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All Clean Energy & Battery Intelligence (Page 11)

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Published Research Papers

Showing 24 of 1398 peer-reviewed translated articles (Page 11 of 59)

Computational-driven design of Ti-based medium entropy alloy for enhanced high-temperature performance above 600 °CGraphical AbstractVerified
SCIENCE CHINA Materials2026

Computational-driven design of Ti-based medium entropy alloy for enhanced high-temperature performance above 600 °C

The development of advanced titanium alloys capable of operating above 600 °C remains a critical challenge for aerospace propulsion systems, where conventional Ti alloys suffer from insufficient high-temperature strength and microstructural instability. Here, we propose a computationally driven design strategy for titanium-based medium-entropy alloys (MEAs) that integrates thermodynamic phase prediction with mechanistically informed strength modeling, enabling systematic exploration of the Ti-Nb-Al-Cr quaternary system. The optimized Ti70Nb10Al15Cr5 MEA exhibits exceptional performance metrics: 18% room-temperature ductility (as-cast), a yield strength of 520.7 MPa at 650 °C (post-aging), and an ultralow density of 4.76 g/cm3 (45% lighter than Inconel 718). Microstructural characterization reveals a metastable single-phase BCC structure in the as-cast state, which transforms into a BCC/Ti3Al dual-phase system upon aging, with temperature-dependent precipitate morphology and phase stability. The alloy demonstrates superior high-temperature strength retention up to 900 °C (>80 MPa yield strength), outperforming commercial titanium alloys (e.g., Ti-1100, TG6) and bridging the performance gap between conventional Ti alloys and nickel-based superalloys. This work establishes a multi-criteria design paradigm for entropy-engineered alloys, offering a viable pathway to lightweight, high-temperature structural materials for next-generation aerospace applications.

Read Full Abstract10.1007/s40843-025-3558-4
In-situ polymer-derived SiOCnws-Cf/SiC(rGO) composites: a potential candidate for EMI shielding and thermal managementGraphical AbstractVerified
SCIENCE CHINA Materials2026

In-situ polymer-derived SiOCnws-Cf/SiC(rGO) composites: a potential candidate for EMI shielding and thermal management

The rapid evolution of aerospace technology necessitates the development of multi-functional composites that combine light weight, mechanical robustness, thermal protection/insulation, and electromagnetic interference (EMI) shielding. C/SiC porous ceramic composites are promising for thermal protection in hypersonic vehicles. Here, we report a facile strategy to fabricate Cf/SiC composite polymer-derived ceramics (PDCs) via re-pyrolysis of high-energy ball-milled polycarbosilane-vinyltriethoxysilane-graphene oxide (PVG) with Cf/SiC(rGO)p blend interleaves. In-situ generated honeycomb-like cellular structures and non-directional channels reduce density and increase porosity. High-quality SiO2 joints, formed from Si-dangling bonds, strengthen interfacial bonding via a brazing effect, while in-situ SiOC nanowires (SiOCnws) create a hierarchically enhanced network, improving fracture toughness and crack resistance. Multi-scale interfacial/dipole polarization enhances EMI shielding. The optimized Cf(0.2)/SiC(rGO) composite exhibits low density (1.49 g cm−3), high fracture toughness (6.32 MPa m1/2), hardness (7.18 GPa), compressive strength (72.67 MPa), and EMI shielding effectiveness of 58.31 dB. It maintains structural stability under butane blowtorch ablation at ~1300 °C for 3600 s. Porous variants show thermal conductivity of 0.211 W m−1 K−1 with 69.74% porosity. These multi-functional composites are promising for thermal protection systems in aerospace applications.

Read Full Abstract10.1007/s40843-025-3588-2
Mechanisms for low temperature densification and enhanced mechanical properties of (Ti, Zr, Hf, Nb, Ta)(C, N) using CrSi2 as an additive: formation of (Ti, Zr, Nb)2Cr4Si5 and grain boundary strengtheningGraphical AbstractVerified
SCIENCE CHINA Materials2026

Mechanisms for low temperature densification and enhanced mechanical properties of (Ti, Zr, Hf, Nb, Ta)(C, N) using CrSi2 as an additive: formation of (Ti, Zr, Nb)2Cr4Si5 and grain boundary strengthening

High-entropy carbonitride ultra-high temperature ceramics (HECN-UHTCs) typically require high densification temperatures, leading to grain coarsening and degraded mechanical properties. This study introduces CrSi2 as a sintering additive for (Ti, Zr, Hf, Nb, Ta)(C, N), effectively reducing the densification temperature by 200 °C. During sintering, interdiffusion and cation exchange result in the formation of an orthorhombic (Ti, Zr, Nb)2Cr4Si5 phase within the ceramic matrix. The resulting dual-phase ceramic exhibits a hardness of 24.65 ± 0.23 GPa and a fracture toughness of 6.03 ± 0.48 MPa m1/2, significantly surpassing most reported HECN-UHTCs. Enhanced mechanical properties are attributed to crack deflection, increased localized lattice strain, and Cr grain boundary segregation. This liquid phase-assisted low-temperature sintering strategy offers a promising pathway for densifying other ultra-high temperature ceramics.

Read Full Abstract10.1007/s40843-025-3771-9
Metastructure Strategies for d33 Enhancement Beyond Intrinsic Limits in 3D-Printed BaTiO3 MetamaterialsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Metastructure Strategies for d33 Enhancement Beyond Intrinsic Limits in 3D-Printed BaTiO3 Metamaterials

High-sensitivity piezoelectric ceramics with high piezoelectric constants (d33) are crucial for miniaturized, low-power, and high-efficiency transducers. However, conventional performance enhancement relies on intrinsic parameter modulation, which is limited and blind. This study introduces a performance-driven metamaterials creation model to develop structure-function-integrated piezoelectric materials. We systematically investigated the effects of metastructure design on d33 across two-dimensional straight rod (SR) structures, three-dimensional dot-matrix (Octa) structures, complex triply periodic minimal surface (TPMS) structures, and hybrid Octa&SR structures. The results demonstrate that metastructures combining high polarization charge conversion efficiency with low compression modulus (stiffness) effectively enhance d33. The SR structure exhibited optimal polarization charge conversion, the Fks-Shellular (FksS) structure within TPMS showed low stiffness, and the Octa&SR structure combined both properties. Notably, all three structures displayed exceptional piezoelectric performance. Specifically, the FksS structure achieved a substantial d33 of 194 pC/N, a 24% enhancement over conventional solid BaTiO3, while maintaining isotropic and stress-insensitive properties. This work elucidates the mechanism for designing piezoelectric metastructures, offering a novel pathway for developing high-performance, high-failure-strength piezoelectric materials.

Read Full Abstract10.1007/s40843-025-3660-5
Molecularly engineered porphyrin photosensitizers featuring multi-anchoring and alkoxy modifications for robust photocatalytic hydrogen productionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Molecularly engineered porphyrin photosensitizers featuring multi-anchoring and alkoxy modifications for robust photocatalytic hydrogen production

A new generation of porphyrin-based photosensitizers (PoTA1–PoTA3) was developed for photocatalytic hydrogen evolution (PHE). Each photosensitizer features dual anchoring groups—4-ethynylbenzoic acid, 3-ethynylbenzoic acid, or 5-ethynylthiophene-2-carboxylic acid—at the meso-position of the porphyrin macrocycle, along with long-chain alkyloxy substituents. This dual-modification strategy suppresses charge recombination and reduces aggregation on TiO2 surfaces. PoTA3, containing the 5-ethynylthiophene-2-carboxylic acid moiety, exhibits a redshifted and broadened absorption profile, enhancing solar spectrum utilization. Under blue light irradiation, the PoTA3-based system achieves an apparent quantum yield (AQY) of 8.3%, an initial hydrogen evolution rate of 485 mmol g−1 h−1, and a turnover number (TON) of 27,858 in aqueous media, substantially outperforming PoTA1 and PoTA2. Under white light, PoTA1 and PoTA3 achieve AQY values of 5.5% and 6.8%, respectively, surpassing the benchmark YD2-o-C8 (AQY = 4.07%). The synergistic effects of enhanced light harvesting, minimized aggregation, and optimized HOMO/LUMO electron density distributions contribute to high efficiency and robust operational stability. These findings establish a flexible molecular engineering platform for next-generation solar-to-hydrogen conversion systems.

Read Full Abstract10.1007/s40843-025-3715-5
Enhancing interfacial bonding and compositional synergy in ANF-PPy/Ag-MXene/ANF-PPy multilayer heterostructures for efficient electromagnetic interference shielding and infrared thermal camouflageGraphical AbstractVerified
SCIENCE CHINA Materials2026

Enhancing interfacial bonding and compositional synergy in ANF-PPy/Ag-MXene/ANF-PPy multilayer heterostructures for efficient electromagnetic interference shielding and infrared thermal camouflage

The proliferation of electronic devices and wireless communications has escalated the demand for materials that simultaneously provide electromagnetic interference (EMI) shielding and infrared (IR) thermal camouflage, a combination critical for military and civilian applications. Traditional metallic shields suffer from high density, poor processability, and cost, while polymer-based alternatives often lack sufficient shielding effectiveness and environmental stability. Here, we report a multilayer composite film fabricated via layer-by-layer vacuum filtration and hot-pressing, integrating modified aramid nanofibers (ANF) and MXene (Ti3C2Tx) nanosheets. The film architecture comprises ANF-polypyrrole (ANF-PPy) as the matrix and Ag-MXene as the functional filler, with in-situ grown Ag nanoparticles intercalating between MXene layers to enhance interlayer spacing and electromagnetic wave scattering. At a thickness of only 33 μm, the film achieves an average EMI shielding effectiveness (SE) of 66.75 dB and a specific shielding effectiveness (SSE/t) of 38432.54 dB cm2 g−1. The multilayer structure promotes multiple internal reflections and interfacial polarization losses, while the tight integration ensures high IR reflectivity. This work establishes a foundation for developing multifunctional protective materials with dual EMI shielding and IR camouflage capabilities, addressing the critical bottleneck of simultaneous performance in ultrathin, flexible formats.

Read Full Abstract10.1007/s40843-025-3664-x
Centrifugal casting-enabled highly oriented MXene-based layered films with dual-shielding against electromagnetic wave and infrared radiationGraphical AbstractVerified
SCIENCE CHINA Materials2026

Centrifugal casting-enabled highly oriented MXene-based layered films with dual-shielding against electromagnetic wave and infrared radiation

MXene-based layered films are promising for electromagnetic interference (EMI) shielding, yet achieving highly ordered structures in scalable production remains challenging. Here, we report a facile centrifugal casting method for fabricating MXene/polyvinyl alcohol (MXene/PVA) films with highly oriented and compact layered structures. During centrifugal casting, the viscous fluid experiences strong shear and centrifugal forces along tangential and normal directions, respectively, inducing compact and oriented arrangement of MXene nanosheets. Consequently, the Herman's orientation factor increases from 0.681 to 0.794 as rotation rate rises from 0 to 4000 r/min. Accordingly, tensile strength and toughness improve from 55.2 to 191.1 MPa and from ~0.8 to 2.5 MJ/m³, respectively. The highly oriented and compact layered structure with ultrathin thickness (~8 μm) enables a high absolute electromagnetic shielding effectiveness (SSE/t) of 21029 dB cm²/g. Moreover, increased orientation reduces infrared emissivity to 0.248, endowing the film with excellent thermal camouflage capability. This work presents an effective strategy for constructing high-performance MXene-based layered films.

Read Full Abstract10.1007/s40843-025-3539-5
Three birds with one stone: dual-interfaces and bulk co-passivation enable >21% efficiency of CsPbI3 solar cells with VOC of 1.27 VGraphical AbstractVerified
SCIENCE CHINA Materials2026

Three birds with one stone: dual-interfaces and bulk co-passivation enable >21% efficiency of CsPbI3 solar cells with VOC of 1.27 V

Inorganic perovskite solar cells (IPSCs) have attracted significant attention due to their excellent light and thermal stability and potential in tandem applications. However, their efficiency and stability are often limited by residual lattice stress and defects at interfaces and within the bulk, causing severe nonradiative recombination. Here, we introduce a zero-dimensional supramolecular complex, (ETP)2SbCl5, as a dual-interface and bulk modifier to regulate CsPbI3 film growth. The modifier exhibits spatial segregation: ETP+ cations anchor at the buried interface, passivating defects on TiO2 and perovskite surfaces; Sb3+ and Cl− ions diffuse into the bulk during annealing, relieving residual stress; and Cl− accumulates on the top surface, passivating cation defects. Consequently, the modified CsPbI3 solar cell achieves a power conversion efficiency (PCE) of 21.71% and an open-circuit voltage (VOC) of 1.27 V, retaining 97.4% of initial efficiency after 500 h of maximum power point (MPP) tracking. This work demonstrates a synergistic strategy to simultaneously address interfacial and bulk defects, advancing high-performance and stable inorganic photovoltaics.

Read Full Abstract10.1007/s40843-025-3547-7
Enhancing NiOx Hole Transport Properties through Planarity Modulation of Organic Small Molecules for Inverted Perovskite Solar CellsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Enhancing NiOx Hole Transport Properties through Planarity Modulation of Organic Small Molecules for Inverted Perovskite Solar Cells

Nickel oxide (NiOx) is widely used as a hole transport material in inverted perovskite solar cells (PSCs). However, its practical application is limited by low intrinsic conductivity and insufficient hole extraction ability, leading to significant interfacial defects that reduce device efficiency and stability. To overcome these issues, two isomeric small organic molecules, 2,6-NOT and 1,5-NOT, were developed and introduced to modify NiOx. These isomers share the same structure but differ in the substitution positions of functional groups, resulting in distinct molecular planarity. Experimental results demonstrate that 1,5-NOT, featuring extended conjugation and enhanced planarity, more effectively enhances the hole extraction/transport capabilities and conductivity of NiOx compared to 2,6-NOT. The NiOx/1,5-NOT-based device achieves a remarkable power conversion efficiency (PCE) of 24.20%, along with excellent long-term stability, surpassing the NiOx control device (18.12%) and the 2,6-NOT-based device (21.87%). These findings indicate that modifying NiOx with small organic molecules significantly improves charge transport performance, and increasing molecular planarity is particularly beneficial for enhancing hole transport and reducing defect density, thereby increasing both efficiency and stability. This work provides a new strategy for NiOx modification via small organic molecules, offering a promising route to high-performance inverted PSCs.

Read Full Abstract10.1007/s40843-025-3605-0
Pyromellitic diimide-mediated bulk passivation for efficient perovskite solar cells with low energy lossGraphical AbstractVerified
SCIENCE CHINA Materials2026

Pyromellitic diimide-mediated bulk passivation for efficient perovskite solar cells with low energy loss

Perovskite solar cells (PerSCs) have achieved remarkable efficiencies, yet their performance is limited by defect states and non-radiative recombination. Here, pyromellitic diimide (PD) is introduced as an additive to passivate bulk defects in perovskite films. PD forms hydrogen bonds with formamidinium (FA+) ions and coordinates with Pb2+ ions, effectively suppressing non-radiative recombination and reducing energy loss. The PD-treated perovskite films exhibit enhanced crystallinity and uniformity. Consequently, 1.55 eV PerSCs achieve a high open-circuit voltage (VOC) of 1.193 V and a power conversion efficiency (PCE) of 25.79%. Moreover, unencapsulated PD-treated devices retain 96% of their initial efficiency after 2000 h under nitrogen atmosphere, whereas control devices retain only 74%. Under ISOS-D-2I accelerated aging (65±5°C in N2), PD-treated devices show less than 5% PCE attenuation after 288 h, compared to ~30% for controls. This work provides a viable strategy for defect passivation in perovskite solar cells, enhancing both efficiency and stability.

Read Full Abstract10.1007/s40843-025-3676-3
High-efficiency hybrid planar/bulk heterojunction organic solar cellsGraphical AbstractVerified
SCIENCE CHINA Materials2026

High-efficiency hybrid planar/bulk heterojunction organic solar cells

Organic solar cells (OSCs) require both a high donor/acceptor (D/A) interfacial area for efficient exciton dissociation and a vertically phase-separated morphology for efficient charge transport. Traditional bulk heterojunctions (BHJs) provide large interfacial areas but lack vertical phase separation, while quasi-planar heterojunctions (QPHJs) achieve vertical separation at the cost of reduced interfacial contact. Here, we introduce an in situ pore-forming strategy for polymer thin films. By incorporating an excess of additives as pore-forming agents into the donor layer, a nanoporous film with a fibrous nano-network is generated. Subsequent deposition of acceptor molecules fills these nanopores, creating a hybrid planar/bulk heterojunction (HP/BHJ) that synergizes the strengths of both architectures. This design enhances performance by: (1) increasing the D/A interfacial area via nanopores, forming a three-dimensional network that accelerates exciton dissociation; (2) promoting close molecular packing that minimizes carrier recombination and establishes low-defect charge transport channels; and (3) fostering vertical phase separation through layer-by-layer deposition. Binary OSCs fabricated with this strategy achieve a power conversion efficiency (PCE) of 20.0%, surpassing conventional BHJ and QPHJ devices by a significant margin. The approach demonstrates general applicability, with analogous improvements observed in D18/BTP-eC9-4F and PM6/L8-BO systems, underscoring its potential for advancing OSC performance.

Read Full Abstract10.1007/s40843-025-3793-9
Porous TPU piezoelectric composites with core-shell structured PZT@CMCS particles for enhanced energy harvestingGraphical AbstractVerified
SCIENCE CHINA Materials2026

Porous TPU piezoelectric composites with core-shell structured PZT@CMCS particles for enhanced energy harvesting

Piezoelectric materials convert mechanical energy into electrical signals, enabling applications in sensors, actuators, and energy harvesting. Inorganic ceramics like PZT and BTO exhibit excellent piezoelectric properties but are brittle, limiting their use in flexible electronics. This work presents a porous composite of PZT@carboxymethyl chitosan (CMCS) in thermoplastic polyurethane (TPU). The core-shell structure enhances interfacial compatibility, while the porous TPU skeleton facilitates stress transfer and amplification, allowing high piezoelectric content. The resulting PZT@CMCS/TPU devices achieve an output voltage of 53 V and current of 13 μA, an 11-fold improvement over conventional PZT composite films. This approach enables flexible piezoelectric devices with high performance.

Read Full Abstract10.1007/s40843-025-3604-1
Anisotropic Liquid Crystalline Hydrogel Actuators with Multi-Stimuli-Responsive Actuation and Multimodal LocomotionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Anisotropic Liquid Crystalline Hydrogel Actuators with Multi-Stimuli-Responsive Actuation and Multimodal Locomotion

Anisotropic hydrogels have attracted significant attention for applications in actuators, soft robotics, and artificial muscles due to their ability to undergo shape morphing and generate anisotropic responses under external stimuli. Here, we report a novel strategy for fabricating anisotropic hydrogels using liquid crystal polymers (LCPs). A series of liquid crystal polyester-polyethylene glycol (LCP-PEG) multiblock copolymers with varying PEG block molecular weights were synthesized via one-pot melt-polycondensation. Upon stretching, LCP-PEG forms a stable, oriented microphase-separated lamellar structure, which enables reversible shape changes driven by melting-induced contraction and crystallization-induced expansion of the oriented PEG crystals. This unique structure imparts anisotropic swelling behavior to the films when exposed to water or humidity. The oriented microphase-separated lamellar structure confers high fracture strength (11.2–14.7 MPa), fracture strain (1600%–2100%), fracture energy (1.7–2.8 MJ m−2), and Young’s modulus (51.2–139.9 MPa). Furthermore, the anisotropic LCP-PEG hydrogel actuators exhibit versatile locomotion modes, including object grabbing and transfer between water and air, object gripping in rainy conditions, walking and somersaulting on ratchet-patterned bases under humidity stimuli, and slope climbing through somersault locomotion under salty water stimuli. These results demonstrate the potential of LCP-based anisotropic hydrogels for advanced soft robotic applications.

Read Full Abstract10.1007/s40843-025-3721-y
Positively Charged Polyamide Membranes with Expanded Ion Passage Channels Enabling Exceptional Lithium Extraction from Battery LeachateGraphical AbstractVerified
SCIENCE CHINA Materials2026

Positively Charged Polyamide Membranes with Expanded Ion Passage Channels Enabling Exceptional Lithium Extraction from Battery Leachate

Polyamide (PA) membranes are promising for lithium extraction from spent lithium-ion battery (LIB) leachate but face a trade-off between selectivity and permeability. Here, we demonstrate that nascent PA membranes post-grafted with triaminoguanidinium (TAG) monomers (PA-TAG membranes) gain expanded ion passage channels (0.8–7.1 Å) and enhanced positive charge, achieving high-performance lithium separation. The PA-TAG membrane exhibits a pure water permeance (PWP) of 15.5 L m−2 h−1 bar−1, superior divalent ion rejection (~98%), and an excellent separation factor (~30), significantly outperforming pristine PA membranes. In a simulated acidic battery leachate, the PA-TAG membrane achieved a relative volumetric lithium recovery rate of 48.2% after a two-stage nanofiltration process, with the Li+/M2+ mass ratio of the second permeate reaching 53.35, 445 times that of the feed (0.12). The membrane maintained stable performance over 45 hours of nanofiltration and resisted acidic conditions (pH=2) for at least 20 days. These results highlight the potential of PA-TAG membranes for efficient lithium extraction from acidic battery leachate, addressing the critical need for sustainable recycling of spent LIBs.

Read Full Abstract10.1007/s40843-025-3559-5
High-resilience, anti-freezing, and vacuum-tolerant eutectogel for self-powered pressure sensing in extreme environmentsGraphical AbstractVerified
SCIENCE CHINA Materials2026

High-resilience, anti-freezing, and vacuum-tolerant eutectogel for self-powered pressure sensing in extreme environments

Triboelectric nanogenerators (TENGs) offer promising solutions for self-powered sensors in the Internet of Things, yet traditional materials suffer from limited mechanical durability, environmental stability, and sensing performance under extreme conditions. This study develops a novel eutectogel composed of a deep eutectic solvent (DES) and a poly(itaconic acid-co-2-hydroxyethyl acrylate) (P(IA-co-HEA)) polymer network. Through careful molecular design and microstructural modification, the eutectogel achieves low hysteresis, excellent resilience (97.8%), high conductivity (48.02 mS m−1), and strong adhesive strength. Benefiting from the low freezing point and low volatility of the DES, the eutectogel retains 75.7% tensile and 69.4% compressive resilience at −40 °C, and shows no significant change in resilience after 24 h storage under −0.1 MPa vacuum. A self-powered TENG pressure sensor incorporating the eutectogel exhibits a fast response time of 16 ms and stable signal output over 16,000 contact-separation cycles. The sensor operates reliably at −60 °C and under vacuum (−0.1 MPa). These attributes make the high-resilience flexible sensor suitable for long-term, reliable pressure monitoring in extreme environments, addressing critical bottlenecks in durability and environmental stability for self-powered sensing technologies.

Read Full Abstract10.1007/s40843-025-3622-0
Quasi-metal 2D Ag2Te nanosheets for high performance surface-enhanced Raman scattering detectionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Quasi-metal 2D Ag2Te nanosheets for high performance surface-enhanced Raman scattering detection

Semiconductor-based surface-enhanced Raman scattering (SERS) substrates have attracted significant attention due to their high uniformity, reproducibility, stability, and cost-effectiveness. However, the Raman enhancement in semiconductors primarily relies on the chemical mechanism (CM), which typically results in a lower enhancement capability compared to traditional noble metals. In this study, we developed a novel two-dimensional (2D) SERS substrate, Ag2Te nanosheets (NSs), synthesized through a simple one-step redox reaction utilizing 2D Te NSs as the template. The 2D Ag2Te NSs not only exhibit strong interfacial interactions with molecules, thereby supporting the CM, but also possess quasi-metallic properties with low resistivity (2.8 × 10−4 Ω cm) and high density of free electrons (4.15 × 10^22 cm−3), giving rise to a significant visible-region surface plasmon resonance (SPR) band and contributing to enormous electromagnetic mechanism (EM). By synergizing CM and EM, the 2D Ag2Te NSs SERS substrate achieved an ultra-low limit of detection (LOD) of 10−10 M with an enhancement factor (EF) of 2.6 × 10^7 for methylene blue (MB), outperforming most semiconductors, even rivaling noble metals. The quasi-metallic properties of 2D Ag2Te NSs also benefit their sensitivity to multiple molecules. The accuracy and reliability were demonstrated in real-sample detections with recoveries of 91.5%–108.3% for various target molecules. These excellent performances, combined with remarkable cost-effectiveness, demonstrate the potential of 2D Ag2Te NSs as a practical SERS substrate with broad applicability. Furthermore, the inherent structural simplicity of these nanosheets creates significant opportunities for further sophisticated nanostructural engineering to advance the SERS performance in the future.

Read Full Abstract10.1007/s40843-025-3585-1
Computational Screening of 2D Pentagonal Materials with Room-Temperature Altermagnetism, Multiferroicity, and Topological StatesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Computational Screening of 2D Pentagonal Materials with Room-Temperature Altermagnetism, Multiferroicity, and Topological States

Two-dimensional planar pentagonal crystals, long pursued for their geometrically frustrated lattice configurations and emergent quantum phenomena, have remained challenging to realize due to the intrinsic incompatibility of regular pentagons with Euclidean tiling. Here, we unveil 37 dynamically stable binary planar pentagonal monolayers through high-throughput computational screening of 1470 stoichiometric candidates. These materials exhibit room-temperature magnetism, including ferromagnetic (Curie temperature up to 521 K), antiferromagnetic (Néel temperature up to 761 K), and altermagnetic (Néel temperature = 984 K) ground states, alongside unprecedented electronic states: Dirac semimetals, Dirac half-metal, nodal-loop semimetal, nodal-loop half-metal, and altermagnetic semiconductors (Mn4N2) with giant spin splitting (0.78 eV). The latter achieves pure spin-polarized transport windows (−0.04 to 0.36 eV) and strain-tunable valley splitting (18.2 meV under 4% uniaxial strain). Intrinsic type-II multiferroicity emerges in Fe4C2 and Mn4C2, featuring in-plane electric polarization (1.4 and 1.6 pC/m), ferroelasticity (0.8% and 1.2% reversible strain), and reversal chirality. Topological band analysis identifies chiral edge states in Dirac semimetal pentagons, alongside a magnetic topological insulator with Chern number |C| = 2 in Mo2S4 and W2Te4. Temperature-driven structural transitions in Os2S4 and Tc2S4 from pentagonal to Lieb lattices accompany topological state switching and metal-to-semiconductor transitions. This work establishes pentagonal lattices as a platform for symmetry-driven multifunctionality, bridging geometric frustration with applications in spintronics, nanoelectronics, and quantum devices.

Read Full Abstract10.1007/s40843-025-3600-1
LEGO-like Three-Dimensional Integrated Stretchable ElectronicsGraphical AbstractVerified
SCIENCE CHINA Materials2026

LEGO-like Three-Dimensional Integrated Stretchable Electronics

Stretchable electronics are pivotal for bio-integrated devices, soft robotics, and wearables, yet their development is constrained by single-layer architectures that limit integration density and by mechanical mismatch between rigid components and soft substrates, which curtails service life. Here, we introduce a LEGO-like modular assembly strategy to construct multilayer three-dimensional (3D) stretchable electronics. Electronic components (ECs) and self-healing polyurethane (SPU) substrates patterned with liquid metal (LM) circuits serve as the modular blocks. This design simplifies fabrication and markedly enhances 3D integration density. The combination of LM circuits and self-healing elastic substrates enables devices to withstand diverse deformations and to autonomously heal after mechanical damage. Notably, the devices can undergo multiple recycling and reuse cycles without significant performance loss. This methodology offers a new paradigm for advanced flexible electronics, addressing critical bottlenecks in integration density, mechanical robustness, and sustainability.

Read Full Abstract10.1007/s40843-025-3615-1
Wearable Interactive System with Uncoded Gesture Recognition Logic Enabled by Deep LearningGraphical AbstractVerified
SCIENCE CHINA Materials2026

Wearable Interactive System with Uncoded Gesture Recognition Logic Enabled by Deep Learning

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.

Read Full Abstract10.1007/s40843-025-3553-7
Reconfiguring hydration shells by rigidly confined interaction within graphene oxide membranes for ultra-efficient anion separationGraphical AbstractVerified
SCIENCE CHINA Materials2026

Reconfiguring hydration shells by rigidly confined interaction within graphene oxide membranes for ultra-efficient anion separation

The understanding of anion transporting behaviors under sub-nanoconfined regimes can guide the design of high-performance anion selective membranes (ASMs), yet it is little known. Here, we build membrane channels that combine physical rigidity with chemical affinity to anions simply through bridging graphene oxide nanosheets with charged linkers. We observe that the rigidly confined interaction imposed by channels to anions can reconfigure hydration shells in varying degrees for different anions via compensating for hydration-induced energy barriers and differentiating their rearrangement behaviors. During the configuration evolution, water molecules within hydration shells would rotate and simultaneously change their distance from the ion center. Based on the big discrepancy in configuration evolution, these membranes can realize ultrahigh selectivity of, for example, 125 for Cl−/SO4^2− and surpass the performance upper bound concerning Cl−/SO4^2− separation by other membranes. The knowledge of the configuration change of hydration shells during the dehydration process will be key to designing next-generation ASMs.

Read Full Abstract10.1007/s40843-025-3538-6
Peritoneum Inspired Janus Barrier with Unilateral Lubrication, Programmable Adhesion and Antiinflammation for Preventing Postoperative Abdominal AdhesionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Peritoneum Inspired Janus Barrier with Unilateral Lubrication, Programmable Adhesion and Antiinflammation for Preventing Postoperative Abdominal Adhesion

Postoperative abdominal adhesion, a complication with morbidity exceeding 90%, imposes severe clinical and economic burdens. Existing bioadhesive barriers often exhibit unreliable adhesion to the slippery abdominal wall, risk mispositioning, and neglect frictional stimuli and inflammation. Inspired by the lubricated peritoneum, we developed a programmable adhesive dual-layer Janus patch (DJP) barrier integrating a lubricated layer and an adhesive matrix. DJP achieves rapid, noncovalent interfacial adhesion, subsequently enhanced 2.81-fold via covalent interactions, enabling repositioning within a short time window to improve surgical fault tolerance. The micron-scale poly(sulfobetaine methacrylamide) brush on the DJP surface provides hydration lubrication with a low coefficient of friction (0.06), mimicking peritoneal lubrication and reducing frictional damage to injured tissue. The catechol-containing copolymer confers antioxidative and anti-inflammatory properties, confirmed in vitro. In a rat model, DJP adhering to the injured site significantly reduced collagen deposition between the abdominal wall and cecum, preventing adhesion and promoting tissue healing compared to commercial barriers. This work provides a guiding reference for developing antiadhesive biomaterials.

Read Full Abstract10.1007/s40843-025-3645-3
Magnetoelectric-bioactive dual functions of MXene regulate macrophage M1-M2 sequential polarization to promote healing of infected woundGraphical AbstractVerified
SCIENCE CHINA Materials2026

Magnetoelectric-bioactive dual functions of MXene regulate macrophage M1-M2 sequential polarization to promote healing of infected wound

Macrophages are pivotal in infection resolution and tissue repair via dynamic M1-to-M2 phenotypic polarization. Although various nano-biomaterials can modulate macrophage polarization, achieving sequential M1-to-M2 transition using a single nanoformulation remains challenging. Here, we propose a strategy employing transition metal carbide/nitride (MXene) nanosheets, internalized by macrophages, as the sole regulator to induce sequential polarization. Under a rotating magnetic field, the high electrical conductivity and magnetoelectric activity of endocytosed MXene generate electrical signals and reactive oxygen species (ROS), driving M1 polarization. Upon magnetic field removal, the inherent bioactivity of MXene facilitates repolarization to the M2 phenotype. Mechanistically, this transition involves inhibition of the NF-κB signaling pathway and activation of the JAK-STAT signaling pathway. In vivo, MXene nanosheets under on-off rotating magnetic field stimulation enabled sequential M1-to-M2 polarization, promoting bacterial clearance and tissue regeneration in infected wounds. This two-step sequential strategy targeting macrophages offers a promising therapeutic approach for infected wound healing.

Read Full Abstract10.1007/s40843-025-3617-x
AB Epoxy Encapsulation-Induced Transparency in Perovskite Films for Light-Emitting Diode ApplicationsGraphical AbstractVerified
SCIENCE CHINA Materials2026

AB Epoxy Encapsulation-Induced Transparency in Perovskite Films for Light-Emitting Diode Applications

Perovskite light-emitting diodes (PeLEDs) are a promising display technology due to high color purity and solution processability, but their operational stability is compromised by environmental degradation. Encapsulation is essential for practical deployment. Here, we report that applying a commercial AB epoxy adhesive as a cover encapsulant induces a striking transparency transition in Cs0.3MA0.7PbBr3 perovskite films, from yellow to optically clear. The effect is attributed to the alkaline hardener (component B, pH 9–10), which engages in Lewis acid-base coordination with Pb2+ and reacts with Br−, as evidenced by Fourier-transform infrared spectroscopy (redshift of C–O–C stretch from 1035.56 to 1018.05 cm−1, Δν ≈ 17.5 cm−1) and X-ray photoelectron spectroscopy (Pb 4f shift of 0.25 eV, Br 3d5/2 shift of 0.45 eV). This chemical interaction refines perovskite grains to tens of nanometers, shifting light scattering from Mie to Rayleigh regime and enhancing transmittance. Encapsulated devices achieve a maximum luminance of 12,643 cd/m2, a low operational current density, and an increased breakdown voltage of 27 V. The work establishes a framework for selecting encapsulation materials that impart transparency, enabling applications in transparent displays, smart windows, and augmented reality.

Read Full Abstract10.1007/s40843-025-3552-2
A hydrogel–textile composite with synapse-inspired ionic multimodal sensingGraphical AbstractVerified
SCIENCE CHINA Materials2026

A hydrogel–textile composite with synapse-inspired ionic multimodal sensing

Flexible and perceptive sensors represent the pinnacle of wearable technology; nevertheless, most current hydrogel-based sensors encounter difficulties in concurrently achieving mechanical durability, biocompatibility, high sensitivity, and scalability. This work introduces an innovative multimodal hydrogel–textile composite sensor (WPU–ChCl hydrogel) developed via free radical polymerization of acrylamide, integrating choline chloride (ChCl), EMIM TFSI ionic liquid, and waterborne polyurethane (WPU) to overcome existing constraints. The resultant hydrogel demonstrates a synergistic network of covalent and dynamic non-covalent connections, with remarkable stretchability (~900%), mechanical toughness (>250 kJ/m3), and ionic conductivity (9.2 mS/cm at 600% strain). Comprehensive morphological and chemical analysis validated uniform structure, increased segmental ordering, and improved heat stability. The hydrogel exhibited swift strain responsiveness (gauge factor = 7.23), quick response/recovery times (~108/114 ms), exceptional durability over 500 cycles, and enhanced self-healing and adherence to various surfaces. Integrated into textiles, the composite demonstrated exceptional real-time touch and motion detection capabilities and retained sensing accuracy after 20 wash cycles. Code transmission and machine learning-based high-accuracy gesture recognition (93.65%) were examples of advanced uses. The wireless-enabled system demonstrated efficacy in IoT-based health monitoring, soft robotics, and human–machine interactions, representing a substantial advancement in next-generation wearable electronics.

Read Full Abstract10.1007/s40843-025-3644-9