High-Performance Indoor Perovskite Solar Cells by Self-Suppression of Intrinsic Defects via a Facile Solvent-Engineering Strategy.

Lead halide perovskite solar cells have been emerging as very promising candidates for applications in indoor photovoltaics. To maximize their indoor performance, it is of critical importance to suppress intrinsic defects of the perovskite active layer. Herein, a facile solvent-engineering strategy is developed for effective suppression of both surface and bulk defects in lead halide perovskite indoor solar cells, leading to a high efficiency of 35.99% under the indoor illumination of 1000 lux Cool-white light-emitting diodes. Replacing dimethylformamide (DMF) with N-methyl-2-pyrrolidone (NMP) in the perovskite precursor solvent significantly passivates the intrinsic defects within the thus-prepared perovskite films, prolongs the charge carrier lifetimes and reduces non-radiative charge recombination of the devices. Compared to the DMF, the much higher interaction energy between NMP and formamidinium iodide/lead halide contributes to the markedly improved quality of the perovskite thin films with reduced interfacial halide deficiency and non-radiative charge recombination, which in turn enhances the device performance. This work paves the way for developing efficient indoor perovskite solar cells for the increasing demand for power supplies of Internet-of-Things devices.

Advancements in Interfacial Engineering for Perovskite Light-Emitting Diodes.

Perovskite light-emitting diodes (PeLEDs) have gained significant attention due to their promising optoelectronic properties and potential applications in the fields of lighting and display devices. Despite their potential, PeLEDs face challenges related to stability, high turn-on voltage, and low external quantum efficiency (EQE) which has restricted their broad acceptance. Most research efforts have predominantly focused on refining the properties of the perovskite films. However, it is becoming more apparent that interfacial layers and device architecture are crucial for achieving stability and high efficiency, making them indispensable components in PeLED development. This perspective highlights remarkable advancements in PeLED devices, with a primary focus on modifying adjacent layers interfacing with the perovskite film.

Unveiling the Role of Water in Heterogeneous Photocatalysis of Methanol Conversion for Efficient Hydrogen Production.

Water molecules, which act as both solvent and reactant, play critical roles in photocatalytic reactions for methanol conversion. However, the influence of water on the adsorption of methanol and desorption of liquid products, which are two essential steps that control the performance in photocatalysis, has been well under-explored. Herein, we reveal the role of water in heterogeneous photocatalytic processes of methanol conversion on the platinized carbon nitride (Pt/C3N4) model photocatalyst. In situ spectroscopy techniques, isotope effects, and computational calculations demonstrate that water shows adverse effects on the adsorption of methanol molecules and desorption processes of methanol oxidation products on the surface of Pt/C3N4, significantly altering the reaction pathways in photocatalytic methanol conversion process. Guided by these discoveries, a photothermal-assisted photocatalytic system is designed to achieve a high solar-to-hydrogen (STH) conversion efficiency of 2.3 %, which is among the highest values reported. This work highlights the important roles of solvents in controlling the adsorption/desorption behaviours of liquid-phase heterogeneous catalysis.

Accelerated Redox Reactions Enable Stable Tin-Lead Mixed Perovskite Solar Cells.

The facile oxidation of Sn2+ to Sn4+ poses an inherent challenge that limits the efficiency and stability of tin-lead mixed (Sn-Pb) perovskite solar cells (PSCs) and all-perovskite tandem devices. In this work, we discover the sustainable redox reactions enabling self-healing Sn-Pb perovskites, where their intractable oxidation degradation can be recovered to their original state under light soaking. Quantitative and operando spectroscopies are used to investigate the redox chemistry, revealing that metallic Pb0 from the photolysis of perovskite reacts with Sn4+ to regenerate Pb2+ and Sn2+ spontaneously. Given the sluggish redox reaction kinetics, V3+ /V2+ ionic pair is designed as an effective redox shuttle to accelerate the recovery of Sn-Pb perovskites from oxidation. The target Sn-Pb PSCs enabled by V3+ /V2+ ionic pair deliver an improved power conversion efficiency (PCE) of 21.22 % and excellent device lifespan, retaining nearly 90 % of its initial PCE after maximum power point tracking under light for 1,000 hours.

Effective Suppressing Phase Segregation of Mixed-Halide Perovskite by Glassy Metal-Organic Frameworks.

Lead mixed-halide perovskites offer tunable bandgaps for optoelectronic applications, but illumination-induced phase segregation can quickly lead to changes in their crystal structure, bandgaps, and optoelectronic properties, especially for the Br-I mixed system because CsPbI3 tends to form a non-perovskite phase under ambient conditions. These behaviors can impact their performance in practical applications. By embedding such mixed-halide perovskites in a glassy metal-organic framework, a family of stable nanocomposites with tunable emission is created. Combining cathodoluminescence with elemental mapping under a transmission electron microscope, this research identifies a direct relationship between the halide composition and emission energy at the nanoscale. The composite effectively inhibits halide ion migration, and consequently, phase segregation even under high-energy illumination. The detailed mechanism, studied using a combination of spectroscopic characterizations and theoretical modeling, shows that the interfacial binding, instead of the nanoconfinement effect, is the main contributor to the inhibition of phase segregation. These findings pave the way to suppress the phase segregation in mixed-halide perovskites toward stable and high-performance optoelectronics.

Photocatalytic Oxidative Coupling of Methane over Au1 Ag Single-Atom Alloy Modified ZnO with Oxygen and Water Vapor: Synergy of Gold and Silver.

C-H dissociation and C-C coupling are two key steps in converting CH4 into multi-carbon compounds. Here we report a synergy of Au and Ag to greatly promote C2 H6 formation over Au1 Ag single-atom alloy nanoparticles (Au1 Ag NPs)-modified ZnO catalyst via photocatalytic oxidative coupling of methane (POCM) with O2 and H2 O. Atomically dispersed Au in Au1 Ag NPs effectively promotes the dissociation of O2 and H2 O into *OOH, promoting C-H activation of CH4 on the photogenerated O- to form *CH3 . Electron-deficient Au single atoms, as hopping ladders, also facilitate the migration of electron donor *CH3 from ZnO to Au1 Ag NPs. Finally, *CH3 coupling can readily occur on Ag atoms of Au1 Ag NPs. An excellent C2 H6 yield of 14.0 mmol g-1 h-1 with a selectivity of 79 % and an apparent quantum yield of 14.6 % at 350 nm is obtained via POCM with O2 and H2 O, which is at least two times that of the photocatalytic system. The bimetallic synergistic strategy offers guidance for future catalyst design for POCM with O2 and H2 O.

A BiVO4 Photoanode with a VOx Layer Bearing Oxygen Vacancies Offers Improved Charge Transfer and Oxygen Evolution Kinetics in Photoelectrochemical Water Splitting.

Sluggish oxygen evolution kinetics are one of the key limitations of bismuth vanadate (BiVO4 ) photoanodes for efficient photoelectrochemical (PEC) water splitting. To address this issue, we report a vanadium oxide (VOx ) with enriched oxygen vacancies conformally grown on BiVO4 photoanodes by a simple photo-assisted electrodeposition process. The optimized BiVO4 /VOx photoanode exhibits a photocurrent density of 6.29 mA cm-2 at 1.23 V versus the reversible hydrogen electrode under AM 1.5 G illumination, which is ca. 385 % as high as that of its pristine counterpart. A high charge-transfer efficiency of 96 % is achieved and stable PEC water splitting is realized, with a photocurrent retention rate of 88.3 % upon 40 h of testing. The excellent PEC performance is attributed to the presence of oxygen vacancies in VOx that forms undercoordinated sites, which strengthen the adsorption of water molecules onto the active sites and promote charge transfer during the oxygen evolution reaction. This work demonstrates the potential of vanadium-based catalysts for PEC water oxidation.

Solvent-derived Fluorinated Secondary Interphase for Reversible Zn-graphite Dual-ion Batteries.

The irreversibility of anion intercalation-deintercalation is a fundamental issue in determining the cycling stability of a dual-ion battery (DIB). In this work, we demonstrate that using a partially fluorinated carbonate solvent can drive a beneficial fluorinated secondary interphase layer formation. Such layer facilitates reversible anion (de-)intercalation processes by impeding solvent molecule co-intercalation and the associated graphite exfoliation. The enhanced reversibility of anion transport contributes to the overall cycling stability for a Zn-graphite DIB-a high Coulombic efficiency of 98.5 % after 800 cycles, with an attractive discharge capacity of 156 mAh g-1 and a mid-point discharge voltage of ≈1.7 V (at 0.1 A g-1 ). In addition, the formed fluorinated secondary interphase suppresses the self-discharge behavior, preserving 29 times of the capacity retention rate compared to the battery with a commonly used carbonate solvent, after standing for 24 hours. This work provides a simple and effective strategy for addressing the critical challenges in graphite-based DIBs and contributes to fundamental understanding to help accelerate their practical application.

Photocatalytic Overall Water Splitting over PbTiO3 Modulated by Oxygen Vacancy and Ferroelectric Polarization.

Ferroelectric materials hold great promise in the field of photocatalytic water splitting due to their spontaneous polarization that sets up an inherent internal field for the spatial separation of photogenerated charges. The ferroelectric polarization, however, is generally accompanied by some intrinsic defects, particularly oxygen vacancies, whose impact upon photocatalysis is far from being fully understood and modulated. Here, we have studied the role of oxygen vacancies over the photocatalytic behavior of single-domain PbTiO3 through a combination of theoretical and experimental viewpoints. Our results indicate that the oxygen vacancies in the negatively polarized facet (001) are active sites for water oxidation into O2, while the defect-free sites prefer H2O2 as the oxidation product. The apparent quantum yield at 435 nm for photocatalytic overall water splitting with PbTiO3/Rh/Cr2O3 is determined to be 0.025%, which is remarkable for single undoped metal oxide-based photocatalysts. Furthermore, the strong correlation among oxygen vacancies, polarization strength, and photocatalytic activity is properly reflected by charge separation conditions in the single-domain PbTiO3. This work clarifies the crucial role of oxygen vacancies during photocatalytic reactions of PbTiO3, which provides a useful guide to the design of efficient ferroelectric photocatalysts and their water redox reaction pathways.

Ligand-Engineered Quantum Dots Decorated Heterojunction Photoelectrodes for Self-Biased Solar Water Splitting.

A cost-effective and high-efficiency photoelectrochemical (PEC) water splitting system based on colloidal quantum dots (QDs) represents a potential solar-to-hydrogen (STH) conversion technology to achieve future carbon neutrality. Herein, a self-biased PEC cell consisting of BiVO4 photoanode and Cu2 O photocathode both decorated with Zn-doped CuInS2 (ZCIS) QDs is successfully fabricated. The intrinsic charge dynamics of the photoelectrodes are efficiently optimized via rational engineering of the surface ligands capped on QDs with controllable chain lengths and binding affinities to the metal oxide electrodes. It is demonstrated that the short-chain monodentate 1-dodecanethiol ligands are beneficial to ZCIS QDs for suppressing charge recombination, which enables the construction of tight heterojunction with coupled metal oxide electrodes, leading to effective photo-induced charge transfer/injection for enhanced PEC performance. The QD decorated BiVO4 and Cu2 O photoelectrodes in pairs demonstrate a self-biased PEC water splitting process, delivering an STH efficiency of 0.65% with excellent stability under AM 1.5 G one-sun illumination. The results highlight the significance of synergistic ligand and heterojunction engineering to build highly efficient and robust QDs-based PEC devices for self-biased solar water splitting.

Graphene-Based Nanomaterials for Solar-Driven Overall Water Splitting.

Water splitting through photocatalysis and photoelectrochemical methods is a promising strategy for solar energy utilization. Graphene is widely used in solar-driven overall water splitting because of its versatile properties. This review summarizes the preparation of graphene-based photocatalysts and photoelectrodes and the functions of graphene, and highlights the challenges and prospects of the future applications of graphene in solar-driven water splitting.

Simultaneous Removal of Antibiotic Resistant Bacteria, Antibiotic Resistance Genes, and Micropollutants by FeS2@GO-Based Heterogeneous Photo-Fenton Process.

The co-occurrence of various chemical and biological contaminants of emerging concerns has hindered the application of water recycling. This study aims to develop a heterogeneous photo-Fenton treatment by fabricating nano pyrite (FeS2) on graphene oxide (FeS2@GO) to simultaneously remove antibiotic resistant bacteria (ARB), antibiotic resistance genes (ARGs), and micropollutants (MPs). A facile and solvothermal process was used to synthesize new pyrite-based composites. The GO coated layer forms a strong chemical bond with nano pyrite, which enables to prevent the oxidation and photocorrosion of pyrite and promote the transfer of charge carriers. Low reagent doses of FeS2@GO catalyst (0.25 mg/L) and H2O2 (1.0 mM) were found to be efficient for removing 6-log of ARB and 7-log of extracellular ARG (e-ARG) after 30 and 7.5 min treatment, respectively, in synthetic wastewater. Bacterial regrowth was not observed even after a two-day incubation. Moreover, four recalcitrant MPs (sulfamethoxazole, carbamazepine, diclofenac, and mecoprop at an environmentally relevant concentration of 10 µg/L each) were completely removed after 10 min of treatment. The stable and recyclable composite generated more reactive species, including hydroxyl radicals (HO•), superoxide radicals (O2• -), singlet oxygen (1O2). These findings highlight that the synthesized FeS2@GO catalyst is a promising heterogeneous photo-Fenton catalyst for the removal of emerging contaminants.

Coordination Chemistry Engineered Polymeric Carbon Nitride Photoanode with Ultralow Onset Potential for Water Splitting.

Construction of an intimate film/substrate interface is of great importance for a photoelectrode to achieve efficient photoelectrochemical performance. Inspired by coordination chemistry, a polymeric carbon nitride (PCN) film is intimately grown on a Ti-coated substrate by an in situ thermal condensation process. The as-prepared PCN photoanode exhibits a record low onset potential (Eonset ) of -0.38 V versus the reversible hydrogen electrode (RHE) and a decent photocurrent density of 242 µA cm-2 at 1.23 VRHE for water splitting. Detailed characterization confirms that the origin of the ultralow onset potential is mainly attributed to the substantially reduced interfacial resistance between the Ti-coated substrate and the PCN film benefitting from the constructed interfacial sp2 N→Ti coordination bonds. For the first time, the ultralow onset potential enables the PCN photoanode to drive water splitting without external bias with a stable photocurrent density of ≈9 µA cm-2 up to 1 hour.

Heterocyclic Conjugated Polymer Nanoarchitectonics with Synergistic Redox-Active Sites for High-Performance Aluminium Organic Batteries.

The development of cost-effective and long-life rechargeable aluminium ion batteries (AIBs) shows promising prospects for sustainable energy storage applications. Here, we report a heteroatom π-conjugated polymer featuring synergistic C=O and C=N active centres as a new cathode material in AIBs using a low-cost AlCl3 /urea electrolyte. Density functional theory (DFT) calculations reveal the fused C=N sites in the polymer not only benefit good π-conjugation but also enhance the redox reactivity of C=O sites, which enables the polymer to accommodate four AlCl2 (urea)2 + per repeating unit. By integrating the polymer with carbon nanotubes, the hybrid cathode exhibits a high discharge capacity and a long cycle life (295 mAh g-1 at 0.1 A g-1 and 85 mAh g-1 at 1 A g-1 over 4000 cycles). The achieved specific energy density of 413 Wh kg-1 outperforms most Al-organic batteries reported to date. The synergistic redox-active sites strategy sheds light on the rational design of organic electrode materials.

Mechanochemically Synthesised Flexible Electrodes Based on Bimetallic Metal-Organic Framework Glasses for the Oxygen Evolution Reaction.

The melting behaviour of metal-organic frameworks (MOFs) has aroused significant research interest in the areas of materials science, condensed matter physics and chemical engineering. This work first introduces a novel method to fabricate a bimetallic MOF glass, through melt-quenching of the cobalt-based zeolitic imidazolate framework (ZIF) [ZIF-62(Co)] with an adsorbed ferric coordination complex. The high-temperature chemically reactive ZIF-62(Co) liquid facilitates the formation of coordinative bonds between Fe and imidazolate ligands, incorporating Fe nodes into the framework after quenching. The resultant Co-Fe bimetallic MOF glass therefore shows a significantly enhanced oxygen evolution reaction performance. The novel bimetallic MOF glass, when combined with the facile and scalable mechanochemical synthesis technique for both discrete powders and surface coatings on flexible substrates, enables significant opportunities for catalytic device assembly.

Nanoconfined Topochemical Conversion from MXene to Ultrathin Non-Layered TiN Nanomesh toward Superior Electrocatalysts for Lithium-Sulfur Batteries.

2D non-layered materials (2DNLMs) featuring massive undercoordinated surface atoms and obvious lattice distortion have shown great promise in catalytic/electrocatalytic applications, but their controllable synthesis remains challenging. Here, a new type of ultrathin carbon-wrapped titanium nitride nanomesh (TiN NM@C) is prepared using a rationally designed nano-confinement topochemical conversion strategy. The ultrathin 2D geometry with well-distributed pores offers TiN NM@C plentiful exposed active sites and rapid charge transfer, leading to outstanding electrocatalytic performance tackling the sluggish sulfur redox kinetics in lithium-sulfur batteries (LSBs). LSBs employing TiN NM@C electrocatalyst deliver excellent rate capabilities (e.g., 304 mAh g-1 at 10 C), greatly outperforming that of using TiN nanoparticles embedded in carbon nanosheets (TiN NPs@C) as a benchmark. More impressively, a free-standing electrode for LSBs with a high sulfur loading of 7.3 mg cm-2 is demonstrated, showing a high peak areal capacity of 5.6 mAh cm-2 at a high current density of 6.1 mA cm-2 . This work provides a new avenue for the facile and controllable fabrication of 2DNLMs with impressive electrocatalysis for LSBs as well as other energy conversion and storage technologies.

1D-2D Synergistic MXene-Nanotubes Hybrids for Efficient Perovskite Solar Cells.

Incorporation of 2D MXenes into the electron transporting layer (ETL) of perovskite solar cells (PSCs) has been shown to deliver high-efficiency photovoltaic (PV) devices. However, the ambient fabrication of the ETLs leads to unavoidable deterioration in the electrical properties of MXene due to oxidation. Herein, sorted metallic single-walled carbon nanotubes (m-SWCNTs) are employed to prepare MXene/SWCNTs composites to improve the PV performance of PSCs. With the optimized composition, a power conversion efficiency of over 21% is achieved. The improved photoluminescence and reduced charge transfer resistance revealed by electrochemical impedance spectroscopy demonstrated low trap density and improved charge extraction and transport characteristics due to the improved conductivity originating from the presence of nanotubes as well as the reduced defects associated with oxygen vacancies on the surface of the SnO2 . The MXene/SWCNTs strategy reported here provides a new avenue for realizing high-performance PSCs.

Interlayer Space Engineering of MXenes for Electrochemical Energy Storage Applications.

The increasing demand for high-performance rechargeable energy storage systems has stimulated the exploration of advanced electrode materials. MXenes are a class of two-dimensional (2D) inorganic transition metal carbides/nitrides, which are promising candidates in electrodes. The layered structure facilitates ion insertion/extraction, which offers promising electrochemical characteristics for electrochemical energy storage. However, the low capacity accompanied by sluggish electrochemical kinetics of electrodes as well as interlayer restacking and collapse significantly impede their practical applications. Recently, interlayer space engineering of MXenes by different chemical strategies have been widely investigated in designing functional materials for various applications. In this review, an overview of the most recent progress of 2D MXenes engineering by intercalation, surface modification as well as heterostructures design is provided. Moreover, some critical challenges in future research on MXene-based electrodes have been also proposed.

Crystal Facet Engineering of Photoelectrodes for Photoelectrochemical Water Splitting.

Photoelectrochemical (PEC) water splitting is a promising approach for solar-driven hydrogen production with zero emissions, and it has been intensively studied over the past decades. However, the solar-to-hydrogen (STH) efficiencies of the current PEC systems are still far from the 10% target needed for practical application. The development of efficient photoelectrodes in PEC systems holds the key to achieving high STH efficiencies. In recent years, crystal facet engineering has emerged as an important strategy in designing efficient photoelectrodes for PEC water splitting, which has yet to be comprehensively reviewed and is the main focus of this article. After the Introduction, the second section of this review concisely introduces the mechanisms of crystal facet engineering. The subsequent section provides a snapshot of the unique facet-dependent properties of some semiconductor crystals including surface electronic structures, redox reaction sites, surface built-in electric fields, molecular adsorption, photoreaction activity, photocorrosion resistance, and electrical conductivity. Then, the methods for fabricating photoelectrodes with faceted semiconductor crystals are reviewed, with a focus on the preparation processes. In addition, the notable advantages of the crystal facet engineering of photoelectrodes in terms of light harvesting, charge separation and transfer, and surface reactions are critically discussed. This is followed by a systematic overview of the modification strategies of faceted photoelectrodes to further enhance the PEC performance. The last section summarizes the major challenges and some invigorating perspectives for future research on crystal facet engineered photoelectrodes, which are believed to play a vital role in promoting the development of this important research field.

Understanding of carrier dynamics, heterojunction merits and device physics: towards designing efficient carrier transport layer-free perovskite solar cells.

The power conversion efficiencies (PCEs) of perovskite solar cells (PSCs) are already higher than those of other thin-film photovoltaic technologies, but the high-efficiency cells are based on complicated device architectures with multiple layers of coating. A promising strategy to commercialize this emerging technology is to simplify the device structure while simultaneously maintaining high-efficiency. Charge transport layers (CTLs) are generally indispensable for achieving high-performance PSCs, but the high cost and possibility of instability hinder the mass production of efficient, stable PSCs in a cost-effective manner. The ambipolar carrier transfer characteristic of perovskite materials makes it possible to fabricate efficient PSCs even in the absence of electron and/or hole transport layers. Encouragingly, the reported PCEs of CTL-free PSCs are already over 20%. However, it is still a mystery about why and how CTL-free devices can work efficiently. Here, we summarize the recent strategies developed to improve the performance of CTL-free PSCs, aiming at strengthening the comprehensive understanding of the fundamental carrier dynamics, heterojunction merits and device physics behind these mysteriously simple yet efficient devices. This review sheds light on identifying the limiting and determining factors in achieving high-efficiency CTL-free devices, and proposes some empirical charge transport models (e.g. p-type doping of perovskites for HTL-free PSCs, n-type doping of perovskites for ETL-free PSCs, constructing efficient p-n heterojunctions and/or homojunctions at one side/interface or employing perovskite single crystal-based lateral geometry for both HTL and ETL-free PSCs, etc.) that are useful to further improve device performance. In addition, an insightful perspective for the future design and commercial development of large-scale, efficient and stable optoelectronic devices by employing carbon electrodes is provided.