SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4425-4
Flexible and weavable alternating-current electroluminescent (ACEL) fiber devices are pivotal for wearable displays and human-computer interfaces, yet their intrinsic lack of color tunability restricts high-density information interaction. This study presents a dynamically color-tunable electroluminescent fiber device with a coaxial winding structure that integrates multiple fiber electrodes emitting the three primary colors. Through simple voltage driving, the device achieves a color gamut covering 131.07% of the sRGB standard, enabling arbitrary full-color tunability, including standard white light with CIE coordinates of (0.31, 0.33). The emission peak is continuously tunable over a 161.7 nm range, a 4-fold enhancement compared to previously reported ACEL fibers. The coaxial winding architecture is compatible with large-scale fabrication, yielding hundred-meter-scale fiber devices with a luminance variation of only 2.76%. The electroluminescent performance remains stable under stringent industrial standards: 10,000 friction cycles, 20 accelerated washing cycles, and 10-day storage at 105 °C and −20 °C. Integration into a smart textile watchband demonstrates real-time heart rate visualization via progress color changes and gesture-controlled color switching, validating its potential as an effective human-computer interface.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4260-5
Lithium-sulfur batteries (LSBs) are recognized as a leading candidate for next-generation energy storage due to their high theoretical specific capacity (1675 mAh g⁻¹). However, the shuttle effect of lithium polysulfides (LiPSs) severely limits cycle life and energy efficiency. Here, we report a multi-interface engineering strategy employing a MnO₂-TiO₂@Ti₃C₂ MXene (MT@MX) heterojunction, synthesized via a facile redox reaction between MXene and KMnO₄, to modulate bidirectional polysulfide conversion. The 2D structure with high conductivity and abundant heterogeneous interfaces facilitates fast ion/electron transfer, reduces reaction energy barriers, and enhances adsorption via d-band center effects. The stepped built-in electric field (BIEF) in MT@MX lowers the migration energy barrier of LiPSs from catalytic MXene to TiO₂ and then to adsorptive MnO₂, enabling reversible migration across multi-interfaces. Optimized heterointerfaces synergistically integrate adsorption, diffusion, and catalytic conversion, yielding excellent cycling stability even at a high sulfur loading of 6.4 mg cm⁻². This work demonstrates that constructing heterojunctions with stepped BIEF offers a feasible approach to modulate interfacial diffusion and provides a new design strategy for high-performance LSB electrocatalysts.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3553-7
Gesture interaction has emerged as a highly effective interface for intelligent human-computer interaction, attributed to its intuitive interaction modality and multi-dimensional control capabilities. However, traditional gesture interaction devices often depend on predefined encoding rules, which substantially limit interaction efficiency and degrade user experience. This study introduces an innovative intelligent finger ring interaction system based on a triboelectric nanogenerator utilizing PDMS/SrTiO3 composite thin film (PS-TENG). The system maps freehand writing gestures directly to textual information input, thereby eliminating the need for complex gesture encoding schemes and offering a user-friendly, low-learning-curve input method. By integrating a deep learning model, the system achieves recognition accuracies of 98.21% for English letters, 96.87% for Arabic numerals, and 96.44% for Chinese characters. Furthermore, it supports secure and encrypted data transmission and enables wireless interaction for gaming control. These findings indicate that the intelligent finger ring interaction system possesses significant potential for practical applications in information input and wireless control.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3860-0
Drug detection is critical for public health and security, yet reversible and highly sensitive sensing materials remain scarce. This study presents a novel ionogel sensor material, poly(ethylene glycol) diacrylate (PEGDA)/1-butyl-3-methylimidazole tetrafluoroborate, for reproducible detection of N-methylphenylethylamine (MPEA), a structural analogue of methamphetamine. The ionogel is fabricated by immobilizing a flowable ionic liquid within a PEGDA network via UV curing, preserving ionic mobility for efficient conduction. Integrated on a flexible poly(ethylene naphthalate) substrate, the sensor exhibits over 72.6% transmittance in the visible spectrum, enabling concealed attachment. Utilizing non-covalent interactions, the sensor achieves reproducible MPEA detection at sub-ppb levels at room temperature, with a theoretical detection limit of 317 ppt. It demonstrates high selectivity and consistency. Ionic conductivity was confirmed via current-voltage tests and impedance spectroscopy, and the sensing mechanism was clarified. The device maintains reliable performance under bending, indicating suitability for dynamic environments. With Bluetooth integration for wireless data transmission, the sensor shows strong potential for practical, discreet drug monitoring in real-world applications.
The Chinese Journal of Process Engineering•2026•DOI: 10.12034/j.issn.1009-606X.225185
Sulfur hexafluoride (SF6), widely used as an insulating gas in high-voltage electrical equipment, possesses a global warming potential (GWP) 25,200 times that of CO2, necessitating efficient degradation technologies. This study employed computational fluid dynamics (CFD) to simulate the thermal catalytic degradation of SF6 in a fixed-bed reactor, integrating models for porous media, heat transfer, turbulence, and chemical kinetics. The simulations revealed significant radial non-uniformities in pressure, velocity, temperature, and species concentration distributions, with temperature identified as the dominant factor influencing degradation efficiency. Radial temperature gradients caused uneven reaction rates, with degradation rates near the wall substantially exceeding those at the central axis, thereby reducing overall SF6 conversion. To address this, structural optimizations were implemented, including reducing the reactor tube diameter and incorporating inert porous media with high thermal conductivity at both ends of the catalytic section. These modifications enhanced radial heat transfer, homogenized the temperature field, and improved the uniformity of reaction rates and species concentrations. Parametric studies on inlet gas velocity showed that both excessively low and high flow rates were detrimental: low velocities led to underutilization of the downstream catalyst and increased energy consumption, while high velocities deteriorated heat transfer and exacerbated radial temperature gradients. The optimal inlet velocity range was determined to be 0.4–0.8 m/s for a reactor tube inner diameter of 10 mm, balancing catalyst utilization, energy consumption, and degradation efficiency. This research provides data-driven guidance for the design and scale-up of SF6 catalytic degradation reactors.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3599-5
Layered transition metal tellurides (TMTs) are promising cathode materials for aqueous zinc ion batteries (AZIBs) due to their graphite-like layered structure and weak van der Waals interactions, which facilitate rapid ion transport. However, their holistic performance—specific capacity, rate capability, and cycling stability—remains insufficient for practical applications. Here, we report a straightforward NaBH4-assisted chemical etching method to introduce abundant Te vacancies on the surface of Bi2Te3 (denoted H-Bi2Te3). Experimental and theoretical analyses reveal that these Te vacancies refine the band structure, enhance electrical conductivity, and significantly reduce the diffusion barrier for Zn2+ ions. Additionally, the vacancies provide increased storage sites for Zn ions. Consequently, H-Bi2Te3 exhibits superior zinc storage performance: a high Zn2+ diffusion coefficient of 3.98×10−11 cm2 s−1, a specific capacity of 325 mAh g−1 at 0.1 A g−1, a rate capability of 217 mAh g−1 at 1 A g−1, and exceptional cycling stability with 70 mAh g−1 retained after 10,000 cycles at 1 A g−1. This work introduces a novel vacancy defect engineering strategy for TMT-based cathodes in AZIBs and expands the potential applications of vacancy-rich TMT materials.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3737-9
The radar stealth performance of weaponry is crucial to their battlefield survivability, jointly determined by the effective absorption bandwidth (EAB) and mechanical properties of microwave-absorbing materials (MAMs). However, conventional MAMs often suffer from narrow EAB and absorption coatings prone to detachment. Herein, inspired by the wing scales of butterfly, we develop a biomimetic concave basalt fiber-reinforced composite (BC-BFRC) that delivers both broadband absorption and superior mechanical performance. Remarkably, the BC-BFRC achieves an EAB (reflection loss < −10 dB) of 14.7 GHz (3.3–18 GHz), which is 26.7% higher than the conventional planar structure (planar BFRC) and covers 91.9% of the S–Ku band. It maintains stable broadband absorption across incidence angles of 0°–45° (reflection loss < −8 dB at 4–18 GHz) and is insensitive to the incident direction. In fact, the broadband absorption originates primarily from impedance gradient between the layers and energy capture induced by the biomimetic concave at bottom. Critically, the composite exhibits a flexural strength of 239.2 MPa, enabled by basalt fiber reinforcement. This work provides a novel biomimetic strategy and feasible pathway for realizing structure-function integration of MAMs, enabling advanced radar stealth and electromagnetic shielding applications.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202605016
BiOX (X=Cl, Br, I) photocatalytic materials were synthesized via a chemical precipitation method. Their structures and properties were characterized using scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, nitrogen adsorption-desorption, and ultraviolet-visible diffuse reflectance spectroscopy. Results showed that BiOBr exhibits a flower-like nanomicrosphere structure composed of nanosheets, providing a more three-dimensional morphology, larger specific surface area, and moderate light absorption range, resulting in superior visible light absorption. Consequently, BiOBr demonstrated the best photocatalytic degradation of NO under xenon lamp irradiation. The study further investigated the effects of light intensity, NO flow rate, and oxygen presence on the NO degradation performance of BiOBr. Optimal NO removal rate of 58% was achieved under conditions of a light source distance of 15 cm, NO flow rate of 15 mL/min, and in the presence of oxygen. The degradation rate constant for BiOBr was 11×10⁻⁴ min⁻¹, significantly higher than that of BiOCl and BiOI. BiOBr also exhibited good reusability and stability. These findings provide an important experimental basis for the application of BiOBr in the photocatalytic degradation of NO.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3814-2
Micro-structured surfaces have attracted increasing attention due to their great potential applications. However, it is still a challenge to continuously fabricate micro-structured surfaces based on thermoplastics by a facile, low-cost, and environmentally-friendly method. Herein, with the help of the extrusion molding method and an elaborately designed mold, micro-grooved fiber (MGF) based on high-density polyethylene (HDPE) is continuously prepared. Theoretically, infinitely long MGFs with feature sizes down to a few microns can be efficiently fabricated because of the continuous fabrication characteristic of the melt extrusion method. Interestingly, left- and right-handed micro-grooves with different helix angles can be produced by applying twisting at the die exit, and the macroscopically MGF springs can be further fabricated via a self-designed three-dimensional helical enwind device. By regulating wettability, MGF can achieve liquid self-transport on predefined paths. In addition, MGF fabric exhibits rapid evaporation behavior, whose evaporation rate is about 4 times higher than that of the Smooth fiber (SMF) fabric and 2 times higher than that of the most popular commercial quick-drying fabric (i.e., Cool-max fabric). This work proposes a facile and environmentally-friendly method for continuously preparing low-cost and flexible MGF, opening a new pathway to develop fiber-based microfluidic systems following the concept of "functionalized processing for thermoplastics".
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3986-2
Organic/molecular ferroelectrics exhibiting spontaneous polarization have attracted increasing attention due to their flexibility, light weight, low-temperature processability, environmental friendliness, and biocompatibility. Among them, organic donor-acceptor cocrystals, self-assembled from two or more components, offer new insights into ferroelectricity. This review systematically examines recent progress in organic donor-acceptor cocrystal ferroelectrics, focusing on microscopic origins of ferroelectricity, structure modulation strategies, and underlying mechanisms. Ferroelectric origin mechanisms, including intermolecular charge transfer, proton transfer, and order-disorder transitions, are analyzed in detail. Structure-property relationships in crystal engineering are summarized, and recent advances in theoretical simulations, experimental characterization techniques, and practical applications are introduced. Finally, current challenges and future research perspectives are outlined. The review highlights that weak intermolecular interactions often lead to low Curie temperatures (Tc), limiting practical applications. Strategies to enhance Tc involve introducing stronger molecular interactions to increase transition energy barriers. Notably, room-temperature ferroelectricity in organic cocrystals has been achieved, as demonstrated by Wiscons et al. (Angew Chem Int Ed, 2018, 57: 9044–9047). The review underscores the potential of organic cocrystal ferroelectrics for flexible and wearable electronics, while addressing the need for higher Tc and robust switching performance.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3944-9
Hard carbon (HC) is a promising anode material for sodium-ion batteries (SIBs) but suffers from low initial Coulombic efficiency (ICE) and unstable solid electrolyte interphase (SEI). Here, we report a dual-functional strategy combining surface engineering and solution chemical pre-sodiation. A graphitic carbon coating on HC acts as a conductive buffer network and shields surface defects, while sodium biphenyl (Na-Bp) pre-sodiation drives sodium ions into the material via a potential difference, inducing a pre-SEI layer that matures into a thin, dense, NaF-rich inorganic SEI during cycling. This approach compensates for irreversible sodium loss and enhances cycling stability. The pre-sodiated electrode (pCH4-HC) achieves an ICE of 99.5% and a reversible capacity of 321.7 mAh g−1, compared to 54.2% for untreated HC. Long-term cycling shows 74.0% capacity retention after 1000 cycles at 300 mA g−1. In full-cells with NaNi1/3Fe1/3Mn1/3O2 (NFM) cathode, pCH4-HC||NFM delivers 81.9 mAh g−1 after 100 cycles, demonstrating excellent stability and rate performance. This dual-strategy approach validates the adaptability of pre-sodiation technology for high-performance SIBs.
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.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(26)60645-7
Volatile organic compounds (VOCs) from diverse sources severely impact atmospheric environment and human health. Manganese (Mn)-based catalysts, with exceptional structural diversity and abundant redox versatility, are widely used in catalytic combustion of VOCs. This review summarizes the catalytic performance of various Mn-based catalysts, emphasizing preparation strategies for high-performance materials and systematically analyzing how active site construction influences VOC combustion. Catalytic oxidation mechanisms are expounded in detail. Key aspects include MnOx polymorphs, doping with alkali metals (e.g., K+), transition metal composites (Co, Cu), and noble metal loading (Pt, Pd, Au). Performance metrics such as T90 values, oxygen vacancy concentrations, and specific surface areas are discussed. The review provides insights into deactivation mechanisms and anti-poisoning strategies, offering practical guidance for VOC pollution remediation.
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/s40843-025-4116-0
The design of solid electrolyte interphases (SEIs) for poly(vinylidene fluoride)-based solid-state batteries has largely focused on solvent-affinity of Li+ to generate robust but ionically sluggish LiF-rich layers, inherently compromising transport kinetics. Here, we establish a paradigm based on quantifiable physicochemical descriptors (ionic potential and donor number) to guide the design of amphitropic ion pairs (AIPs). These AIPs are engineered to simultaneously tailor both the solvent-affinity and anion-affinity of Li+: a solvent-philic cation with high ionic potential (Al3+) first sequesters reactive solvents, clearing the path for a high-donor-number, lithium-philic anion (NO3−) to remodel solvation. This rationally guided, sequential mechanism enables the in situ synthesis of a LiF/Li3N heterostructured SEI, where dendrite-suppressing LiF domains are seamlessly integrated with ultra-fast Li3N ion channels. This design heterogeneity effectively enhances stability and kinetics, yielding a robust and highly conductive interface. Consequently, Li|Li cells achieve >2000 h of stable cycling, and Li|LiNi0.8Co0.1Mn0.1O2 full cells surpass 600 cycles.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4145-0
Conductive fibers face a fundamental trade-off between high electrical conductivity and substantial mechanical stretchability, which critically undermines their reliability under extreme or dynamic mechanical conditions. To overcome this challenge, we report a bio-inspired, hierarchically structured conductive fiber engineered by mimicking the parallel-fibril architecture and integrated matrix of skeletal muscle. This fiber is constructed from multiple parallel spandex yarns as the elastic core, a continuous liquid metal (LM) layer as the conductive pathway, and a composite waterborne polyurethane (WPU)/fluoropolymer (FP) sheath as the protective matrix. This unique architecture concurrently delivers exceptional stretchability (>3500%), high electrical conductivity (3.76 × 10^5 S m−1), and outstanding stability against water and mechanical abrasion. Leveraging its excellent conductivity and mechanical compliance, the fiber can be woven into textiles and function as a receiving coil for efficient wireless power transfer. Additionally, a twisted-pair capacitive strain sensor fabricated from this fiber demonstrates a broad, linear response up to 1000% strain. When integrated into garments, the sensor effectively monitors a wide range of physiological activities, from gross joint movements to subtle biological signals, including wrist pulse, vocal vibration, ballistocardiogram, and respiration. This work presents a conductive fiber that integrates high conductivity, ultra-stretchability, waterproofness, and long-term durability, offering a robust material platform and a scalable fabrication strategy for advancing all-weather health-monitoring systems, smart textiles, and next-generation wearable electronics.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4064-1
Bacterial infections and the accelerating rise of antimicrobial resistance (AMR) demand innovative antibacterial strategies beyond conventional antibiotics. Copper single-atom catalysts (Cu-SACs), featuring atomically dispersed active sites and tunable electronic structures, offer potent multimodal catalytic antibacterial functions. This review summarizes recent advances in the design, mechanisms and applications of Cu-SACs in antimicrobial technologies. We first outline four major synthesis routes: thermal activation, solvent-mediated strategies, energy-intensive methods and template-etching approaches, enabling high loading, stable anchoring and scalable, environmentally compatible production. We then dissect the multimodal antibacterial mechanisms of Cu-SACs: functioning as nanozymes to catalyze reactive oxygen species (ROS) generation; acting as photosensitizers to enable photocatalytic and photothermal bactericidal activity; and integrating these pathways with gas therapy, controlled ion release and immune modulation to construct multidimensional antimicrobial networks capable of eradicating drug-resistant bacteria and biofilms. We further discuss the substantial potential of Cu-SACs across three application domains: chemical-free, high-efficiency disinfection and real-time monitoring in water purification; durable self-disinfecting performance in antimicrobial textiles; and precision infection management in biomedical settings through integrated “bactericidal-anti-inflammatory-tissue-repair” therapeutic frameworks for both superficial and deep-tissue infections. Finally, we examine the challenges and future directions for the clinical translation and precise antimicrobial deployment of Cu-SACs, providing a conceptual foundation and practical guidance for advancing atomically engineered antibacterial materials from laboratory research to industrial applications.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4216-7
Flexible Cu2ZnSn(S,Se)4 (CZTSSe) solar cells are promising for lightweight and mechanically pliable photovoltaics, yet their performance is limited by severe non-radiative recombination and residual stress. Here, we report a sealed constant temperature (SCT) annealing strategy that simultaneously optimizes the CZTSSe/CdS heterojunction and alleviates stress. Under uniform mild thermal conditions (85°C, 5 h), SCT annealing promotes gradient diffusion of Cd2+ into the absorber, partially substituting Zn2+, which optimizes band alignment, passivates interface defects, and suppresses near-interface CuZn defects. This reduces open-circuit voltage loss and improves fill factor. The flexible device achieves a power conversion efficiency of 13.07%, a significant improvement over the reference (12.1%). The SCT strategy also enhances mechanical flexibility by reducing residual stress. Our findings provide a controllable route to advance both efficiency and flexibility of flexible CZTSSe solar cells.