Spatial Charge Research Articles

Fast microwave synthesis of WO2.9–W18O49/carbon particles for near infrared-driven photocatalytic water remediation

Photocatalytic water remediation is gaining much attention as a cost-efficient and environmentally friendly technology. We designed WO2.9–W18O49/carbon composite particles to overcome the drawbacks of semiconductor-based photocatalysts by extending light absorption capacity to the near-infrared region and achieving efficient charge separation. A 2.45 GHz microwave plasma successfully upgraded commercially available WO3 and polystyrene powders to the composite particles through a fast reaction with the typical heating and cooling rates of 30 and 470 °C/s, respectively. The synthesized composite particles exhibited broad absorption in the UV–Vis-NIR range and outstanding electrical properties. Besides, excellent NIR-driven photocatalytic performance was demonstrated for the degradation of organic water pollutants (rhodamine B), with the WO2.9–W18O49 homojunction contributing to sufficient spatial charge separation, resulting in considerably enhanced degradation rates by more than two orders of magnitude.

Study on space charge accumulation characteristics of silicone elastomer under DC voltage

AbstractThe electric field distortion caused by the accumulation of space charge in the insulating dielectric is easy to lead to accelerated ageing and even breakdown. In this paper, the space charge characteristics and the interfacial electric field change with time of silicone elastomer under different polarity DC voltages are studied. The results show that the homopolar charge injection is dominant in the silicone elastomer, and the electric field threshold is less than 4 kV/mm. The accumulation of homopolar charge weakens the interfacial electric field, resulting in the reduction of charge injection, and the interfacial electric field and spatial charge distribution gradually stabilise over time. In addition, the electric field at the interface does not decrease to the charge injection field threshold when it reaches stability. A time‐varying electric field model of the metal‐dielectric interface under a direct current field is derived and a calculation method for the time of charge accumulation to stabilise is proposed, based on the Schottky injection model and the relation between current density and volume charge density. The accuracy of the model is verified by comparing it with the experimental results of the stability time of silicone elastomer. This model is used to estimate the time when space charge accumulation reaches stability by means of the electric field threshold and the interface barrier, which can provide reference for the experimental measurement of space charge.

Efficient Perovskite Nanograin Light-Emitting Diodes in Green-to-Blue Gamut with Co-Additive Engineering.

Perovskite nanograins exceeding the Bohr exciton diameter show great potential for high-performance light-emitting diodes (LEDs) owing to their bandgap homogeneity, spatial charge confinement, and nonlocal interaction. However, it is challenging to directly synthesize proper nanograins along with reduced crystal defects on functional substrate, and the corresponding high-efficiency perovskite LEDs (PeLEDs) have rarely been reported. In this study, crystallization modulation for perovskites with an effective co-additive system, including lithium bromide, p-fluorophenethylammonium bromide, and 18-crown-6, is performed. Furthermore, it is demonstrated that the proposed co-additive system can synergistically retard perovskite crystallization and reduce crystal defects. Consequently, high-quality perovskite nanograin solids (≈22.8nm) are obtained with a high photoluminescence quantum yield (≈88%). These superior optical properties contribute to developing efficient green PeLEDs with a champion external quantum efficiency (EQE) of 28.4% and an average EQE of 27.1%. The co-additive system can be universally applied to mixed-halide perovskite nanograin LED, presenting a maximum EQE of 24.4%, 21.6%, 17.5%, and 11.1% for the blue device at 496, 488, 478, and 472nm, respectively, along with a narrow spectral linewidth (17-14nm) and stable color. These results supplement the research on high-efficiency perovskite nanograin LEDs for multicolor displays and lighting.

Impact of a Lightly Branched Star Polyelectrolyte Architecture on Polyelectrolyte Complexes.

The effect of charge density in blocky and statistical linear polyelectrolytes on polyelectrolyte complex (PEC) properties has been studied with the finding that increased charge density in a polyelectrolyte tends to increase the salt resistance and modulus of a PEC across various polyelectrolyte pairs. Here, we demonstrate the ability to orthogonally alter PEC salt resistance while maintaining rheological properties and internal structure by going from linear to lightly branched architectures with similar total degrees of polymerization. Using a model system built around glycidyl methacrylate (GMA) and thiol-epoxy "click" functionalization, we create a library of homologous linear, 4-armed, 6-armed, and 8-armed star polyelectrolytes. The PECs formed from these model polyelectrolyte pairs are then characterized via optical microscopy, rheology, and small-angle X-ray scattering to evaluate their salt resistance, mechanical properties, and internal structure. We argue that our results are due to the difference between linear charge density or charge per unit length along backbone segments for each polyelectrolyte and spatial charge density, the number of charges per unit volume of the polyelectrolyte prior to complexation. Our findings suggest that linear charge density is the dominant factor in determining intermolecular interactions of the complex, leading to identical rheological and structural behavior, whereas the spatial charge density primarily influences the stability of the complexes. These distinct mechanisms for altering various sought-after PEC properties offer greater potential applications in precision design of polyelectrolyte complex materials.

Selenium doping to improve internal electric field for excellent photocatalytic efficiency of g-C3N4 nanosheets

Graphitic carbon nitride is a promising photocatalyst to address environmental issues and energy applications. Herein, we develop an efficient defect-containing functionalized system of 2D selenium doped g-C3N4 porous nanosheets via one pot with two-step temperature for the first time. During heat treatment, Se-infused g-C3N4 nanosheets loosen stacking and form thinner nanosheets, which could effectively shorten the electronic path of charge migration. The introduction of nitrogen vacancies creates a midgap energy state below the CB, which improves the light-harvesting efficiency. Moreover, the dual effect of N vacancy and Se doping provides a driving force for the dissociation of excitons and achieves an effective spatial charge separation. High specific surface area (104.1 m2/g), suitable bandgap (2.65 eV), and good photocurrent response (0.45 µA cm−2) help to enhance the photocatalytic efficiency of 1-SeCN remarkably. Henceforth, high photocatalytic H2 production rate of 5441 µmol g−1 h−1 and CO evolution rate of 31.5 µmol g−1 h−1 verifies the effective Se doping enhances the photocatalytic efficiency of g-C3N4. Furthermore, DFT calculations are consistent with experimental results and this facile engineering strategy provides a scalable way to develop a novel, efficient g-C3N4-based photocatalyst for H2 production and CO2 reduction.

DeepSP: Deep learning-based spatial properties to predict monoclonal antibody stability

Therapeutic antibody development faces challenges due to high viscosities and aggregation tendencies. The spatial charge map (SCM) and spatial aggregation propensity (SAP) are computational techniques that aid in predicting viscosity and aggregation, respectively. These methods rely on structural data derived from molecular dynamics (MD) simulations, which are computationally demanding. DeepSCM, a deep learning surrogate model based on sequence information to predict SCM, was recently developed to screen high-concentration antibody viscosity. This study further utilized a dataset of 20,530 antibody sequences to train a convolutional neural network deep learning surrogate model called Deep Spatial Properties (DeepSP). DeepSP directly predicts SAP and SCM scores in different domains of antibody variable regions based solely on their sequences without performing MD simulations. The linear correlation coefficient between DeepSP scores and MD-derived scores for 30 properties achieved values between 0.76 and 0.96 with an average of 0.87. DeepSP descriptors were employed as features to build machine learning models to predict the aggregation rate of 21 antibodies, and the performance is similar to the results obtained from the previous study using MD simulations. This result demonstrates that the DeepSP approach significantly reduces the computational time required compared to MD simulations. The DeepSP model enables the rapid generation of 30 structural properties that can also be used as features in other research to train machine learning models for predicting various antibody stability using sequences only. DeepSP is freely available as an online tool via https://deepspwebapp.onrender.com and the codes and parameters are freely available at https://github.com/Lailabcode/DeepSP.

Engineered 3D Vortex Array with Customized Energy and Topological Charges for Multi‐View Display

AbstractArrays of multiple vortex beams enhance parallel processing capabilities from particle manipulation to information communication. However, the spatial position, topological charge, and energy parameters of the vortex beams within the array have yet to be precisely controlled, posing significant challenges to the realization of multi‐view 3D Orbital Angular Momentum (OAM) display using vortex arrays as information carriers. To address this issue, a method for generating vortex arrays based on a phase‐only hologram, customizing the array by using the energy and OAM spectrum of each vortex beam as the loss function is developed. Experimental results indicate that a 2D array generates 100 vortex beams in the spatial frequency domain, while a 3D array in the Fresnel zone produces 252 vortex beams across 7 planes, each with 36 unprecedentedly controllable energy and topological charge vortex beams. Subsequently, images of 4 views using the 3D vortex arrays and decoded through coordinate transformation to achieve a multi‐view 3D OAM display are encoded. The results demonstrate imaging quality with Mean Peak Signal‐to‐Noise Ratio (MPSNR) of 12.7, 13.0, 13.4, and 12.2 dB in 4 views, respectively, offering promising opportunities for applications in 3D optical manipulation, high‐capacity communication, and 3D OAM holography.

Hollow SrTiO3 photocatalyst with spatially separated OER and HER cocatalysts for photocatalytic overall water splitting

Overcoming the challenge of sluggish charge separation and the concurrent occurrence of overall water splitting (OWS) half reactions at the same catalytic sites is crucial for achieving efficient photocatalysis. This issue often leads to a high recombination rate and the back reaction of OWS. In this study, we addressed this challenge by enhancing interfacial spatial charge separation. Specifically, we designed hollow SrTiO3 spheres and spatially segregated the hydrogen and oxygen evolution sites on the outer and inner surfaces, respectively, for OWS. The spatially distributed Pt/SrTiO3/CoOx catalysts exhibited exceptional separation of photogenerated charges, resulting in 3-times higher stoichiometric OWS compared to Pt/SrTiO3. This work underscores the effectiveness of a well-tailored spatially distributed structure in promoting charge separation in photocatalysis, thereby opening avenues for the development of efficient artificial photosynthesis systems.

Efficient photocatalytic hydrogen production of Ni-Co layered double hydroxides (Ni-Co LDHs) anchored with reduced graphene oxide (rGO) hybrid composite

Using a suitable co-catalyst to boost photocatalytic H2 evolution from water splitting is crucial. Herein, we designed pristine NiCo-LDH and reduced graphene-oxide supported nickel-cobalt layered double hydroxide nanosheets (NiCo-LDH/rGO) as photocatalyst for the first time to evaluate the hydrogen production performance. Adding graphene has the potential to significantly increase electrical conductivity, and the supported NiCo-LDH has the potential to significantly reduce the likelihood of graphene self-aggregation. The effectiveness of its photocatalytic hydrogen generation was analyzed using a set of characterizations. The H2 evolution rates for pure rGO were 345.2 μmolh−1g−1, whereas those for Ni-Co LDH/rGO were 578.2 μmolh−1g−1. Average hydrogen generation per hour for the Ni-Co LDH/rGO composite material was 2032.1 μmolh−1g−1, which was 5.8 and 3.5 times that of rGO and Ni-Co LDH/rGO, respectively, NiCo-LDH@rGO's synergistic impact on the NiCo-LDH boosts the H2 generation pathway by increasing the catalyst's stability as well as performance by exposing active sites and speeding up electron transport. The produced nanocomposite shows excellent spatial charge separation and quicker electron transport across the conductive network of rGO, as shown by the photocurrent response test and photoluminescence (PL) spectra. The results of this study provide a fresh perspective on the practical use and synthesis of the inexpensive and effective NiCo-LDH/rGO, demonstrating the standard deviation of logical planning and preparation of high-performance photocatalysts.

Staggered band alignment – direct Z-scheme for photocatalytic activity in Stibnite/rGO layered nanohybrids

Type-II staggered band aligned layered nanohybrids (LNHs) satisfy the unique characteristics required for photocatalysts. Here, the spin-assisted layer-by-layer deposition (SA-LBL) of stibnite/reduced graphene oxide (Sb2S3/rGO) LNHs are fabricated and their structural, morphological, electrical, and optical properties are reported. From the FESEM analysis, it was found that with increasing rGO content, the morphology of Sb2S3 nanoparticles changed from the granular to nanorods which might be due to Ostwald ripening or microstructural coarsening effect. Further, Raman spectroscopy proves that the B1 g and Ag of Sb2S3 decrease by the addition of rGO mainly due to the electron-phonon interaction. Based on the estimation of valence band edge and conduction band edge of Sb2S3/rGO LNHs using X-ray photoelectron spectroscopy and optical studies, we propose that the interface in Sb2S3/rGO LNHs is a type-II staggered band alignment Direct Z-scheme. The increased spatial charge separation and carrier lifetime of Sb2S3/rGO LNHs materials results in opening a new pathway to explore and extend their applications as photocatalysts.

The construction of Cs3MoxSbyBr9/BiVO4 S-scheme heterojunction photocatalyst for efficient photocatalytic N2 fixation

Synergistic nitrogen (N2) reduction with water (H2O) oxidation is meaningful but challenging owing to the inertness of the N2 molecule and the sluggish kinetics of H2O oxidation. Herein, a simutaneous-promotion strategy of redox capacities is presented for constructing a lead-free Cs3Sb2Br9-based S-scheme heterojunction, by decorating Mo-functionalized Cs3Sb2Br9 nanocrystals (Cs3MoxSbyBr9) on BiVO4 nanosheet through an in-situ plane-to-point growth manner. The Mo-functionalization for Cs3Sb2Br9 enables the regulation of the d-band center position, greatly improving surface reaction kinetics for N2 reduction. Furthermore, the construction of the S-scheme heterojunction enhances the driving force for H2O oxidation and spatial charge separation of photocatalysts. As anticipated, the resultant Cs3MoxSbyBr9/BiVO4 exhibits an excellent photocatalytic N2 reduction activity under ambient atmosphere, achieving ammonia (NH3) production at a rate of 300 ± 5 μmol g−1 h−1 under simulated sunlight illumination (100 mW cm−2), which is nearly 20-fold higher than that of pristine Cs3Sb2Br9.

Enhanced charge separation via ZnIn2S4@S-doped-C3N4 S-scheme heterojunction for efficient photocatalytic water splitting under visible light

Heterojunction photocatalysts possess high efficiency in photogenerated electron-hole separation, which give significant advantages in the field of solar hydrogen production. Herein, a novel ZnIn2S4@S doped g-C3N4 (ZIS@SCN) heterojunction with mesoporous structure was prepared for photocatalytic water splitting under visible light. Characterization showed that the element of S was successfully introduced into g-C3N4 (CN) by replacing N to form C–S–C bonds and significantly enhanced the visible light absorption ability. The constructed heterojunction exhibited excellent photocatalytic hydrogen evolution under visible light. The best performance belonged to the sample of ZIS@100SCN. The corresponding H2 production rate reached 9.3 mmol h−1 g−1, which was 1.87-fold higher than that of the undoped one. More importantly, the heterojunction realized overall water splitting of H2 and O2 evolution simultaneously with good stability. The mechanism analysis indicted that introducing the element of S could regulate the band structure of CN and induce the charge transfer switching of a ZnIn2S4@g-C3N4 (ZIS@CN) photocatalyst from Ⅰ-type to S-scheme, which promoted the efficient spatial charge separation and maintained the high redox ability of the ZIS and SCN. This work provides an insight in construction high performance S-scheme heterojunction for water splitting with a doping method.

Modeling of semiconductor heterostructures for energy converters and sensors

A set of modeling programs for constructing a sequence of energy zones of heterojunctions is presented for analyzing the distribution of charge carriers in the heterostructure and internal characteristics, for describing the processes of charge transfer and accumulation. Wolfram Mathematica analytical system and Delphi programming language were used. The main elements of materials are semiconductors, metals of contact structures and injection regions of nonequilibrium carriers. The programs allow determining the structural characteristics of materials, active zones and spatial charge regions, calculating quasi-Fermi levels and built-in potentials, as well as the efficiency of heterostructures in general and for separation-charge collection, charge accumulation, determining the type of metallization of barrier or ohmic contact.

Cocatalyst activity mapping for photocatalytic materials revealed by the pattern-illumination time-resolved phase microscopy.

Photocatalytic water-splitting represents a promising avenue for clean hydrogen production, necessitating an in-depth understanding of the photocatalytic reaction mechanism. The majority of the photocatalytic materials need cocatalysts to enhance the photo-oxidation or reduction reactions. However, the working mechanism, such as collecting charge carriers or reducing the reaction barrier, is not clear because they disperse inhomogeneously on a surface, and it is difficult to follow the local charge carrier behavior. This study employs the pattern-illumination time-resolved phase microscopy (PI-PM) method to unravel the spatial charge carrier behavior in photocatalytic systems, utilizing time-resolved microscopic image (refractive index change) sequences and their clustering analyses. This approach is robust for studying the change in local charge carrier behavior. We studied two major cocatalyst effects on photocatalysts: TiO2 with/without Pt and hematite with/without CoPi. The PI-PM method, supported by charge type clustering and the effects of scavengers, allowed for the analysis of local activity influenced by cocatalysts. This approach revealed that the introduction of cocatalysts alters the local distribution of charge carrier behavior and significantly impacts their decay rates. In TiO2 systems, the presence of Pt cocatalysts led to a local electron site on the micron scale, extending the lifetime to a few tens of microseconds from a few microseconds. Similarly, in hematite films with CoPi, we observed a notable accumulation of holes at cocatalyst sites, emphasizing the role of cocatalysts in enhancing photocatalytic efficiency. The study's findings highlight the complexity of charge carrier dynamics in photocatalytic processes and the significant influence of cocatalysts.

In-situ anion-exchange construction of Z-scheme Ag3PO4/AgI, derived AgCl/Ag3PO4/AgI and Ag2CO3/Ag3PO4/AgI composites with multiple redox energy bands and charge transfer pathways for efficient absorption and sonocatalytic properties

Z-scheme Ag3PO4/AgI composites were synthesized by facile in-situ anion-exchange method at room temperature (RT). All the catalysts have excellent affinity to dyes and adsorb larger than 70 % of Methyl blue. The fastest adsorption equilibrium of Ag3PO4 (qe: 25.9278 mg/g) with low specific surface area (SSA: 4.6624 m2/g) can be rapidly attained for 6 min. The best color removal efficiency (RE) for Methyl blue over all the composites can rapidly increase to 100 % within 45 min. Meanwhile, the highest RE for RhB over S3 is 98.9 % for 60 min, and corresponding rate constant (k) is 0.07018 min−1. After adding NaCl or Na2CO3 into sonocatalysis, because of the formation of novel ternary AgCl/Ag3PO4/AgI and Ag2CO3/Ag3PO4/AgI during sonocatalytic process, the best REs for RhB over S3 composite increase from 89.8 % (no scavenger) to 98.2 % (1.2 mM NaCl), or to 97.6 % (1.8 mM Na2CO3) for 30 min, respectively, and the REs for Methyl blue over S3 are about 100 % for 10 min. From single Ag3PO4 to binary Ag3PO4/AgI, and to ternary Ag2CO3/Ag3PO4/AgI or AgCl/Ag3PO4/AgI, REs are significantly enhanced. New redox energy bands and charge transfer channels lead to efficiently spatial charge separation and further activation of hole (h+), superoxide anions (·O2−), hydroxyl radicals (·OH). Additionally, the relation among oxygen vacancies (Ov), Zeta potential and RE was discussed in detail. Density functional theory (DFT) calculations were used to make clear charge transfer and sonocatalytic mechanism. The evaluation of used samples, adsorption kinetics and modes, diverse degradation pathways and sonocatalytic mechanisms were also discussed in detail. The work provides a novel in-situ strategy for real-time control of catalytic performance by rapidly forming new phase during catalysis at RT. Furthermore, the strategy obviously facilitates real-time development of rare more than ternary composites for enhanced catalytic performance.

Synergistic effect of homojunction and Ohmic junctions in CdS boosting spatial charge separation for U(VI) photoreduction

Synergistic effect of homojunction and Ohmic junctions in CdS boosting spatial charge separation for U(VI) photoreduction

Performance limiting inhomogeneities of defect states in ampere-class Ga2O3 power diodes

Impacts of spatial charge inhomogeneities on carrier transport fluctuations and premature breakdown were investigated in Schottky ampere-class Ga2O3 power diodes. Three prominent electron traps were detected in Ga2O3 epilayers by a combination of the depth-resolved capacitance spectroscopy profiling and gradual dry etching. The near-surface trap occurring at 1.06 eV below the conduction band minimum (EC), named E3, was found to be confined within a 180 nm surface region of the Ga2O3 epilayers. Two bulk traps at EC − 0.75 eV (E2*) and at EC − 0.82 eV (E2) were identified and interconnected with the VGa- and FeGa-type defects, respectively. In the framework of the impact ionization model, employing the experimental trap parameters, the TCAD simulated breakdown characteristics matched the experimental breakdown properties well, consistently with inverse proportionality to the total trap densities. In particular, the shallowest distributed E3 trap with the deepest level is responsible for higher leakage and premature breakdown. In contrast, Ga2O3 Schottky diodes without E3 trap exhibit enhanced breakdown voltages, and the leakage mechanism evolves from variable range hopping at medium reverse voltages, to the space-charge-limited conduction at high reverse biases. This work bridges the fundamental gap between spatial charge inhomogeneities and diode breakdown features, paving the way for more reliable defect engineering in high-performance Ga2O3 power devices.

Boosting Spatial Charge Storage in Ion-Compatible Pores of Carbon Superstructures for Advanced Zinc-Ion Capacitors.

Capacitive carbon cathodes deliver great potential for zinc-ion hybrid capacitors (ZHCs) due to their resource abundance and structural versatility. However, the dimension mismatch between the micropores of carbons and hydrated Zn2+ ions often results in unsatisfactory charge storage capability. Here well-arranged heterodiatomic carbon superstructures are reported with compatible pore dimensions for activating Zn2+ ions, initiated by the supramolecular self-assembly of 1,3,5-triazine-2,4,6-triamine and cyanuric acid via in-plane hydrogen-bonds and out-of-plane π-π interactions. Flower-shaped carbon superstructures expose more surface-active motifs, continuous charge-transport routes, and more importantly, well-developed pores. The primary subnanopores of 0.82nm are size-exclusively accessible for solvated Zn2+ ions (0.86nm) to maximize spatial charge storage, while rich mesopores (1-3nm) allow for high-kinetics ion migration with a low activation energy. Such favorable superstructure cathodes contribute to all-round performance improvement for ZHCs, including high energy density (158Whkg-1), fast-charging ability (50Ag-1), and excellent cyclic lifespan (100000cycles). An anion-cation hybrid charge storage mechanism is elucidated for superstructure cathode, which entails alternate physical uptake of Zn2+/CF3SO3 - at electroactive pores and bipedal chemical binding of Zn2+ to electronegative carbonyl/pyridine motifs. This work expands the design landscape of carbon superstructures for advanced energy storage.

Construction of an all-organic S-scheme heterostructure based on PEDOT immobilized g-C3N4 nanosheets by electrostatic self-assembly with enhanced visible-light photocatalytic hydrogen production

Inspired by photosynthesis in nature, exploring all-organic S-scheme heterojunction photocatalysts for efficient H2 production is of great significance in addressing energy shortage issues. In this paper, poly(3,4-ethylenedioxythiophene) (PEDOT) immobilized g-C3N4(CN) nanosheets were constructed by an electrostatic self-assembly strategy to obtain an all-organic S-scheme heterojunction, significantly enhancing the visible-light photocatalytic H2 production performance of g-C3N4. The optimized 5PEDOT/CN exhibits the highest H2 production rate of 3.15 mmol g−1h−1, a 31.5-fold enhancement over pristine CN. According to the staggered energy band positions of two components and the results of electron spin resonance tests, the S-scheme heterojunction electron-transfer mechanism is confirmed, which greatly facilitates the spatial charge separation and retains the strong reducing ability of high-energy potential electrons for efficient photocatalytic H2 production. Based on the results of FT-IR spectra, XPS spectra, fluorescence spectra, hydroxyl radical tests and time-resolved photoluminescence spectra, it is confirmed that the significantly improved photocatalytic activity is mainly attributed to the enhanced charge separation by the S-scheme heterojunction and the tightly contacted interface dependent on N···S interactions in PEDOT immobilized CN nanosheet heterojunctions, along with the enhanced visible-light absorption ability. This work presents a novel approach to the design and fabrication of all-organic S-scheme heterojunction photocatalysts for solar-light-driven energy production.

Hollow Cu2-xS@NiFe Layered Double Hydroxide Core-Shell S-Scheme Heterojunctions with Broad-Spectrum Response and Enhanced Photothermal-Photocatalytic Performance.

Designing a reasonable heterojunction is an efficient path to improve the separation of photogenerated charges and enhance photocatalytic activity. In this study, Cu2-xS@NiFe-LDH hollow nanoboxes with core-shell structure are successfully prepared. The results show that Cu2-xS@NiFe-LDH with broad-spectrum response has good photothermal and photocatalytic activity, and the photocatalytic activity and stability of the catalyst are enhanced by the establishment of unique hollow structure and core-shell heterojunction structure. Transient PL spectra (TRPL) indicates that constructing Cu2-xS@NiFe-LDH heterojunction can prolong carrier lifetime obviously. Cu2-xS@NiFe-LDH shows a high photocatalytic hydrogen production efficiency (5176.93µmolh-1g-1), and tetracycline degradation efficiency (98.3%), and its hydrogen production rate is ≈10-12 times that of pure Cu2-xS and NiFe-LDH. In situ X-ray photoelectron spectroscopy (XPS) and electron spin resonance (ESR) provide proofs of the S-scheme electron transfer path. The S-scheme heterojunction achieves high spatial charge separation and exhibits strong photoredox ability, thus improving the photocatalytic performance.