Solar Energy Conversion Efficiency Research Articles

Interface-modulated kinetic differentials in electron and hole transfer rates as a key design principle for redox photocatalysis by Sb2VO5/QD heterostructures.

The efficient conversion of solar energy to chemical energy represents a critical bottleneck to the energy transition. Photocatalytic splitting of water to generate solar fuels is a promising solution. Semiconductor quantum dots (QDs) are prime candidates for light-harvesting components of photocatalytic heterostructures, given their size-dependent photophysical properties and band-edge energies. A promising series of heterostructured photocatalysts interface QDs with transition-metal oxides which embed midgap electronic states derived from the stereochemically active electron lone pairs of p-block cations. Here, we examine the thermodynamic driving forces and dynamics of charge separation in Sb2VO5/CdSe QD heterostructures, wherein a high density of Sb 5s2-derived midgap states are prospective acceptors for photogenerated holes. Hard-x-ray valence band photoemission spectroscopy measurements of Sb2VO5/CdSe QD heterostructures were used to deduce thermodynamic driving forces for charge separation. Interfacial charge transfer dynamics in the heterostructures were examined as a function of the mode of interfacial connectivity, contrasting heterostructures with direct interfaces assembled by successive ion layer adsorption and reaction (SILAR) and interfaces comprising molecular bridges assembled by linker-assisted assembly (LAA). Transient absorption spectroscopy measurements indicate ultrafast (<2ps) electron and hole transfer in SILAR-derived heterostructures, whereas LAA-derived heterostructures show orders of magnitude differentials in the kinetics of hole (<100ps) and electron (∼1ns) transfer. The interface-modulated kinetic differentials in electron and hole transfer rates underpin the more effective charge separation, reduced charge recombination, and greater photocatalytic efficiency observed for the LAA-derived Sb2VO5/CdSe QD heterostructures.

Development of Bio-Photoelectrochemical Hybrids for Solar Energy Conversion

Recent advancements in solar energy conversion have identified bio-photoelectrochemical hybrids as one of the most promising sustainable techniques. This study integrates BiVO4 and TiO2 semiconductors with photoautotrophic microorganisms (e.g., Algae) to enhance solar energy conversion. Thin films of these materials were prepared and characterized, revealing a relatively smooth surface for BiVO4 while structures for TiO2 thin films deposited as nanorods. Optical properties showed band gaps of ≤ 3.1 and 2.4 eV for TiO2 and BiVO4, respectively. The point of zero charge of materials was investigated, indicating that naturally occurring biofilm formation might not be favorable for as-prepared materials. To overcome this challenge, we aimed to use polyelectrolytes to enhance attachment of cells on the surface of semiconductor and in this regards we determined the biocompatibility of using this approach. Photoelectrochemical (PEC) measurements were conducted to evaluate solar energy conversion efficiency. This study offers insights into optimizing biosystem attachment, biofilm stability, and PEC performance of coupled semiconductors with photoautotrophic microorganisms as one photoelectrode in PEC cell, advancing sustainable solar energy conversion technologies.

Innovations in Photocatalytic and Photoelectrocatalytic Water Splitting: Pathways to Efficiently Convert Biomass into Renewable Energy and Chemicals

AbstractThis review comprehensively explores the integration of photocatalytic (PC) and photoelectrocatalytic (PEC) technologies for hydrogen production via water splitting, in synergy with the efficient conversion of biomass resources. This synergistic strategy significantly boosts hydrogen production rates in both PC and PEC systems and enhances solar energy conversion efficiency. Furthermore, it enables selective conversion of cost‐effective biomass via precise modulation of catalyst structures, paving a novel pathway for green hydrogen generation and synthesis of high‐value chemicals. Specifically, the manuscript highlights recent progress in the oxidation and coupling reactions of biomass derivatives, such as methanol, ethanol, glycerol, and 5‐hydroxymethylfurfural, in PC/PEC systems. It reveals their potential to enhance hydrogen production efficiency and the synthesis of high‐value organic compounds. Future research should focus on employing in‐situ characterization techniques and theoretical simulations to deeply understand reaction mechanisms, thus advancing the field of biomass conversion through photocatalytic/photoelectrocatalytic methods.

Unlocking high stability in perovskite solar cells through vacuum-deposited Cs3Bi2I9 thin layer

Perovskite solar cells (PSCs) show great potential for efficient solar energy conversion, but their long-term stability is still a concern. To address this issue, we developed a vacuum-deposited bismuth-based perovskite-like material (Cs3Bi2I9), which forms a high-quality thin film showing remarkable stability over 150 days of air exposure. When combined with a solution-processed MAPbI3 perovskite, the resulting device exhibits improved stability under varying environmental conditions. However, the power conversion efficiency (PCE) drops by 70% compared to the reference MAPbI3-based PSC. An advanced multiphysics optoelectrical device simulation combining 3D FDTD and FEM methods validates these findings, yielding results in excellent agreement with the experimental data. The study also provides insight into the device’s optics and electronic properties, revealing the factors that limit its performance. An optimized device design is proposed to reach an 18.81% PCE, higher than the reference device. The findings have significant implications for developing next-generation solar cells, including high-performance tandem solar cells.

Electron-parking engineering assisted ZnIn2S4/Mo2TiC2-Ru photocatalytic hydrogen evolution for efficient solar energy conversion and storage

The electron utilization efficiency in photocatalytic hydrogen evolution (PHE) is crucial for solar energy conversion and storage. Prolonged lifetime and effective use of accumulated electrons based on the storage-release behavior is a potential strategy to regulate the electronic utilization efficiency. Herein, this study utilized Mo2TiC2-Ru as the “electron-parking” to construct a ZnIn2S4/Mo2TiC2-Ru photocatalyst. The ZnIn2S4/Mo2TiC2-Ru exhibits a visible light-driven PHE rate of 5.72 mmol·g−1·h−1, and maintains a PHE rate of ∼1.67 mmol·g−1·h−1 under dark conditions. The photogenerated electrons could be directionally stored in Mo2TiC2-Ru to create an electron-rich environment, this can inhibit backflow and recombination of electrons, and could regulate the water dissociation and hydrogen adsorption kinetics. Importantly, the stored electrons could release in the dark, increasing the quantity of electrons and overcoming intermittent sunlight and regional environmental influences. This work provides insights and references for the development of capacitive cocatalysts with an “electron-parking” engineering for efficient and sustained PHE reactions.

Boosting photocatalytic activity in ternary lamellar hierarchical structured ZnFe2O4/polymeric carbon nitride by constructing an electronic bridge

Photocatalytic technology is one of the ideal approaches for clean energy production and environmental pollution control in the future. However, the rapid recombination of photo-generated charge carriers is a bottleneck problem of low solar energy conversion efficiency. Herein, a magnetic ZnFe2O4/Pt/polymeric carbon nitride (PCN) semiconductor catalyst is designed and prepared for high-performance photocatalytic hydrogen production reaction and photocatalytic degradation rate of RhB. It exhibits 339.31 μmol·g−1·h−1 hydrogen production rate and 96.08 % photocatalytic degradation rate of RhB within 120 min under visible light. The introduction of Pt, constructing an electronic bridge, accelerated the transfer of photo-generated carriers, meanwhile, the smaller band gap of the ternary composites enabled the generation of more photo-generated electrons. The internal electric field accelerated the accumulation of electrons and holes in the conduction band of ZnFe2O4 and valence band of PCN, thus photocatalytic activity is greatly enhanced. The electron-hole separation is also improved and the transport of photo-generated electrons is facilitated by the special structure of the heterojunction and the unique morphology of PCN. In addition, the used catalyst can be recovered through magnetic fields, and this magnetic catalytic system has great application prospects in the fields of photocatalytic hydrogen production and pollutant degradation.

Manufacturing porous BaTaO2N nanosheet via nitridation of a novel oxyhalide precursor for boosted photocatalytic water oxidation reaction

BaTaO2N (BTON) with a generous adsorption edge of ca. 660 nm and high theoretical solar-to-hydrogen conversion efficiency of ca. 20.6% has been extensively investigated for photocatalytic water splitting. In this study, we have successfully prepared a porous BTON nanosheet via employing Ba2Bi3Ta2O11Cl (BBTOC) oxyhalide as a novel nitridation precursor. The oxygen evolution rate of the BTON nanosheet is 108 μmol·h−1, which is three times higher than that of BTON (25.9 μmol·h−1) prepared by conventional solid-state method. The successful construction of porous BTON nanosheet is due to the structural transformation of BBTOC nanosheet precursor and facile evaporation of Bi and Cl elements. The porous nanosheet morphology of BTON can not only promote the transfer of photogenerated charge carriers but also provide abundant reaction sites for the oxygen evolution reaction. This work demonstrates a novel and efficient strategy for preparing oxynitride for efficient solar energy conversion.

Steering charge flow in hierarchical ZnIn2S4/TiO2/Ti3C2 heterojunction for noble-metal-free photocatalytic hydrogen production

The construction of effective photogenerated charge transfer channels through interface engineering is the key to achieving the highly efficient of photocatalysts. Herein, sandwich-like ZnIn2S4/TiO2/Ti3C2 nanosheets integrated type-II heterostructure with Schottky junction are reasonably fabricated by low temperature in-situ growth method. Benefitting from the intensive visible light absorption of ZnIn2S4, the fast electron transport of TiO2, the rich active sites in Ti3C2, as well as the intimate interface coupling and the matched band alignment among ternary components, enhanced hydrogen production can be achieved with ZnIn2S4/TiO2/Ti3C2 hierarchical photocatalyst under visible light irradiation in the absence of noble metal co-catalysts. The concept of coupling type-II heterostructure with the Schottky barrier can steer the charge flow and boost the charge carrier separation and transfer across the interfacial domain, which may spark new ensemble design for efficient solar energy harvesting and conversion.

Design and hardware verification of photovoltaic converter based on adaptive P&amp;O with snubber and BJT circuits

The efficient utilization of renewable energy is a key technology area of high domestic and international concern, and the research and development of DC–DC photovoltaic converters with high conversion efficiency is of great significance for improving performance and reducing the cost of solar power generation systems. In order to improve the conversion efficiency of solar energy, this paper proposes the design of a high-efficiency photovoltaic DC–DC converter with a non-isolated DC–DC converter as the object of the study. Solar power conversion is accomplished by designing a simple and reliable snubber circuit and a triode auxiliary circuit and tracking the maximum power point by combining the perturbation observation method with variable step size. The snubber circuit can effectively suppress the problems of pulse spikes and oscillations, and the triode auxiliary circuit prevents the reverse current and improves the switching speed, which reduces the switching loss and combines with the perturbation observation method with variable step size for fast and stable tracking of the maximum power point. In order to verify the feasibility of the converter, a 600 W prototype is designed. The experimental results show that using the snubber circuit reduces the pulse spike by 4.2 V and the overshoot is reduced by 4.3%. The maximum conversion efficiency is increased by 0.88% with the use of the transistor-assisted circuit, and the tracking efficiency of the MPPT is still stable under cloudy conditions. The maximum conversion efficiency of the prototype is finally measured to be up to 98.12%.

Spontaneous enhanced photocatalytic overall water splitting on AlO/WSi2N4 vdW heterojunction

Completely achieving spontaneous water splitting without sacrificing co-catalysts poses a significant challenge, as factors such as electrical, optical, and catalytic activity can limit the conversion efficiency of solar energy to hydrogen. Herein, we propose a type-II van der Waals heterostructure composed of vertically stacked AlO and WSi2N4, and systematically investigate its mechanism and potential for catalyzing water splitting. Photon-induced photocatalytic water splitting takes advantage of the staggered energy bands of the heterojunction, effectively promoting the separation of photogenerated carriers and thus enhancing catalytic efficiency. In neutral water environment, the band edge position of AlO/WSi2N4 aligns with the redox potential required for water decomposition. Thermodynamic analysis of the oxygen and hydrogen evolution reactions indicates that the external potential provided by photogenerated carriers is expected to trigger spontaneous water decomposition. Moreover, with its high electron mobility (4800.62 cm2/Vs) and a solar-to-hydrogen energy conversion efficiency of up to 19.98 %, the AlO/WSi2N4 heterojunction demonstrates substantial potential as a photoelectric catalyst. This research introduces a promising avenue for efficient photocatalytic production of clean energy.

Electrochemistry of 2D-materials for the remediation of environmental pollutants and alternative energy storage/conversion materials and devices, a comprehensive review

This review article explores into the complicated relationship between electrochemistry and 2D materials, exploring their mutual influences and the consequential advancements in energy conversion, storage, and environmental applications. Electrochemical reactions, manifested through oxidations and reductions at submerged electrodes, form the linchpin connecting the electrochemistry of 2D materials with their practical utility. Various electrochemical cell topologies are investigated for their role in enhancing material flexibility, operational states, energy conversion efficiency, and device design adaptability. The comprehensive discussion extends to diverse applications, emphasizing the pivotal roles of 2D materials in environmental remediation, alternate energy storage and conversion, and chemical reactivity. Noteworthy applications include pollutant detection, adsorption and absorption of pollutants, elimination of both organic and inorganic pollutants, and photocatalytic degradation. The review also addresses materials synthesis via electrochemical processes, detailing functionalization, handling, and deposition techniques. Particular focus is directed towards local electrochemical techniques enabling the analysis and local alteration of 2D materials. Moreover, this paper concludes the article published in the recent years with this topic and most significant trends observed in 2022 and 2023 with electrochemistry of materials for the remediation of environmental pollutants. While the trends of article publishing increased from 2020 to 2023 with topic alternative energy storage/conversion materials. Finally, offering a comprehensive overview of the synergistic relationship between electrochemistry and 2D materials and their transformative potential in sustainable technologies. Broader contextThe decreasing availability of energy resources and the contamination of the environment are two significant worldwide concerns that need immediate attention. The focus on 2D materials and associated technologies is important for the efficient conversion of solar energy into chemical energy. These materials have diverse applications in fields such as energy (e.g., water splitting), synthesis (e.g., production of valuable chemicals and N2 reduction), and the environment (e.g., CO2 reduction and environmental remediation). Furthermore, Electrochemical energy storage and conversion (EESC) technologies are widely acknowledged as the most viable solutions to address the escalating energy crisis and environmental degradation because to their exceptional energy efficiency and little environmental footprint. Currently, there have been several reports discussing the use of 2D-materials in energy applications and wastewater treatment. However, there is a lack of comprehensive reviews that summarize the electrochemistry of 2D-materials, their preparation strategies, modification techniques, and related properties. Furthermore, there is a need for detailed analysis of the progress in applying 2D-materials for environmental pollution remediation, electrocatalytic performance, energy storage, and conversion technologies and devices. In this paper, we systematically and comprehensively review the electrochemistry of 2D-materials and innovatively analyze the design principles and difficulties of 2D-materials. We discussed comprehensively the remediation of environmental pollutants through 2D-materials in water treatment fields such as photocatylsts, adsorption/absorption and dyes removal as an entry point and provide an in-depth knowledge and outlook on the current status and development potential of specific applications of energy storage and conversion materials and devices.

Upgrading structural conjugation in covalent organic framework with spatial dual sites enables boosting solar-to-H2O2-to-•OH for environmental remediation

Designing photocatalysts with well-defined structure-function relationships is imperative for propelling the progression of desired photocatalytic oxidation. Herein, the efficient conversion of solar energy to H2O2 and subsequently to hydroxyl radicals (•OH) is achieved through a synergistic interplay between olefin linkage (-CC-) and spatially separated benzene-triazine dual reaction sites within covalent organic frameworks (COFs). The upgraded -CC- can increase the conjugation degree of COFs, which establishes an expanded superstructure for boosting charge separation/transfer and stability. This precise modulation renders more opportunities for the hot electrons to migrate to the benzene site for solar-to-H2O2 generation, and to the triazine site for H2O2-to-•OH, separately. The optimized •OH generation pathway enables remarkable oxidation performances against recalcitrant organic pollutants, and pathogenic microorganisms under visible light irradiation. This work provides new insights for tuning the synergistic interactions of various building blocks within the COFs for the selective generation of highly reactive •OH for environmental remediation.

Interplay of intermolecular and intramolecular vibrations mediates ultrafast singlet fission

Singlet fission (SF) is an exciton multiplication process that splits a singlet exciton in organic semiconductors into two triplet excitons and thus, can overcome the Shockley–Queisser limit to improve the solar energy conversion efficiency in photovoltaics. In this paper, we construct a unified model for the ultrafast primary step of the SF process. To achieve this, we investigate the dynamics of vibrational modes and their interactions with the relevant electronic excited states in prototypical SF materials, pentacene (exothermic SF) and tetracene (endothermic SF) single crystals. Additionally, the functional role of the charge transfer (CT) state is also examined. Using the refined parameters obtained from the reported experimental results, we deduce that the intermolecular vibrations mediate the SF in pentacene with the assistance from strong vibronic couplings to intramolecular modes, which drives the SF process to occur within 100 fs. In this timescale, the CT state has a limiting role towards the SF process in pentacene. However, the CT state plays an important role in a relatively slower SF process in tetracene. Our results disentangle the role of underlying vibrational coherences and clarify the importance of the CT state in tetracene crystal. Hence, with our unified model, we can study the coherent dynamics of the SF process, which can principally be extended to other SF materials as well.

Strong Interactions between Au Nanoparticles and BiVO4 Photoanode Boosts Hole Extraction for Photoelectrochemical Water Splitting.

Strong metal-support interaction (SMSI) is widely proposed as a key factor in tuning catalytic performances. Herein, the classical SMSI between Au nanoparticles (NPs) and BiVO4 (BVO) supports (Au/BVO-SMSI) is discovered and used innovatively for photoelectrochemical (PEC) water splitting. Owing to the SMSI, the electrons transfer from V4+ to Au NPs, leading to the formation of electron-rich Au species (Auδ-) and strong electronic interaction (i.e., Auδ--Ov-V4+), which readily contributes to extract photogenerated holes and promote charge separation. Benefitted from the SMSI effect, the as-prepared Au/BVO-SMSI photoanode exhibits a superior photocurrent density of 6.25 mA cm-2 at 1.23 V versus the reversible hydrogen electrode after the deposition of FeOOH/NiOOH cocatalysts. This work provides a pioneering view for extending SMSI effect to bimetal oxide supports for PEC water splitting, and guides the interfacial electronic and geometric structure modulation of photoanodes consisting of metal NPs and reducible oxides for improved solar energy conversion efficiency.

Strong Interactions between Au Nanoparticles and BiVO4 Photoanode Boosts Hole Extraction for Photoelectrochemical Water Splitting

AbstractStrong metal‐support interaction (SMSI) is widely proposed as a key factor in tuning catalytic performances. Herein, the classical SMSI between Au nanoparticles (NPs) and BiVO4 (BVO) supports (Au/BVO‐SMSI) is discovered and used innovatively for photoelectrochemical (PEC) water splitting. Owing to the SMSI, the electrons transfer from V4+ to Au NPs, leading to the formation of electron‐rich Au species (Auδ−) and strong electronic interaction (i.e., Auδ−‐Ov‐V4+), which readily contributes to extract photogenerated holes and promote charge separation. Benefitted from the SMSI effect, the as‐prepared Au/BVO‐SMSI photoanode exhibits a superior photocurrent density of 6.25 mA cm−2 at 1.23 V versus the reversible hydrogen electrode after the deposition of FeOOH/NiOOH cocatalysts. This work provides a pioneering view for extending SMSI effect to bimetal oxide supports for PEC water splitting, and guides the interfacial electronic and geometric structure modulation of photoanodes consisting of metal NPs and reducible oxides for improved solar energy conversion efficiency.

Harnessing fluorescence resonance energy transfer for improved solar still performance with zinc oxide nanoparticles and activated carbon

The Single Slope Corrugated Wick type Solar Distillers (SWS) have attracted significant research funding owing to their simple preparation process and excellent durability against heat and moisture. However, there is a recognized need to enhance their solar energy conversion efficiency. The utilization of ZnO nanoparticles (Z) in SWS is limited by their light absorption capacity, resulting in suboptimal thermal energy conversion and solar energy absorption. In this investigation, we propose an innovative method known as Fluorescence Resonance Energy Transfer (FRET), combining crystallized Z with activated carbon (AC) derived from areca nut shells. This novel approach substantially boosts the thermal efficiency of solar energy utilization in SWS by facilitating efficient energy transfer from ZAC to water.The FRET technique enables the effective transfer of energy from ZAC to water and is comprehensively analyzed. By utilizing Z as donors and AC as acceptors, the photoluminescence emitted by ZAC can be absorbed by both components, thereby increasing the carrier population as of Corrugated Wick-type towards the condenser face within SWS. The evaporation rate from water to the condensing surface is significantly higher in SWS with ZAC compared to conventional wick-type solar stills (CWS), attributed to the efficient heat transfer facilitated through multi-dimensional heterojunctions within ZAC. The energy and charge transfer processes are optimized for both summer and winter operating conditions. The ZAC-based SWS exhibits exceptional resilience in various ambient conditions, resulting in a substantial 33.989 % enhancement in distillation efficiency during summer and a notable 31.199 % improvement in winter. The incorporation of ZAC elevates the production of distillate water to 6.325 liters/m2 per day in summer and 5.840 liters/m2 per day in winter (24 h). The energy distribution among particle components is extensively scrutinized using the FRET mechanism.

High‐Temperature Semiconductor CuO/SiC‐Based Catalyst for Artificial Photosynthesis

AbstractArtificial photosynthesis can convert CO2 and H2O into hydrocarbons via solar energy. However, the extremely low process efficiency is a major obstacle to this application. The photocatalyst is considered to be the key factor to raise the overall solar energy conversion efficiency. Much research focused on co‐catalysts, but less attention has been paid on the high‐temperature semiconductor. Herein, a strategy is proposed involving high‐temperature semiconductor to design target photocatalyst dealing with the artificial photosynthesis at high temperature. Based upon this strategy, a CuO/SiC catalyst with single atom characteristic was designed, prepared and the activity of CO2 photoreduction with H2O was tested in a high temperature environment. Above 150 °C, the catalyst activity was boosted and unprecedented performance values were attained. Under the irradiation condition delivered by a 1000 W Xe light and at 350 °C, the obtained yields of CH4, C2H4, and C2H6 were 2041.4 μmol ⋅ g−1, 15.2 μmol ⋅ g−1, and 63.6 μmol ⋅ g−1, respectively. The overall CO2 conversion reached 24.6 % and the maximum solar energy conversion efficiency was 2.3 % without any sacrificed agents. This strategy will be helpful to overcome the current limitations for the industrialization of artificial photosynthesis and accelerate the related research on photothermal catalysis.

Application of Metamaterial in Renewable Energy: A Review

Metamaterial advancements hold promise for compact renewable energy harvesting, capturing acoustic, electromagnetic, mechanical, and solar energy on a modest scale across global industries. Engineered structures surpass natural material limitations, offering capabilities unattainable in traditional counterparts. This investigation explores metamaterials' manipulation of acoustic, electromagnetic, mechanical, and solar energy. Mechanical metamaterials convert strain into electrical energy, applicable from interstellar travel to terrestrial infrastructure. Precision-configured acoustic metamaterials efficiently harness dispersed acoustic energy, improving renewable energy methodologies. Integration into photovoltaic cells showcases metamaterials' solar potential, with innovative designs enhancing solar energy conversion efficiency. Electromagnetic metamaterials efficiently absorb and convert frequencies into usable energy from communications and monitoring systems, in the agricultural and environmental sectors. Comparative analyses highlight noteworthy efficiency advancements, underscoring metamaterials' transformative influence on renewable energy. As they redefine the sector, implications extend to both small-scale devices and large-scale applications, positioning them as pivotal contributors. The paper critically evaluates metamaterial effectiveness in harnessing diverse energy sources, guiding future research. Metamaterial adaptability to different sizes and integration into technology reveals possibilities for compact energy sources. Ongoing research addresses scientific and economic challenges, paving the way for scaling metamaterial applications to commercial operations and emphasizing their importance in incorporating renewable energy into our technological milieu.

Biomimetic Design of 3D Fe3O4/V-EVOH Fiber-Based Self-Floating Composite Aerogel to Enhance Solar Steam Generation Performance.

An interfacial solar steam generation evaporator for seawater desalination has attracted extensive interest in recent years. Nevertheless, challenges still remain in relatively low evaporation rate, unsatisfactory energy conversion efficiency, and salt accumulation. Herein, we have demonstrated a biomimetic bilayer composite aerogel consisting of bottom hydrophilic and vertically aligned EVOH channels and an upper hydrophobic conical Fe3O4 array. Thanks to the design merits, the 3D Fe3O4/V-EVOH evaporator exhibits a high evaporation rate of ∼2.446 kg m-2 h-1 and an impressive solar energy conversion efficiency of ∼165.5% under 1 sun illumination, which is superior to those of state-of-the-art evaporators reported so far. Moreover, the asymmetrical wettability not only allows the evaporator to self-float on the water but also facilitates the salt ion diffusion in the channels; thus, the evaporator shows no salt crystals on its surface and only a 6% decrease in evaporation performance even after the salt concentration increases from 0 to 10.0 wt %.

Double S-scheme Cu2−xSe/twinned-Cd0.5Zn0.5S homo-heterojunctions with surface plasmon effects for efficient photocatalytic H2 evolution

The enhancement of charge separation and utilization efficiency in both the bulk phase and interface of semiconductor photocatalysts, as well as the expansion of light absorption range, are crucial research topics in the field of photocatalysis. To address this issue, twinned Cd0.5Zn0.5S (T-CZS) homojunctions consisting of wurtzite Cd0.5Zn0.5S (WZ-CZS) and zinc blende Cd0.5Zn0.5S (ZB-CZS) were synthesized via a hydrothermal method to facilitate the bulk-phase charge separation. Meanwhile, Cu2−xSe with localized surface plasmon resonance effect (LSPR) generated by Cu vacancies was also obtained through a hydrothermal process. Due to their opposite electronegativity, a solvent evaporation strategy was employed to combine Cu2−xSe and T-CZS by intermolecular electrostatic. After optimization, the photocatalytic hydrogen (H2) evolution rate of 5 wt% Cu2−xSe/T-CZS reached an impressive value of 60 mmol∙h−1∙g−1, which was 4.6 and 66.6 times higher than that of pure Cu2−xSe and T-CZS, respectively. Furthermore, this composites demonstrated a remarkable rate of 0.46 mmol∙h−1∙g−1 under near-infrared (NIR) wavelength (>800 nm). The enhanced performance observed in Cu2−xSe/T-CZS can be attributed to its unique and efficient double S-scheme charge transfer mechanism which effectively suppresses rapid recombination of electron-hole pairs both within the bulk phase and at the surface interfaces; this conclusion is supported by Density Functional Theory (DFT) calculations as well as electron paramagnetic resonance spectroscopy analysis. Moreover, incorporation of Cu2−xSe enables effective utilization ultraviolet visible-near infrared (UV–Vis-NIR) light by the composites while facilitating injection “hot electrons” into T-CZS for promoting photocatalytic reactions. This study provides a potential strategy for achieving efficient solar energy conversion through synergistic integration of non-stoichiometric plasmonic materials with photocatalysts with twinned-twinned structures.