SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4316-0
The rapid development of small molecule acceptors (SMAs) has enabled organic photovoltaics (OPVs) to achieve power conversion efficiencies exceeding 21%. Structural asymmetry has emerged as a particularly effective approach for boosting acceptor performance. This review provides a comprehensive overview of asymmetric SMAs from the molecular scale to the nanoscale and macroscale. The main text is organized into four sections: molecular design strategies for structural asymmetry, crystal structure evolution from symmetry breaking, morphological characteristics revealed by advanced characterization techniques, and energy loss mechanisms involving asymmetric SMAs. At the molecular scale, asymmetry enables precise modulation of dipole moments and intermolecular interactions, directly affecting crystalline packing and charge-transport networks. At the nanoscale, it further regulates domain purity, phase continuity, and molecular orientation. Asymmetric designs can also help mitigate non-radiative voltage loss through modulation of charge-transfer state energetics. Overall, asymmetric molecular design introduces additional structural and electronic tunability, offering new opportunities for overcoming the trade-offs that limit OPV performance. Finally, we discuss ongoing challenges and outline future perspectives to guide continued development and innovation in asymmetric SMA design.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3706-3
Aprotic lithium-oxygen (Li-O2) batteries are severely limited by slow cathode reaction kinetics and large polarization. Herein, we design and prepare a Mott-Schottky catalyst by uniformly embedding ultrafine Ru nanoparticles on nitrogen-doped carbon (Ru@NC) nanoflakes to accelerate oxygen redox kinetics of Li-O2 batteries. The Mott-Schottky effect of Ru@NC drives spontaneous electron rearrangement in the NC matrix and induces a strong built-in electric field at heterointerfaces, which accelerates the activation and conversion of oxygen intermediates. The obtained Ru@NC possesses rich Mott-Schottky heterointerfaces and defective carbon structures, which provide extensive adsorption and nucleation sites. More importantly, Ru@NC manifests moderate affinity for the intermediate LiO2, inducing formation of unique nanosheet-like Li2O2 with low Li2O2/cathode interfacial impedance, which further enhances oxidation kinetics. These enable the Li-O2 battery with Ru@NC to deliver a remarkably reduced polarization of 0.89 V, superior rate performance, and prolonged lifespan of over 200 cycles. This work will provide valuable guidelines for engineering advanced electrocatalysts for high-performance Li-O2 batteries and beyond.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3727-0
Lead halide perovskites are promising scintillators for X-ray imaging due to high X-ray absorption efficiency, excellent luminescence, and facile synthesis. However, their ionic nature challenges simultaneous high photoluminescence efficiency and environmental robustness. This work introduces a multilevel encapsulation strategy: CsPbBr3 quantum dots (QDs) are sequentially coated with Cs4PbBr6, SiO2, and polydimethylsiloxane (PDMS). Cs4PbBr6 passivates surface defects, while SiO2 and PDMS provide barriers against moisture, heat, and radiation. The resulting CsPbBr3@Cs4PbBr6/SiO2/PDMS flexible films exhibit a photoluminescence quantum yield (PLQY) of 85%, outstanding mechanical flexibility, and durability under stretching, bending, and compressing. Films retain emission stability under elevated temperatures, prolonged X-ray irradiation, and extended water immersion. X-ray imaging demonstrates spatial resolution of 12 lp/mm, enabling distortion-free imaging of curved objects; superior water resistance allows long-term underwater imaging. This work highlights hierarchical encapsulation in balancing luminescence efficiency and stability, offering a pathway toward practical flexible perovskite scintillators.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202510089
Microplastics (MPs) are frequently detected in various water bodies, posing increasing environmental risks. This study synthesized magnetic Fe3O4@MIL-100(Fe) microspheres via an in-situ one-step hydrothermal method and investigated their adsorption removal mechanisms for polystyrene (PS) and polylactic acid (PLA) microplastics. The composite exhibited a core-shell structure with a high specific surface area of 848.6 m2·g−1. Adsorption kinetics showed that PLA followed a pseudo-second-order model, while PS fitted both pseudo-first-order and pseudo-second-order models. Equilibrium data for both MPs were well described by the Freundlich isotherm. Removal efficiencies for PLA and PS increased from 58.18% and 49.66% to 98.90% and 98.58%, respectively, as pH decreased, and from 64.24% and 21.58% to 97.05% and 94.63% with increasing ionic strength. The removal mechanism involved synergistic physical-chemical interactions: hydrogen bonding dominated for PLA, with some complexation, while π–π interactions and hydrogen bonding were primary for PS. The material demonstrated excellent reusability over multiple cycles. These findings highlight the potential of Fe3O4@MIL-100(Fe) for efficient removal of MPs from water, offering a novel approach for controlling emerging contaminants.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3850-3
Chiral nanomaterials have attracted considerable attention for antibacterial applications due to their unique chiroptical properties. Here, we report a novel spatiotemporally precise synergistic photodynamic therapy (PDT) and photothermal therapy (PTT) strategy using circularly polarized light (CPL)-activated chiral molybdenum-doped carbon dots (L-Mo-CDs and D-Mo-CDs). These chiral carbon dots were synthesized using chiral tartaric acid as a precursor. Notably, D-Mo-CDs selectively respond to left-handed CPL (LCP), while L-Mo-CDs respond to right-handed CPL (RCP). Under CPL irradiation, D-Mo-CDs exhibit enhanced reactive oxygen species (ROS) generation and a higher photothermal conversion efficiency (PCE) compared to L-Mo-CDs. In vitro antibacterial assays demonstrate that D-Mo-CDs possess excellent bactericidal efficacy against both Gram-positive and Gram-negative bacteria. In vivo wound healing studies in a mouse model reveal remarkable therapeutic efficacy, attributed to reduced inflammation, accelerated angiogenesis, and enhanced collagen deposition. This work introduces a paradigm for utilizing chiral carbon dots in precision antibacterial therapy, addressing the limitations of conventional chiral nanomaterials such as poor biocompatibility and low photothermal conversion. The findings underscore the potential of metal-doped chiral carbon dots for advanced biomedical applications, offering a spatiotemporally controllable approach to combat bacterial infections without promoting resistance.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3879-5
Stimuli-responsive circularly polarized luminescence (CPL) materials are pivotal for investigating excited-state chirality and advancing optoelectronic applications. However, achieving comprehensive modulation of chiroptical properties within a single system under a single external stimulus remains a significant challenge. Here, electric-field-responsive helical ferroelectric liquid crystals are developed by incorporating diverse chiral emitter dopants into the prototypical liquid crystal mesogen 2,3′,4′,5′-tetrafluoro-[1,1′-biphenyl]-4-yl 2,6-difluoro-4-(5-propyl-1,3-dioxan-2-yl)benzoate (DIO), known for its high dielectric anisotropy and multiple mesophases. By co-doping different types of chiral molecules with opposite handedness, a competitive chiral field is generated that responds differentially to the applied voltage, enabling continuous modulation of the helical pitch and reversible inversion of handedness. This work provides the integrated demonstration of single-stimulus regulation of on/off gating, magnitude tuning, and reversible sign inversion in a single liquid-crystal system, opening a pathway toward intelligent chiroptical materials.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202509051
Recyclables constitute a significant fraction of municipal solid waste (MSW) and hold substantial potential for resource utilization and greenhouse gas (GHG) emission reduction, contributing to carbon peak and carbon neutrality goals. However, reported GHG emission factors (EFs) for various recyclables vary widely across databases and literature, ranging from -19,110 to -125 kgCO2-eq·t⁻¹, with significant differences both among categories and within the same category, complicating accurate accounting. This study systematically integrates literature data on EFs for different recyclable categories, focusing on identifying factors causing intra-category variability. Data were collected from global databases (ecoinvent, WARM, CPCD, NAEI) and peer-reviewed studies over the past two decades, normalized to a functional unit of 1 tonne of recyclable. Statistical analysis (mean ± standard deviation) provided reference ranges for each category. Results show paper recyclables EFs range from -3,140 to 270 kgCO2-eq·t⁻¹, with corrugated cardboard and writing paper exhibiting higher absolute values than packaging paper due to structural strength and resource value. Plastic recyclables EFs range from -3,096 to -566 kgCO2-eq·t⁻¹, with EPS showing the highest reduction potential, followed by PET and PVC, then HDPE, LDPE, PP, and other plastics. Key influencing factors include functional unit definition, accounting scenario, system boundary, electricity emission factor selection, and calculation assumptions. The study recommends selecting EFs matching the specific accounting scenario and performing error analysis. Data gaps remain for LDPE, EPS, and other plastics, necessitating further experimental or field data. To enhance accuracy, calibration methods such as process-level and life-cycle inventory data calibration are proposed. This work provides a scientific basis for EF selection and calibration in GHG accounting of recyclables.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3787-x
Circumventing the tumor's defensive antioxidant system and achieving precision cancer therapy remain major challenges in high-efficacy tumor treatments. Here, we propose a synergistic strategy integrating non-oxidative physical ablation and oxidative chemical intervention. An acid-responsive self-collapsing nanomineral PCSB is constructed, comprising poly(acrylic acid)-modified calcium sulfite (CaSO3) and a pH-responsive photoacoustic (PA) therapeutic molecule, aza-BDP. In the tumor acidic microenvironment, PCSB decomposes, releasing PA agents and SO2/Ca2+, thereby enabling combined non-oxidative mechanical damage from PA therapy and oxidative chemical damage from SO2 gas and Ca2+ ions. This dual-action approach effectively reduces resistance conferred by tumor antioxidant mechanisms and improves treatment precision. The study presents a synergistic physical-chemical strategy with significant potential for solid tumor elimination.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202512025
Persulfate (PS) is a common oxidant in in-situ chemical oxidation (ISCO) for groundwater organic contamination, but its vertical concentration stratification may lead to inefficient remediation of light non-aqueous phase liquids (LNAPLs). To investigate the vertical stratification characteristics of PS in porous aquifers and its impact on LNAPLs remediation, static water column experiments and flowing water sand tank experiments were conducted. The migration behavior of PS under non-slow-release and slow-release conditions was compared, with Br− as a reference tracer and benzene, toluene, and xylene (BTX) as LNAPLs contaminants. Results showed that in static water columns, Br− exhibited weak vertical migration, short migration distance, and a low decay rate (0.009 d−1), consistent with a stable tracer. In contrast, PS showed strong vertical migration, with concentrations increasing with depth; under slow-release conditions, the concentration difference between the top and bottom of the column could reach two orders of magnitude. Br− migration was dominated by molecular diffusion (effective diffusion coefficient 2.2×10−9 m2·s−1), while PS migration was driven by both diffusion and density. Under slow-release conditions, the average PS decay rate was 0.072 d−1, slightly higher than the non-slow-release rate (0.059 d−1). In both column and sand tank experiments, BTX exhibited a distinct shallow-layer distribution, contrasting with PS. When the aquifer thickness is large, PS stratification limits its contact with LNAPLs contaminants, increasing remediation cost and difficulty. These findings provide theoretical reference for PS-based ISCO remediation of LNAPLs in porous aquifers.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202608006
Organic waste is a potential phosphorus reservoir, and understanding the dynamics of available phosphorus (AP) during its resource utilization is critical for efficient phosphorus recovery. Composting, a key route for organic waste valorization, involves complex transformations of phosphorus alongside organic matter degradation and humification. However, the long duration and high cost of composting experiments, coupled with multifactorial influences, hinder efficient elucidation of AP dynamics via conventional methods. This study compiled data from 33 publications, constructing a dataset of 647 samples. Data preprocessing included iterative imputation, one-hot encoding, and standardization. A stacking ensemble learning model was developed to predict AP generation during composting. The optimal ensemble comprised XGBoost and SVR as base learners and ElasticNet as the meta-learner, achieving R² values of 0.954 and 0.928 on training and test sets, respectively, with low overall error. SHAP analysis revealed that key factors influencing AP content, in descending order of importance, were feedstock type, bulking agent type, turning interval, pH, electrical conductivity (EC), and C/N ratio. Notably, livestock manure as feedstock and straw-based bulking agents contributed positively to AP predictions. Partial dependence plots indicated that lower pH and C/N ratios generally favored AP accumulation throughout composting. During the initial stage, higher moisture content and lower EC enhanced AP; in the thermophilic phase, higher temperatures corresponded to higher AP; and during cooling and maturation, maintaining moisture below 48% and C/N below 14, while extending composting beyond 43 days, promoted AP accumulation. This study demonstrates accurate AP prediction via stacking ensemble learning and identifies critical factors, offering support for optimizing phosphorus management in composting engineering.