SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4279-0
Inkjet printing has emerged as a viable additive manufacturing route for organic light-emitting diodes (OLEDs), offering drop-on-demand patterning, high material utilization, and compatibility with large-area flexible substrates. This review critically examines the formulation science, printhead physics, and drying kinetics that govern the quality of inkjet-printed organic layers. We analyze the rheological window required for stable jetting, typically 1–20 mPa·s viscosity and 25–45 mN/m surface tension, and the dimensionless Ohnesorge number (0.1 < Z < 1) that defines satellite-free droplet formation. The coffee-ring effect, driven by capillary flow and solvent evaporation gradients, remains the dominant failure mode for pixel non-uniformity; binary solvent systems and substrate temperature control (40–60 °C) mitigate this. We survey recent progress in printed hole-transport, emissive, and electron-transport layers, with particular attention to cross-linkable hole-transport materials that resist interlayer dissolution. Device performance metrics from printed OLEDs now reach external quantum efficiencies of 15–20% for fluorescent emitters and >25% for phosphorescent systems, with operating lifetimes (T95) exceeding 1,000 hours at 1,000 cd/m². We identify remaining bottlenecks: nozzle clogging from aggregated nanoparticles, film thickness variation across large panels, and the absence of standardized ink formulations. The review concludes with a roadmap for industrial adoption, emphasizing in-line metrology and closed-loop process control as prerequisites for yield parity with vacuum-deposited OLEDs.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4342-3
Electron acceptors containing single-bond-linked building blocks offer attractive advantages for organic solar cells owing to their synthetic simplicity and structural modularity. However, achieving backbone planarity without compromising electronic compatibility remains a persistent challenge. Conventional conformational locking strategies based on alkoxy substitution can effectively suppress torsional freedom but often elevate the highest occupied molecular orbital energy level, limiting compatibility with widely used donor polymers. Here, we report a partially fused electron acceptor design that achieves intrinsic backbone planarity through heterocycle selection rather than side-chain-assisted conformational locking. By incorporating a benzodifuran core and furan-thiophene linkages, the resulting acceptors exhibit a near-coplanar backbone geometry as revealed by density functional theory calculations, without the need for electronically perturbing alkoxy groups. Devices based on the optimized acceptor (BDF-1) deliver a binary power conversion efficiency of 12.2%, and further improvement to 19.5% is achieved in a ternary blend with PM6 and BTP-eC9. The enhanced performance is accompanied by favorable morphology, balanced charge transport, and suppressed recombination losses. This work provides molecular-level insight into partially fused acceptor design and demonstrates that heteroatom-guided conformational locking offers a viable strategy for expanding the design space of acceptors with single-bond-linked building blocks while maintaining compatibility with mainstream donor systems.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4183-3
Excessive ultraviolet (UV) radiation poses significant risks to human health, necessitating highly sensitive detection systems. Organic photodetectors (OPDs) offer high sensitivity and tunable spectral response, but their UV performance is constrained by conventional glass/indium tin oxide (ITO) substrates and electrodes, and insufficient photoactive layer responsivity. Here, we report high-performance UV-OPDs achieved through UV-transparent window and active-layer optimization. Replacing glass/ITO with a UV-transparent window comprising a quartz substrate and PH1000 electrode enhances UV transmittance. Integrating the high UV-responsive blend PM6:Y6:PC71BM as the active layer, the optimal ternary UV-OPD exhibits external quantum efficiency (EQE) exceeding 53% across 280–400 nm, with a peak EQE of 78.29% and responsivity of 214.68 mA/W at 340 nm, alongside a rapid response time of 2.6/2.1 μs. This performance represents the best combination of responsivity and response time reported to date in the UV region. We demonstrate the potential of these UV-OPDs for outdoor real-time UV monitoring. This work presents a promising strategy for developing high-performance UV-OPDs through transparent substrate and electrode engineering, and active-layer optimization.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3629-3
Electrically pumped lasers with reduced physical dimensions are critical for future optical information processing, storage, and photonic integrated circuits. However, electrical injection in perovskite lasers faces challenges including material instability, non-radiative losses, and Joule heating. Here, we demonstrate an ultralow-threshold perovskite microlaser decorated with gold nanoparticles (AuNPs), enabling simultaneous optical pumping and current injection at ambient temperature. The lasing threshold is reduced to 8.6 μJ/cm², approximately 44% lower than that of pristine devices (15.3 μJ/cm²). The AuNPs, with optimized size, enhance both lasing performance and electrical properties, achieving a current injection density of 2.98 kA/cm². AuNPs accelerate hot-carrier cooling, reducing non-radiative recombination and mitigating Joule heating. The threshold decreases progressively with increasing electrical assist fraction. Stability tests confirm excellent resistance to aging and humidity, with stable lasing output under co-excitation in ambient air. This work underscores the feasibility of electrically driven perovskite microlasers, offering a pathway toward electrically pumped microlaser diodes.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3712-2
Electrochemical potential and ion diffusion of electrode materials restrain the energy and power densities of lithium-ion batteries, and these challenges also remain in the intercalation-type Li3VO4 (LVO). In this work, the local [VO4] coordination symmetry in LVO is broken by a higher concentration of oxygen vacancies (Vö), resulting in an increased average V–O bond length and a larger ligand field splitting. These alterations reduce the energy level of the lowest unoccupied orbitals (e*) and lift the electrochemical potential, resulting in a higher voltage output. Additionally, the broken local symmetry in Vö-LVO is found to reduce the band gap and expand the ion transport channels, which favors enhancing electronic conductivity and facilitates ion diffusion, thereby improving the electrochemical kinetics in the energy storage process. The local symmetry broken sample (Vö-LVO) achieves a significantly improved capacity of 532 mAh/g at 0.1 A/g in comparison with 394 mAh/g of pristine LVO, and long cycling stability with retained capacity of 398 mAh/g at 1 A/g over 500 cycles compared with 236 mAh/g of the pristine LVO. The fundamental understanding paves the way to exploit high-performance electrodes via ligand field engineering for next-generation rechargeable batteries.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3682-6
Metal single-atoms with optimized coordination structure on highly accessible substrate can maximize the metal utilization efficiency along with enhancing catalytic activities. Herein, axial nitrogen-coordinated Fe-N5 sites on N-doped carbon (denoted as FeN5@N-C) hollow microplates are fabricated via a unique Fe3+-chelated polydopamine assisted hollowing strategy using ZIF-L microplates as multifunctional templates. Due to the powerful chelating and adhesive ability of polydopamine, this hollow-carbon strategy can be extended to fabricate single-atom Fe-N-C hollow structures with different shapes and encapsulate other transition-metal single atoms (Ni, Co, Mn, and Cu) into the N-doped carbon hollow microplates. The FeN5@N-C hollow microplates exhibit outstanding oxygen reduction reaction (ORR) capability with an impressive half-wave potential of 0.93 V vs. reversible hydrogen electrode and high stability, which can serve as air-cathode catalysts for high-performance Zn-air batteries with high peak power density of 225.3 mW cm−2 and stable cyclability of up to 400 h. Comprehensive analysis and theoretical calculations elucidate that axial nitrogen coordination in Fe-N5 catalytic sites, unlike the planar Fe-N4 configuration, can compete well with the bonding of OH* through additional 3d-2p orbital hybridization, thereby giving moderate bonding strength to enhance the ORR activity.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3722-3
Magnesium alloys are promising biodegradable bone implant materials due to their biocompatibility and mechanical compatibility, but rapid degradation and postoperative bacterial infection limit clinical application. Here, zeolitic imidazolate framework-8 (ZIF-8) and 3,4,9,10-perylenetetracarboxylic diimide (PD) composite coatings (ZIF-8@PD) were fabricated in situ on micro-arc oxidation (MAO) coated AZ31 alloys via two-step and one-step (OS) methods. The MAO/ZIF-8@PD and MAO/ZIF-8@PD (OS) coatings reduced corrosion current density by three and two orders of magnitude, respectively, compared to MAO coating, due to the physical barrier of the 2D-co-3D MOF structure. Under 808 nm near-infrared laser irradiation, photothermal and photodynamic effects from PD, combined with contact killing by released Zn2+ ions, achieved bactericidal rates ≥99.5% against E. coli and S. aureus. Photothermal conversion efficiencies were 44.01% and 48.57% for the two-step and one-step coatings, respectively. The distinct Zn2+ sources led to different 2D-co-3D MOF structures, influencing degradation and antibacterial behavior. These coatings offer a strategy to enhance corrosion resistance and antibacterial activity of Mg alloys for biomedical applications.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(25)60617-7
The global energy landscape is undergoing a profound transformation, with wind energy gaining increasing prominence due to its clean and renewable nature. However, as installed wind power capacity expands, disposal of waste wind turbine blades (WWTB) has emerged as a significant challenge. These blades are predominantly composed of epoxy resin (EP) polymers, carbon fibers (CFs), and glass fibers (GFs). Improper disposal exacerbates environmental concerns and leads to loss of valuable resources, particularly carbon-based materials. Pyrolysis technology, a versatile and environmentally sustainable method for resource recovery, has garnered considerable attention for WWTB disposal. This work presents a comprehensive review of pyrolytic recycling of WWTB, focusing on principles and classifications of pyrolysis technology, key factors influencing the pyrolysis process, as well as pyrolysis methods, equipment, products, and their applications. Through in-depth analysis of current research, this review identifies critical unresolved issues and provides a forward-looking perspective on emerging research trends. The review highlights that pyrolysis can effectively recover glass fibers and carbon fibers with mechanical property retention depending on process conditions, and that catalytic pyrolysis can enhance the quality of recovered products. Economic analysis indicates that collaborative disposal methods can improve cost-effectiveness. Future research should focus on optimizing process parameters for large-scale industrial application and developing more efficient catalysts to improve product selectivity and fiber quality.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202604015
Shale gas extraction generates hazardous oily sludge, necessitating effective in-situ treatment. Microemulsion technology offers low energy consumption, cost efficiency, and high oil removal without heating. This study investigates single-surfactant microemulsions using sodium dodecyl sulfate (SDS) and alpha-olefin sulfonate (AOS), and composite microemulsions with sodium silicate (Na2SiO3). Phase behavior and effects of surfactant, alcohol, and salt concentrations on oil removal were examined. Optimal single formulations achieved removal rates of 86.33% for SDS (SDS:alcohol:NaCl = 2.72%:13.21%:2.17% mass ratio) and 87.45% for AOS (SDS:alcohol:NaCl = 2.72%:15.41%:2.17%). SDS microemulsions showed superior phase stability despite slightly lower removal efficiency. Composite SDS-Na2SiO3 microemulsion achieved 92.47% oil removal, outperforming single systems, and could be recycled five times while meeting national secondary reuse standards. AOS-Na2SiO3 exhibited better salt resistance, whereas SDS-Na2SiO3 showed better alcohol resistance. This work provides a novel approach for in-situ oily sludge treatment.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3882-y
Organic semiconductor crystals with well-defined morphologies are highly desirable for high-performance optoelectronic devices, yet precise control over their growth remains a challenge. Here, a novel donor-acceptor (D-A) molecule, TQDPT, has been successfully developed, featuring a rigid π-conjugated acceptor core composed of thiazoloquinoxaline and naphthalene, coupled with phenylphenothiazine donors. This study presents a temperature-mediated crystallization strategy for precisely controlling the morphology and carrier transport properties of TQDPT single crystals. By systematically investigating the growth kinetics across a controlled temperature range (15–35°C), we reveal a distinct transition from needle-like structures to plate-like crystals, with tunable average widths spanning from around 2.8 to 30.1 μm. This morphological evolution is driven by temperature-dependent molecular diffusion and nucleation kinetics. Significantly, the plate-like crystals grown at 25°C exhibit an order-of-magnitude enhancement in mobility compared to needle-like counterparts, while higher temperatures of 35°C yield broader crystals with improved carrier mobility and device stability. This work highlights the critical role of temperature as a pivotal parameter in the dimensional and electronic optimization of organic crystals, offering an attractive approach to optimize functional materials for advanced optoelectronics.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025012302
Phosphorus (P) loss from paddy fields contributes to eutrophication in Chaohu Lake. This study evaluated the effects of novel fertilizers and P reduction on P loss and rice yield. Seven treatments were established: no P (CK), rice-specific fertilizer (ZYF), slow-release blended fertilizer (SRF), Xinjutian compound fertilizer (XJT), enhanced loss-controlled fertilizer (CRF), CRF with 10% P reduction (CRF-10P%), and CRF with 30% P reduction (CRF-30P%). Results showed that novel fertilizers and P reduction significantly reduced concentrations of total phosphorus (TP), dissolved phosphorus (DP), and particulate phosphorus (PP) in surface water and leachate. The first 5 days after basal fertilization and heavy rainfall were high-risk periods for P loss. Rainfall increased TP concentrations by 417.74%–432.86% and 94.85%–351.35% in surface water and leachate, respectively; DP increased by 120.80%–322.44%, and PP by 280.66%–501.77% and 80.23%–297.55%. Compared with ZYF, SRF, XJT, and CRF reduced TP loss by 15.43%–33.95%, with SRF showing the lowest loss. Under P reduction, CRF-10P% and CRF-30P% reduced TP loss by 31.48% and 37.04%, respectively, with CRF-30P% achieving the lowest loss. Notably, CRF-10P% increased rice yield by 22.37% relative to ZYF, indicating that moderate P reduction with enhanced loss-controlled fertilizer can maintain or increase yield while reducing environmental risk. The study concludes that CRF-10P% offers a promising strategy for sustainable rice production in the Chaohu Lake watershed.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(26)60641-X
Polycarbonate (PC) is a widely utilized engineering plastic, but its accumulation in waste streams poses environmental and health risks due to the leaching of toxic bisphenol A (BPA). This study presents a catalyst-free methanolysis route for the chemical recycling of waste PC into BPA under mild conditions. At 160 °C, complete depolymerization of PC (100.0% conversion) was achieved with a high BPA yield of 95.0% without any catalyst or auxiliary solvent. A scaled-up experiment with 10 g PC demonstrated a facile separation process, recovering BPA with over 85.0% yield. The method proved effective for various commercial PC grades and mixed plastics, including ABS-PC blends, as well as other polyesters such as polylactic acid, polyglycolic acid, and polyethylene terephthalate. Based on SEM and GPC analyses, a probable alcoholysis depolymerization mechanism was proposed, involving initial swelling and gradual breakdown of PC into soluble macromolecules with broad molecular weight distribution, ultimately yielding BPA. This work offers a facile, green, and efficient approach for the alcoholysis recovery of polyester plastics, addressing both environmental concerns and sustainable resource utilization.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3869-7
Iontronic capacitive pressure sensors (ICPSs) are pivotal for wearable technology, yet their performance is constrained by an inherent trade-off between sensitivity and detection range. Here, we introduce a micro-electric double layer (micro-EDL) engineering strategy to overcome this limitation. This is realized through a nanocomposite dielectric where multi-walled carbon nanotubes (MWCNTs) form a percolated network, generating a dense array of pressure-responsive nano-capacitors. Synergistically integrating a hierarchical MoS2/NiCo-LDH electrode provides abundant pseudocapacitive interfaces. The resulting sensor exhibits an ultrahigh sensitivity of 67,095 kPa−1 at 1 kHz, a broad detection range up to 1.3 MPa, rapid response and recovery times of 4 ms and 5 ms, respectively, and outstanding durability exceeding 18,000 cycles. Practical validation demonstrates 100% classification accuracy in recognizing complex gestures and gait patterns, underscoring its real-world applicability. These findings establish micro-EDL engineering as a promising route for advancing next-generation iontronic devices, offering insights into their electrochemical mechanisms.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(26)60653-6
Carbon deposition caused by mass transfer limitations is a key challenge for traditional microporous ZSM-5 zeolites in coal tar catalytic cracking. To address this, benzene was used as a model compound. Parent ZSM-5 (NL-ZSM-5) was modified with tetraethylammonium hydroxide (TEAOH) to prepare hierarchical ZSM-5 zeolites with different mesopore sizes. Characterization (XRD, FT-IR, BET, TEM) confirmed successful mesopore introduction via selective desilication while retaining the MFI structure. At TEAOH concentration of 0.4 mol/L (ZSM-5-C), total pore volume increased from 0.24 to 0.43 cm3/g, and Brønsted acid amount increased from 0.28 to 0.67 mmol/g, with improved acid site accessibility. Catalytic experiments and carbon deposition analysis showed that hierarchical pore structure inhibits coking via a synergistic effect of diffusion enhancement and adsorption-site regulation. The coke amount of ZSM-5-C was 4.0%, only one-third of that of NL-ZSM-5 (11.9%). Molecular dynamics simulations confirmed that the diffusion coefficient of benzene in a 3.0 nm mesopore model is an order of magnitude higher than in a 2.0 nm model. Adsorption capacity decreases with increasing mesopore size, shortening residence time. Increasing temperature enhances diffusion but exponentially intensifies surface condensation reactions (Arrhenius effect), which dominates coke formation; hierarchical pores mitigate this negative effect. This research provides a theoretical basis for designing high-efficiency, coke-resistant catalysts for coal tar conversion.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3920-1
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.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3967-x
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.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3907-0
Passive radiative cooling dissipates heat through the atmospheric transparency window (8–13 μm) into cold outer space, offering energy-free building cooling. However, its performance degrades substantially in humid environments; for instance, in Singapore, where average relative humidity is ~80%, achievable cooling power can be as low as ~20 W/m², far below the theoretical maximum of ~150 W/m² under dry conditions. Restricted sky view factor on building facades further curtails efficiency. Evaporative cooling, leveraging water's high latent heat of vaporization (~2256 J/g), provides an omnidirectional heat dissipation pathway but porous materials like hydrogels suffer from swelling, poor adhesion, and structural degradation. Here, we report a cement-based integrated cooling paint (CCP) that synergistically combines radiative and evaporative cooling. The paint utilizes a calcium silicate hydrate (C-S-H) porous network matrix with barium sulfate nanoparticles, polyvinyl alcohol (PVA), and lithium chloride (LiCl). The optimized formulation (CCP-30) achieves high solar reflectance of ~93% in the dry state and maintains ~89% reflectance when wetted. Its high emissivity (~95%) within the atmospheric window ensures efficient radiative heat dissipation. PVA and LiCl inhibit plastic shrinkage and promote continued hydration, yielding a denser, robust microstructure. The interconnected porous structure and hygroscopic components enable passive water capture from rainfall and ambient moisture, driving sustained evaporative cooling. Field tests in Singapore showed a ~5°C lower surface temperature on CCP-coated facades compared to commercial radiative cooling paint, and an ~8°C reduction on a proximate black absorber, indicating mitigation of local heat island effects. Building energy simulations indicated 30–40% more savings in air conditioning electricity consumption. The paint is prepared via a simple one-pot method compatible with standard production, indicating excellent commercialization potential.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202511043
Zero-valent iron (ZVI) suffers from surface passivation and low electron utilization in reductive removal of nitrobenzene (NB). To address these issues, a ball-milled iron/digestate biochar composite (BM-Fe/DBC) was prepared and compared with a physically mixed counterpart (PM-Fe/DBC). Characterization revealed that ball milling tightly embedded ZVI particles into the carbon matrix, forming Fe–C chemical bonds and a strong interfacial coupling structure that established efficient electron transfer channels. This structure significantly enhanced the micro-galvanic effect between iron and carbon, yielding superior reduction performance across a wide pH range (3–9). Under optimal conditions (Fe:C mass ratio 2:1, dosage 1.0 g·L−1, pH 5), BM-Fe/DBC achieved 79.9% NB removal, and the generation of aniline (AN) was 1.85 times that of PM-Fe/DBC. Mechanistic studies indicated that the intimate Fe–C interfacial coupling promoted sustained ZVI corrosion and enhanced the production of indirect reducing species, including adsorbed Fe(II) and atomic hydrogen (H*). Electrochemical analyses showed that BM-Fe/DBC exhibited a lower corrosion potential, a higher corrosion current density (approximately 2.15 times higher), and lower charge transfer resistance, kinetically confirming its superior electron transfer capability. These findings reveal that constructing strong interfacial coupling in iron–carbon composites via mechanochemical methods can effectively overcome key limitations of ZVI in reduction reactions, providing a theoretical basis and practical pathway for designing high-performance water treatment materials.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025041805
Selenium (Se) is an essential trace element for mammals, yet no universally applicable method exists for assessing soil Se bioavailability. This study validated the feasibility of diffusive gradients in thin-films (DGT) technology for accurately evaluating Se bioavailability in paddy soils under natural conditions, and analyzed Se migration in the soil-plant system, soil kinetic characteristics, and the influence of physicochemical properties on Se bioavailability. Rice plants and corresponding rhizosphere soil samples were collected and analyzed using three traditional extraction methods alongside DGT. Results showed that 96.7% of soil samples and 66.7% of rice samples met the selenium-rich standard, and Se content measured by DGT most accurately reflected soil Se bioavailability. The bioconcentration factor (BCF) of different rice plant parts indicated generally low Se enrichment in grains, with primary enrichment in rice roots. Correlation analysis revealed that adjustments in soil pH, organic matter (SOM), cation exchange capacity (CEC), and sulfur (S) content could effectively improve soil Se bioavailability. These findings underscore DGT's superiority over conventional extraction methods for predicting Se uptake, offering a robust tool for managing selenium-rich agricultural resources.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202608023
Zinc-containing steel dust sludge, a by-product of steelmaking, contains high levels of chlorine (Cl) along with valuable metals such as Fe, Zn, K, and Na. When recycled into the steel production process, Cl accumulates, causing sintering instability and severe corrosion of blast furnace linings. This study investigated water leaching for Cl removal from zinc-containing steel dust sludge. Under optimal conditions (liquid-to-solid ratio 5 mL/g, temperature 70 °C, time 60 min, rotation speed 160 r/min), the Cl leaching rate reached 87%. Furthermore, a three-stage countercurrent water washing process at a liquid-to-solid ratio of 6 mL/g and room temperature for 45 min achieved a Cl leaching rate exceeding 90%. The water washing also reduced the leaching toxicity of metals in the sludge to a certain extent. Characterization via XRD, SEM, FT-IR, and XPS revealed that water washing primarily dissolved soluble chlorides (NaCl, KCl, etc.), increasing the specific surface area from 2.71 to 10.11 m²/g and average pore size from 12.83 to 16.29 nm. These findings provide theoretical and technical support for efficient Cl removal from zinc-containing steel dust sludge, facilitating its safe resource utilization.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4060-5
Organic solar cells (OSCs) offer unique advantages for wearable electronics due to their light weight and mechanical flexibility. However, achieving both high optoelectronic performance and mechanical robustness in organic semiconductors remains challenging, compromising the efficiency and durability of stretchable OSCs. Here, we report a cross-linked conjugated polyelectrolyte (CPE)-polyoxometalate (POM) anode interlayer (AIL), PTN-POM, constructed via strong electrostatic interactions between ammonium groups and POM. The PTN-POM film exhibits an electrical conductivity of 3.30×10−3 S/m and high stretchability, significantly outperforming the classic PEDOT:PSS AIL in mechanical strength. Binary OSCs modified with PTN-POM achieve a power conversion efficiency (PCE) of 19.59%, the highest reported for OSCs using a cross-linked AIL. Notably, PTN-POM enables fabrication of water-proof OSCs that show no performance degradation after underwater storage for 42 days. Furthermore, stretchable OSCs incorporating PTN-POM demonstrate enhanced mechanical robustness, retaining 81% of initial PCE under a large tensile strain of 50%. This work significantly enhances the photovoltaic, waterproof, and mechanical properties of OSCs, advancing their potential for wearable photovoltaics.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3951-4
Silicon anodes offer an ultrahigh theoretical capacity (4200 mAh g−1) but suffer from >300% volumetric expansion during cycling and unstable solid electrolyte interphase (SEI) formation, leading to rapid capacity fading. Here, we design a hierarchical composite p-cSi@aSi@MgSiN2@C featuring a porous crystalline-amorphous silicon core (p-cSi@aSi), an in-situ MgSiN2 transition layer, and an outer nitrogen-doped carbon shell. The 3D interconnected pores accommodate volume expansion, while amorphous silicon enables isotropic lithiation-induced strain, eliminating crystalline phase transition barriers. The MgSiN2 layer transforms into a tough Li3N-rich SEI with ultra-fast ion channels, and the carbon shell provides mechanical confinement and electronic conductivity. This synergistic interface engineering achieves an initial coulombic efficiency (ICE) of 81.4%, a charge transfer resistance of 16.4 Ω after 200 cycles (64% reduction), and a Li+ diffusion coefficient of 1.72×10−11 cm2 s−1. The anode delivers 1719.3 mAh g−1 at 0.2 C after 200 cycles and 823.8 mAh g−1 at 0.5 C after 500 cycles. The molten salt electrolysis synthesis achieves a current efficiency of 68.12% and specific energy consumption of 12.76 kWh kg−1, with an estimated electricity cost of 1154.69 USD ton−1, only 20% of commercial Si/C anodes. This work resolves the ICE-cycle life trade-off and provides a scalable, cost-effective approach for next-generation high-energy batteries.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4109-2
The fabrication of high-efficiency organic solar cells (OSCs) under ambient conditions remains a formidable challenge due to the sensitivity of active layer morphology to environmental factors. We propose an innovative approach for air-processed devices that combines spontaneous water-spreading film formation with layer-by-layer (LBL) deposition. This method enables the fabrication of donor- and acceptor-dominant bulk heterojunction blend films near the anode and cathode interfacial layers, respectively, optimizing vertical phase separation and enhancing charge transfer efficiency. In the D18:L8-BO system, the device achieves a power conversion efficiency (PCE) of 19.02% with an exceptionally narrow efficiency distribution. Even for devices with an area of 1 cm2, a PCE of 16.56% is attained. After a 1000-hour decay test, the efficiency retains 84.1%. This novel method offers a promising pathway for advancing the industrial application of large-area, highly stable devices with narrow efficiency distribution under ambient conditions.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4067-4
Confined growth of metal halide perovskite quantum dots (QDs) in porous matrices yields improved stability and sensitivity for their implementation in luminescent chemical sensing applications. Here, we realized the synthesis of highly stable (water, photo, and thermal) and luminescent CsPbX3 QDs within nanoporous glass (NG). This is achieved by a nano-confined aqueous synthesis of CsPbBr3 QDs in Pb-anchored NG. Benefiting from strong Pb–O–Si chemical bonding between the perovskite QDs and the NG matrix, the stability of the encapsulated perovskite QDs is significantly enhanced. The emission of the perovskite NG can be tuned from 440 to 760 nm. By integrating green- and red-emitting perovskite NG onto a blue LED chip, stable WLEDs were successfully fabricated. This facile approach enables the integration of ultra-stable perovskite QDs within transparent porous monoliths toward diverse luminescent chemical sensing applications.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4072-3
All-inorganic, hole-transport-material-free (HTM-free), carbon-based perovskite solar cells (C-PSCs) have attracted significant attention due to their exceptional stability and low cost. However, their performance and commercial potential are constrained by poor interfacial contact, insufficient crystallinity, and energy level misalignment. In this work, we address these challenges via a molecular engineering strategy by introducing tetrakis(4-ethynylphenyl)methane (TEPM) as a multifunctional additive. The alkynyl moiety (C≡C) in TEPM coordinates with Pb2+ ions in perovskite precursors, synergistically slowing crystallization kinetics to regulate crystal growth and passivate deep-level defects. Consequently, CsPbI3 films exhibit larger grain sizes, improved crystallinity, and lower defect densities. Devices modified with TEPM achieved a record power conversion efficiency (PCE) of 20.01% (certified 19.58%). Additionally, unencapsulated devices retained 87.6% of their initial efficiency after 1080 h under ambient conditions (25 °C, 30% relative humidity), and maintained 94.0% of their initial efficiency after 730 h of continuous AM 1.5G illumination in air. This work sets a new efficiency benchmark for inorganic HTM-free C-PSCs and provides a versatile molecular engineering strategy for developing high-performance, stable perovskite photovoltaics.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4123-0
Aqueous aluminum-ion batteries (AAIBs) are promising for large-scale energy storage due to safety, sustainability, and theoretical high capacity. However, sluggish electron/ion transport in conventional cathodes limits rate capability. Here, we first propose high-entropy engineering of metal oxides (HEOs) as cathodes in AAIBs, leveraging the 'cocktail effect' and abundant electron transport pathways to enhance rate-capacity. Atomic-level interactions between different metal atoms broaden the d-band with reduced electronic level degeneracy, facilitating rapid electron transport, achieving one of the best rate capabilities (119.4 mAh g−1 at 10.0 A g−1) among metal-oxide cathodes. The disordered layered oxides formed with a high-entropy framework alleviate electrostatic repulsion between aluminum ions and the fixed lattice, mitigating structural degradation and imparting excellent cycling stability (over 95.1 mAh g−1 after 500 cycles at 2.0 A g−1). The optimized HEO-Cr cathode (Fe0.6Co0.6Ni0.6Mn0.6Cr0.6O4) exhibits outstanding rate performance and cycling stability. DFT simulations and electrochemical tests reveal that multi-transition metal incorporation, bandgap narrowing, and unique lattice structure drastically enhance electron transport efficiency. The layered phase formed after cycling, based on a high-entropy framework, overcomes challenges from high charge density aluminum ions, significantly enhancing cycling stability. This work paves the way for high-performance AAIBs and other aqueous multivalent metal ion batteries by rationally designing high-entropy engineering.