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/s40843-025-3582-9
Perovskite quantum dots (PQDs) hold great potential for brain-like neuromorphic computing. However, the development of PQDs-based synaptic devices is hindered by interfacial defects and limited stability. Here, we demonstrate a high-performance Cs2AgBiBr6 QDs/organic single crystal heterojunction synaptic device, fabricated via a novel space-confined vertical growth technique combined with a polymer-free transfer process. Vertically grown organic single crystals enable superior carrier mobility and facilitate the formation of low-defect interfaces with PQDs. The heterojunction exhibits remarkable photosensitivity (7.22 × 10^5 at 425 nm) and detectivity (2.15 × 10^15 Jones), owing to the strong optical absorption of PQDs coupled with the superior charge transport characteristics of organic single crystals. Notably, the device achieves dual-functional light adaptation, emulating synaptic behaviour under blue light while exhibiting photo-switching under green/red light. This unique capability enables smart blue-light hazard protection. This work not only provides a versatile platform for high-performance PQDs-based synaptic devices but also advances the development of brain-inspired neuromorphic systems for next-generation computing and intelligent sensing.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3805-1
The sluggish kinetics of oxygen reduction and evolution reactions (ORR/OER) at the air electrode impede the practical deployment of fiber zinc-air batteries (FZABs) for wearable electronics. Conventional bifunctional catalysts suffer from an inherent activity trade-off due to the distinct mechanisms of ORR and OER. Here, we propose a spatial decoupling strategy to overcome this limitation by engineering isolated Fe single atoms and Fe–Ir dual-atom pairs on a nitrogen-doped carbon matrix (Fe/FeIr-NC). In this architecture, Fe single atoms serve as ORR centers, while Fe–Ir pairs with tunable spacing are tailored for OER, enabling complete functional separation and independent optimization. The catalyst exhibits an ORR half-wave potential of 0.91 V and an OER overpotential of 250 mV at 10 mA cm−2, yielding a record-low bifunctional gap (ΔE = 0.57 V) that outperforms all reported single- and dual-atom catalysts. A flexible fiber zinc-air battery based on this catalyst delivers a peak power density of 3920 W kg−1, along with a 1.4-fold increase in energy efficiency and a 2.6-fold extension in cycle life compared to the commercial Pt/C + IrO2 benchmark. This work not only breaks the traditional activity trade-off in bifunctional catalysis but also offers a promising route toward high-performance power sources for wearable electronics.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202605001
The lower reaches of the Yangtze River Basin, as a concentrated area of China's C5 petroleum resin industry, face critical bottlenecks in green and low-carbon transformation due to high-pollution, refractory wastewater and high carbon emissions. Traditional petrochemical wastewater treatment technologies suffer from low efficiency, high energy consumption, and insufficient resource utilization. This paper systematically analyzes the sources of wastewater in C5 petroleum resin production from principles and processes, and reviews research progress and carbon reduction potential of current technologies in three aspects: new materials, new equipment, and new processes. Integrated processes centered on efficient pretreatment, biological enhancement, and multi-technology coupling show significant advantages in improving treatment efficiency, reducing energy consumption and cost, and strengthening resource recovery. The study also prospects future research priorities for pollution and carbon mitigation through green technological innovation and intelligent upgrading, providing new solutions for 'near-zero discharge' and resource recycling of C5 petroleum resin wastewater, thereby promoting the green and low-carbon transformation of the petrochemical industry.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3786-8
Conventional cancer diagnostic techniques, such as tissue sampling and microscopy, are invasive and prone to misdiagnosis, driving the need for non-invasive, precise alternatives. Chiral biophotonics, exploiting circularly polarized light (CPL), offers unique polarization-selective interactions with biological tissues, enabling higher imaging contrast and molecular-level discrimination. However, current CPL detection technologies are passive and single-mode, lacking dynamic tunability and parallel processing capabilities. Meanwhile, AI-assisted diagnostics rely on separated sensing and computing units, suffering from poor integration and transmission inefficiency. Here, we report a near-infrared (NIR) chiral organic synaptic photodiode with electrically tunable dual-mode operation, enabling simultaneous CPL detection and neuromorphic processing. Under negative bias, the device operates as a highly sensitive CPL detector for chiroptical signal acquisition. Under positive bias, it exhibits history-dependent synaptic behavior with photocurrent dissymmetry factor (g_ph) dynamically tunable up to -0.06. By integrating this device into an optical convolutional neural network (OCNN), we achieved intelligent cancer detection with CPL-based imaging. Experimental results demonstrate that CPL detection accuracy reaches 83%, approaching the theoretical 87%, significantly outperforming natural light detection at 65%. The device enhances image contrast and feature extraction, laying a foundation for intelligent, adaptive diagnostic systems.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3863-x
Lead-free double perovskites are promising for optoelectronic applications due to their tunable optical properties, stability, and non-toxicity. However, achieving efficient ultrabroadband near-infrared (NIR) emission and X-ray radioluminescence (RL) simultaneously remains challenging. Here, we report a Mo4+-doped Cs2(Na0.4Ag0.6)InCl6 double perovskite that exhibits efficient blue-light-excitable NIR emission with a near-unity photoluminescence quantum yield. The emitter demonstrates robust thermal stability, retaining 84% of its initial emission intensity at 420 K relative to 300 K. Under X-ray irradiation, the material shows bright NIR RL with a high light yield of 39,400 ± 1100 photons/MeV. A flexible film of Mo4+-doped Cs2(Na0.4Ag0.6)InCl6/polydimethylsiloxane (PDMS) was fabricated and applied as an NIR light source and X-ray scintillator. A dual-functional platform for cooperative NIR and X-ray imaging was established using a bullfrog palm as the target, achieving pixel-level fusion of NIR and X-ray images without spatial mismatch or complex image processing. The fused image simultaneously visualizes blood vessels and skeleton textures under the skin tissue. This work provides a viable strategy for lead-free double perovskites in advanced optoelectronic devices, particularly for multispectral imaging.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3943-y
Biodegradable polymers are promising for bioelectronic materials, yet simultaneously improving their mechanical, electrical, and optical performance remains a major challenge. Poly(3-hydroxybutyrate-co-4-hydroxyvalerate) (P34HB), a microbially synthesized polyhydroxyalkanoate (PHA), exhibits excellent biocompatibility and degradability but suffers from poor chain length control, limiting its functional performance. Here, we report a low-temperature, non-destructive supercritical ethyl alcohol-assisted polymerization (SEAP) strategy to enhance P34HB at the molecular level. Operating at 40 °C and 1500 psi, SEAP combines the permeability of supercritical CO2 with ethanol-mediated catalysis to promote in situ dehydration polymerization and efficiently remove impurities. Post-treatment, P34HB exhibits a 16% increase in number-average molecular weight, along with a record-high Young's modulus of 51.08 GPa and a 144% increase in elongation at break, overcoming the conventional trade-off between stiffness and ductility. Optical performance is also improved, with transmittance rising by 44% and refractive index increasing to 1.2. Material analyses confirm a higher ester group density and reduction of residual impurities. Electrical insulation is notably enhanced, with leakage current reduced by 50% to below 1 pA and reduced dielectric loss to 0.06. Cytotoxicity assays further verify excellent biocompatibility. This work establishes SEAP as a sustainable strategy for functionalizing P34HB, enabling its deployment in next-generation bioelectronics and flexible electronics.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4107-x
Aqueous fiber zinc-iodine batteries (FZIBs) with four-electron redox exhibit inherent safety and high energy density for wearable electronics. Nevertheless, their practical implementations are hindered by unsatisfactory cycling stability and low realistic energy density, mainly caused by severe H2O-induced nucleophilic attack toward iodine species and poor zinc anode reversibility. Here, we report a quaternary ammonium-mediated coordination strategy to simultaneously address the irreversible cathode/anode redox behavior and thus promote the electrochemical performance of four-electron FZIBs. The cationic choline ion (Ch+) induces complexation with ICl2− via electrostatic interaction, homogenizing the electron cloud density and suppressing irreversible hydrolysis of I+ species, enabling a reversible near-theoretical high capacity of 418.3 mAh g−1. Meanwhile, preferentially adsorbed Ch+ on the zinc anode surface creates positively charged shielding layers, mitigating the tip effect caused by localized electric field and achieving robust zinc stripping/plating. The enhanced cathode/anode reversibility and improved interfacial stability enable stable FZIBs operation for over 20,000 cycles at 20.0 A g−1. Moreover, successful integration of FZIBs into electronic textiles with glucose and cardiac rhythm sensors demonstrates great potential for next-generation wearable electronics.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202512059
Recovery of palladium from Pd-bearing wastewater is economically and environmentally significant. Adsorption is a promising method due to its simplicity, low cost, and high efficiency. In this study, a novel thiol-modified adsorbent (CHT-SH) was synthesized via one-step functionalization of inexpensive chitin (CHT) with thioglycolic acid. At room temperature and pH=2, CHT-SH exhibited an experimental adsorption capacity of 223.67 mg·g−1 for Pd(II), which was approximately 7 times higher than that of pristine CHT (30.6 mg·g−1). Kinetic and isotherm studies indicated that the adsorption process followed the pseudo-second-order kinetic model and the Langmuir isotherm model, with a maximum theoretical adsorption capacity of 248.89 mg·g−1, suggesting monolayer chemisorption. Characterization (FTIR, SEM, XPS, XRD) and density functional theory (DFT) calculations revealed that the adsorption mechanism primarily involved synergistic coordination of nitrogen and sulfur atoms, along with electrostatic interactions. Furthermore, CHT-SH demonstrated good reusability, retaining stable adsorption capacity after five adsorption-desorption cycles. Compared to other adsorbents that rely on redox mechanisms and are costly, CHT-SH offers comprehensive advantages. This work provides a cost-effective and efficient adsorbent for Pd(II) recovery from wastewater, offering technical support and theoretical reference for practical applications.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4036-4
Alkaline water electrolysis is a pivotal technology for large-scale green hydrogen production, yet its efficiency is constrained by sluggish hydrogen evolution reaction (HER) kinetics at industrial current densities. Here, we propose a synergistic dual-doping strategy to lower kinetic barriers for both Volmer and Heyrovsky steps. A robust amorphous NiCoV nanosheet electrode was synthesized via scalable one-step electrodeposition. In situ spectroscopic and kinetic characterizations reveal that hydrophilic V species optimize interfacial water by disrupting the hydrogen bond network, ensuring rapid supply of free water at the inner Helmholtz plane. Co dopants modulate electronic structure to facilitate electron transfer and optimize intermediate adsorption energetics. The NiCoV electrode requires an ultralow overpotential of 253 mV at -400 mA cm−2, surpassing most Pt-based catalysts, and maintains stability for over 200 h. Industrial validation in a scaled-up electrolyzer demonstrates a cell voltage of 1.89 V at 400 mA cm−2, achieving energy savings of 0.12 kWh m−3 H2 compared to commercial benchmarks. This translates to annual electricity savings of 1.33 × 10^6 kWh for a medium-scale demonstration project, highlighting immense potential for sustainable industrial applications.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(26)60684-6
Tungsten trioxide (WO3) is a transition metal oxide of significant interest in heterogeneous catalysis due to its environmental friendliness, cost-effectiveness, and favorable electrical properties. The catalytic performance of WO3 is strongly dependent on its exposed crystal facets, which exhibit distinct physicochemical properties including charge separation efficiency, reactant adsorption capacity, and redox activity. These differences arise from variations in atomic arrangement, electronic structure, and surface energy. This review systematically examines the facet effect of WO3 across photocatalysis, electrocatalysis, photoelectrocatalysis, and thermal catalysis. Theoretical calculations are integrated to elucidate the intrinsic mechanisms underlying facet-dependent behavior from an atomic structure perspective. The paper synthesizes general rules governing the WO3 facet effect across these applications, critically assesses current research limitations, and outlines future directions. Key findings highlight that facet engineering enables precise tuning of catalytic activity and selectivity, with specific facets such as {001}, {110}, and {010} demonstrating enhanced performance in various reactions. The review underscores the importance of morphology control in optimizing WO3-based catalysts and identifies challenges in achieving facet-selective synthesis and stability under operational conditions. Future research should focus on advanced characterization techniques and computational modeling to further unravel facet-dependent mechanisms and guide rational catalyst design.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4147-9
Fiber-shaped zinc-air batteries (FZABs) with aqueous electrolytes combine intrinsic safety, high energy density (1086 Wh kg−1), and environmental compatibility, making them attractive for wearable applications. However, free water in the electrolyte induces severe anode degradation while being a critical reactant for cathode redox, presenting a dilemma between anode stability and cathode functionality. The semi-open structure of FZABs allows airborne water to permeate and migrate to the anode, causing interfacial instability, while high surface area accelerates solvent evaporation, leading to increased internal resistance and salt crystallization. Consequently, typical cycle life is limited to <50 h. To overcome these challenges, we report a polymer electrolyte that captures atmospheric water as a solvent through the semi-open structure, achieved by introducing acetamide (AA), identified via unsupervised clustering algorithms, into the poly(vinylidene fluoride-hexafluoropropylene)/zinc trifluoromethanesulfonate (PVDF-HFP/Zn(OTf)2) system. AA incorporation preserves solvent-retention capability while reconstructing the Zn2+ coordination structure, promoting salt dissociation and polymer-segment mobility. Low adsorption energy of AA on zinc surfaces suppresses parasitic reactions from ambient moisture, and preferential adsorption across zinc crystal planes directs Zn2+ deposition along the (002) face, leading to uniform plating morphology. The exogenous aqueous polymer electrolyte exhibits superior mechanical properties, enabling stable output even after compression by a 1.7-t vehicle. As proof-of-concept, FZABs integrated with fiber solar cells and sensors in clothing enabled real-time health monitoring and sustainable energy utilization, demonstrating promising practical applications.