specific evolution. In addition, catalysts reported so far, are also benchmarked based on their performance separately for different electrolytes used.     

Design and Fabrication of a Precious Metal‐Free Tandem Core–Shell p+n Si/W‐Doped BiVO4 Photoanode for Unassisted Water Splitting

Tandem photoelectrochemical water splitting cells utilizing crystalline Si and metal oxide photoabsorbers are promising for low‐cost solar hydrogen production. This study presents a device design and a scalable fabrication scheme for a tandem heterostructure photoanode: p⁺n black silicon (Si)/SnO₂ interface/W‐doped bismuth vanadate (BiVO₄)/cobalt phosphate (CoPi) catalyst. The black‐Si not only provides a substantial photovoltage of 550 mV, but it also serves as a conductive scaffold to decrease charge transport pathlengths within the W‐doped BiVO₄ shell. When coupled with cobalt phosphide (CoP) nanoparticles as hydrogen evolution catalysts, the device demonstrates spontaneous water splitting without employing any precious metals, achieving an average solar‐to‐hydrogen efficiency of 0.45% over the course of an hour at pH 7. This fabrication scheme offers the modularity to optimize individual cell components, e.g., Si nanowire dimensions and metal oxide film thickness, involving steps that are compatible with fabricating monolithic devices. This design is general in nature and can be readily adapted to novel, higher performance semiconducting materials beyond BiVO₄ as they become available, which will accelerate the process of device realization.     

Recent Progress on Multimetal Oxide Catalysts for the Oxygen Evolution Reaction

Hydrogen is a promising alternative fuel for efficient energy production and storage, with water splitting considered one of the most clean, environmentally friendly, and sustainable approaches to generate hydrogen. However, to meet industrial demands with electrolysis‐generated hydrogen, the development of a low‐cost and efficient catalyst for the oxygen evolution reaction (OER) is critical, while conventional catalysts are mostly based on precious metals. Many studies have thus focused on exploring new efficient nonprecious‐metal catalytic systems and improving the understandings on the OER mechanism, resulting in the design of catalysts with superior activity compared with that of conventional catalysts. In particular, the use of multimetal rather than single‐metal catalysts is demonstrated to yield remarkable performance improvement, as the metal composition in these catalysts can be tailored to modify the intrinsic properties affecting the OER. Herein, recent progress and accomplishments of multimetal catalytic systems, including several important groups of catalysts: layered hydroxide, spinel, and amorphous metal oxides along with the theoretical principles of activity enhancement in multimetal systems are reviewed. Finally, this is concluded by discussing remaining challenges to achieve further improvements of OER catalyst activities.     

Retarded Charge–Carrier Recombination in Photoelectrochemical Cells from Plasmon‐Induced Resonance Energy Transfer

N‐type metal oxides such as hematite (α‐Fe₂O₃) and bismuth vanadate (BiVO₄) are promising candidate materials for efficient photoelectrochemical water splitting; however, their short minority carrier diffusion length and restricted carrier lifetime result in undesired rapid charge recombination. Herein, a 2D arranged globular Au nanosphere (NS) monolayer array with a highly ordered hexagonal hole pattern (hereafter, Au array) is introduced onto the surface of photoanodes comprised of metal oxide films via a facile drying and transfer‐printing process. Through plasmon‐induced resonance energy transfer, the Au array provides a strong electromagnetic field in the near‐surface area of the metal oxide film. The near‐field coupling interaction and amplification of the electromagnetic field suppress the charge recombination with long‐lived photogenerated holes and simultaneously enhance the light harvesting and charge transfer efficiencies. Consequently, an over 3.3‐fold higher photocurrent density at 1.23 V versus reversible hydrogen electrode (RHE) is achieved for the Au array/α‐Fe₂O₃. Furthermore, the high versatility of this transfer printing of Au arrays is demonstrated by introducing it on the molybdenum‐doped BiVO₄ film, resulting in 1.5‐fold higher photocurrent density at 1.23 V versus RHE. The tailored metal film design can provide a potential strategy for the versatile application in various light‐mediated energy conversion and optoelectronic devices.     

Boosting Photoelectrochemical Water Splitting by TENG‐Charged Li‐Ion Battery

The need for cost‐effective and sustainable power supplies has spurred a growing interest in hybrid energy harvesting systems, and the most elementary energy production process relies on intermittent solar power. Here, it is shown how the ambient mechanical energy leads to water splitting in a photoelectrochemical (PEC) cell boosted by a triboelectric nanogenerator (TENG). In this strategy, a flexible TENG collects and transforms mechanical energy into electric current, which boosts the PEC water splitting via the charged Li‐ion battery. Au nanoparticles are deposited on TiO₂ nanoarrays for extending the available light spectrum to visible part by surface plasmon resonance effect, which yields a photocurrent density of 1.32 mA cm^?2 under AM 1.5 G illumination and 0.12 mA cm^?2 under visible light with a bias of 0.5 V. The TENG‐charged battery boosts the water splitting performance through coupling electrolysis and enhanced electron–hole separation efficiency. The hybrid cell exhibits an instantaneous current more than 9 mA with a working electrode area of 0.3 cm², suggesting a simple but efficient route for simultaneously converting solar radiation and mechanical energy into hydrogen.     

MOF‐Based Transparent Passivation Layer Modified ZnO Nanorod Arrays for Enhanced Photo‐Electrochemical Water Splitting

This study introduces zeolitic imidazolate framework‐8 (ZIF‐8) as the first metal‐organic framework based transparent surface passivation layer for photo‐electrochemical (PEC) water splitting. A significant enhancement for PEC water oxidation is demonstrated based on the in situ seamless coating of ZIF‐8 surface passivation layer on Ni foam (NF) supported ZnO nanorod arrays photoanode. The PEC performance is improved by optimizing the ZIF‐8 thickness and by grafting Ni(OH)₂ nanosheets as synergetic co‐catalyst. With respect to ZnO/NF, the optimized Ni(OH)₂/ZIF‐8/ZnO/NF photoanode exhibits a two times larger photocurrent density of 1.95 mA cm^?2 and also a two times larger incident photon to current conversion efficiency of 40.05% (350 nm) at 1.23 V versus RHE (V_RHE) under AM 1.5 G. The synergetic surface passivation and the co‐catalyst modification contribute to prolonging the charge lifetime, to promoting the charge transfer, and to decreasing the overpotential for water oxidation.