SinoGreenTech Academic Portal
📚 Peer-Reviewed Translated Literature

All Clean Energy & Battery Intelligence (Page 45)

Browse complete peer-reviewed translations from top indexed Chinese clean energy & battery intelligence journals. Read verified previews and download authentic research reports verified by SinoGreenTech.

Published Research Papers

Showing 24 of 1398 peer-reviewed translated articles (Page 45 of 59)

Circularly Polarized Light Detection in Achiral Organic Semiconductors via Chiral Plasmonic ResonanceGraphical AbstractVerified
SCIENCE CHINA Materials2026

Circularly Polarized Light Detection in Achiral Organic Semiconductors via Chiral Plasmonic Resonance

Circularly polarized light (CPL) detection is critical to emerging technologies in optical communication, chiral sensing, and bio-inspired imaging. However, current devices rely on intrinsically chiral semiconductors that are synthetically complex and costly to scale. Here, we demonstrate robust CPL detection in achiral organic semiconductors by exploiting chiral plasmonic resonance (CPR). A self-assembled monolayer of L-phenylalanine–modified gold nanoparticles imparts optical chirality to adjacent semiconductors while enhancing photocurrent through plasmon-induced hot-carrier processes. The resulting hybrid devices exhibit nearly tenfold responsivity enhancement and a high dissymmetry factor of 0.35 at 515 nm. Mechanistic analysis reveals a field-driven, hot-carrier-assisted route to helicity sensitivity. This solution-processable approach merges plasmonic chirality with organic semiconductor versatility, providing a scalable platform for next-generation on-chip chiroptoelectronic and polarization-imaging technologies.

Read Full Abstract10.1007/s40843-025-3916-3
Spatial Distribution Characteristics of Typical Contaminants in Municipal Solid Waste Landfills under Water-Soil Interactions in Alluvial-Diluvial StrataGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Spatial Distribution Characteristics of Typical Contaminants in Municipal Solid Waste Landfills under Water-Soil Interactions in Alluvial-Diluvial Strata

The Holocene alluvial-diluvial stratum of the Quaternary is characterized by high soil hydraulic conductivity and intense surface water-groundwater interaction, which leads to rapid and extensive migration of contaminants from landfills. To investigate the contaminant characteristics of a municipal solid waste (MSW) landfill in such strata, a case study was conducted at a landfill in southwestern China. Methods including the Nemerow pollution index and the potential ecological risk index were employed to systematically analyze the contamination of groundwater and soil, as well as the spatial distribution of organic matter and heavy metals. The results showed that the groundwater was severely contaminated (PI > 3). The maximum exceedance multiples for total bacterial count, ammonia nitrogen (NH4+-N), and total coliforms relative to the standard limits were 36, 9.5, and 8, respectively. The composition of the contaminants in groundwater was highly consistent with the characteristics of landfill leachate. For the soil, the concentrations of six heavy metals (Cu, Pb, Cd, Ni, Hg, and As) were all below the Class II screening values of the standard GB 36600—2018. Both the Nemerow pollution index (PI < 0.7) and the potential ecological risk index (RI < 150) indicated that the soil environment was safe. Regarding soil dissolved organic matter (DOM), humic-like substances (22.9% to 34.9%) and fulvic-like substances (22.4% to 27.5%) were the dominant components, and their fluorescence intensities exhibited an exponential decay trend with increasing soil depth. The speciation of Cu, Pb, As, Hg, and Ni was dominated by the residual fraction (52.33% to 90.32%). However, over 70% of Cd existed in active forms (exchangeable + Fe/Mn oxide-bound), suggesting a high migration risk. The horizontal distribution of heavy metals showed regional specificity, with high-value areas mainly concentrated in the screening waste and soil stacking areas. Vertically, Cu and Cd exhibited surface enrichment, while As, Hg, Pb, and Ni were enriched in the groundwater fluctuation zone. These findings indicate that groundwater in alluvial-diluvial strata is highly susceptible to leachate contamination, while soil heavy metal contamination is not significant, with low levels in the aquifer but a tendency to accumulate at the water-soil interface. It is recommended that during landfill remediation, attention be paid to anti-seepage measures in waste excavation and stacking areas, as well as the interception and remediation of the groundwater fluctuation zone, to prevent secondary contamination of soil and groundwater.

Read Full Abstract10.13205/j.hjgc.202607025
Circularly polarized electroluminescence achieved in achiral emitters via chiral nematic liquid crystalsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Circularly polarized electroluminescence achieved in achiral emitters via chiral nematic liquid crystals

Developing circularly polarized organic light-emitting diodes (CP-OLEDs) that simultaneously achieve a high electroluminescence dissymmetry factor (g_EL) and a high external quantum efficiency (EQE) remains a central challenge in polarized optoelectronics. Here, we report a general composite strategy for constructing full-color CP-OLEDs by integrating a 5CB-based chiral nematic liquid crystal (N*-LC) layer with OLEDs based on achiral emitters. The resulting CP-OLEDs exhibit both high polarization purity and high electroluminescence efficiency, with |g_EL| values of up to 1.9, EQEs reaching 26.9%, and Q-factors as high as 0.48. Notably, contrary to the conventional assumption that N*-LC integration causes severe optical losses (>50%) due to Bragg reflection, the EQE of the devices is preserved mainly in this composite architecture. This behavior is attributed to an internal photon-recycling process enabled by the reflection of light within the device structure. To the best of our knowledge, these CP-OLEDs represent the highest comprehensive performance reported to date. Furthermore, the practical utility of these high-performance devices is demonstrated through the encryption and decryption of information based on circularly polarized electroluminescence.

Read Full Abstract10.1007/s40843-025-3957-y
Electrocaloric Devices for Solid-State Refrigeration: Design Strategies and ApplicationsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Electrocaloric Devices for Solid-State Refrigeration: Design Strategies and Applications

Refrigeration is essential for modern society, supporting applications from household appliances and industrial manufacturing to microelectronics and biopharmaceutical cold chains. Conventional refrigeration technologies are constrained by environmental impact and low energy efficiency, emphasizing the importance of developing sustainable alternatives. Solid-state caloric refrigeration, particularly electrocaloric (EC) devices, offers a promising route owing to their high cooling efficiency, rapid electric-field-driven response, and potential for miniaturization. Significant progress has been achieved in various EC device configurations. However, EC devices still face challenges in achieving large temperature spans, high cooling power, and effective integration for specific applications. This review systematically summarizes these developments, focusing on device design and performance enhancement. It elucidates the fundamental and shared design strategies, classifies EC devices into fluid-based heat-transfer type, solid-based heat-transfer type, and thermal-resistance-modulated heat-switch architectures, and analyzes representative device structures, performance metrics, and application scenarios. Finally, energy-recovery strategies and future optimization directions toward more efficient EC systems are discussed. This work provides a comprehensive reference for the design innovation and practical implementation of EC-based solid-state refrigeration technologies.

Read Full Abstract10.1007/s40843-025-3983-4
Gd3+ Synergistic Sensitization in Tb3+-Doped LBSO Glasses: Influence of Cluster Dispersion and Energy Transfer on Luminescence and X-ray DetectionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Gd3+ Synergistic Sensitization in Tb3+-Doped LBSO Glasses: Influence of Cluster Dispersion and Energy Transfer on Luminescence and X-ray Detection

Gd3+-sensitized Tb3+-based glasses are high light-yield scintillators. Energy transfer sensitization between Gd3+ and Tb3+ is well-recognized. Gd3+ ions are also found to typically modulate the interionic distances of Tb3+ ions; however, the mechanism why this effect enhances the latter’s photoluminescence still remains unclear. This work focuses on Gd3+, Tb3+ co-doped La2O3-B2O3-SiO2 (LBSO), first demonstrating Tb3+ clusters via spectroscopy. LBSO’s optimal Tb3+ single-doping concentration is 37%, rising to 50% with 20% Gd3+. The LBSO:20%Gd3+,50%Tb3+ sample exhibits a 542 nm emission intensity 2.22 times that of the 37%Tb3+ single-doped sample, 38% scintillation efficiency (vs. BGO), and >20 lp mm−1 X-ray resolution. The introduction of Gd3+ increases the interionic distance between Tb3+ ions within the clusters, thereby suppressing the concentration quenching effect and enhancing the fluorescence emission. We propose this mechanism as “cluster-dispersion sensitization effect”. This effect was further confirmed in other glass systems (LBSO:Lu3+, Tb3+, LBSO:Y3+, Tb3+, Bi-based:Lu3+, Tb3+, etc.). Spectroscopic analysis shows Gd3+-Tb3+ energy transfer efficiency up to 80%. In conclusion, Gd3+ synergistically enhances Tb3+ fluorescence via both effects. These findings not only fully elucidate the sensitization mechanism of Gd3+ ions in Gd3+, Tb3+ co-doped scintillating glasses but also provide new insights for researching the manipulation of activator ion clusters in luminescent materials. In search for novel scintillators, cluster-dispersion sensitization effect may greatly improve their spatial resolution via intrinsic architectures design in glasses, ceramics, thin films, and nanoparticles.

Read Full Abstract10.1007/s40843-025-4025-y
Enhancing Sludge Dewatering and Filtrate Carbon Source Recovery via Typical Bioenzymatic ConditioningGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Enhancing Sludge Dewatering and Filtrate Carbon Source Recovery via Typical Bioenzymatic Conditioning

This study systematically investigated the effects of single and composite conditioning with lysozyme, amylase, and protease on sludge dewatering performance and carbon source recovery in filtrate from residual sludge of a water treatment plant in Foshan City. Results indicated that lysozyme significantly improved sludge dewatering by reducing specific resistance of filtration (SRF), capillary suction time (CST), and water content of the filtered sludge cake (Wc). While amylase and protease decreased Wc, they elevated SRF and CST, deteriorating sludge filtration properties. Among combined enzyme treatments, lysozyme and protease exhibited synergistic effects. The asynchronous addition strategy (protease/amylase followed by lysozyme) demonstrated the best performance in reducing Wc, while simultaneous addition was more effective in improving SRF and CST. Mechanistic analysis revealed that all three enzymes reduced sludge particle size. Lysozyme primarily targeted cell lysis and wall disruption, releasing intracellular substances, reducing viscosity, and enhancing sludge hydrophobicity. Meanwhile, amylase and protease mainly disrupted extracellular polymeric substances (EPS), leading to release of proteins and polysaccharides into slime EPS, increasing viscosity and hydrophilicity. Furthermore, all three enzymes effectively promoted carbon source release, increased soluble chemical oxygen demand (SCOD) of filtrate, and transformed recalcitrant humic acid-like organic matters into readily bioavailable tryptophan-like and tyrosine-like substances. These findings provide a basis for optimizing enzyme-based sludge conditioning to achieve simultaneous dewatering enhancement and carbon source recovery.

Read Full Abstract10.13205/j.hjgc.202607024
Effects of Municipal Sludge Application on Composition and Microbial Communities of Mine Waste Rock SoilGraphical AbstractVerified
Journal of Environmental Engineering Technology2026

Effects of Municipal Sludge Application on Composition and Microbial Communities of Mine Waste Rock Soil

The rapid population growth and accelerating urban development have made the comprehensive utilization of municipal sludge (MS) an urgent challenge. MS contains substantial organic matter and essential nutrients for crop growth, making it a promising soil amendment for the ecological restoration of mine waste rock. However, research evaluating the impact of MS application on soil health and ecological safety from a soil microbiology perspective remains understudied. Therefore, this study investigated the effects of MS and composted municipal sludge (CMS) on the ecological restoration of mine waste rock soil through pot experiments. High-throughput sequencing technology was employed to analyze changes in soil microbial community structure and diversity. Finally, network analysis and correlation heatmaps were utilized to elucidate the microbial driving mechanisms. The results indicated that after MS and CMS application, organic matter content increased from 20.38 g/kg (Level 3) to 38.52 g/kg (Level 2). The levels of available nitrogen, phosphorus, and potassium rose from Level 4, 6, 2, to Level 1, 4, 1, respectively. Fresh weight, aboveground height, root length, and stem diameter of ryegrass all increased significantly. Venn diagram and heatmap analyses indicated that lower application rates (<1.5 kg/m²) enhanced microbial community richness and diversity. This study confirms municipal sludge as an effective amendment for mine waste rock soil. It is recommended to limit application rates below 1.5 kg/m² in practical mine ecological restoration projects, with particular attention to long-term dynamics of heavy metals and salinity to ensure safe and sustainable land reuse.

Read Full Abstract10.13205/j.hjgc.202607023
In-situ growth of ZnIn2S4 nanosheets on a Ti-based MOF to form a core-shell heterojunction for enhanced photocatalytic hydrogen evolutionGraphical AbstractVerified
SCIENCE CHINA Materials2026

In-situ growth of ZnIn2S4 nanosheets on a Ti-based MOF to form a core-shell heterojunction for enhanced photocatalytic hydrogen evolution

Photocatalytic hydrogen evolution reaction (HER) from pure water is a promising strategy to address critical challenges in energy sustainability and environmental remediation. However, HER over single-component photocatalysts is intrinsically limited by inefficient carrier separation and relatively poor photostability. Forming abundant interfaces between two components is an effective approach for solving these issues. Herein, a series of hierarchical core-shell heterojunction photocatalysts, designated as F@Z-X, was rationally constructed by in situ growing ZnIn2S4 (ZIS) nanosheets on a Ti-based metal-organic framework (FIR-125), demonstrating remarkable structural stability. Due to the abundant intimate contact interfaces and well-matched band structure, the F@Z-X series exhibit enhanced HER performance. Among them, the optimized heterojunction [email protected] shows a photocatalytic hydrogen evolution rate of 3789.45 μmol g−1 h−1, which is about 4.4 and 264.4 times higher than that of pristine ZIS (859.57 μmol g−1 h−1) and FIR-125 (15.32 μmol g−1 h−1), respectively. Moreover, the photocatalyst manifests excellent reusability and durability, maintaining its performance over five consecutive cycles and sixteen hours of continuous reaction. The outstanding performance of [email protected] may be ascribed to an optimal balance among three fundamental photocatalytic processes: sufficient light absorption, exceptional carrier separation, and appropriate surface reaction. This work offers valuable insights into the rational design and controllable synthesis of novel heterojunction photocatalysts for efficient hydrogen evolution.

Read Full Abstract10.1007/s40843-025-3875-1
Zn dilution-directed synthesis of Pt nanoclusters on porous nickel-carbon microspheres for hydrogen evolutionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Zn dilution-directed synthesis of Pt nanoclusters on porous nickel-carbon microspheres for hydrogen evolution

The development of low platinum-loading catalysts for the economically viable hydrogen evolution reaction (HER) remains challenging. Herein, a precursor dilution strategy is used to fabricate Pt nanoclusters anchored on Ni-embedded porous carbon microspheres. The approach begins with the facile synthesis of Zn/Ni-based coordination polymers (Ni-BTC-Zn) due to the isomorphic substitution of Zn2+ and Ni2+. During pyrolysis, the evaporation of zinc species results in a highly porous carbon structure with well-dispersed nickel nanoparticles. Subsequent solvothermal treatment allows for the uniform deposition of Pt nanoclusters to form the final bimetallic PtNi catalysts (PtNi-BTC-C). Among them, the optimized PtNi-BTC-C10 exhibits exceptional alkaline HER performance, requiring an overpotential of only 41 mV to achieve 10 mA cm−2 and a low Tafel slope of 31.1 mV dec−1. It also demonstrates outstanding durability with a current retention of 90.7% after 70 h, far exceeding Pt/C. Extensive characterization confirms that moderate Zn dilution optimally modulates the Ni particle size and dispersion, leading to maximized active sites and enhanced charge transfer. Combined with DFT calculations, the Pt-Ni-cluster model for PtNi-BTC-C10 possesses an optimized electronic structure with a shifted d-band center, which facilitates water dissociation and optimizes H* desorption with the most favorable energetics (0.262 eV). This work provides a fundamental understanding of precursor dilution engineering and offers a versatile pathway for designing advanced noble-metal-based bimetallic electrocatalysts.

Read Full Abstract10.1007/s40843-025-3966-0
Co-electrosynthesis of ammonia and formic acid over nitrogen-doped carbon-supported Bi<sub>2</sub>O<sub>3</sub> and NiO catalystsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Co-electrosynthesis of ammonia and formic acid over nitrogen-doped carbon-supported Bi<sub>2</sub>O<sub>3</sub> and NiO catalysts

Co-electrosynthesis of ammonia and formic acid over nitrogen-doped carbon-supported Bi<sub>2</sub>O<sub>3</sub> and NiO catalysts

Read Full Abstract10.1007/s40843-025-3940-y
N-vacancy engineering Zn single-atom site boosts efficient photosynthesis of hydrogen peroxideGraphical AbstractVerified
SCIENCE CHINA Materials2026

N-vacancy engineering Zn single-atom site boosts efficient photosynthesis of hydrogen peroxide

Photocatalytic oxygen reduction reaction (ORR) for hydrogen peroxide (H2O2) production via the two-electron pathway offers an environmentally friendly oxidant and a clean fuel. However, challenges exist in optimal oxygen (O2) adsorption capacities and maintaining O–O bond during O2 activation. Herein, we present a zinc single-atom catalyst (Zn/VN-CN) incorporating nitrogen vacancies (VN), designed to modulate the electronic structure of the photocatalyst, leading to optimized O2 adsorption energy and a remarkable enhancement in H2O2 yield. Benefiting from the synergistic effect between nitrogen vacancies and Zn single atoms, the optimized Zn/VN-CN catalyst exhibits a photocatalytic H2O2 production rate of 2.399 mmol g−1 h−1 under visible-light irradiation, representing a 12-fold enhancement compared to pristine g-C3N4 (CN), along with a high H2O2 selectivity of 87.4%. Combined experimental and theoretical studies indicate that the Zn-N3 sites act as highly active reaction centers, while nitrogen vacancies increase the charge density and downshift the d-band center of the Zn sites, thereby moderating O2 adsorption strength, lowering the activation energy barrier for the formation of *H2O2, and further converting it to H2O2. This work proposes an effective strategy for tuning O2 adsorption behavior to achieve highly selective and active photocatalytic H2O2 production.

Read Full Abstract10.1007/s40843-025-3950-x
Isolated Mn2+-activated near-infrared phosphors under nephelauxetic effects and strong crystal fieldGraphical AbstractVerified
SCIENCE CHINA Materials2026

Isolated Mn2+-activated near-infrared phosphors under nephelauxetic effects and strong crystal field

Broadband near-infrared (NIR) phosphors with longer wavelengths are critically needed for deep-tissue biomedical imaging and other emerging applications. However, the detailed mechanism of Mn2+-activated NIR emission remains elusive. Guided by the nephelauxetic effect theory, sulfide phosphors with strong covalent bonding are promising for achieving long-wavelength Mn2+ luminescence. This work reports a series of M(Ga, In)2S4:Mn2+ (M = Ca, Sr, Ba) phosphors featuring strong crystal field environments, and for the first time the luminescence behaviors of Mn2+-doped MIn2S4 (M = Sr, Ba). Preferential site occupancy leads to significant differences between MGa2S4:Mn2+ (M = Ca, Sr) and MIn2S4:Mn2+ (M = Sr, Ba) despite the same crystal structure. Severe polyhedral distortion enhances ultrawideband deep-red to NIR luminescence (600–850 nm, FWHM ≈ 123–257 nm), far superior to similar materials. Fabricated pc-LED devices demonstrate excellent vascular imaging and plant illumination capabilities. This study provides new insights into the NIR luminescence of isolated Mn2+.

Read Full Abstract10.1007/s40843-025-3939-4
Atomically dispersed Pt species anchored on Al3+-doped SrTiO3 for photocatalytic overall water splittingGraphical AbstractVerified
SCIENCE CHINA Materials2026

Atomically dispersed Pt species anchored on Al3+-doped SrTiO3 for photocatalytic overall water splitting

Single-atom co-catalysts on semiconductor substrates offer a cost-efficient route to enhance photocatalytic performance with minimal precious metal loading. However, precise tuning of local coordination environments and construction of efficient single-atom co-catalysts remain challenging for overall water splitting. Here, we employ an icing-assisted photochemical reduction strategy to anchor atomically dispersed Pt species as hydrogen evolution co-catalysts on Al3+-doped SrTiO3 (Pt SA-STO). The optimized Pt SA-STO exhibits remarkable activity, with hydrogen and oxygen evolution rates of 13.62 and 6.71 mmol h−1 g−1, respectively, and a turnover frequency (TOF) of 2114.5 h−1. We pioneer the use of nuclear magnetic resonance (NMR) spectroscopy to quantitatively track the temporal evolution of Pt4+ to Pt2+ under continuous irradiation during the icing-assisted photoreduction. Advanced characterizations and theoretical calculations confirm that single-atom Pt co-catalysts facilitate directional transfer and extraction of photogenerated charge carriers, effectively suppressing surface recombination. This work provides insights into designing novel single-atom co-catalysts by deepening understanding of electronic configurations and active sites in photocatalytic overall water splitting.

Read Full Abstract10.1007/s40843-025-3892-2
Transparent oxyhalide glass-ceramic scintillators containing lead-free chloride perovskite nanocrystals for high-resolution and stable X-ray imagingGraphical AbstractVerified
SCIENCE CHINA Materials2026

Transparent oxyhalide glass-ceramic scintillators containing lead-free chloride perovskite nanocrystals for high-resolution and stable X-ray imaging

Lead-free halide perovskites are promising scintillators due to strong X-ray attenuation and high internal quantum efficiency (IQE), but their application is hindered by moisture sensitivity. Here, CsSrCl3:Eu2+ nanocrystals were grown in situ in a specially designed inorganic glass matrix. By employing [PO4]-modification and controlled crystallization, a transparent CsSrCl3:Eu2+ glass-ceramic (GC) scintillator was obtained, combining high crystallinity (15.9%) with excellent optical transparency (85.3% at 432 nm). The GC exhibits outstanding photoluminescence (PL) performance, including a high IQE of 87.6% and superior thermal stability (74% intensity retention at 493 K relative to 303 K). Benefiting from the robust glass matrix, the GC retains 99% of its initial PL intensity after 14 days of water immersion. Under X-ray excitation, it shows blue X-ray excited luminescence (XEL), with peak and integrated intensities reaching 117% and 25.1% of those of Bi4Ge3O12 crystal, respectively. The scintillator achieves a high spatial resolution of 20 lp mm−1 and an X-ray detection limit of 3.7 μGy s−1. Furthermore, it demonstrates exceptional operational stability in humid environments, maintaining clear X-ray image contrast even after 48 h of water submersion. This study provides an effective strategy for stabilizing hygroscopic halide scintillators in a durable [PO4]-modified fluoroaluminate glass matrix and demonstrates the potential of CsSrCl3:Eu2+ GC for high-resolution and stable X-ray imaging.

Read Full Abstract10.1007/s40843-025-3920-1
Broad-Temperature-Range Thermoresponse of Cu(I)-Based Organic-Inorganic Hybrid Metal Halides with Multimode Dynamic LuminescenceGraphical AbstractVerified
SCIENCE CHINA Materials2026

Broad-Temperature-Range Thermoresponse of Cu(I)-Based Organic-Inorganic Hybrid Metal Halides with Multimode Dynamic Luminescence

Organic-inorganic hybrid metal halides (OIMHs) based on Cu(I) ions exhibit broad application prospects in stimulus-responsive luminescent materials due to their rich structural diversity and highly adjustable electronic states. However, achieving sensitive and broad-temperature-range thermal responses remains a significant challenge. Here, we synthesize a zero-dimensional warm white-light emitting OIMH, MPC-W ((C9H20N2O)4(Cu2I4)(Cu2I6)(H2PO2)2), using 4-morpholinopiperidine (4-MP) and CuI. MPC-W features hybrid structures of [Cu2I4]2− and [Cu2I6]4−. The coexistence of three luminescent mechanisms—organic cluster luminescence (CL), self-trapped exciton (STE) emission of [Cu2I6]4−, and cluster-centered (CC) state luminescence of [Cu2I4]2−—endows MPC-W with temperature- and excitation-wavelength-dependent dynamic luminescence. From 77 to 297 K, the luminescence color continuously tunes from blue to cyan, green, yellow-green, and white. In the range of 217–463 K, MPC-W exhibits abnormal luminescence enhancement with increasing temperature. Upon chemical stimuli, MPC-W reversibly transforms into blue-emitting MPC-B ((C9H20N2O)Cu2I4) and yellow-emitting MPC-Y ((C9H18N2O)7Cu8I8). These dynamic luminescent properties position MPC-W for applications in temperature sensing, optical anti-counterfeiting, and password locks. This work provides new insights for developing wide-temperature-responsive multifunctional intelligent luminescent materials.

Read Full Abstract10.1007/s40843-025-3989-4
Cost-effective organic solar cells consisting of homogeneously passivated metal oxidesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Cost-effective organic solar cells consisting of homogeneously passivated metal oxides

Organic solar cells (OSCs) have achieved power conversion efficiencies (PCEs) exceeding 20% in laboratory-scale devices, yet challenges persist in developing cost-effective charge-transporting materials (CTMs) that ensure high performance and long-term stability. Conventional organic CTMs such as PEDOT:PSS and PDINN suffer from thermal instability due to molecular diffusion and phase segregation. Solution-processed metal oxides (MOs) offer excellent stability and cost-effectiveness but are plagued by surface defects, particularly hydroxyl groups, which act as recombination centers and photocatalytic sites, degrading device interfaces. Here, we develop an organic-inorganic hybrid strategy to homogeneously passivate solution-processible semiconducting MOs. By first synthesizing MOs rich in surface hydroxyl groups and then introducing organic molecules, we achieve chemically homogeneous passivation that mitigates surface defects. This approach enables favorable interfacial energy level alignment, enhanced charge extraction, and tunable surface energy. Employing these passivated MOs as electron transport layers (ZnO) and hole transport layers (NiOx), we achieve a champion PCE of 20.22% for all-MO CTM-based OSCs, the highest reported to date. Scalability is demonstrated via ambient blade-coating, yielding 18.33% PCE for large-area cells (1.44 cm2) and 16.03% for modules (20.05 cm2), with material costs estimated at only 4% of organic counterparts. Furthermore, devices exhibit outstanding stability, retaining over 80% of initial PCE after 1300 h of maximum power point tracking and over 1000 h of thermal annealing at 85°C. This work establishes a new benchmark for cost-effective, high-performance organic photovoltaics.

Read Full Abstract10.1007/s40843-025-3980-y
Dual-mode Förster resonance energy transfer for color-tunable and stimulus-responsive organic afterglowGraphical AbstractVerified
SCIENCE CHINA Materials2026

Dual-mode Förster resonance energy transfer for color-tunable and stimulus-responsive organic afterglow

Achieving flexible polymer-based organic afterglow materials with color-tunable and stimulus-responsive capabilities is significant in diverse optoelectronic fields, especially in next-generation wearable full-color display applications, yet remains a great challenge. Here, we report polymer-based dual-mode afterglow systems that realize long-lived color-tunable afterglow with full-color gamut of blue, green, orange, red, and even white-light emissions with ultralong lifetimes up to 2.42 s. This unique performance is enabled by a universal strategy of dual-mode afterglow-assisted Förster resonance energy transfer (FRET) that utilizes seconds-long dual-mode afterglow materials as energy donors and permits efficient synchronous transfer of singlet and triplet excitons from energy donors to the fluorescent dye acceptors. More impressively, the dual-mode afterglow-assisted FRET efficiency reaches up to 99%, with the lifetime of the energy acceptor reaching 1.55 s. Associated with the abundant hydrogen-bonding interactions within the polymer system, the doped afterglow films exhibit water/thermal stimulus responsiveness and recyclability. Furthermore, these full-color dual-mode afterglow materials are employed for multicolor screen-printing, optical anti-counterfeiting, and high-level information encryption, demonstrating considerable application potential in advanced anti-counterfeiting technologies.

Read Full Abstract10.1007/s40843-025-3906-2
Phase Distribution Control in Thermally Evaporated Perovskite Films for Speckle-Free Laser ImagingGraphical AbstractVerified
SCIENCE CHINA Materials2026

Phase Distribution Control in Thermally Evaporated Perovskite Films for Speckle-Free Laser Imaging

Metal-halide perovskites exhibit exceptional optical gain, narrow emission linewidths, and high emission efficiency, positioning them as promising candidates for next-generation lasers. Thermal evaporation, a mature semiconductor fabrication technique, offers scalability, yet monitoring phase distribution during deposition remains challenging. This study systematically investigates and regulates thermally evaporated FAxCs0.8PbBr3 perovskite films by tuning formamidinium (FA) content to optimize phase distribution. At intermediate FA content, films achieve a balanced distribution of n=2 to n=5 quantum-well phases, facilitating ultrafast carrier transfer (<0.31 ps) and suppressing nonradiative recombination. FA+ actively incorporates as an A-site cation, promoting ordered crystallization and reducing defect densities. The optimized films exhibit a net modal gain of 1041 cm−1 and a gain lifetime of 129 ps. Benefiting from efficient internal scattering, the threshold for cavity-free random lasing is reduced to below 5 μJ/cm2 at room temperature. The low spatial coherence of random lasing enables speckle-free imaging with a speckle contrast as low as 0.011 and improved contrast-to-noise ratios across all spatial frequencies. This work provides a scalable strategy for perovskite composition-phase engineering, advancing speckle-free laser imaging systems compatible with semiconductor-grade, large-area manufacturing.

Read Full Abstract10.1007/s40843-025-3967-x
Nitrogen-Substitution Engineering Enabling Efficient H2O2 PhotosynthesisGraphical AbstractVerified
SCIENCE CHINA Materials2026

Nitrogen-Substitution Engineering Enabling Efficient H2O2 Photosynthesis

The transition from laboratory-scale to industrial hydrogen peroxide (H2O2) production hinges on achieving ultra-high photocatalytic efficiency. Herein, we demonstrate a nitrogen-substitution engineering strategy for photocatalysts by replacing partial carbon atoms in benzene-1,3,5-triamine with nitrogen atoms, showing dual synergistic effects: (1) electronic structure modification upon electronegativity and dipole moment of the building blocks, creating built-in electric fields that promote charge separation and interfacial electron transfer; (2) enhancement in adsorption of reaction intermediates significantly boosting oxygen reduction reaction (ORR) and water oxidation reaction (WOR) kinetics. This dual-modification system exhibits broadband light absorption extending to 700 nm (near-infrared), enabling outstanding performance under ambient conditions with a H2O2 production rate of 12099 μmol g−1 h−1 from water and O2 without any sacrificial agent, an apparent quantum efficiency (AQE) of 19% at 500 nm, and a solar-to-chemical energy (SCC) efficiency of 1.38%. This work establishes atom-engineered nitrogen substitution as a general approach for designing high-performance photocatalysts, offering a viable pathway for large-scale H2O2 production with solar-driven chemical synthesis paradigm.

Read Full Abstract10.1007/s40843-026-4076-x
Lignin-Based Carbon Nanofibrous Scaffold: Constructing a Mechanically Robust Bi2WO6/ZnIn2S4 Z-Scheme Heterojunction Membrane for Enhanced Pollutant Degradation and Stable CyclabilityGraphical AbstractVerified
SCIENCE CHINA Materials2026

Lignin-Based Carbon Nanofibrous Scaffold: Constructing a Mechanically Robust Bi2WO6/ZnIn2S4 Z-Scheme Heterojunction Membrane for Enhanced Pollutant Degradation and Stable Cyclability

Sustainable bio-sourced functional materials are pivotal for advancing wastewater treatment technologies. This study reports a lignin-based carbon nanofiber (CNF) scaffold engineered with a Bi2WO6 (BWO) and ZnIn2S4 (ZIS) Z-scheme heterojunction via coaxial electrospinning and hydrothermal synthesis. The resulting all-component photocatalytic nanomembrane exhibits superior mechanical robustness under wet conditions, with a Young's modulus of 20.38 MPa and toughness of 2.48 kJ/m3. Stabilization kinetics are accelerated 10-fold (1°C/min), yielding significant energy savings. Using methylene blue (MB) as a model pollutant, the CNFs@BWO/ZIS membrane achieves 94.4% degradation efficiency (k = 0.01664 min−1) after 120 min of solar irradiation, maintaining excellent recyclability over five successive cycles. Systematic mechanistic studies elucidate the Z-scheme charge-transfer pathway, which optimizes interfacial photoexcited carrier separation and reduces energy loss. This work demonstrates a sustainable biomass-derived photocatalytic system with high mechanical integrity and catalytic performance, offering a viable route for efficient wastewater treatment and contributing to carbon neutrality goals.

Read Full Abstract10.1007/s40843-025-3990-6
Oxygen Anion-Mediated Electron Pump Suppressed Iron Segregation in Cobalt-Iron Catalyst Boosts Ampere-Scale Seawater ElectrolysisGraphical AbstractVerified
SCIENCE CHINA Materials2026

Oxygen Anion-Mediated Electron Pump Suppressed Iron Segregation in Cobalt-Iron Catalyst Boosts Ampere-Scale Seawater Electrolysis

Electrochemical seawater electrolysis powered by renewable energy is a highly promising route toward sustainable hydrogen production, mitigating both energy shortages and carbon emissions. However, chloride-induced corrosion and competitive chlorine evolution reactions lead to metal site dissolution, severely impairing durability, especially at industrial-level current densities. Here, we report a nitrite-incorporated cobalt-iron layered double hydroxide (CoFe-NO2−-LDH) electrocatalyst that exhibits exceptional activity and stability for seawater splitting. The nitrite anion acts as an electronic pump: it accepts electrons to facilitate the formation of high-valence Fe species essential for initial OER activation, and donates electrons under high potential to suppress oxidative dissolution. Moreover, the negatively charged nitrite generates an electrostatic repulsion field that effectively repels chloride ions, protecting metal active sites from corrosion and segregation. The in situ characterization confirms that nitrite doping weakens the Fe–O covalency, which suppresses lattice oxygen participation and promotes a stable adsorbate-evolving mechanism, consequently leading to significantly enhanced operational stability. When used as an anode, the CoFe-NO2−-LDH catalyst achieves over 1000 h of stable operation at 1000 mA cm−2 in seawater electrolysis, demonstrating great potential for practical applications.

Read Full Abstract10.1007/s40843-025-3918-x
Nitrogen vacancy-modified Fe3O4 for efficient visible-light-driven CO2 photoreduction to syngasGraphical AbstractVerified
SCIENCE CHINA Materials2026

Nitrogen vacancy-modified Fe3O4 for efficient visible-light-driven CO2 photoreduction to syngas

Photocatalytic reduction of CO2 to syngas (CO and H2) is pivotal for Fischer-Tropsch synthesis and carbon neutrality, yet suffers from rapid charge carrier recombination. Here, we report a solvent-induced defect engineering strategy to fabricate nitrogen vacancy (Nv)-modified Fe3O4 (Fe3O4-Nv-12h). Under visible light (λ ≥ 420 nm), Fe3O4-Nv-12h achieves a total syngas production rate of 43.55 mmol g−1 h−1 with a near 1:1 CO/H2 ratio, representing an 805.2-fold enhancement over pristine Fe3O4 and surpassing state-of-the-art systems. Electron paramagnetic resonance (EPR) and X-ray photoelectron spectroscopy (XPS) confirm that Nv introduction modulates the electronic structure, acting as electron traps to suppress recombination and enhance charge transport. In situ Fourier transform infrared (FTIR) spectroscopy identifies *COOH and *CO as key intermediates for CO formation. This work establishes an effective nitrogen vacancy modification strategy for efficient photocatalytic CO2 conversion to syngas, offering new avenues for high-performance catalyst design.

Read Full Abstract10.1007/s40843-025-3922-2
Molecular Tailoring Modulates Coordination of Deep Eutectic Electrolytes for Dendrite-Free Rechargeable Aluminum BatteriesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Molecular Tailoring Modulates Coordination of Deep Eutectic Electrolytes for Dendrite-Free Rechargeable Aluminum Batteries

Rechargeable aluminum batteries (RABs) are promising for large-scale energy storage due to high theoretical capacity, inherent safety, and abundant aluminum reserves. However, conventional AlCl3-based ionic liquid electrolytes suffer from high cost, uncontrolled dendrite growth, and severe anode corrosion. Here, a molecular-level ligand engineering strategy is proposed, employing nitrogen-containing cyclic amides with tunable N–H functionalities to modulate the coordination environment of deep eutectic electrolytes (DEEs). Combined experimental and theoretical investigations reveal that the α-pyrrolidone-based DEE (PDEE) possesses a wider electrochemical window, higher ionic conductivity, and lower polarization. Precise N–H regulation optimizes cationic ligand and chloroaluminate anion interactions, accelerating ion transport to facilitate uniform Al deposition without dendrites. The amine functionalities enable in situ construction of a uniform inorganic-organic bilayer solid electrolyte interphase, mitigating anode corrosion and enhancing long-term interfacial stability. As a result, Al//Al symmetric batteries with PDEE achieve stable cycling for over 2000 hours, while Al-graphite full batteries demonstrate negligible capacity decay after 6000 cycles. This study establishes that ligand molecular engineering offers an effective strategy for optimizing DEEs, enabling durable and high-performance RABs.

Read Full Abstract10.1007/s40843-025-3984-5
Correlating the dielectric properties with chain packing density of polar functionalities in hyperbranched polyimidesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Correlating the dielectric properties with chain packing density of polar functionalities in hyperbranched polyimides

Polymer-based dielectric materials with high energy density and thermal stability are critical for modern electric/electronic industries. Polyimide (PI) based materials are promising due to their high temperature resistance and chemical inertness, yet their inherently low dielectric constant and limited charge-discharge energy density restrict applications in film capacitors. While incorporating ferroelectric or conductive fillers can enhance dielectric performance, batch-to-batch inconsistency and physical deterioration remain problematic. This study focuses on molecular structure design and modulation, preparing hyperbranched polyimides with different dianhydride monomers and branching degrees. The effects of chain packing density with polar groups on dielectric and energy storage performances were systematically investigated via experimentation and molecular simulation. Results demonstrate a significant correlation between monomers' electrical distribution and packing density in polymer systems. Molecular simulation further elucidated the underlying mechanism. This work establishes a foundation for designing polymer-based dielectric materials with high dielectric and energy storage performances at the molecular level.

Read Full Abstract10.1007/s40843-025-3825-x