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All Clean Energy & Battery Intelligence (Page 54)

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Published Research Papers

Showing 24 of 1398 peer-reviewed translated articles (Page 54 of 59)

Influence of Structural Isomerism in Multicomponent Covalent Organic Frameworks on Their Photocatalytic H2O2 ProductionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Influence of Structural Isomerism in Multicomponent Covalent Organic Frameworks on Their Photocatalytic H2O2 Production

Constitutional isomerism in covalent organic frameworks (COFs) has emerged as a powerful strategy to tailor material properties for photocatalytic applications. Here, we report the design and synthesis of two isomeric multicomponent COFs (MC-COFs) via Schiff-base condensation followed by Povarov reaction, converting imine linkages into quinoline structures. These isomeric MC-COFs exhibit opposing C=N bond orientations and distinct phenyl group alignments within the COF pores, leading to different torsion angles in the COF layers. Structural analyses reveal that enhanced planarity promotes π-π stacking and electron delocalization, resulting in favorable band structures and reduced exciton binding energies. Consequently, the optimized COF achieves a superior hydrogen peroxide (H2O2) production rate of 3128 μmol g−1 h−1 under visible light irradiation. This work underscores the critical influence of structural isomerism on the photocatalytic efficiency of MC-COFs and provides insights for rational design of high-performance COF-based photocatalysts.

Read Full Abstract10.1007/s40843-025-3998-8
Cryogenic Tribological Breakthroughs in Medium-Entropy Alloy Composites via Regulated Partial RecrystallizationGraphical AbstractVerified
SCIENCE CHINA Materials2026

Cryogenic Tribological Breakthroughs in Medium-Entropy Alloy Composites via Regulated Partial Recrystallization

The pursuit of advanced wear-resistant materials for cryogenic applications is often hindered by a fundamental trade-off between enhancing strength and damage tolerance. CoCrNi-based medium-entropy alloys (MEAs), while excellent in cryogenic toughness, suffer from this very limitation. Although second-phase reinforcement boosts strength, the strain incompatibility between phases inevitably triggers cracking, which is severely exacerbated at low temperatures. This work introduces a novel microstructural design strategy based on regulated partial recrystallization to overcome this long-standing challenge. By tailoring the thermomechanical processing of a (CoCrNi)90Mo10 MEA, we engineered a unique architecture where a fully recrystallized FCC phase is homogeneously embedded within a continuous skeleton of a hard, non-recrystallized σ phase. The alloy with this optimized microstructure achieved a remarkably low wear rate at 113 K that is less than half of its as-cast and fully recrystallized counterparts. The experimental and modeling results indicate the underlying synergy: the σ skeleton provides robust structural support and distributes stress deeply, while the recrystallized FCC phase, with its high density of grain boundaries and annealing twins, acts as a compliant strain-accommodating medium, effectively suppressing interfacial cracking. This combined 'skeleton effect' and 'recrystallization effect' not only delivers exceptional cryogenic wear resistance but also offers a practical strategy for designing high-performance, crack-resistant dual-phase composites for extreme environments.

Read Full Abstract10.1007/s40843-025-4018-6
Facile Construction of VS2@GNSs Composites with 1D/2D Hierarchical Structures for Efficient Electromagnetic Wave AbsorptionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Facile Construction of VS2@GNSs Composites with 1D/2D Hierarchical Structures for Efficient Electromagnetic Wave Absorption

The proliferation of electronic devices has exacerbated electromagnetic pollution, necessitating advanced electromagnetic wave (EMW) absorbing materials. In this study, VS2 nanorods were uniformly grafted onto graphene nanosheets (GNSs) via a facile ball milling method, constructing 1D/2D hierarchical VS2@GNSs composites with superior EMW absorption properties. The minimal reflection loss (RLmin) reached -49.83 dB at a thickness of 1.83 mm, while an ultra-broad effective absorption bandwidth (EAB) of 6.72 GHz was achieved at 1.96 mm. These performances are attributed to enhanced impedance matching and EMW attenuation capacities. Computer simulation technology (CST) full-wave simulations confirmed remarkable radar cross-section (RCS) suppression, with a reduction value of up to 20.38 dB m2 compared to a metallic substrate. This work provides theoretical and experimental guidance for designing high-performance stealth materials.

Read Full Abstract10.1007/s40843-025-4047-0
Kinetic separation of hydrogen isotopes over lignin-rich biomass-derived carbon molecular sievesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Kinetic separation of hydrogen isotopes over lignin-rich biomass-derived carbon molecular sieves

Deuterium (D2) is indispensable for isotope tracing, neutron scattering, and fusion reactions, yet its separation from hydrogen (H2) remains challenging due to their nearly identical physicochemical properties. Adsorptive separation exploiting the kinetic quantum sieving (KQS) effect at cryogenic temperatures offers a promising route, but demands precise pore engineering. Here, we report a biomass-derived carbon molecular sieve that permits rapid D2 transport while imposing a significant diffusion barrier for H2, enabling effective separation from D2/H2 mixtures. The molecular sieving micropores are generated by transforming cellulose components into slit-type carbon micropores, with lignin acting as a pore-size modifier. At 77 K, the diffusion rate of D2 is 1.8 times that of H2, leading to a D2 concentration in the recovered gas approximately 10% higher than that achieved with conventional microporous carbons. Aspen adsorption simulations demonstrate that D2 can be enriched to 90.1% from a 1.0% D2/H2 mixture within 12 successive cycles following a two-bed cryogenic pressure swing adsorption process. These findings advance the development of effective adsorbents for kinetic D2/H2 separation, offering a sustainable, low-cost route to deuterium enrichment.

Read Full Abstract10.1007/s40843-025-4059-3
A Knittable, Muscle-Fiber-Inspired Fiber with Ultra-Stretchability, Waterproof Property and High Conductivity for Wireless Power and Wide-Range SensingGraphical AbstractVerified
SCIENCE CHINA Materials2026

A Knittable, Muscle-Fiber-Inspired Fiber with Ultra-Stretchability, Waterproof Property and High Conductivity for Wireless Power and Wide-Range Sensing

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.

Read Full Abstract10.1007/s40843-025-4145-0
Constructing porous magnetic Ni@C-anchored carbon foams for excellent magnetic-dielectric synergy to develop integrated microwave absorbers with efficient thermal insulation and antibacterial propertiesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Constructing porous magnetic Ni@C-anchored carbon foams for excellent magnetic-dielectric synergy to develop integrated microwave absorbers with efficient thermal insulation and antibacterial properties

The escalating electromagnetic (EM) pollution necessitates the development of high-performance microwave absorbers (MAs) with integrated functionalities. However, it is still a difficult problem to integrate more related high performances into the designed MAs. Herein, a sustainable strategy was reported for fabricating three-dimensional (3D) porous magnetic Ni@C-anchored carbon foams (Ni@C/CFs) with abundant heterointerfaces and magnetic Ni@C nanoparticles using 3D porous chitosan foams and Ni-nitrilotriacetic acid chelate (Ni-NAC) as precursors. The modulation of carbonization temperature and concentration of Ni-NAC solution contributed to the tunable carbon graphitization, Ni crystallinity and magnetic Ni@C nanoparticles loading, which effectively improved their EM properties and EM wave absorption performances (EMWAPs). The optimized 3D porous magnetic Ni@C/CFs not only exhibited exceptional EMWAPs with a minimum reflection loss (RL min) of −27.58 dB and an ultra-wide effective absorption bandwidth (EAB) of 7.20 GHz, but also presented efficient thermal insulation and strong antibacterial activity (>95% inhibition against E. coli), which mainly originated from their excellent magnetic-dielectric synergies and unique 3D hierarchical porous structures. Consequently, this work delivers a coherent design strategy for next-generation multifunctional absorbers with potential applications in EM protection, thermal management, and adaptive stealth technologies.

Read Full Abstract10.1007/s40843-025-4003-7
Realizing Broad-Range Thermoelectric Performance in PbS through Distorting Rock-Salt LatticeGraphical AbstractVerified
SCIENCE CHINA Materials2026

Realizing Broad-Range Thermoelectric Performance in PbS through Distorting Rock-Salt Lattice

Lattice distortion via entropy engineering can significantly optimize thermoelectric performance by intensifying phonon scattering. However, excessive lattice distortion in high-entropy materials inevitably hinders carrier transport, limiting the wide-temperature average ZT (ZTave). To enhance the wide-temperature thermoelectric performance of low-cost PbS-based compounds, this work introduces moderate lattice distortion by controlling entropy around 1.0R (R is the gas constant) to balance phonon and carrier transport, alleviating restrictions on carrier mobility. Substantial Se and Te alloying in PbS induces rock-salt lattice distortion, effectively impeding phonon propagation, thus suppressing lattice thermal conductivity (κlat) from 2.41 W m−1 K−1 in PbS to 0.66 W m−1 K−1 in PbS0.5Se0.35Te0.15 at 300 K. Additionally, Cu interstitials are introduced into the lattice-distorted PbS0.5Se0.35Te0.15 to further optimize carrier density and weighted carrier mobility (μW), leading to significant improvement in μW/κlat parameter at 300–773 K. Finally, a room-temperature ZT of 0.53 and a maximum ZT of 1.44 are obtained in PbS0.5Se0.35Te0.15-1%Cu sample, contributing to an impressive ZTave of 1.08 at 300–773 K and a maximum power generation efficiency (ηmax) of 7.5%. The results outperform previously reported cost-effective PbS-based compounds and highlight the importance of lattice distortion regulation in enhancing wide-temperature thermoelectric performance.

Read Full Abstract10.1007/s40843-025-4017-y
Room-Temperature Sensitive Electromechanical Magnetization Reversal with Modulation Capability Approaching 100%Graphical AbstractVerified
SCIENCE CHINA Materials2026

Room-Temperature Sensitive Electromechanical Magnetization Reversal with Modulation Capability Approaching 100%

Developing efficient strategies for electrically manipulating two-dimensional magnetism at room temperature is a key challenge in contemporary spintronics. In this study, we demonstrate giant electromechanical control over the magnetism of the room-temperature van der Waals ferromagnet Fe3GaTe2 by integrating it with the ferroelectric α-In2Se3. Modest gate voltages lead to an almost complete suppression of the coercive field by 96.5%, corresponding to a remarkable peak modulation sensitivity of ~8.1 mT V−1, which stands out among existing van der Waals magnetoelectric systems. Importantly, this substantial magnetoelectric response is predominantly unaffected by voltage polarity, as both positive and negative gate voltages induce similar magnetic modulation effects. To elucidate the underlying mechanism, we tracked the voltage-induced Raman spectral changes, revealing a peak shift of 1.7 cm−1 that accurately represents an effective in-plane tensile strain of ~1.42% under an equivalent bias, demonstrating polarity independence as well. The synchronized magnetic response and strain variation unequivocally indicate that the induced tensile strain serves as the fundamental physical driver behind the magnetic modulation. Additionally, density functional theory calculations corroborate that the reduction in magnetic anisotropy induced by tensile strain results in a decrease in the coercive field. Our work establishes a novel and efficient approach for achieving voltage control of magnetism at room temperature in van der Waals multiferroic heterostructures, highlighting their significant potential for applications in ultra-low-power magnetic logic and sensing technologies.

Read Full Abstract10.1007/s40843-025-4144-y
Construction of an acid-tolerant cationic COF by Zincke reaction for efficient recovery of gold from e-waste via anion exchange and chemical reductionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Construction of an acid-tolerant cationic COF by Zincke reaction for efficient recovery of gold from e-waste via anion exchange and chemical reduction

Recovering gold from electronic waste (e-waste) is critical for sustainable resource management, yet conventional adsorbents suffer from poor acid stability and slow kinetics. Here, we report an acid-resistant cationic covalent organic framework (COF), TAPT-TNV, synthesized via irreversible Zincke reaction. TAPT-TNV exhibits exceptional stability in concentrated acids, retaining crystallinity and porosity after exposure to 12 M HCl and 6 M HNO3. The cationic skeleton, balanced by Cl− counterions, enables rapid and selective capture of AuCl4− through anion exchange, complemented by chemical reduction at triazine units. Adsorption kinetics are fast, reaching equilibrium within 30 minutes, with a maximum capacity of 1835.5 mg g−1 at pH 1. In real e-waste leachate, TAPT-TNV achieves a gold recovery rate of 99.42%, demonstrating high selectivity over competing metal ions. This work introduces a robust COF platform for precious metal recovery, addressing the limitations of hydrolytically unstable frameworks.

Read Full Abstract10.1007/s40843-026-4282-y
Covalent Organic Frameworks Functionalized with Thioether or Vinyl Groups for Efficient and Rapid Capture of Multiple Iodine PollutantsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Covalent Organic Frameworks Functionalized with Thioether or Vinyl Groups for Efficient and Rapid Capture of Multiple Iodine Pollutants

Efficient sequestration of radioactive iodine species (I2, CH3I, I3−) is vital for nuclear safety and environmental protection. However, developing multifunctional adsorbents that remain effective under diverse conditions remains a significant challenge. Herein, we report two functionalized PD-COFs (PD-WS and PD-WY) with moderate crystallinity, outstanding thermal stability, and robust chemical resistance. They exhibit superior adsorption performance in both gas and liquid phases. Specifically, at 75°C, PD-WY achieves capacities of 4.88 g g−1 for I2, 1.55 g g−1 for CH3I, and 5.55 g g−1 for the I2/CH3I mixture, while high capacities are also retained at room temperature. In solution, PD-WY adsorbs up to 3.56 g g−1 of I3− in water and 2.00 g g−1 of iodine in cyclohexane. These COFs display rapid kinetics (K80% = 3.25 g g−1 h−1 for I2 and 7.89 g g−1 h−1 for I3−) and excellent selectivity. Mechanistic studies indicated that the excellent iodine affinity of PD-COFs arises from their rich electronic structures, abundant active sites, and charge transfer interactions. These findings position PD-COFs as highly promising adsorbents for nuclear waste treatment and environmental remediation.

Read Full Abstract10.1007/s40843-025-4044-3
Ni5.75SnTe5 as a Reliable Contact Layer for SnTe-Based Thermoelectric DevicesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Ni5.75SnTe5 as a Reliable Contact Layer for SnTe-Based Thermoelectric Devices

SnTe-based thermoelectric materials have demonstrated significant improvements in performance and are considered a promising, less-toxic alternative to PbTe. However, a substantial gap persists between experimental device efficiencies and those predicted from material performance metrics, primarily due to extra resistance in the contact layers. To fully realize the potential of SnTe thermoelectrics at the device level, it is critical to develop contact layers that ensure strong interfacial bonding, high thermal stability, and low electrical contact resistance. Although Ni is the most commonly used contact material for SnTe devices, it exhibits significant interdiffusion with SnTe, which can degrade interfacial integrity and ultimately lead to long-term device failure. Here, a reliable contact layer for SnTe through thermodynamic analysis of the SnTe-Ni3Te2 phase diagram is identified, Ni5.75SnTe5 selected as a promising candidate. A single-leg thermoelectric device based on Sn0.96Bi0.04Te0.98Se0.02 with Ni5.75SnTe5 as a contact layer is fabricated, achieving a contact resistivity of approximately 3.7 μΩ cm2. This contact layer selection strategy shows great promise for application to other thermoelectric materials.

Read Full Abstract10.1007/s40843-025-3972-9
Unveiling strength-ductility synergy in eutectic high-entropy alloys via directional solidificationGraphical AbstractVerified
SCIENCE CHINA Materials2026

Unveiling strength-ductility synergy in eutectic high-entropy alloys via directional solidification

Eutectic high-entropy alloys (EHEAs) combine multi-principal-element compositions with regular lamellar microstructures, offering exceptional high-temperature stability and mechanical properties. However, conventional casting yields random solidification microstructures and inhomogeneous phase distributions, constraining strength-ductility synergy. This study employs directional solidification (DS) on Al19Fe20Co20Ni41 EHEA to achieve precise microstructural control, constructing a multi-level lamellar architecture with a herringbone-like alternating arrangement. This tailored microstructure refines interlamellar spacing, eliminates detrimental isolated B2 phases, and promotes slip continuity at interfaces, enhancing coordinated dislocation motion and uniform distribution across multiple slip systems. Consequently, the DS EHEA exhibits superior mechanical properties compared to most reported thermomechanically processed and directionally solidified HEAs. Micro-mechanistic analysis reveals that homogenized geometrically necessary dislocation (GND) density, interface-assisted crack deflection, and multi-stage strain-hardening from sequential dislocation activation collectively contribute to outstanding strength-ductility synergy. This work demonstrates that programming solidification paths enables design of unique multi-level lamellar architectures, serving as intrinsic microstructural composites that optimize dislocation management and crack propagation, offering a novel paradigm for developing ultra-robust EHEAs for extreme service environments.

Read Full Abstract10.1007/s40843-025-4068-2
Tetralactam Macrocycle-Based Polymers for Efficient and Rapid Adsorption of Radioactive IodineGraphical AbstractVerified
SCIENCE CHINA Materials2026

Tetralactam Macrocycle-Based Polymers for Efficient and Rapid Adsorption of Radioactive Iodine

The release of radioactive iodine from nuclear accidents and nuclear medicine poses significant environmental and health risks. Here, we report the design and synthesis of two cross-linked macrocycle-based porous organic polymers (P1 and P2) with different functionalities for efficient and rapid capture of radioactive iodine. P1 achieves complete iodine adsorption within 5 minutes, with an exceptional adsorption rate constant (k_obs) of 18.92 g g−1 min−1 (8.24 g g−1 min−1 for P2), representing a record-high iodine removal rate among state-of-the-art porous organic polymers. P1 demonstrates superior iodine adsorption efficacy in dynamic flow-through experiments, achieving a remarkable efficiency of 96.4% for radioactive 131I removal, greatly minimizing radiation contamination. Experimental and modelling techniques reveal that the superior iodine adsorption performance originates from electron-rich functional groups, hydrophobic surface, and porous structure of P1, thus exhibiting remarkable iodine capture capabilities through charge transfer, halogen bonding, and hydrophobic effects. The adsorbents show excellent stability and performance under complex and harsh conditions (pH 2–10) and can be easily regenerated, confirming their excellent reusability and potential for practical applications.

Read Full Abstract10.1007/s40843-025-4045-x
All-Optically Controlled Positive and Negative Photoresponses for Artificial Visual Adaptation and ProtectionGraphical AbstractVerified
SCIENCE CHINA Materials2026

All-Optically Controlled Positive and Negative Photoresponses for Artificial Visual Adaptation and Protection

In the era of artificial intelligence, efficient perception and processing of massive visual information demand advanced machine vision systems. Inspired by human visual adaptation, various optoelectronic devices have been developed, yet most rely on external gate voltages or complex circuits for dynamic sensitivity modulation. This work demonstrates an all-optically controlled biomimetic sensor based on a one-dimensional ZnO/MAPbBr3 heterojunction, achieving both positive and negative photoconductivity effects. By modulating oxygen vacancy states with ultraviolet light, the competition between intrinsic photoconduction and trap-mediated carrier capture is regulated, enabling dynamic control of visible-light photoresponse within a single device. This tunable behavior mimics scotopic adaptation (photopigment regeneration under weak illumination), photopic adaptation (photopigment bleaching in bright environments), and eyelid-like self-protection against intense light. The device operates without external gate bias or cascaded circuits, offering a promising strategy for next-generation intelligent biomimetic sensors in machine vision.

Read Full Abstract10.1007/s40843-025-4030-y
Biomimetic Visual Perception System Based on InAlZnO Optoelectronic Neuromorphic Array for Static Image Processing and Dynamic Trajectory PerceptionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Biomimetic Visual Perception System Based on InAlZnO Optoelectronic Neuromorphic Array for Static Image Processing and Dynamic Trajectory Perception

Vision is a vital means for humans to perceive the environment, with 80% of information from visual perception. Developing visual systems approaching or surpassing human-level vision plays an indispensable role in advancing autonomous driving, intelligent security, and other fields. Optoelectronic neuromorphic devices, integrating sensing and memory, are promising for emulating human vision. This study constructs a biomimetic visual system based on a 16 × 16 InAlZnO optoelectronic neuromorphic array with oxygen vacancy gradients. Under multi-factor modulation (oxygen vacancy concentration differences, Ag ions, heterojunction interfaces), the device achieves electrical/optical conductance tunability. Integrated with external circuits and a field-programmable gate array, the system successfully emulates human vision capabilities: image memory, denoising, attention mechanism, and motion state perception (direction, speed, color). Image digit recognition based on visual attention reaches 97.15% accuracy, and motion state recognition reaches 100%. This system will promote bionic vision development and application, paving the way for high-performance neuromorphic vision systems surpassing the human eye.

Read Full Abstract10.1007/s40843-025-4019-1
An Event-Driven Sensor Based on Colloidal Quantum Dots for Contactless Human-Machine InteractionGraphical AbstractVerified
SCIENCE CHINA Materials2026

An Event-Driven Sensor Based on Colloidal Quantum Dots for Contactless Human-Machine Interaction

Contactless human-machine interaction (HMI) is rapidly evolving, yet it remains constrained by the latency, redundancy, and power consumption inherent in conventional frame-based vision sensors. While bio-inspired event-driven sensors offer a low-power alternative, existing architectures are often complex or fail to accurately encode the magnitude of light intensity changes. Herein, we report a solution-processed, two-terminal event-driven sensory device based on CuIn(Se,S)2 colloidal quantum dots (QDs) integrated with an Sb-doped TiO2 layer. Unlike traditional dynamic vision sensors (DVS), this device exhibits a transient photoresponse that encodes both the polarity and the magnitude of light intensity variations into the output current amplitude. This preservation of magnitude information significantly enhances the feature extraction capability, leading to faster convergence and superior clustering performance in gesture recognition. Based on these unique optoelectronic properties, we constructed a hierarchical HMI system that synergizes the strengths of event-based and frame-based sensing. The system utilizes the event-driven sensor for low-latency gesture control of an unmanned aerial vehicle (UAV) and a frame-based sensor for high-precision gaze control of an unmanned ground vehicle (UGV). The proposed system achieves a gesture recognition accuracy of more than 92.5% while substantially reducing data redundancy, offering a promising strategy for efficient, robust, and low-cost intelligent interaction systems.

Read Full Abstract10.1007/s40843-025-3997-9
Bio-inspired synergistic interfacial anchoring for highly stable graphite lubricantsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Bio-inspired synergistic interfacial anchoring for highly stable graphite lubricants

Graphite lubricants are critical for high-quality and high-efficiency drawing of refractory metal wires, yet inadequate dispersion stability frequently challenges their practical application. Inspired by the bio-surfactant synergic mechanism that combines different bio-surfactants to collectively reduce surface energy and friction, a binary anionic surfactant system comprising sodium dodecyl benzene sulfonate (SDBS) and sodium lignosulfonate (SL) was engineered to enhance dispersion and stability via a synergistic effect. The synergistic parameter β was calculated to be −2.34, indicating strong synergism. The resulting graphite lubricants maintained homogeneous dispersion for up to 60 days. Molecular dynamics (MD) simulations combined with density functional theory (DFT) calculations confirmed that the synergistic effects originate from steric hindrance, electrostatic repulsion, π-π stacking, and hydrogen bonding. These hierarchical secondary interactions collectively increased the interfacial formation energy at the graphite/surfactant/water tri-phase interface, thereby effectively wetting particle powders and enhancing stability. During metal wire drawing, the graphite lubricants reduced the friction coefficient between the die and metal wires to 0.06, ultimately enabling drawn tungsten wires with superior surface integrity, expanded loop diameter, and enhanced tensile strength relative to single-surfactant benchmarks. This study provides experimental and theoretical guidance to design effective graphite lubricants for high-quality drawn metal wires.

Read Full Abstract10.1007/s40843-025-4051-x
Developing flexible BaTiO3-based ceramic memristors through entropy engineeringGraphical AbstractVerified
SCIENCE CHINA Materials2026

Developing flexible BaTiO3-based ceramic memristors through entropy engineering

Flexible memristors are pivotal for advancing neuromorphic computing in wearable electronics, yet the intrinsic brittleness of inorganic oxides poses a critical challenge. Here, we employ an entropy-engineering strategy to control the amorphization of oxide compositions, yielding a precisely controlled crystalline/amorphous microstructure in a BaTi0.25Sn0.25Hf0.25Zr0.25O3 thin film. This film withstands bending angles up to 180°, enabling an Au/BaTi0.25Sn0.25Hf0.25Zr0.25O3/ITO/Mica device that functions as a memristor. Entropy engineering increases oxygen vacancy concentration, imparting stable resistive switching behavior under both flat and bent conditions. The device exhibits exceptional endurance and reproducibility over multiple bending cycles, demonstrating a significant strategy for advancing flexible memristor technologies and holding promise for next-generation high-performance flexible electronics.

Read Full Abstract10.1007/s40843-025-4077-0
Heterojunction-Enhanced Photodynamic Uterine Scaffold Mediated by Upconversion for Treating Infectious InjuriesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Heterojunction-Enhanced Photodynamic Uterine Scaffold Mediated by Upconversion for Treating Infectious Injuries

Bacterial infection following endometrial injury delays tissue regeneration and may progress to endometritis and other reproductive disorders. Photodynamic therapy (PDT) offers a promising antibacterial strategy in the post-antibiotic era, yet its efficacy is often limited by rapid recombination of photogenerated charge carriers and poor penetration of visible excitation light. Here, we report a previously unexplored upconversion-mediated, Type I dominant photodynamic antibacterial uterine scaffold specifically designed for infection-associated endometrial injury. The core innovation is the construction of a Schottky Ag0-Ag2S heterojunction on NaYF4:Yb,Tm nanoparticles using ZIF-8 as a sacrificial precursor, enabling efficient charge separation and oxygen-independent hydroxyl radical generation, overcoming the oxygen dependence of conventional Type II PDT under hypoxic uterine conditions. The upconversion core permits deep-tissue-penetrable near-infrared (NIR) activation. Beyond instantaneous PDT, dynamic release of Ag+ ions provides synergistic bactericidal activity, enabling spatiotemporally coordinated biofilm disruption. These nanostructures were incorporated into patient-customizable, biodegradable poly(L-lactic acid) (PLLA) scaffolds fabricated by selective laser sintering, achieving simultaneous antibacterial therapy and endometrial regeneration in a single platform. This integration of an oxygen-independent PDT mechanism, MOF-templated heterojunction engineering, and 3D printed personalized uterine implants constitutes a comprehensive therapeutic strategy not previously reported for treating infection and endometrial injury.

Read Full Abstract10.1007/s40843-025-4058-4
Electrospray Self-Healing Porous Polymer Microspheres for Multimode Imaging and Combined Photothermal/Chemodynamic Therapy of Nasopharyngeal CarcinomaGraphical AbstractVerified
SCIENCE CHINA Materials2026

Electrospray Self-Healing Porous Polymer Microspheres for Multimode Imaging and Combined Photothermal/Chemodynamic Therapy of Nasopharyngeal Carcinoma

Nasopharyngeal carcinoma (NPC) poses a therapeutic challenge due to its anatomical complexity and the limitations of conventional treatments in achieving precise targeting and sufficient efficacy. Here, we report a multifunctional platform based on heat-triggered electrospray self-healing porous poly(lactic-co-glycolic acid) (PLGA) microspheres encapsulating indocyanine green (ICG), sequentially coated with a tannic acid-Fe3+ (TAF) metal-phenolic network and fibronectin (FN) for targeted photothermal/chemodynamic combination therapy. The resulting functional microspheres (PI-TAF@FN) exhibit an average size of 1.9 μm, excellent colloidal stability, heat-induced self-healing performance, and a high photothermal conversion efficiency of 51.4%. These microspheres specifically target NPC cells via FN-mediated integrin recognition, enabling ICG/TAF-mediated photothermal therapy under 808-nm laser irradiation and TAF-mediated chemodynamic therapy, leading to enhanced cancer cell apoptosis in vitro. In a mouse NPC model, the combined photothermo-chemodynamic therapy achieved effective tumor treatment with minimal systemic toxicity. Furthermore, the dual TAF and ICG components allow multimode FN-targeted T1-weighted magnetic resonance/fluorescence/thermal imaging for precision NPC management. This electrospray self-healing porous microsphere platform offers a unique theranostic strategy that can integrate diverse therapeutic and diagnostic components for precision oncology.

Read Full Abstract10.1007/s40843-025-4037-1
A Layered Ferrous Silicate for Ion-Exchange-Driven Chemodynamic TherapyGraphical AbstractVerified
SCIENCE CHINA Materials2026

A Layered Ferrous Silicate for Ion-Exchange-Driven Chemodynamic Therapy

Nanoparticle-based therapeutics have been intensively explored for tumor treatment. However, developing convenient and specific strategies that do not rely on exogenous energy-guided activation remains challenging. Herein, an ion-exchange-driven chemodynamic therapy is proposed based on the TME K+-mediated cation exchangeability of layered ferrous silicates (LFSs). LFSs were prepared by a facile "in situ 3D-to-2D structural transformation" strategy through valence bond transition from SiO–H–OSi to Fe–O, providing extensive convenience compared to conventional exfoliation methods. The structure-activity relationship and mechanism between surrounding TME ions and the cation exchange behavior of LFSs were revealed by both experimental investigation of the cation-exchange process and DFT calculations of the adsorption hydration behavior. As a result, the interlayered Fe ions were selectively and preferentially exchanged by TME K+ rather than surrounding TME Na+, Mg2+, Ca2+, or Cl−, thereafter activating specific Fenton reaction together with TME H+, H2O2, and glutathione, demonstrating highly precise catalytic therapeutic efficacy both in vitro and in vivo. This study proposes an original tumor-specific therapy modality with high precision and safety through taking advantage of ionic exchangeability of layered silicate, and provides enlightenment to reverse the TME K+ disorder.

Read Full Abstract10.1007/s40843-025-4056-1
Dark-Current-Suppressed Semimetal-Based ZrTe3/CuInP2Se6 Heterostructure Photodetector for Information Encryption and DecryptionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Dark-Current-Suppressed Semimetal-Based ZrTe3/CuInP2Se6 Heterostructure Photodetector for Information Encryption and Decryption

Photodetectors are critical components in modern optoelectronic systems, underpinning applications in optical communication, low-altitude economy, environmental monitoring, and national defense. Layered two-dimensional (2D) materials such as MoS2, WS2, black phosphorus (BP), and ReS2 have attracted extensive attention due to their remarkable electronic and optical properties, including facile mechanical exfoliation and tunable characteristics via thickness engineering. The absence of dangling bonds enables the construction of van der Waals (vdW) heterostructures free from lattice-matching constraints, promoting efficient charge transport, enhanced light absorption, and suppressed dark current. Among layered materials, semimetals such as graphene, PdTe2, MoTe2, and TaIrTe4 exhibit narrow or zero bandgaps, enabling ultrabroadband spectral responses from ultraviolet (UV) to terahertz (THz). ZrTe3, a layered gapless semimetal, demonstrates pronounced carrier transport features, including robust excitons and ultrafast carrier relaxation times, making it an ideal candidate for photodetection. However, pure ZrTe3-based photodetectors suffer from substantial dark current due to the absence of an energy bandgap, degrading signal-to-noise ratio and specific detectivity (D*). This work reports a high-performance broadband photodetector based on a ZrTe3/CuInP2Se6 heterostructure. By exploiting an asymmetric contact configuration that introduces a Schottky barrier, the device effectively suppresses dark current while enhancing photoresponse. The photodetector exhibits broad spectral sensitivity from UV to near-infrared (355–1177 nm), microsecond-level response speed, and high responsivity and specific detectivity. Beyond conventional photodetection, an optoelectronic information encryption-decryption application is demonstrated, where modulated light and bias voltage serve as dual input channels to encode and decode ASCII signals. This study resolves the challenge of high dark current in semimetal-based photodetectors and introduces a multifunctional platform for secure optoelectronic communication, highlighting the potential of ZrTe3 for next-generation photonic and quantum information technologies.

Read Full Abstract10.1007/s40843-025-4033-1
Multifunctional mitochondria-targeting energy disruptor for enhancing imaging-guided low-temperature photothermal therapy of melanomaGraphical AbstractVerified
SCIENCE CHINA Materials2026

Multifunctional mitochondria-targeting energy disruptor for enhancing imaging-guided low-temperature photothermal therapy of melanoma

The evolution of precision medicine has propelled multimodal imaging-guided phototheranostics to the forefront for precise tumor diagnosis and therapy. Low-temperature photothermal therapy (PTT) offers a promising approach for the treatment of melanoma due to its non-invasiveness and minimal damage to normal tissues. However, its efficacy is limited by cancer cell thermal tolerance. To address this, a new type of multifunctional energy disruptor (CAMeO-Q NPs) is developed featuring homologous targeting and mitochondria targeting, and synergistically enhancing low-temperature PTT in melanoma by reversing heat shock protein 90 (Hsp90)-mediated thermal tolerance and blocking mitochondrial adenosine triphosphate (ATP) biosynthesis. The multifunctional energy disruptor enables precise trimodal imaging (fluorescence imaging/FLI, photoacoustic imaging/PAI, and photothermal imaging/PTI) guidance for low-temperature PTT. Comprising a mitochondria-targeting photothermal agent and an Hsp90 inhibitor, CAMeO-Q NPs induce selective mitochondrial damage under 660 nm laser irradiation and downregulate cellular HSP expression by ATP inhibition and Hsp90 inhibitor. This multifunctional energy disruptor provides a novel strategy for enhancing multimodal imaging-guided low-temperature photothermal therapy through combined homologous targeting, mitochondria-targeting, and Hsp90 inhibition.

Read Full Abstract10.1007/s40843-025-4081-y
A covalent tumor-targeted theranostic system for NIR imaging-guided photodynamic-ferroptosis synergistic therapy of lung cancerGraphical AbstractVerified
SCIENCE CHINA Materials2026

A covalent tumor-targeted theranostic system for NIR imaging-guided photodynamic-ferroptosis synergistic therapy of lung cancer

Lung cancer, particularly non-small cell lung cancer (NSCLC), remains a leading cause of cancer-related mortality, with conventional therapies hampered by poor tumor specificity, low drug accumulation, and suboptimal efficacy. To address these challenges, we rationally designed a tumor-targeted, ferrocene-bearing, covalently immobilizable theranostic probe, dIR-CDF, for near-infrared (NIR) imaging-guided photodynamic-ferroptosis synergistic therapy. The probe exploits the overexpression of sulfenated proteins in the tumor microenvironment to specifically target integrin αvβ3-positive NSCLC cells and undergo covalent anchoring via the reaction between 1,3-cyclohexanedione and sulfenic acid, thereby enhancing tumor accumulation and retention. Under 808 nm irradiation, dIR-CDF generates singlet oxygen (1O2) for photodynamic therapy (PDT), while the sustained release of ferrocene catalyzes Fenton reactions to produce hydroxyl radicals (·OH), inducing ferroptosis. The synergistic action of PDT and ferroptosis amplifies lipid peroxidation and disrupts antioxidant defenses, leading to efficient suppression of NSCLC tumors in living mice. This work presents a universal and powerful theranostic platform for precise cancer diagnosis and treatment, with the covalent targeting strategy offering enhanced specificity and retention.

Read Full Abstract10.1007/s40843-025-4008-2