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All Clean Energy & Battery Intelligence (Page 39)

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Published Research Papers

Showing 24 of 1398 peer-reviewed translated articles (Page 39 of 59)

Supercritical-Assisted Chain Engineering of Biodegradable Polyhydroxyalkanoates for Simultaneous Mechanical, Optical and Dielectric EnhancementGraphical AbstractVerified
SCIENCE CHINA Materials2026

Supercritical-Assisted Chain Engineering of Biodegradable Polyhydroxyalkanoates for Simultaneous Mechanical, Optical and Dielectric Enhancement

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.

Read Full Abstract10.1007/s40843-025-3943-y
Solvent-Driven Dual-Network Entanglement for Organo-Hydrogels with High Strength and ToughnessGraphical AbstractVerified
SCIENCE CHINA Materials2026

Solvent-Driven Dual-Network Entanglement for Organo-Hydrogels with High Strength and Toughness

The development of hydrogels that simultaneously achieve high strength and good toughness remains a critical challenge in soft material science, particularly for applications in flexible electronics, soft robotics, and biomedical devices. Conventional approaches often suffer from a trade-off between mechanical robustness and functional performance. In this work, we present a novel solvent-driven dual-network entanglement strategy to fabricate a strong and tough poly(vinyl alcohol) (PVA)-based organo-hydrogel by synergistically combining isopropanol (IPA) solvent substitution to induce dense polymer chain entanglement and a sodium alginate (SA) ionic crosslinked network as a dynamic energy-dissipation phase. The resulting organo-hydrogel exhibits excellent mechanical performance with a tensile strength of 3.18 MPa and a toughness of 16.65 MJ/m3, representing increases of approximately 17 and 49 times that of conventional PVA hydrogels, respectively. Furthermore, the organo-hydrogel displays superior swelling resistance and long-term stability in aqueous environments, enabling reliable operation in challenging conditions such as underwater motion sensing and wearable strain detection. Morphological analyses reveal the critical role of solvent-mediated chain reorganization and dual-network interactions in achieving these properties. This work not only provides a versatile platform for designing robust gel materials but also offers fundamental insights into solvent-network interactions for advanced soft material engineering.

Read Full Abstract10.1007/s40843-025-3809-y
Collapsed nanomineral inducing oxidation-enhanced photoacoustic mechanical damage for elimination of solid tumorGraphical AbstractVerified
SCIENCE CHINA Materials2026

Collapsed nanomineral inducing oxidation-enhanced photoacoustic mechanical damage for elimination of solid tumor

Circumventing the tumor's defensive antioxidant system and achieving precision cancer therapy remain major challenges in high-efficacy tumor treatments. Here, we propose a synergistic strategy integrating non-oxidative physical ablation and oxidative chemical intervention. An acid-responsive self-collapsing nanomineral PCSB is constructed, comprising poly(acrylic acid)-modified calcium sulfite (CaSO3) and a pH-responsive photoacoustic (PA) therapeutic molecule, aza-BDP. In the tumor acidic microenvironment, PCSB decomposes, releasing PA agents and SO2/Ca2+, thereby enabling combined non-oxidative mechanical damage from PA therapy and oxidative chemical damage from SO2 gas and Ca2+ ions. This dual-action approach effectively reduces resistance conferred by tumor antioxidant mechanisms and improves treatment precision. The study presents a synergistic physical-chemical strategy with significant potential for solid tumor elimination.

Read Full Abstract10.1007/s40843-025-3787-x
Optimizing Oxygen and Water Affinity in Aliphatic Acylhydrazone Covalent Organic Frameworks for Efficient H2O2 Photosynthesis from Water and AirGraphical AbstractVerified
SCIENCE CHINA Materials2026

Optimizing Oxygen and Water Affinity in Aliphatic Acylhydrazone Covalent Organic Frameworks for Efficient H2O2 Photosynthesis from Water and Air

Photocatalytic production of hydrogen peroxide (H2O2) via oxygen reduction reaction (ORR) and water oxidation reaction (WOR) from water and air offers a sustainable alternative to conventional anthraquinone processes. However, the intrinsic kinetic mismatch—fast ORR (microseconds to milliseconds) versus sluggish WOR (seconds)—limits overall efficiency. Here, we report aliphatic acylhydrazone covalent organic frameworks (AA-COFs) synthesized by coupling aliphatic hydrazides with benzotrithiophene motifs via acylhydrazone linkages. The pore walls are decorated with abundant S, O, and N heteroatoms, enhancing affinity toward both O2 and H2O, thereby improving the kinetics of both half-reactions. Through single-carbon atomic engineering, the optimized AA-COF achieves a trade-off between ORR and WOR kinetics, enabling efficient overall H2O2 photosynthesis from water and air without sacrificial agents. The material exhibits a H2O2 production rate of 4777 μmol g−1 h−1 and an O2 utilization/conversion efficiency of 99.3%. This work demonstrates that rational design of heteroatom-rich COFs can synchronize ORR and WOR, overcoming a major bottleneck in artificial photosynthesis.

Read Full Abstract10.1007/s40843-025-3885-8
Distributed and stretchable tactile sensing for dexterous robotic hands based on a crosslinked interpenetrating networkGraphical AbstractVerified
SCIENCE CHINA Materials2026

Distributed and stretchable tactile sensing for dexterous robotic hands based on a crosslinked interpenetrating network

Tactile sensing for dexterous robotic hands is essential for achieving human-like precision in manipulation. However, current tactile sensors face challenges such as insufficient durability, limited coverage, and poor conformability to curved, jointed surfaces. This study presents a stretchable distributed tactile sensor array designed for dexterous robotic hands. The array comprises 18 sensing units distributed across the hand, incorporating quasi-homogeneous functional layers interconnected by crosslinked interpenetrating networks, and composite electrodes combining high conductivity with stretchability. This design yields a thin, soft, transparent, and stretchable sensor array that integrates seamlessly with a commercial dexterous hand. The sensor array exhibits high interlayer tensile strength, high sensitivity, low hysteresis, and excellent long-term reliability over 10,000 loading cycles. Experimental results demonstrate accurate detection of tactile force across the entire robotic hand during object grasping. Using convolutional neural network algorithms, the sensor array identifies different object types with 90.1% accuracy, with results displayed in real time on a digital twin interface. The proposed sensor array holds significant potential for embodied intelligence and robotics in adaptive grasping, safe manipulation, and remote teleoperation.

Read Full Abstract10.1007/s40843-025-3840-3
Multifunctional Permeable Electrodes for Synchronous Temperature-Electrophysiological Signals Monitoring and Intelligent Arrhythmia DiagnosisGraphical AbstractVerified
SCIENCE CHINA Materials2026

Multifunctional Permeable Electrodes for Synchronous Temperature-Electrophysiological Signals Monitoring and Intelligent Arrhythmia Diagnosis

The rapid expansion of home-based digital health monitoring necessitates electrodes capable of simultaneous, accurate acquisition of electrophysiological signals and body temperature. Conventional single-function electrodes, including metal block, gel, and Ag/AgCl types, suffer from limitations such as restricted movement, skin irritation, signal degradation over time, and poor permeability for prolonged use. To overcome these challenges, we developed a low-cost, multifunctional flexible electrode enabling concurrent body temperature and electrophysiological signal monitoring without cross-interference. Body temperature is assessed via visual colorimetric evaluation and precisely measured using a custom smartphone application. The electrode features high air permeability, ultra-thin architecture, superior flexibility, antibacterial properties, and strong skin adhesion, while maintaining low interfacial impedance for stable, long-term acquisition of high-fidelity signals such as electrocardiography (ECG) and surface electromyography (sEMG). Integrated with a Raspberry Pi platform and a hybrid convolutional neural network-long short-term memory (CNN-LSTM) algorithm, the system achieves intelligent arrhythmia detection with 99.30% accuracy. This novel electrode provides a powerful tool for multifunctional sensing of temperature and physiological electrical signals, with significant potential for wearable physiological tracking applications.

Read Full Abstract10.1007/s40843-025-3792-6
Concentration-Driven Ion Transport Regulated Perovskite Nanocrystal Memristors Enable Reliable Neuromorphic Sensing, Logic Gate Circuits, and Data SecurityGraphical AbstractVerified
SCIENCE CHINA Materials2026

Concentration-Driven Ion Transport Regulated Perovskite Nanocrystal Memristors Enable Reliable Neuromorphic Sensing, Logic Gate Circuits, and Data Security

Memristors, which leverage ion migration for resistance switching, offer breakthroughs in bionic perception, information security, and edge computing but face bottlenecks in functional integration and stability. Herein, we explore all-inorganic Cu3SbI6 nanocrystals (NCs) & PMMA composite memristors (Ag/PMMA&Cu3SbI6/ITO) regulated by NCs doping (0–15 wt%). The devices operate via electric field-induced Ag+ ion migration and conductive filament dynamics, where NCs act as local electric field enhancers. At a doping concentration of 4 wt%, stable bipolar switching (Ron/Roff > 2 × 10^3, cycling endurance > 700 cycles) enables the simulation of biological nociception/Pavlovian reflexes and the construction of basic logic gates. At 2 wt%, sparse NCs induce random filament formation for encryption key extraction, which integrates with 4 wt% logic gates to enable efficient encryption/decryption of text/image data. This work provides a strategy for designing multifunctional memristors by regulating ion transport through nanocrystal concentration, offering references for related functional integration and cross-disciplinary applications.

Read Full Abstract10.1007/s40843-025-3900-8
Bio-camouflaged nanoreactors with spatiotemporally controlled Cu2+-Fenton catalysis for enhanced starvation-augmented mild photothermal therapyGraphical AbstractVerified
SCIENCE CHINA Materials2026

Bio-camouflaged nanoreactors with spatiotemporally controlled Cu2+-Fenton catalysis for enhanced starvation-augmented mild photothermal therapy

Triple-negative breast cancer (TNBC) remains a formidable clinical challenge due to its high invasiveness and adaptive resistance. We report a bio-mimetic nanoplatform (HMPB-GOx@HSA-Cu2+) integrating starvation therapy, Fenton/Fenton-like catalysis, and mild photothermal therapy (mPTT) for synergistic TNBC treatment. The nanoreactor comprises a hollow mesoporous Prussian blue (HMPB) core loaded with glucose oxidase (GOx), encapsulated in a human serum albumin (HSA) shell covalently functionalized with Cu2+ ions. This design enables spatiotemporal control of Cu2+-mediated Fenton catalysis, responding to the tumor microenvironment (TME) to generate cytotoxic hydroxyl radicals (·OH). GOx catalyzes glucose depletion, elevating H2O2 levels and acidity, thereby enhancing catalytic efficiency. Concurrently, mPTT at ~43–45°C accelerates the Fenton reaction and suppresses heat shock protein (HSP) expression, overcoming thermal tolerance via ATP depletion. In vitro and in vivo studies demonstrate significant anti-tumor efficacy through reactive oxygen species (ROS) accumulation and metabolic disruption, with excellent biocompatibility. This work presents a highly integrated strategy for precise TNBC therapy, addressing limitations of conventional monotherapies.

Read Full Abstract10.1007/s40843-025-3937-7
Synergistic innate-adaptive chemo-immunotherapy through a high-payload nanoplatformGraphical AbstractVerified
SCIENCE CHINA Materials2026

Synergistic innate-adaptive chemo-immunotherapy through a high-payload nanoplatform

The synergistic strategy combining chemotherapy and immunotherapy has recently demonstrated significant promise in cancer treatment. However, the substantial physicochemical disparities between chemotherapeutic agents and small-molecule immune adjuvants pose considerable challenges for co-delivery strategies. In this study, we designed a reactive oxygen species-responsive paclitaxel prodrug, PTX-PBA, which markedly enhanced drug encapsulation stability and dual-drug loading efficiency by various polymeric delivery systems. The resultant nanosystem (NanoPR) exhibited excellent physicochemical properties and ROS-triggered release profiles, effectively inducing immunogenic cell death in tumor cells while promoting dendritic cell maturation and CD8+ T cells activation. In murine models of 4T1 breast cancer and CT26 colon carcinoma, NanoPR achieved significant tumor growth inhibition and elicited durable immune memory responses. Collectively, this work provides an innovative molecular design strategy for the co-delivery of chemotherapeutics and immunomodulators, offering a robust foundation for the clinical translation of chemo-immunotherapy.

Read Full Abstract10.1007/s40843-025-3783-x
WO3−x:N/ZnO:N Broadband Optoelectronic Synapse for Object Detection in Edge ComputingGraphical AbstractVerified
SCIENCE CHINA Materials2026

WO3−x:N/ZnO:N Broadband Optoelectronic Synapse for Object Detection in Edge Computing

Broadband optoelectronic memristors with high computational efficiency and low power consumption are pivotal for neuromorphic computing at the edge. This work presents a Ag/WO3−x:N/ZnO:N/ITO memristor exhibiting dual-modal synaptic plasticity. Electronic synaptic properties emulate biological plasticity, while photoresponse to multiple wavelengths, including simultaneous dual-wavelength stimulation, yields composite photocurrents. Leveraging these characteristics, single- and dual-wavelength artificial vision arrays simulate human visual perception. An artificial neural network integrated with a Field Programmable Gate Array (FPGA) forms a floating-point arithmetic system for object detection. The edge computing system achieves a 103-fold reduction in power consumption, addressing computational power limitations and enabling floating-point operations in embedded neuromorphic deployments. This work advances broadband optoelectronic synapses for efficient, low-power edge computing.

Read Full Abstract10.1007/s40843-025-3839-4
Micro-EDL Engineered Ionogels Enable Ultra-Sensitive Iontronic Pressure Sensing over a Broad RangeGraphical AbstractVerified
SCIENCE CHINA Materials2026

Micro-EDL Engineered Ionogels Enable Ultra-Sensitive Iontronic Pressure Sensing over a Broad Range

Iontronic capacitive pressure sensors (ICPSs) are pivotal for wearable technology, yet their performance is constrained by an inherent trade-off between sensitivity and detection range. Here, we introduce a micro-electric double layer (micro-EDL) engineering strategy to overcome this limitation. This is realized through a nanocomposite dielectric where multi-walled carbon nanotubes (MWCNTs) form a percolated network, generating a dense array of pressure-responsive nano-capacitors. Synergistically integrating a hierarchical MoS2/NiCo-LDH electrode provides abundant pseudocapacitive interfaces. The resulting sensor exhibits an ultrahigh sensitivity of 67,095 kPa−1 at 1 kHz, a broad detection range up to 1.3 MPa, rapid response and recovery times of 4 ms and 5 ms, respectively, and outstanding durability exceeding 18,000 cycles. Practical validation demonstrates 100% classification accuracy in recognizing complex gestures and gait patterns, underscoring its real-world applicability. These findings establish micro-EDL engineering as a promising route for advancing next-generation iontronic devices, offering insights into their electrochemical mechanisms.

Read Full Abstract10.1007/s40843-025-3869-7
Bioinspired voltage-gated multi-state ion channels in MXene nanoconfinement for emulating synaptic plasticityGraphical AbstractVerified
SCIENCE CHINA Materials2026

Bioinspired voltage-gated multi-state ion channels in MXene nanoconfinement for emulating synaptic plasticity

Biological ion channels exhibit multistate transport behavior beyond simple binary open-closed conformations, enabling dynamic control of neural signaling and transmembrane substance transport. Inspired by this, we synthesized a triphenylamine-ketone donor-acceptor (D-A) type poly(aryl amine-ketone) with multiple redox sites, allowing continuously tunable electrochemical states via hierarchical electron transfer. Combining this polymer with two-dimensional conductive MXene, we constructed a biomimetic nanofluidic transistor. Through side-group tuning to optimize redox matching, the polymer undergoes reversible conformation switching via intramolecular charge transfer at voltages below 1 V. The field-driven conformational changes induce electrostatic attraction, promoting reversible contraction of MXene interlayers. Synergistic coupling of interlayer spacing variation and dynamic interfacial charge rearrangement enables precise hierarchical control of ion flux. The device achieves three switchable ion transport states—closed, partially open, and fully open—with an ion switching ratio of 10 and outstanding cycling stability. Furthermore, synaptic plasticity features emulate fundamental attributes of biological signaling, providing a foundation for bioinspired neuromorphic devices.

Read Full Abstract10.1007/s40843-026-4148-3
Multifunctional Melamine Foam Composites Featuring Asymmetric Conductive Networks for Highly Absorptive EMI Shielding and Infrared StealthGraphical AbstractVerified
SCIENCE CHINA Materials2026

Multifunctional Melamine Foam Composites Featuring Asymmetric Conductive Networks for Highly Absorptive EMI Shielding and Infrared Stealth

The escalating demand for lightweight, multifunctional stealth materials in modern protective applications necessitates integrated solutions against electromagnetic interference (EMI), infrared (IR) detection, and incendiary threats. This study presents an innovative melamine foam (MF)-based composite featuring an asymmetric dual-nano conductive network, achieving absorption-dominated EMI shielding, IR stealth, and flame retardancy. Inspired by the Salisbury screen, the composite employs MF as an interlayer and flame-retardant thermoplastic polyurethane (TPU) nanofiber membrane as a substrate. The architecture comprises a carbon nanotubes (CNTs)-modified impedance matching nanofiber layer as the top absorber and a silver nanoparticles (AgNPs)-modified nanofiber layer as the highly conductive reflective bottom. Precise control of CNTs content and interlayer thickness enables tunable electromagnetic wave (EMW) absorption, yielding a low reflection coefficient of 0.03 and a high EMI shielding effectiveness of 79.23 dB at a total thickness of 4.40 mm. Even at 1.40 mm, effective absorption-dominated shielding is maintained. The performance remains stable under ultrasonic, compression, and bending tests, demonstrating high durability. The mechanism underlying absorption-dominated EMI shielding at reduced thickness, relying on destructive interference of EMWs enabled by the asymmetric dual-nano conductive network, is thoroughly elucidated. Additionally, the composite exhibits superior IR stealth and self-extinguishing properties. This work offers a feasible strategy for designing high-performance stealth materials with strong potential for personnel and communication equipment protection.

Read Full Abstract10.1007/s40843-025-3873-7
Effects of the partially fluorinated side-chain positions on the charge mobility and photovoltaic performance of M-series acceptorsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Effects of the partially fluorinated side-chain positions on the charge mobility and photovoltaic performance of M-series acceptors

Incorporating fluorinated side-chains into M-series acceptors enhances the fill factor (FF) and power conversion efficiency (PCE) of organic solar cells (OSCs). However, the impact of fluorinated side-chain positions on charge mobility and photovoltaic performance remains unexplored. Here, we synthesize a partially fluorinated alkyl chain, 7-butyl-1,1,1,2,2-pentafluoro-octyl, and attach it to either the oxygen or nitrogen atoms of the M-series acceptor backbone, yielding two new acceptors, O5F and N5F. Compared to O5F, N5F exhibits closer π-π stacking and higher charge mobility. Consequently, PM6:N5F-based devices achieve a PCE of 18.8% with an FF of 80.7%, surpassing PM6:O5F counterparts (PCE 17.8%, FF 79.2%). The 18.8% PCE is among the highest reported for A-D-A-type small-molecule acceptors. Notably, PM6:N5F devices show significantly improved operational stability, with a T80 lifetime of 1084 hours under one-sun illumination, versus 123 hours for PM6:O5F. This work demonstrates that positioning partially fluorinated side-chains on nitrogen atoms optimizes intermolecular packing and carrier transport, enhancing both efficiency and stability. It underscores the potential of partially fluorinated side-chains in designing high-performance NFAs.

Read Full Abstract10.1007/s40843-025-3914-7
Achieving wide linear range and high sensitivity in capacitive pressure sensors via a stretchable nanofilm with interlocked hierarchyGraphical AbstractVerified
SCIENCE CHINA Materials2026

Achieving wide linear range and high sensitivity in capacitive pressure sensors via a stretchable nanofilm with interlocked hierarchy

Capacitive pressure sensors have garnered significant attention in electronic skin, human-machine interaction, health monitoring, and medical devices due to their remarkable properties like highly sensitive pressure perception, good repeatability, and rapid response capabilities. However, manufacturing capacitive pressure sensors that simultaneously achieve a broad linear detection range and high sensitivity remains a significant challenge. Herein, a novel hierarchically interlocked capacitive pressure sensor (HI-CPS) was designed by integrating a stretchable polyethylene glycol (PEG)-based nanofilm dielectric layer with hierarchically interlocked microstructures, demonstrating excellent linearity and high sensitivity over a wide sensing range. HI-CPS based on a one-layer nanofilm exhibits ultrahigh sensitivity (9.40 kPa−1) and an ultralow detection limit (0.1 Pa). When the dielectric layer comprises two layers of stacked nanofilms, the sensor not only maintains high sensitivity (3.17 kPa−1) but also achieves excellent linearity (R2 = 0.999) over a broad working range (<5 kPa), along with remarkable stability even after 10,000 cycles. Benefitting from the outstanding comprehensive performance, HI-CPS has been proven to be successfully implemented in monitoring various human biological signals, sign language recognition, and basketball shooting gesture correction. This strategy of assembling the tailored nanofilm with structural engineering has significant potential application in building high-performance pressure detection and recognition devices.

Read Full Abstract10.1007/s40843-025-3925-5
Unique Role of High-Entropy Metallic Glasses as Multifunctional Electrocatalytic MaterialsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Unique Role of High-Entropy Metallic Glasses as Multifunctional Electrocatalytic Materials

High-entropy alloys (HEAs) and metallic glasses (MGs) are promising electrocatalysts but suffer from inherent limitations: HEAs lack corrosion resistance and uniform surfaces due to their crystalline nature, while MGs have limited compositional flexibility, restricting active-site diversity and electronic-structure tuning. High-entropy metallic glasses (HEMGs) integrate the structural disorder of MGs with the multi-principal-element chemistry of HEAs, offering a unique combination of robust corrosion resistance, homogeneous surfaces, and abundant tunable active sites. Using Pd20Pt20Cu20Ni20P20 as a model HEMG, we investigate its electrocatalytic performance for alcohol oxidation and hydrogen evolution. The HEMG exhibits superior activity and stability compared to conventional HEAs and MGs, attributed to its disordered structure and high configurational entropy, which promote optimized adsorption energies and accelerated charge transfer. This work bridges the performance gap between HEAs and MGs, demonstrating HEMGs as multifunctional electrocatalytic materials with potential for industrial applications.

Read Full Abstract10.1007/s40843-025-3952-5
Interfacial Molecular Engineering for Stable Lead-Free Tin Perovskite Solar Cells: A Paradigm Shift in Buried Interface OptimizationGraphical AbstractVerified
SCIENCE CHINA Materials2026

Interfacial Molecular Engineering for Stable Lead-Free Tin Perovskite Solar Cells: A Paradigm Shift in Buried Interface Optimization

The advancement of lead-free perovskite photovoltaics, particularly tin-based devices, has been hindered by interfacial instability and energetic mismatches at the buried interface. This study, building on the foundational work of Qi and co-workers, establishes a clear paradigm: the path to stable, lead-free perovskite photovoltaics depends not only on material composition but also on interfacial engineering at the molecular scale. By transforming a historically problematic buried interface into a structurally coherent and energetically optimized contact, the research sets a new benchmark for tin-based devices. The work demonstrates that molecular design of self-assembled monolayers (SAMs) on nickel oxide (NiOx) hole transport layers can significantly enhance device performance and stability. Specifically, the use of phosphonic acid-based SAMs, such as MBP, results in improved surface wettability, reduced contact angle with the perovskite precursor, and superior current density-voltage characteristics. The findings underscore the critical role of interfacial chemistry in achieving high-efficiency, durable tin perovskite solar cells. This research brings perovskite solar cells closer to the long-sought balance of sustainability, efficiency, and durability, essential for real-world adoption. The study also highlights the importance of replacing acidic PEDOT:PSS with non-acidic alternatives to prevent device degradation. Overall, this work provides a comprehensive strategy for interfacial engineering that can be universally applied to other perovskite systems, paving the way for commercial viability of lead-free perovskite photovoltaics.

Read Full Abstract10.1007/s40843-025-3832-2
Entropy stabilization and effect of A-site ionic size in bilayer nickelatesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Entropy stabilization and effect of A-site ionic size in bilayer nickelates

The discovery of high-temperature superconductivity in bilayer nickelate La3Ni2O7−δ (La-327) under high pressure and in thin films at ambient pressure has opened new avenues in superconductivity research. However, La-327 exhibits a narrow phase stability range, leading to stacking faults that suppress bulk superconductivity. Chemical substitutions, particularly at the A-site with smaller rare-earth ions, have been shown to enhance phase purity and reduce stacking faults, while also increasing the orthorhombic distortion and chemical pressure. In this work, we apply the high-entropy (HE) strategy to stabilize the 327 phase with reduced average A-site ionic radius (rA). We successfully synthesized medium-entropy La1.2Pr0.6Nd0.6Sm0.6Ni2O7−δ (ME-327) and high-entropy La0.67Pr0.67Nd0.67Sm0.33Eu0.33Gd0.33Ni2O7−δ (HE-327) polycrystalline samples. These compositions satisfy medium- and high-entropy criteria, with rA values of 1.181 Å and 1.164 Å, respectively. The samples are phase-pure and homogeneous. HE-327 exhibits the lowest cell volume, largest orthorhombicity, and shortest interlayer Ni-Ni distance among reported bilayer nickelates. Physical property measurements reveal low electrical conductivity and a high density-wave (DW) transition temperature. Under high pressure, HE-327 shows a resistivity anomaly at 103 K under 31 GPa, suggesting a possible superconducting transition. Extrapolation indicates that Tc under high pressure exceeds 100 K for HE-327, correlating with reduced rA and enhanced interlayer coupling. Our results demonstrate the ionic size effect and the effectiveness of the HE approach in stabilizing bilayer nickelates, providing a new avenue for developing superconducting materials.

Read Full Abstract10.1007/s40843-025-3976-x
Removal of iodine from water in seconds using nonporous naphthobipyrrole-based organic cagesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Removal of iodine from water in seconds using nonporous naphthobipyrrole-based organic cages

The rapid and efficient removal of radioactive iodine species from water is critical for nuclear waste treatment, particularly given the short half-life of 131I (8.02 days). Traditional porous inorganic materials exhibit low uptake capacities (<1 g g−1), while porous frameworks such as MOFs and COFs achieve high capacities (>5 g g−1) but suffer from slow removal kinetics, often requiring hours to capture 80% of iodine. This study introduces nonporous naphthobipyrrole-based organic cages (NBP-Cages) that demonstrate ultrafast iodine removal from water. Among the materials tested, type-II Me-NBP-Cage and Et-NBP-Cage, prepared via reprecipitation, exhibit amorphous morphology with small particle sizes (2–6 μm) and low BET surface areas (33.4 and 2.3 m2 g−1, respectively). Despite their nonporosity, these materials achieve >99% iodine removal within seconds, outperforming previously reported sorbents. The adsorption performance correlates with particle size and morphology: amorphous, small particles with effective surface gaps show superior kinetics. The materials are recyclable; for instance, Et-NBP-Cage can be regenerated by washing with acetonitrile, maintaining removal efficiency over five cycles. This work highlights the potential of nonporous organic cages as high-performance iodine sorbents, addressing the critical need for materials that combine high uptake capacity with rapid removal kinetics.

Read Full Abstract10.1007/s40843-026-4053-5
Light-Induced Dramatic Enhancement of Magnetization in Methylviologen-Prussian Blue HybridsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Light-Induced Dramatic Enhancement of Magnetization in Methylviologen-Prussian Blue Hybrids

The dynamic modulation of magnetic properties by external stimuli represents a paradigm shift in materials science, enabling non-contact, reversible control of spin states for applications in optical switching, sensing, and low-power spintronics. Prussian blue analogues (PBAs) are versatile platforms for photo-responsive magnetism, yet their photomagnetic response is highly sensitive to transition metal selection, alkali ions, vacancies, and water content, complicating targeted synthesis. Here, we introduce a generalizable strategy by incorporating the photo-responsive organic cation methyl viologen (MV2+) into PBA frameworks, yielding hybrids MVPB, MVPB-Co, and MVPB-Ni. Upon Xe lamp irradiation, MV2+ undergoes reduction to the radical cation MV+•, which acts as a spin carrier coupling to the magnetic moments of the metal ions. This mechanism decouples the photomagnetic response from the inorganic lattice, overcoming stoichiometric limitations. Irradiation leads to a substantial enhancement of magnetization, followed by partial relaxation under prolonged exposure, attributed to the generation and accumulation of MV+• radicals. These radicals function as dynamic magnetic modifiers, distinct from conventional light-induced charge transfer in PB frameworks. The approach is applicable across diverse cyanide-bridged metal pairs, irrespective of alkaline cations, vacancies, or water content, establishing a robust route for designing light-responsive magnetic materials.

Read Full Abstract10.1007/s40843-025-4061-5
Ultrastable Supported Oxygen Evolution Electrocatalyst Formed by Ripening-Induced EmbeddingGraphical AbstractVerified
SCIENCE CHINA Materials2026

Ultrastable Supported Oxygen Evolution Electrocatalyst Formed by Ripening-Induced Embedding

The oxygen evolution reaction (OER) is a critical bottleneck in electrochemical water splitting, yet the stability of supported OER electrocatalysts under industrial conditions remains a formidable challenge. Here, we report an ultrastable supported OER electrocatalyst fabricated via a ripening-induced embedding strategy. This approach leverages controlled Ostwald ripening to embed catalytically active nanoparticles into a conductive oxide support, dramatically enhancing mechanical and electrochemical adhesion. The resulting catalyst exhibits an overpotential of only 245 mV at 10 mA cm−2 in 1 M KOH, with negligible degradation after 1000 hours of continuous operation at 100 mA cm−2, representing a 50-fold improvement in durability compared to conventional supported catalysts. Structural analyses reveal that the embedded architecture mitigates nanoparticle detachment and coalescence, preserving a high electrochemically active surface area (ECSA) of 85 m² g−1. Furthermore, the catalyst demonstrates exceptional performance in a proton exchange membrane (PEM) electrolyzer, achieving a cell voltage of 1.72 V at 1 A cm−2 with a decay rate of only 0.12 mV h−1 over 500 hours. This work provides a generalizable route to design robust OER electrocatalysts for industrial-scale water electrolysis, addressing the critical stability bottleneck that has hindered the deployment of renewable hydrogen production.

Read Full Abstract10.1007/s40843-025-3811-6
Coupled Ion-Electron Transfer Mechanism in Lithium-Ion BatteriesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Coupled Ion-Electron Transfer Mechanism in Lithium-Ion Batteries

Lithium-ion batteries (LIBs) are pivotal in portable electronics, electrified transportation, and smart grids, where energy conversion and delivery hinge on the coupled transfer of electrons and lithium ions (Li+). Charge transfer at the electrode-electrolyte interface, involving solvated Li+ interacting with the solid electrode, dictates overpotential—the excess energy required to drive reactions—directly impacting energy loss, voltage fade, and power limitations. Despite decades of research, interfacial kinetics remain incompletely understood, hindering advances in energy density, fast charging, and cycling life. Two classical models—electron transfer (ET) and ion transfer (IT)—have been treated as mutually exclusive. The ET model posits quantum tunneling of electrons as rate-determining, with solvated Li+ residing at the outer Helmholtz plane; activation energy is modulated by overpotential, and current-overpotential behavior follows the Butler-Volmer equation. Marcus-Hush-Chidsey theory extends this to high overpotentials, explaining weak temperature dependence in Tafel curvature. Conversely, the IT model identifies physical desolvation of Li+ as the energy-consuming, rate-limiting step, with desolvation barriers (ΔG_desolv) typically tens of kJ/mol, far exceeding electron tunneling activation energies. Strategies to lower IT barriers include electrolyte design, electric field modulation, electrode surface engineering, and alloying. This paper critically examines both models, proposing a coupled ion-electron transfer mechanism to reconcile discrepancies and guide future interfacial engineering.

Read Full Abstract10.1007/s40843-025-3824-8
Sub-thermionic organic thin-film tunnel transistors for beyond-thermionic electronicsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Sub-thermionic organic thin-film tunnel transistors for beyond-thermionic electronics

Organic thin-film transistors (OTFTs) are fundamental building blocks for flexible electronics, offering mechanical flexibility, biocompatibility, chemical tunability, and compatibility with large-area, cost-effective fabrication. However, their widespread adoption in high-density integrated systems is hindered by the thermionic limit of carrier injection, which constrains the subthreshold swing (SS) to a minimum of 60 mV/dec at room temperature, posing a critical barrier to ultra-low-power operation. In a groundbreaking study published in Nature Electronics, Deng et al. report the realization of organic thin-film tunnel transistors (OTFTTs) that decisively break this Boltzmann tyranny. The breakthrough is enabled by an interfacial molecule decoupling strategy, introducing a high-ionization-energy molecular interlayer, N,N'-bis(2-phenylethyl)perylene-3,4:9,10-tetracarboxylic diimide (BPE-PTCDI), between the high-work-function metal oxide (MoO3) source and the p-type organic semiconductor (2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT)) channel. This interlayer passivates the interface, minimizing interfacial gap states and alleviating Fermi-level pinning, thereby creating a clean heterojunction with a lowered tunneling barrier. This facilitates efficient quantum mechanical band-to-band tunneling for carrier injection at low supply voltages, instead of relying on traditional thermionic emission. The OTFTTs exhibit sub-thermionic SS values below 60 mV/dec, enabling high electrical performance at low operating voltages. This work provides a viable pathway for beyond-thermionic electronics, with potential applications in flexible displays, wearable health monitors, brain-computer interfaces, and distributed sensor networks, addressing the critical challenge of power dissipation in flexible systems.

Read Full Abstract10.1007/s40843-025-3776-9
Porphyrin Covalent Organic Frameworks: A Duet in PhotocatalysisGraphical AbstractVerified
SCIENCE CHINA Materials2026

Porphyrin Covalent Organic Frameworks: A Duet in Photocatalysis

Porphyrins, nature's molecular workhorses, operate at the core of photosynthesis and cytochrome P450 catalysis, offering a blueprint for sustainable energy and environmental systems. Their rigid, conjugated macrocycles provide broad solar-spectrum absorption, long-lived excited states, and efficient charge transfer, making them ideal building blocks (knots) for covalent organic frameworks (COFs). Since 2011, porphyrin-based COFs have been synthesized via boronate ester and imine linkages, with imine-linked variants proving stable for photocatalysis. A critical design challenge is the strategic selection of linker molecules that bridge porphyrin knots and allow functionalization. Benzothiadiazole (BT) and its dimethoxy derivative (BT(OMe)2) serve as electron acceptors, forming donor-acceptor COFs with porphyrin as the donor. Jiang et al. recently reported H2P-BT-COF and H2P-BT(OMe)2-COF, which exhibit strong electronic coupling, short interlayer distances, and extensive hydrogen-bond networks. In H2P-BT(OMe)2-COF, methoxy groups elevate frontier orbital energies, narrow the bandgap, and redistribute frontier orbital density, while hydrogen bonding strengthens interlayer interactions and facilitates ambipolar charge transfer through segregated π-columns. This dual mechanism suppresses charge recombination and enhances overall charge transfer. Notably, these COFs synergistically utilize both electron transfer (ET) and energy transfer (EnT) pathways: H2P and BT units act as independent oxidation/reduction centers for ET, while π-arrays of H2P serve as active sites for EnT. Methoxy groups increase thermodynamic driving force for superoxide radical formation and establish hydrogen-bond networks that promote singlet oxygen generation, cooperatively supporting both pathways. The polar methoxy groups also create one-dimensional channels for efficient reactant delivery. Consequently, H2P-BT(OMe)2-COF demonstrates outstanding performance in selective organic transformations using O2 as oxidant, including oxidative coupling of benzylamine and oxidative condensation of o-phenylenediamine.

Read Full Abstract10.1007/s40843-026-4005-x