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All Clean Energy & Battery Intelligence (Page 60)

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Showing 24 of 1498 peer-reviewed translated articles (Page 60 of 63)

A Hetero-Cross-Linking Strategy for Versatile Artificial Muscles with Superior Electromechanical SensitivityGraphical AbstractVerified
SCIENCE CHINA Materials2026

A Hetero-Cross-Linking Strategy for Versatile Artificial Muscles with Superior Electromechanical Sensitivity

Dielectric elastomer actuators (DEAs) are promising artificial muscle technologies due to their large actuation strains, high energy density, and fast response. However, their practical application is hindered by a trade-off between increasing the relative dielectric constant (εr) and decreasing the Young's modulus (Y), which limits electromechanical sensitivity (εr/Y) to below 110 MPa⁻¹. Here, we report a hetero-cross-linking strategy to fabricate a semiseparated biphasic bicontinuous dielectric elastomer (SBE) using two commercial silicone elastomers: Elastosil P7676 (mechanical phase, M-phase) and Sylgard 170 (dielectric phase, D-phase). The M-phase provides an ultralow Young's modulus (~10 kPa), while the D-phase offers a high dielectric constant (3.6). With only 10% D-phase content (SBE-1), the material achieves a record-high electromechanical sensitivity of 360 MPa⁻¹. Under an electric field of 35 V μm⁻¹ without prestretching, SBE-1 exhibits a 90% area strain, significantly outperforming pure phases and previously reported DEAs. The interpenetrating phase structure also enhances breakdown strength. SBE-based artificial muscles demonstrate large displacement at high frequencies, achieving a power density of 2250 W kg⁻¹ at resonance (>200 Hz), surpassing natural muscle and prior DEA artificial muscles. A human-like robotic arm with one rotational joint and four pure-shear SBE-based artificial muscles was developed, capable of extending and bending actions. This work provides a versatile strategy for high-performance DEAs, advancing soft robotics applications.

Read Full Abstract10.1007/s40843-025-3970-1
Catching an Optical Photograph via a Focus-Tunable Real-Time Imaging SystemGraphical AbstractVerified
SCIENCE CHINA Materials2026

Catching an Optical Photograph via a Focus-Tunable Real-Time Imaging System

Visual systems are the primary interface for humans to perceive the external environment. Mimicking the human eye, which integrates adjustable lenses with a curved retina, bio-inspired curved image sensors effectively mitigate field curvature and vignetting. To realize focus-tunable imaging, sensors must possess dynamic curvature while maintaining high sensitivity and mechanical stability. However, transitioning from rigid architectures to flexible devices often results in poor surface conformity through simple bending. Flexible sensors have explored intrinsic and structural designs for better flexibility and less stress concentration. Recent advances suggest that ultrathin devices with mesh-inspired designs offer a superior strategy, achieving seamless alignment with the curved surface without compromising optoelectronic performance. He et al. have developed a focus-tunable real-time curved imaging system inspired by the human visual system, based on an ultrathin perovskite curved image sensor with a hierarchical mesh architecture. They introduced an ultrathin image sensor with 5.4 μm thickness and soft interconnections, enabling it to be readily deformed into a hemispherical geometry. The ultrathin structure significantly reduces intrinsic mechanical behaviors, while interconnections effectively release twisting and stretching stress among pixels under various curvature conditions. As a result, the curved sensor array achieves a low detection limit of 10 nW cm−2, approaching the light sensitivity level of human photoreceptors. The focus-tunable imaging system integrates a curved image sensor with a shape-tunable convex lens, forming a conformal, skin-like architecture on a hemispherical surface. Finite element analysis revealed that when deformed to a curvature radius of 17.8 mm, the maximum strain on the Parylene C substrate reaches 5.72% and is primarily localized at pixel interconnections and edge regions. The curved image sensor achieves an overall thickness of approximately 5.4 μm and integrates a perovskite photodetector array comprising 127 pixels, enabling mechanically robust operation under pronounced curvature.

Read Full Abstract10.1007/s40843-025-3958-8
Generative AI Empowers Minimalist Wearable Personalized Human-Machine InterfaceGraphical AbstractVerified
SCIENCE CHINA Materials2026

Generative AI Empowers Minimalist Wearable Personalized Human-Machine Interface

The seamless integration of electronics with the human body is pivotal for next-generation human-machine interfaces (HMI) and personalized healthcare. Traditional high-density sensor arrays, while capable of capturing complex biomechanical data, impose significant power and comfort penalties. This study introduces the Generative EMG Network (GenENet), a framework that synergizes generative artificial intelligence with soft bioelectronics to reduce hardware complexity. By leveraging a 32-channel stretchable sensor array as a 'teacher' dataset, GenENet employs a masked autoencoder architecture to learn spatiotemporal correlations within high-density electromyography (EMG) data. The trained model enables a simplified 6-channel wearable band to replicate the performance of the full 32-channel array. The sensor device utilizes a polydimethylsiloxane (PDMS) substrate, liquid metal (EGaln) interconnects, and a conductive PEDOT:PSS hydrogel interface, achieving low skin-contact impedance and high signal-to-noise ratios under mechanical strain. This approach addresses the bottleneck of data throughput and power consumption in wearable HMIs, offering a path toward minimalist, personalized devices for applications such as sign language decoding and gait analysis. The findings underscore the potential of generative AI to transform wearable bioelectronics by shifting computational burden from hardware to software.

Read Full Abstract10.1007/s40843-025-3911-7
Control Strategy for Mercury Emissions from Coal-Fired Flue Gas in ChinaGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Control Strategy for Mercury Emissions from Coal-Fired Flue Gas in China

Mercury emissions from coal combustion are highly toxic, volatile, and bioaccumulative, posing long-term threats to ecosystems and human health. This review systematically examines the current status and control policies of mercury emissions from coal combustion in China, analyzing distribution characteristics and transformation mechanisms during combustion, with emphasis on collaborative removal in pollution control devices after ultra-low emission retrofitting. A progressive strategy of 'synergistic enhancement–deep purification–resource recycling' is proposed, comprising three tiers: optimizing operational parameters of existing control systems to enhance synergistic mercury removal; developing efficient adsorption and catalytic oxidation technologies for industrial application; and advancing integrated mercury removal and recovery technologies, such as magnetosphere-based sorbents and recovery processes, focusing on high-value utilization. The paper also outlines future research directions aligned with international compliance and domestic environmental tax policies, providing theoretical and technical support for China's commitments to near-zero emissions of coal combustion pollutants.

Read Full Abstract10.1016/S1872-5813(26)60708-6
Research Progress on Hydrogen and Carbon Materials Production from Methane PyrolysisGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Research Progress on Hydrogen and Carbon Materials Production from Methane Pyrolysis

The escalation of global warming and climate change necessitates the development of clean energy carriers. Hydrogen, with a high combustion value of 120 MJ/kg and net-zero carbon emissions, is a promising alternative. Catalytic methane pyrolysis offers a route to produce high-purity hydrogen and functional carbon materials simultaneously. However, challenges persist in catalyst deactivation due to carbon deposition and the efficient separation and valorization of carbon byproducts. This review systematically examines recent progress in solid and molten-medium catalysts for methane pyrolysis. It highlights strategies to enhance catalyst stability, including precise control of active sites, alloying, support optimization, and tuning the carbon-catalyst interface. The introduction of molten media catalytic systems, which feature dynamically refreshed gas-liquid interfaces, can fundamentally mitigate deactivation and facilitate continuous carbon separation. The paper discusses reaction mechanisms, catalytic performance, and control of carbon morphology, along with strategies for efficient separation and purification of carbon products in molten media. High-value applications of the produced carbon materials are also explored. The review underscores the potential of methane pyrolysis as a low-carbon technology for hydrogen production, while identifying key research directions for industrial scalability.

Read Full Abstract10.1016/S1872-5813(26)60681-0
AI for Electrocatalytic Energy Conversion: From Atoms to IndustryGraphical AbstractVerified
SCIENCE CHINA Materials2026

AI for Electrocatalytic Energy Conversion: From Atoms to Industry

Achieving carbon neutralization relies heavily on green hydrogen and electrochemical carbon-nitrogen cycles. However, the complexity of these systems and the cost of traditional Edisonian trial-and-error methods hinder rapid progress. Artificial intelligence (AI) has emerged as a transformative tool, enabling high-throughput data processing and dynamic adaptation. This review surveys the landscape of AI-driven electrochemistry, bridging the gap from atomic-scale design to industrial-scale implementation. Specifically, we focus on three areas: atomic structure-function decoding, fully automated “self-driving” laboratories, and macro-scale simulations for device durability. Furthermore, we elucidate the critical challenges in integrating AI with materials science. By mapping current trends and future directions, this work aims to unlock the full transformative potential of AI in next-generation energy storage and conversion.

Read Full Abstract10.1007/s40843-025-4074-6
Reaction mechanisms and cracking performance of CH4 provoked by non-equilibrium plasmaGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Reaction mechanisms and cracking performance of CH4 provoked by non-equilibrium plasma

Methane cracking driven by electric power holds significant promise in the context of the rapid development of renewable energy. The effects of carrier gas ratio, input power, and inlet gas flow rate on CH4 cracking performance were systematically investigated in a dielectric barrier discharge (DBD) reactor. The variation of temperature distribution and reaction energy intensity were also examined. The experimental results indicate that CH4 conversion and gaseous product formation are promoted by increasing the DBD input power or decreasing the inlet gas flow rate. At an input power of 90 W and an inlet gas flow rate of 200 mL/min, the single-pass CH4 conversion reaches 46.6%, with an H2 yield of 23.3%, demonstrating that CH4 cracking is governed by electron induced reactions. While the Joule heating from the inner and outer electrodes is relatively limited. The reaction energy intensity increases as the CH4 conversion decreases. When the inlet gas flow rate increases from 200 to 800 mL/min, the energy intensity rises by approximately 2.8 times, indicating that higher inlet gas flow rates enhance the convective heat transfer and shorten the gas residence time, thereby suppressing deep CH4 cracking. Moreover, BOLSIG+ calculations further reveal that CH4 activation is dominated by electron induced vibrational excitation, in which stepwise energy accumulation drives C–H bond dissociation. The energy transfer and species transformation pathways of overall CH4 cracking process, which comprises electron energy injection, vibrational excitation, stepwise dissociation, radical chain extension, and final product formation, can be summarized into three stages, i.e. methane activation, radical evolution, and product formation.

Read Full Abstract10.1016/S1872-5813(26)60690-1
Emerging Janus/gradient anode structures for high-performance lithium-metal batteriesGraphical AbstractVerified
SCIENCE CHINA Materials2026

Emerging Janus/gradient anode structures for high-performance lithium-metal batteries

Lithium (Li)-metal batteries (LMBs) are promising next-generation energy storage systems due to their high theoretical capacity (3860 mAh g−1) and low electrochemical potential (−3.04 V vs. standard hydrogen electrode). However, uncontrollable Li dendrite growth and volume fluctuations during cycling cause low Coulombic efficiency, safety hazards, and rapid capacity decay. Conventional 3D current collectors mitigate these issues by increasing surface area and providing void space, but they suffer from top-heavy deposition and underutilization of internal space. Emerging Janus/gradient anode structures, featuring asymmetric or gradient properties in lithiophilicity, conductivity, or porosity, enable bottom-up Li plating and efficient space utilization. This review systematically summarizes design principles, operational mechanisms, and recent progress in lithiophilic-lithiophobic Janus designs, conductivity-gradient frameworks, and dual-gradient configurations. These structures collectively improve Coulombic efficiency, cyclic longevity, and safety. The review concludes with future research directions, underscoring the potential of Janus/gradient anodes for high-energy-density and durable LMBs.

Read Full Abstract10.1007/s40843-025-4099-2
Calcination Atmosphere-Engineered Cu/SiO2 Catalysts for Efficient Hydrogenation of Dimethyl Succinate to 1,4-ButanediolGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Calcination Atmosphere-Engineered Cu/SiO2 Catalysts for Efficient Hydrogenation of Dimethyl Succinate to 1,4-Butanediol

The catalytic hydrogenation of biomass-derived dimethyl succinate (DMS) to 1,4-butanediol (BDO) is a pivotal route for producing high-value C4 chemicals in green chemistry. Cu/SiO2 catalysts are known for high selectivity in hydrogenating ester groups, with performance correlated to copper species microstructure. Although calcination critically defines this active structure, systematic influence of calcination atmosphere remains underexplored. Here, Cu/SiO2 catalysts were prepared via urea-assisted hydrothermal method and calcined under different atmospheres to elucidate effects on physicochemical properties and hydrogenation performance. Comprehensive characterization (N2 physisorption, FT-IR, H2-TPR, XRD, TEM, N2O pulse chemisorption, XPS, NH3-TPD) revealed that calcination atmosphere profoundly alters metal-support interaction, regulating dispersion and chemical state of copper species. Specifically, air calcination promoted stronger metal-support interaction, enhancing copper dispersion and increasing proportion of key active Cu+ species. Consequently, air-calcined catalyst achieved 92.37% DMS conversion and 64.15% BDO yield under optimized conditions (210 °C, 5.0 MPa, WHSV 0.6 h−1, H2/DMS molar ratio 100). This work underscores calcination atmosphere engineering as potent strategy for optimizing metal-support interactions in heterogeneous catalysts for efficient hydrogenation.

Read Full Abstract10.1016/S1872-5813(26)60663-9
Harnessing Anion Intercalation to Activate Layered Double Hydroxides for Efficient and Stable Seawater SplittingGraphical AbstractVerified
SCIENCE CHINA Materials2026

Harnessing Anion Intercalation to Activate Layered Double Hydroxides for Efficient and Stable Seawater Splitting

Direct seawater electrolysis offers a sustainable route to green hydrogen, yet is hindered by the competing chlorine evolution reaction and severe catalyst corrosion. Layered double hydroxides (LDHs), with tunable host layers and exchangeable interlayer galleries, are promising for the oxygen evolution reaction (OER) in seawater, but their intrinsic activity and chloride tolerance need enhancement. Anion intercalation engineering has emerged as a powerful strategy to address these challenges. By inserting functional anions—from simple inorganic ions and polyoxometalates to organic molecules—into LDH interlayers, it is possible to expand interlayer spacing for improved mass transport, modulate the electronic structure of metal centers to boost intrinsic OER activity, and create a negatively charged interfacial microenvironment that selectively enriches OH−. This review comprehensively examines design principles, mechanistic insights, and catalytic performance of various anion-intercalated LDHs for seawater splitting. It highlights representative breakthroughs in material design, discusses integration strategies in practical electrolyzer devices, and evaluates long-term stability under industrial operating conditions. Finally, it outlines key challenges and future directions for rational design and scalable deployment of high-performance, durable LDH-based catalysts for sustainable hydrogen production from seawater.

Read Full Abstract10.1007/s40843-025-4066-x
Synthesis of Plate-Like Alumina via Synergistic Activation from Co-Combustion Ash of Coal Gangue and Corn StalkGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Synthesis of Plate-Like Alumina via Synergistic Activation from Co-Combustion Ash of Coal Gangue and Corn Stalk

This study reports a streamlined route for synthesizing plate-like α-Al2O3 via co-combustion activation of coal gangue and corn stalk, enabling high-value utilization of solid wastes. The introduction of corn stalk significantly reduces the apparent activation energy of coal gangue combustion and increases the acid leaching yield of aluminum to 81.9%. Mechanism analysis reveals that titanium and iron ions in the co-combustion ash leachate act as natural morphology regulators, facilitating the formation of a plate-like structure in the alumina product, with titanium exhibiting leaching behavior consistent with that of aluminum. Furthermore, a high content of AlO6 structural units in the precursor effectively promotes the direct conversion into dense α-Al2O3 crystals during thermal treatment, thereby enhancing product density. Under optimized conditions (800 °C, 1 h), the as-prepared α-Al2O3 exhibits a plate-like morphology, with a median particle size (d50) of 5.70 μm and a density of 4.94 g/cm3. This work provides a new approach for the synergistic resource utilization of coal gangue and biomass waste.

Read Full Abstract10.1016/S1872-5813(26)60686-X
Advances in Piezoelectric Materials with Diverse Crystal Structures: From Design to ApplicationsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Advances in Piezoelectric Materials with Diverse Crystal Structures: From Design to Applications

Piezoelectric materials underpin modern electromechanical energy conversion, serving as critical components in sensors, actuators, and energy harvesters. Their performance is intrinsically governed by the piezoelectric coefficient, yet optimizing this property remains challenging due to the profound influence of diverse microscopic structures. This review systematically examines three fundamental crystalline architectures—perovskite, wurtzite, and fluorite—and critically analyzes performance optimization strategies tailored to each structure. We explore five principal modification approaches: defect engineering, elemental doping, heterostructure film fabrication, composite film design, and buffer layer incorporation, with emphasis on the underlying physical mechanisms that drive property enhancements. By providing a cross-structural comparison, this review establishes clear structure–property relationships, offering a foundational guide for material selection and design. Furthermore, we highlight the implications of these advanced materials for next-generation applications in energy harvesting and smart devices. Finally, we present a forward-looking roadmap, outlining emerging research directions and addressing key technical challenges to guide the development of next-generation high-performance piezoelectric materials.

Read Full Abstract10.1007/s40843-025-4334-9
Influence of Si/Al ratio of MFI zeolites on the microstructure and catalytic performance of Co-based catalyst for N2O decompositionGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Influence of Si/Al ratio of MFI zeolites on the microstructure and catalytic performance of Co-based catalyst for N2O decomposition

A series of Co-based molecular sieve catalysts with varying Si/Al ratios was synthesized via impregnation. Microstructural properties of Co active sites were characterized by XRD, TEM, Raman, H2-TPR, Py-FTIR, and XPS. Results indicate that surface Co species predominantly exist as CoOx nanoclusters and isolated Co2+, with the latter exhibiting superior N2O decomposition activity. Decreasing the Si/Al ratio of the MFI zeolite promotes the formation of isolated Co2+ active sites, thereby enhancing catalytic performance. Compared to Co/S-1 (pure silica support), the Co/HZ60 catalyst (low Si/Al ratio ZSM-5) lowers the temperature for complete N2O decomposition by 80 °C and demonstrates excellent resistance to O2 and NO. The strong interaction between the zeolite framework and Co2+ inhibits oxidation to Co3+, improving N2O adsorption and activation. This work provides a rational design strategy for efficient and stable Co-based catalysts for N2O abatement in industrial tail gases.

Read Full Abstract10.1016/S1872-5813(26)60668-8
Progress of Biomass/Coal-Based Carbon Materials as Electrocatalysts for Oxygen Reduction ReactionGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Progress of Biomass/Coal-Based Carbon Materials as Electrocatalysts for Oxygen Reduction Reaction

The oxygen reduction reaction (ORR) is a critical cathode reaction in fuel cells and metal-air batteries, yet its sluggish kinetics and high overpotential severely limit device performance. Conventional platinum-based catalysts suffer from prohibitive cost (accounting for up to 40% of total fuel cell system cost), scarce reserves, and poor tolerance to methanol and carbon monoxide, impeding large-scale commercialization. This review systematically summarizes recent advances in biomass/coal-based carbon materials as ORR electrocatalysts, focusing on raw material characteristics, preparation methods, structural regulation, and performance evaluation. Biomass and coal precursors offer advantages of low cost, abundant availability, and natural heteroatom doping (N, P, S), enabling the design of high-performance, metal-free catalysts. Key challenges include ensuring raw material homogeneity, precise control of active sites, and scalable synthesis. Future research directions emphasize optimizing pore structure and surface chemistry to enhance four-electron selectivity and stability. The review provides theoretical guidance for developing cost-effective ORR catalysts to replace platinum, thereby accelerating the deployment of clean energy technologies.

Read Full Abstract10.3724/2097-213X.2026.JFCT.0006
In-depth Research on Atomic-Level Issues in the Field of Single-Atom Catalyst SynthesisGraphical AbstractVerified
SCIENCE CHINA Materials2026

In-depth Research on Atomic-Level Issues in the Field of Single-Atom Catalyst Synthesis

Single-atom catalysts (SACs) represent a frontier in catalytic science, offering theoretically 100% atom utilization, tunable electronic structures, and coordination microenvironments, with broad prospects in energy conversion and high-end chemical synthesis. However, atomic-scale challenges—disordered active site distribution, constrained electronic structures, metal atom agglomeration, limited loading capacity, and insufficient coordination environment precision—severely restrict performance optimization and practical deployment. This review systematically analyzes the mechanistic interconnections among these challenges, framing them as a multi-level, coupled systemic problem rather than isolated issues. It summarizes recent regulation strategies including support engineering, coordination regulation, spatial confinement, and dynamic synthesis, emphasizing the value of multi-strategy synergy for performance breakthroughs. Future research directions include developing in-situ characterization with high spatial and temporal resolution, exploring multi-site synergistic catalytic mechanisms, and constructing standardized databases and rational design platforms. These efforts aim to enable large-scale advances in clean energy and green chemical processes.

Read Full Abstract10.1007/s40843-026-4101-5
Hydrothermal Liquefaction of Alkaline Lignin with In Situ Hydrogen Supply from Formic AcidGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Hydrothermal Liquefaction of Alkaline Lignin with In Situ Hydrogen Supply from Formic Acid

Alkali lignin, a high-volume byproduct from pulp and paper manufacturing and biomass refining, is a promising feedstock for aromatic hydrocarbon production in liquid fuels due to its high energy density and abundant aromatic moieties. However, its highly cross-linked polymeric structure hinders efficient valorization. This work investigates catalytic conversion of alkali lignin into bio-oil under in situ H2 supply from formic acid. A series of Ni-Mo/h-BN bimetallic catalysts with varied metal ratios were synthesized by impregnation and characterized by XPS, XRD, and other techniques. The effects of reaction parameters on H2 production via aqueous-phase reforming (APR) of formic acid were evaluated. Optimal H2 yield was achieved at a formic acid-to-water molar ratio of 1:10 and a Ni/Mo atomic ratio of 3:1. H2 yield increased monotonically with temperature from 220 to 280 °C, reaching a maximum of 38.48 mmol. Subsequently, influences of reaction temperature and residence time on bio-oil production were examined. The highest heavy bio-oil yield (18.93%) and maximum relative content of aromatic hydrocarbons (13.81%) were both achieved at 280 °C. Prolonged reaction time reduced heavy bio-oil yield and aromatic hydrocarbon abundance while favoring furan derivatives. This work demonstrates good synergy between in situ hydrogen generation from formic acid and lignin hydrogenation in the temperature range 240–280 °C.

Read Full Abstract10.1016/S1872-5813(26)60717-7
An Insight into Conductive Metal-Organic Frameworks for Chemical SensingGraphical AbstractVerified
SCIENCE CHINA Materials2026

An Insight into Conductive Metal-Organic Frameworks for Chemical Sensing

Chemical sensing technology is pivotal in modern industry and daily life, with sensor performance critically reliant on nanomaterials. While sensors based on traditional nanomaterials, such as inorganic semiconductors and organic conductive polymers, have achieved commercialization, they face persistent challenges. As an emerging subclass, conductive metal-organic frameworks (c-MOFs) not only inherit the core advantages of traditional MOFs—high specific surface area, porosity, and tunable composition/structure—but also offer adjustable electrical conductivity, rendering them ideal for sensing applications. This review systematically elucidates the construction and properties of c-MOFs across microscopic crystalline and macroscopic micro-nano structural scales. Special emphasis is placed on the structural design and regulation of c-MOFs for analytical sensing, and the intrinsic structure-performance relationship is clarified to achieve higher sensitivity, selectivity, response speed, and long-term stability, as well as other performance metrics. Finally, we comprehensively summarize the typical applications of c-MOFs-based sensors, covering environmental and safety monitoring, photoelectric detection, and health monitoring and diagnosis. At the same time, the key challenges existing in this field, such as the controllable preparation of high-quality single-crystal materials, the theoretical analysis of intrinsic electrically conductive mechanisms, and the balance between macroscopic material stability and the processing performance of devices, were evaluated. The future research directions should focus on developing new ligands and metal combinations to optimize the band structure, deepening the exploration of the mechanisms of emerging physical effects such as piezoelectricity, and promoting the integration and application of materials in practical scenarios such as flexible electronics and wearable devices.

Read Full Abstract10.1007/s40843-025-4029-4
Effect of UiO-66 Precursors with Different Ce/Zr Ratios on the Performance of Pt-Based Catalysts in Dry Methane Reforming ReactionsGraphical AbstractVerified
Journal of Fuel Chemistry and Technology2026

Effect of UiO-66 Precursors with Different Ce/Zr Ratios on the Performance of Pt-Based Catalysts in Dry Methane Reforming Reactions

Dry reforming of methane (DRM) converts CH4 and CO2 into syngas with a unity H2/CO ratio, but suffers from catalyst deactivation via sintering and carbon deposition at high temperatures. This study addresses these challenges by employing UiO-66 as a precursor to modify Pt-based catalysts. A series of Pt/CeO2-ZrO2 catalysts were synthesized via incipient wetness impregnation using supports with varying Ce/Zr ratios prepared hydrothermally. Comprehensive characterization—including CO2-TPD, CH4-TPD, XPS, XAFS, in situ DRIFTS, TG, and Raman spectroscopy—revealed a volcano-type correlation between DRM performance and Ce/Zr ratio. Optimal activity and stability were achieved with Pt/3CeO2-ZrO2 (Ce/Zr = 3:1). This catalyst features highly dispersed platinum, primarily as single atoms and thermally stable PtOx clusters. It exhibits the highest concentration of Ce3+ and Zr3+ species, abundant oxygen vacancies, and high defect density, indicating strong metal-support interaction. Mechanistically, stable DRM is facilitated by oxygen-assisted CH4 dissociation and hydrogen-assisted CO2 dissociation. At 800 °C, CH4 and CO2 conversions reached 86% and 93%, respectively, with H2/CO ratio near unity. A 10 h stability test showed no detectable carbon deposition. These results confirm that the catalyst enhances reaction kinetics while demonstrating superior activity, stability, and resistance to coking and sintering.

Read Full Abstract10.1016/S1872-5813(26)60669-X
Additively manufactured metal matrix composites: a review of fatigue and creep resistance for in-service conditionsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Additively manufactured metal matrix composites: a review of fatigue and creep resistance for in-service conditions

Metal additive manufacturing (AM) enables the fabrication of arbitrary three-dimensional structures with unprecedented design freedom. However, components must withstand extreme in-service conditions, including high temperatures, fatigue, and creep, necessitating materials with multifunctional properties. Metal matrix composites (MMCs), comprising reinforcing particles embedded in metallic matrices, offer promising solutions for such harsh environments. Nevertheless, the non-equilibrium nature of AM processes introduces complex phase diffusion, reactions, and melt flow dynamics, making microstructural design and production challenging. This review focuses on the fatigue and creep resistance of additively manufactured MMCs under in-service conditions, emphasizing how composite strategies influence these properties. The underlying mechanisms responsible for property enhancements via AM are interpreted and discussed. Key findings indicate that AM enables refined microstructures, improved particle dispersion, and the formation of in-situ reinforcing phases, which collectively enhance fatigue life and creep resistance. For instance, TiC-reinforced steels exhibit improved wear resistance after heat treatment, and boron-phosphorus interactions in Inconel 718 enhance creep properties. The review provides insights into future directions for developing AM MMCs for critical applications, highlighting the need for tailored microstructures and process optimization to achieve balanced mechanical performance.

Read Full Abstract10.1007/s40843-025-4083-9
Ambient Fabrication of Over 19% Efficient Organic Solar Cells via Spontaneous Water-Spreading and Layer-by-Layer DepositionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Ambient Fabrication of Over 19% Efficient Organic Solar Cells via Spontaneous Water-Spreading and Layer-by-Layer Deposition

The fabrication of high-efficiency organic solar cells (OSCs) under ambient conditions remains a formidable challenge due to the sensitivity of active layer morphology to environmental factors. We propose an innovative approach for air-processed devices that combines spontaneous water-spreading film formation with layer-by-layer (LBL) deposition. This method enables the fabrication of donor- and acceptor-dominant bulk heterojunction blend films near the anode and cathode interfacial layers, respectively, optimizing vertical phase separation and enhancing charge transfer efficiency. In the D18:L8-BO system, the device achieves a power conversion efficiency (PCE) of 19.02% with an exceptionally narrow efficiency distribution. Even for devices with an area of 1 cm2, a PCE of 16.56% is attained. After a 1000-hour decay test, the efficiency retains 84.1%. This novel method offers a promising pathway for advancing the industrial application of large-area, highly stable devices with narrow efficiency distribution under ambient conditions.

Read Full Abstract10.1007/s40843-026-4109-2
Inorganic Biomaterials as Immunomodulators: Dual Strategies for Activation and SuppressionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Inorganic Biomaterials as Immunomodulators: Dual Strategies for Activation and Suppression

Precise regulation of the immune system is essential for maintaining physiological homeostasis and treating disease. Insufficient immune activation leads to tumor development, whereas excessive immune responses cause autoimmune diseases or chronic inflammation. Inorganic biomaterials, owing to their unique intrinsic properties such as enzyme-mimicking catalytic functions, tunable composition and morphology, degradability, and inherent bioactivity, have transformed from conventional carriers into versatile platforms capable of actively regulating immune responses. This review summarizes recent progress in immunoregulatory inorganic biomaterials, highlighting their dual capacities to induce immune activation or immune suppression. For immune activation, inorganic materials serve as adjuvants to enhance antigen presentation, induce immunogenic cell death (ICD), and reprogram immune cell metabolism, enabling applications in tumor treatment. For immune suppression, specific inorganic materials effectively eliminate excessive reactive oxygen species (ROS), modulate the functions of inflammatory cells such as neutrophils, and promote the development of immunosuppressive cell populations, including regulatory T cells and M2 macrophages, thereby re-establishing immune tolerance in autoimmune diseases. Despite remaining challenges in mechanistic verification, long-term biosafety, and clinical translation, inorganic biomaterials offer a promising multifunctional platform for achieving precise immune interventions across cancer immunotherapy, tissue regeneration, and autoimmune disease management.

Read Full Abstract10.1007/s40843-025-4001-x
Copper-based single-atom catalysts for synergistic antibacterial action: synthesis, mechanisms, and multifunctional applicationsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Copper-based single-atom catalysts for synergistic antibacterial action: synthesis, mechanisms, and multifunctional applications

Bacterial infections and the accelerating rise of antimicrobial resistance (AMR) demand innovative antibacterial strategies beyond conventional antibiotics. Copper single-atom catalysts (Cu-SACs), featuring atomically dispersed active sites and tunable electronic structures, offer potent multimodal catalytic antibacterial functions. This review summarizes recent advances in the design, mechanisms and applications of Cu-SACs in antimicrobial technologies. We first outline four major synthesis routes: thermal activation, solvent-mediated strategies, energy-intensive methods and template-etching approaches, enabling high loading, stable anchoring and scalable, environmentally compatible production. We then dissect the multimodal antibacterial mechanisms of Cu-SACs: functioning as nanozymes to catalyze reactive oxygen species (ROS) generation; acting as photosensitizers to enable photocatalytic and photothermal bactericidal activity; and integrating these pathways with gas therapy, controlled ion release and immune modulation to construct multidimensional antimicrobial networks capable of eradicating drug-resistant bacteria and biofilms. We further discuss the substantial potential of Cu-SACs across three application domains: chemical-free, high-efficiency disinfection and real-time monitoring in water purification; durable self-disinfecting performance in antimicrobial textiles; and precision infection management in biomedical settings through integrated “bactericidal-anti-inflammatory-tissue-repair” therapeutic frameworks for both superficial and deep-tissue infections. Finally, we examine the challenges and future directions for the clinical translation and precise antimicrobial deployment of Cu-SACs, providing a conceptual foundation and practical guidance for advancing atomically engineered antibacterial materials from laboratory research to industrial applications.

Read Full Abstract10.1007/s40843-025-4064-1
Remarkable roles of electron-rich Mo and electron-deficient Ni active pairs in MoN/Ni heterostructures in promoting efficient urea oxidation reactionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Remarkable roles of electron-rich Mo and electron-deficient Ni active pairs in MoN/Ni heterostructures in promoting efficient urea oxidation reaction

The urea oxidation reaction (UOR) offers a low-energy pathway for hydrogen production via water electrolysis, but Ni-based catalysts suffer from Ni self-oxidation reaction (NSOR) that wastes energy and poisons active sites via strong CO2 adsorption. Here, we design MoN/Ni heterostructures to optimize the electronic structure of Ni sites, suppressing NSOR. X-ray photoelectron spectroscopy and X-ray absorption spectroscopy confirm the formation of electron-rich Mo and electron-deficient Ni active pairs. In-situ spectroscopy, electrochemical tests, and density functional theory calculations reveal that electron-rich Mo sites enhance urea adsorption, while electron-deficient Ni sites prevent NSOR, facilitating urea activation, intermediate conversion, and CO2 desorption. The synergistic effect yields a current density of 100 mA cm−2 at only 1.39 V vs. RHE in 1 M KOH + 0.33 M urea, outperforming many NiOOH-based catalysts. This work introduces a novel high-performance catalyst with electron-rich/electron-deficient active pairs for efficient UOR.

Read Full Abstract10.1007/s40843-025-4162-0
Giant Optical Anisotropy in the Edge Surfaces of Layered Crystals: Unveiled by Direct Measurements of Out-of-Plane Optical ConstantsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Giant Optical Anisotropy in the Edge Surfaces of Layered Crystals: Unveiled by Direct Measurements of Out-of-Plane Optical Constants

Large optical anisotropy is paramount for efficient light manipulation in optoelectronic devices. Van der Waals layered materials, exhibiting large structural contrast between in-plane and out-of-plane directions, are inherently anisotropic in 3D space. However, measurements of their optical constants have been limited to 2D planes. Here, we directly measure reflectance spectra from the edge and basal surfaces of layered MoS2, NbOCl2, and WTe2 crystals to compare out-of-plane and in-plane optical constants in the 500–1000 nm range. Results show that out-of-plane refractive indices are smaller than in-plane values. Out-of-plane extinction coefficients are zero for MoS2 and NbOCl2 but nonzero for WTe2, confirmed by transient reflection spectroscopy. The nonzero extinction in WTe2 arises from symmetry of transition dipole moments and density of states dictated by crystal structure. Out-of-plane optical constants of MoS2 and NbOCl2 exhibit less dispersion than in-plane, whereas WTe2 shows enhanced out-of-plane dispersion around 2.14 eV, attributed to increased optical transition probability from larger density of states. These parameters indicate giant birefringence (>1.8 for MoS2, >0.6 for NbOCl2, >0.5 for WTe2) and linear dichroism (up to 100% for MoS2 and NbOCl2, 40.7% for WTe2) on edge surfaces. Results enable prediction of optical response at arbitrary incidence angles, aiding polarization-related optoelectronic devices.

Read Full Abstract10.1007/s40843-026-4149-1