SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4351-8
Breaking intrinsic structural symmetry is a fundamental prerequisite for pronounced nonlinear optical responses. Low-symmetry semiconductors with inherent anisotropy enable self-powered optoelectronic conversion and polarization-sensitive functionalities. This work reports the synthesis of low-dimensional van der Waals chain TeSe2 crystals with intrinsic inversion and C3 symmetry breaking. Angle-resolved polarized Raman spectroscopy and second-harmonic generation measurements confirm crystalline anisotropy and nonlinear optical performance. Electrical transport studies reveal p-type conduction with a room-temperature field-effect mobility of 122 cm2 V-1 s-1. The TeSe2 photodetector achieves self-powered detection and linearly polarized light detection across 405–1064 nm, with a photoresponsivity of 77.3 mA/W at 532 nm. The linear photogalvanic effect response is effectively modulated by gate voltage. Density functional theory calculations attribute p-type doping to Te and Se vacancies, while the nonlinear optical origin is linked to strong Berry curvature. Applications in polarization encoding communication and polarization imaging are demonstrated, indicating potential for low-energy-consuming, highly sensitive, on-chip integrated linear polarized photodetectors.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4303-7
Sodium-ion batteries (SIBs) are promising for grid-scale storage and low-speed electric vehicles, yet their electrochemical behavior is governed by intricate mechanical-electrochemical coupling effects, rendering failure mechanisms not fully understood. Here, we develop an in-situ pressure-electrochemical monitoring system and reveal the failure mechanism of commercial Ah-level NaNi1/3Fe1/3Mn1/3O2//hard carbon (NNFMO//HC) sodium-ion pouch cells. Under an initial external pressure of 500 kPa, the full cell retains 90.07% of its capacity after 500 cycles at 0.5 C. Operating at the optimal pressure of 500 kPa effectively avoids heterogeneous sodium deposition in HC anodes, suppresses gas evolution from electrolyte decomposition, and prevents irreversible phase transitions in NNFMO cathodes during long-term cycling, thereby mitigating capacity degradation. Deviation from this optimal pressure leads to spatially non-uniform sodium deposition, accelerated electrolyte decomposition, and irreversible cathode phase transitions, collectively accelerating capacity fade. This work establishes a quantitative relationship between external pressure and pouch cell degradation, advancing SIBs development and application.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3637-6
Traditional optical fiber communication encryption methods lack sufficient dynamic adaptability and hardware flexibility, while reconfigurable logic gates can overcome this limitation, thereby significantly improving the flexibility of encryption systems. This study reports a reconfigurable optoelectronic logic gate (OELG) system based on hafnium-zirconium oxide (HZO) ferroelectric thin films. Through ultra-low temperature atomic layer deposition technique, the fabricated HZO thin films demonstrate an exceptional pyroelectric coefficient of 1835.91 μC m−2 K−1 and robust multi-level polarization stability, enabling efficient broadband photon-to-current conversion. By leveraging the pyroelectric effect and tunable polarization states, the OELG device achieves dynamic optical signal modulation and logic processing. The OELG device supports five fundamental logic operations (AND, OR, NAND, NOR, NOT) via electrical bias and polarization control, without requiring hardware modifications. The OELG device demonstrates stable performance over 10^9 cycles with no degradation, meeting practical application requirements. Furthermore, a convolutional neural network (CNN)-integrated image encryption-decryption framework was validated, achieving 95.01% recognition accuracy on decrypted data, while unauthorized decryption attempts resulted in significant feature loss. This study addresses security challenges in optical communication networks by proposing an innovative solution that integrates pyroelectric materials with reconfigurable logic gate technology, offering a new pathway to enhance physical-layer security.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2024110202
Anaerobic digestion (AD) is an environmentally friendly biochemical technology for waste treatment and renewable energy production, yet its methane conversion efficiency remains suboptimal. This study employed flux balance analysis (FBA) to determine the optimal temperature for methane production in AD, and subsequently regulated key flexible nodes in the metabolic pathway to maximize methane flux. At the optimal temperature of 40 °C, up-regulating the acetyl-CoA flexible node increased methane flux by 48.5%, while up-regulating the acetate node increased it by 36.6%. The higher improvement via acetyl-CoA regulation is attributed to the fact that 40 °C is unfavorable for hydrogen-producing acetogenic bacteria, making acetyl-CoA the critical control point. These findings demonstrate that flexible node regulation can overcome the limitations of temperature optimization alone. The FBA methodology provides a reliable, cost-effective approach for optimizing target product yields in AD and other fermentation systems, requiring only input and output measurements to resolve intermediate metabolic fluxes.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3819-7
Selective solar-driven aerobic oxidation of biomass derivatives into valuable chemicals under ambient conditions is pivotal for sustainable chemical manufacturing but faces challenges from the conflict between O2 activation kinetics and selective C–H bond cleavage. This work demonstrates a spatial decoupling strategy in a precisely-engineered 2D/2D g-C3N4/ZnIn2S4 architecture, where ZnIn2S4 domains selectively activate O2, while adjacent g-C3N4 modulates electron transfer to O2 and tailors 5-hydroxymethylfurfural (HMF) binding configuration for selective C–H bond cleavage. This enables efficient selective conversion of HMF to 2,5-diformylfuran (DFF) via ambient aerobic photooxidation. When used alone, ZnIn2S4 produces mixed reactive oxygen species (·O2−/·OH) due to uncontrolled electron transfer during O2 activation. In-situ spectroscopy, Kelvin probe force microscopy (KPFM) and density functional theory (DFT) calculations demonstrate that the 2D/2D heterojunction, driven by its directed electric field, selectively activates O2 into ·O2− at ZnIn2S4 domains while suppressing ·OH generation by moderate electron transfer, mitigating over-oxidation. Adjacent g-C3N4 domains precisely anchor HMF via –OH group interactions, steering selective DFF formation. This spatial decoupling achieves a remarkable HMF-to-DFF photo-conversion rate of 1517.5 μmol g−1 h−1 with 99.4% selectivity under ambient air, outperforming many reported state-of-the-art catalysts and maintaining durable cycling performance. The work establishes a spatial decoupling principle to overcome O2 activation kinetics and site competition thermodynamics, paving the way for advanced catalyst design for sustainable energy and the environment.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3933-9
The global cold chain consumes vast amounts of energy and emits greenhouse gases, while many regions lack proper refrigeration. To address this, we developed a dual-layer electrospun membrane (PZ-PML) for energy-free fruit preservation. The top PVDF-HFP/ZIF-8 layer offers 97.64% solar reflectance and 92.5% mid-infrared emissivity, providing 70 W/m2 radiative cooling. The bottom PAN/MIL-101/LiCl layer, with 2.18 g/g water uptake at 80% RH, delivers ~156 W/m2 evaporative cooling, lowering surface temperature by 6.1 °C under ~400 W/m2 irradiation. The membrane also shows ≥99% antibacterial efficiency against E. coli and S. aureus. Applied to strawberries, it reduced dehydration to 20.2% after 9 days, compared to 68.2% and 74.4% in controls. Additionally, it demonstrates durability, superhydrophobicity, and UV stability. This scalable solution offers energy-free fruit cooling, reducing postharvest losses while maintaining quality and safety.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202509095
Biotrickling filtration (BTF) is a promising technology for treating volatile organic compounds (VOCs), but its application to hydrophobic alkanes like isohexane is hindered by mass transfer limitations, low degradation efficiency, and high operational costs. To address these bottlenecks, this study developed composite fillers by incorporating biochars derived from coffee grounds (CG), coconut shells (CS), corn cobs (CC), and activated carbon (AC) into a polyvinyl alcohol-sodium alginate (PVA-SA) hydrogel matrix. The fillers were systematically characterized for water retention, pore structure, surface functional groups, crystalline phase, and acid-base resistance. Adsorption capacity, biofilm formation, and isohexane degradation were evaluated using the strain Rhodococcus ruber ZYH-ZY. Among the composites, CG@PVA-SA exhibited superior performance: water retention of 358 mg·g−1 (vs. 280 mg·g−1 for control), enhanced mesoporosity (specific surface area 4.77 m2·g−1, pore volume 11.46 cm3·kg−1, 10–30% higher than control), and robust acid-base stability (mass loss 21.37% at pH 2 and 31.98% at pH 10). Its saturated adsorption capacity reached 201.02 mg·kg−1 (vs. 114.24 mg·kg−1 for control), and it promoted bacterial colonization with a survival rate of 79.0% (vs. 37.2% for control). Static degradation tests showed 96.59% removal of 10 μL isohexane within 24 h. The abundant polar functional groups and suitable mesoporous structure of coffee ground biochar synergized with the PVA-SA matrix, enhancing water retention, mass transfer, and microbial colonization, thereby significantly improving isohexane purification. CG@PVA-SA is an ideal filler for BTF treatment of alkane VOCs, offering a cost-effective and efficient solution for industrial VOC control.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4098-8
Fluorescence image-guided photodynamic therapy (PDT) enables real-time monitoring of photosensitizer biodistribution and metabolism for optimized treatment timing. However, its application remains limited by reliance on high-end imaging systems. To address this, we designed three novel small-molecule photosensitizers (TTNb, TTAn, TTPh) based on a 2-vinylbenzoic acid scaffold, functionalized at the 5-position with nitro, amino, or hydrogen groups. Replacing the nitro group with amino or hydrogen switched aggregation behavior from aggregation-induced emission (AIE) to aggregation-caused quenching (ACQ), accompanied by a red-to-green fluorescence shift and subcellular relocation from liposomes to lysosomes. These findings establish design principles for ratiometric nitroreductase probes and enable systematic comparison between AIE and ACQ photosensitizers. Among these, TTAn exhibited superior cellular uptake (2800 times higher than Ce6 in Eca-109 cells), specific lysosomal targeting, balanced reactive oxygen species (singlet oxygen/superoxide anion) generation, and intense fluorescence. Under white light irradiation, TTAn achieved an IC50 of 21 nM, surpassing Ce6 by 50-fold. Notably, TTAn produced strong fluorescence in mice tumors under both one- and two-photon excitation, detectable using conventional imaging tools (smartphones, DSLR cameras) or even visible to the naked eye, confirming outstanding tumor specificity. Leveraging these advantages, TTAn enabled successful image-guided two-photon PDT in Eca-109 tumor-bearing mice with a single treatment, demonstrating potent therapeutic efficacy and biosafety. This work provides a strategic blueprint for developing small-molecule theranostic agents that operate without complex fluorescence imaging systems.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3348-1
Chemotherapy induces immunogenic cell death (ICD) but is compromised by elevated cholesterol in the tumor microenvironment (TME), which activates myeloid-derived suppressor cells (MDSCs) and exhausts CD8+ T cells. A poly(lactide-co-glycolide) (PLGA)-based nanoplatform (COD/MTO@PLGA@FA) co-loading mitoxantrone (MTO) and cholesterol oxidase (COD) was engineered to respond to acidic TME, releasing MTO and COD. MTO kills tumor cells and triggers ICD; COD consumes cholesterol, downregulating PD-1 on tumor-infiltrating CD8+ T cells and inhibiting MDSC activation. In 4T1 tumor-bearing mice, COD/MTO@PLGA@FA plus αPD-L1 increased splenic CD4+ and CD8+ T cells from 63.4% to 72.3% and 25.7% to 32.5%, respectively. CD8+PD-1+ T cells decreased to 5.93% versus 35.9% (PBS), 31.4% (αPD-L1), 29.0% (MTO@PLGA), 23.0% (COD/MTO@PLGA), and 12.2% (COD/MTO@PLGA@FA). MDSC infiltration dropped from 16.3% to 2.25% (combination) and 6.14% (COD/MTO@PLGA@FA alone). DC maturation in tumor-draining lymph nodes reached 35.3% with the combination. The platform reverses CD8+ T cell exhaustion and remodels the immunosuppressive TME, significantly inhibiting tumor growth. This strategy offers a practical approach to enhance chemo-immunotherapy by targeting cholesterol metabolism.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3392-8
Electroreduction-derived Cu-based two-dimensional materials are promising catalysts for CO2 conversion to C2+ products, yet the role of reconstructed interface structures remains ambiguous. We fabricate interface-engineered Cu nanosheets via in situ pre-electrolysis of kilogram-scale brochantite nanosheet precursors. Lead underpotential deposition and OH− electrosorption analysis confirm abundant Cu(100)/Cu(110) interfaces. In situ attenuated total reflection-surface enhanced infrared absorption spectroscopy reveals C–C coupling pathways involving hydrogenation of *CO to *CHO, followed by coupling to *COCHO. Operando Raman spectra demonstrate that these interfaces provide sufficient *CO surface coverage, facilitating deep coupling reactions. Density-functional-theory calculations indicate that Cu(100)/Cu(110) interfaces reduce the energy barrier of the rate-determining hydrogenation step by 0.16 eV and promote *CO and *CHO coupling. Consequently, the Cu nanosheets achieve a C2+ Faradaic efficiency of 80.4% at an industrial current density of 800 mA cm−2, surpassing most reported Cu-based catalysts. This work establishes a molecular-level understanding of interface engineering for CO2 electroreduction, leveraging scalable precursor synthesis and precise characterization.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3516-2
Iron-based mixed phosphates are considered promising cathode materials for sodium-ion batteries (SIBs) due to low cost, non-toxicity, and high structural stability. However, their electrochemical performance is limited by poor electronic conductivity and sluggish ion diffusion. This study presents Na4Fe3(PO4)2(P2O7) with porous coral-like S-doped carbon (NFPP-U0.5%) as cathode material for SIBs. The porous coral-like structure of the S-doped carbon layer, along with C–S–Fe interaction, significantly enhances electronic conductivity and sodium ion diffusion. NFPP-U0.5% delivers excellent rate performance, achieving 80.3 mAh g−1 at 20 C. In-situ X-ray diffraction analysis reveals that the C–S–Fe interaction, combined with the unique carbon structure, contributes to a small lattice volume change during cycling. NFPP-U0.5% reached an ultra-long cycling life with capacity retention of 82.66% after 25,000 cycles at 20 C. The outstanding electrochemical performances and unique interface interaction demonstrate that S-doped carbon coating NFPP is of high potential as a cathode material for low cost and long-lasting cyclability energy storage systems.