SinoGreenTech Academic Portal
📚 Peer-Reviewed Translated Literature

All Clean Energy & Battery Intelligence (Page 17)

Browse complete peer-reviewed translations from top indexed Chinese clean energy & battery intelligence journals. Read verified previews and download authentic research reports verified by SinoGreenTech.

Published Research Papers

Showing 24 of 1398 peer-reviewed translated articles (Page 17 of 59)

Laminated self-healing thermochromic gel for visualizing thermal managementGraphical AbstractVerified
SCIENCE CHINA Materials2026

Laminated self-healing thermochromic gel for visualizing thermal management

Thermochromic soft materials are flexible functional materials that adaptively tune optical properties (transmittance, reflectance, or scattering) with temperature for thermal modulation. Herein, a laminated thermochromic gel (DEE-DA) is synthesized by encapsulating a thermochromic hydrogel (DA) between two hydrophobic ionogels (DEE) in a stacked configuration. The synergy of multiple dynamic bonds endows the DEE-DA gel with exceptional mechanical properties and remarkable self-healing capability (98.8% at 30 °C). More importantly, attributed to the temperature-responsive reversible cleavage and recombination of hydrogen bonds and borate ester bonds, DEE-DA gel demonstrates tunable transmittance with a light modulation efficiency of 85.45%. In response to the various external conditions, the gel can auto-adjust the optical properties to avoid sun irradiation or heat loss. Accordingly, the gel enables efficient dual-mode thermal modulation across a broad temperature range to realize thermal management. The research proposes gel thermochromism and laminated durability enhancement for adaptive materials in smart buildings and wearables.

Read Full Abstract10.1007/s40843-025-3747-3
Synergistic Additive Engineering with Sulfur-Terminated Ti3C2Tx MXene towards Efficient and Stable Perovskite Solar CellsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Synergistic Additive Engineering with Sulfur-Terminated Ti3C2Tx MXene towards Efficient and Stable Perovskite Solar Cells

Two-dimensional MXene Ti3C2Tx demonstrates great promise in perovskite solar cells (PSCs). Herein, sulfur-terminated Ti3C2Tx (S-Ti3C2Tx) is developed by modifying Ti3C2Tx via a facile hydrothermal method using thioacetamide. As a perovskite additive, S-Ti3C2Tx outperforms pristine Ti3C2Tx by (1) significantly promoting grain growth, enhancing carrier mobility, and reducing defect density; (2) optimizing energy level alignment to lower interfacial energy barriers and minimize interface non-radiative recombination; (3) stabilizing uncoordinated Pb2+ and [PbI6]4− octahedra via Pb–S bonds while alleviating bulk lattice strain, as this Pb–S interaction exerts a “tape-like” effect. Based on this synergistic mechanism, PSCs with S-Ti3C2Tx achieve a champion efficiency of 25.51%—outperforming control (23.46%) and pristine Ti3C2Tx-based devices (24.54%)—with enhanced stability. This work highlights terminal group engineering as a critical strategy for advancing high-performance PSCs and their potential for emerging photovoltaic technologies.

Read Full Abstract10.1007/s40843-025-3795-x
Redefining selectivity paradigms in electrochemical nitrogen reduction reaction on confined dual-atom catalystsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Redefining selectivity paradigms in electrochemical nitrogen reduction reaction on confined dual-atom catalysts

The premature decay of electrochemical nitrogen reduction reaction (eNRR) performance at low electrode potentials remains a major obstacle to practical applications, primarily due to competition from the hydrogen evolution reaction (HER). A new paradigm capable of transcending current selectivity constraints is urgently required to advance eNRR toward industrial implementation. In this work, we propose two practical selectivity descriptors (ΔΔG and ΔU) based on a systematic investigation of the potential-dependent competition between eNRR and HER on confined dual-atom catalysts. The descriptor ΔΔG (ΔG_N2 − ΔG_H) identifies the potential range where N2 adsorption dominates over H adsorption, while ΔU (U_cross – U_eNRR) specifies the potential range to trigger direct eNRR, offering a quantitative benchmark for rational catalyst design. Ideal catalysts should maintain N2-preferential adsorption across a broad potential window to facilitate direct eNRR. Guided by this insight, we demonstrate that confined dual-atom configurations with optimized interatomic distances can simultaneously achieve both overwhelming N2 adsorption and sufficient activation, thereby overcoming conventional selectivity limitations. This strategy enables ammonia synthesis with industrially relevant production rates and current density even at elevated potentials. Our mechanistic insights not only elucidate the root causes of performance limitations in eNRR but also offer a rational design framework for developing high-performance catalysts across a broad range of electrochemical transformations.

Read Full Abstract10.1007/s40843-025-3739-8
Impedance-Matchable 3D MXene Sponge/NiFe@NC Heterostructure with Tunable Pores for Efficient Electromagnetic Wave Absorption and Thermal ResistanceGraphical AbstractVerified
SCIENCE CHINA Materials2026

Impedance-Matchable 3D MXene Sponge/NiFe@NC Heterostructure with Tunable Pores for Efficient Electromagnetic Wave Absorption and Thermal Resistance

The proliferation of 5G/6G communications and radar systems has intensified electromagnetic wave (EMW) leakage, interference, and thermal management challenges. This study presents a 3D MXene sponge/NiFe@NC heterostructure with tunable pore architecture, fabricated by pyrolyzing a polyurethane (PU) foam template uniformly coated with NiFe-decorated Ti3C2Tx MXene nanosheets. The resulting porous dielectric-magnetic network integrates interconnected MXene pathways with uniformly dispersed NiFe@NC nanoparticles, enabling synergistic dielectric-magnetic loss via conduction loss, dipole/interface polarization, and magnetic loss. Precise pore structure design enhances impedance matching and promotes multi-scattering and internal reflection of EMWs. An 'EMW-pore matching' mechanism is proposed, where pore size governs impedance matching at specific frequencies, enabling tunable absorption performance. The optimized absorber achieves a reflection loss (RL) of -67.84 dB, while radar cross-section (RCS) simulations confirm exceptional attenuation and stealth potential. Additionally, the 3D skeleton derived from PU foam confers remarkable thermal resistance and flame retardancy. This pore-regulation strategy provides a scalable route to designing lightweight, broadband, and thermally stable EMW absorbers for next-generation communication and stealth applications.

Read Full Abstract10.1007/s40843-025-3887-6
Synergistic dual supramolecular interactions enhance ionic thermoelectric performance in dilute-electrolyte hydrogelsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Synergistic dual supramolecular interactions enhance ionic thermoelectric performance in dilute-electrolyte hydrogels

Converting body heat into electricity presents an appealing route for sustainably powering wearable electronics; however, conventional thermoelectric materials face significant drawbacks, including high ionic concentrations, toxicity, and limited thermoelectric efficiency. Here, we report an ionic thermoelectric hydrogel designed through precise supramolecular chemistry, utilizing dual molecular interactions: host-guest complexation of α-cyclodextrin (α-CD) with I3− ions and hydrogen bonding between polyvinyl alcohol (PVA) polymer chains and I3−. This molecularly tailored approach markedly amplifies thermoelectric performance, achieving a high thermopower of 2.21 mV/K and a tenfold enhancement in peak power output at an exceptionally low iodine concentration (10 mmol/L I− + 2.5 mmol/L I3−). The hydrogel maintains excellent biocompatibility and mechanical robustness, suitable for direct skin contact. Demonstrated applications include flexible thermoelectric devices generating nearly 100 mV from body heat and sensor arrays capable of motion and spatial temperature sensing. These results underscore the substantial potential of supramolecularly designed ionic thermoelectric hydrogels for wearable energy harvesting, personalized healthcare monitoring, and advanced human-computer interfaces.

Read Full Abstract10.1007/s40843-025-3689-9
Polarization-Sensitive Air-Stable Photodetector Based on Ternary Layered Compound FeIn2Se4Graphical AbstractVerified
SCIENCE CHINA Materials2026

Polarization-Sensitive Air-Stable Photodetector Based on Ternary Layered Compound FeIn2Se4

Layered chalcogenide compounds have attracted considerable attention for optoelectronic applications due to their rich structural diversity and unique physical properties, including high carrier mobility, ferromagnetism, ferroelectricity, and outstanding optoelectronic and thermoelectric performance. Their tunable bandgaps and strong light absorption render them highly suitable for next-generation photodetectors. However, the environmental instability of many 2D chalcogenides poses a critical challenge for practical applications. In this work, we report a high-performance, polarization-sensitive photodetector based on an air-stable ternary chalcogenide FeIn2Se4. Angle-resolved polarized Raman spectroscopy reveals that the four characteristic Raman modes exhibit a 60° periodic variation in intensity, highlighting the material's pronounced in-plane anisotropy. Benefiting from its strong absorption over a broad spectral range (510–1028 nm), the FeIn2Se4-based device demonstrates reliable photoresponse under multiple excitation wavelengths (405, 473, 515, and 638 nm), showcasing its wideband detection capabilities. Furthermore, XPS measurements after prolonged air exposure confirm the enhanced chemical stability of FeIn2Se4 compared to binary chalcogenides. These findings demonstrate that 2D ternary FeIn2Se4 is an excellent candidate for advanced anisotropic optoelectronic devices, offering broadband photodetection, robust polarization sensitivity, and excellent environmental resilience.

Read Full Abstract10.1007/s40843-025-3760-y
PANoptosis-Driven Immunogenic Cell Death by a Single NIR Laser-Triggered Nanoplatform for Cancer PhototherapyGraphical AbstractVerified
SCIENCE CHINA Materials2026

PANoptosis-Driven Immunogenic Cell Death by a Single NIR Laser-Triggered Nanoplatform for Cancer Phototherapy

Immuno-phototherapy faces a critical bottleneck: achieving high singlet oxygen (1O2) quantum yield and efficient photothermal conversion simultaneously under a single near-infrared (NIR) laser. Here, we report an acceptor-donor-acceptor (A-D-A) structured molecule, 3,9-bis(2-methylene-((3-(1,1-dicyanomethylene)-6/7-methyl)-indanone))-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d:2',3'-d']-s-indaceno[1,2-b:5,6-b']-dithiophene (m-ITIC), formulated into nanoparticles (NPs) via self-assembly with DSPE-PEG-NH2. The NPs exhibit strong NIR absorption and fluorescence at 688 and 768 nm, respectively. Under single-laser irradiation, they generate heat, superoxide anion (O2•−), and 1O2, with a 1O2 quantum yield of 56.8% and photothermal conversion efficiency (PCE) of 27.4%. This enables NIR fluorescence imaging-guided synergistic photodynamic therapy (PDT) and photothermal therapy (PTT). Notably, the nanoplatform induces PANoptosis—a coordinated cell death program integrating pyroptosis, apoptosis, and necroptosis—in tumor cells, amplifying immunogenic cell death (ICD). This triggers robust dendritic cell activation, macrophage polarization toward M1 phenotype, elevated CD8+ T cell infiltration, and suppression of immunosuppressive Treg cells, leading to significant tumor growth inhibition and prevention of lung metastasis in vivo. Therapeutic efficacy was validated in patient-derived tumor organoids, underscoring translational potential. This study presents a novel single-laser-activated nanoplatform that simultaneously mediates efficient photothermal and photodynamic effects and induces PANoptosis-driven ICD for synergistic cancer immunotherapy.

Read Full Abstract10.1007/s40843-025-3665-2
Dislocations in Motion: Engineering Mechanoluminescence via Pressure-Driven Phase TransitionsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Dislocations in Motion: Engineering Mechanoluminescence via Pressure-Driven Phase Transitions

Mechanoluminescent (ML) materials that emit light under mechanical stress are attracting growing attention for their potential in next-generation sensing, display, and energy-harvesting technologies. Among these, Mn/Cu-doped zinc sulfide (ZnS) has emerged as a leading candidate due to its bright emission, low activation threshold, and remarkable self-recovery over thousands of cycles. Despite these advantages, the fundamental mechanisms governing ML remain unresolved, with ongoing debate between two primary models: the piezoelectric effect and the triboelectric effect. The piezoelectric effect is generally associated with scenarios where ML materials emit light directly under external pressure and exhibit self-recoverable performance, whereas the triboelectric effect dominates when emission occurs at the interface of layered materials. Previous research on ZnS-based ML systems has focused on phase transitions from the sphalerite phase to the wurtzite phase, as the latter is widely recognized as critical for ML activity. A recent study published in Advanced Materials introduces a transformative approach that not only enhances ML performance but also provides new insights into its underlying mechanism. The authors demonstrate that controllable phase transitions can be used to tune and optimize ML properties in ZnS. For the first time, they report a gradual and reversible transition between hexagonal wurtzite (wt-ZnS) and cubic sphalerite (sp-ZnS) phases at room temperature using low uniaxial pressure in the range of 0–30 MPa, a striking departure from the extreme conditions traditionally required for such transformations. Applying modest pressure with a standard tableting machine converts wt-ZnS into sp-ZnS without the need for high-temperature or high-pressure environments, while subsequent thermal annealing reverses the process, enabling reversible structural cycling. High-resolution transmission electron microscopy reveals that this phase transition is mediated by dislocations: a 1/3⟨1120⟩ screw dislocation decomposes into two 30° Shockley partial dislocations, 1/3⟨1010⟩ and 1/3⟨0110⟩, whose glide converts portions of the wt-ZnS lattice into the sp-ZnS structure. These dislocation-driven rearrangements introduce stacking faults and localized lattice distortions that exert a profound influence on luminescence behavior. Under dynamic loading, charged dislocations facilitate carrier transport toward Mn2+ luminescent centers by altering the energy transfer pathways. Regions undergoing phase transition exhibit stronger mechanoluminescence due to an enhanced local piezoelectric field compared to areas without phase transition. The study further uncovers strikingly different responses for Mn and Cu dopants under pressure. For Mn-doped ZnS, ML intensity increases by up to 2.7 times at moderate pressures around 10 MPa, an enhancement attributed to stronger local piezoelectric fields and more efficient carrier transport. In contrast, Cu-doped ZnS exhibits pronounced ML quenching under similar conditions, underscoring the fundamentally different energy transfer pathways associated with these dopants. Pressure-thermal cycling enables tunable ML and photoluminescence (PL) properties, opening new opportunities for adaptive optical devices. The manuscript also reports on the ML behavior of Mn, Cu co-doped ZnS, which exhibits similar pressure-responsive characteristics to Cu-doped ZnS, but with the emission predominantly originating from Mn2+ centers. The authors propose a dislocation-mediated ML mechanism in which charged dislocations generate local electric fields that alter carrier migration and complexation. Under dynamic loading, the piezoelectric field in ZnS separates carriers, which become trapped at defect levels and subsequently recombine at luminescent centers, leading to light emission.

Read Full Abstract10.1007/s40843-025-3711-8
Green Separation Membranes for Water Sustainability: A Breakthrough in Biodegradable Nanofiltration TechnologyGraphical AbstractVerified
SCIENCE CHINA Materials2026

Green Separation Membranes for Water Sustainability: A Breakthrough in Biodegradable Nanofiltration Technology

Water scarcity, exacerbated by organic micropollutant contamination and climate change, necessitates energy-efficient, eco-friendly purification technologies. Membrane separation has emerged as a transformative solution, outperforming energy-intensive processes such as distillation. Traditional chemical separations, dominated by distillation, consume 10%–15% of global energy, whereas advanced membrane technologies can reduce energy use by up to 90%. However, membrane separation is hampered by reliance on toxic petrochemical feedstocks and persistent microplastic pollution from nonbiodegradable end-of-life membranes. Shao's group addresses both gaps with a sustainable nanofiltration membrane (SNFM) crafted entirely from low-hazard, renewable components. The substrate polylactic acid (PLA), a biodegradable polyester derived from corn starch, is processed via modified nonsolvent-induced phase separation (NIPS) to form a porous yet strong support. For the selective layer, toxic aromatic monomers are replaced with xylitol (a plant sugar alcohol) and dopamine (DA, a biogenic amine), and green solvents such as dimethyl sulfoxide are used to avoid volatile organic compound emissions. Compared with commercial alternatives, this design yields a membrane with exceptional dual functionality: it maintains high separation performance (928% greater permeance, 92% bisphenol A rejection, and 89% Na2SO4 rejection) and low fouling (protein adsorption ≤12 μg cm−2) over 30 days. A life cycle assessment reveals a 62% reduction in carbon footprint compared with petrochemical-based membranes, whereas soil biodegradation tests confirm 90% breakdown within 6 months, driven by Delftia and Tissierella microbes. By eliminating microplastic waste and toxic inputs, this SNFM bridges the divide between performance and environmental responsibility, offering a scalable blueprint for next-generation green membranes in water treatment and beyond.

Read Full Abstract10.1007/s40843-025-3730-3
Tetrahedral Framework Nucleic Acid Loaded Celastrol Ameliorates Skin Fibrosis by Epithelial-Mesenchymal Transition PreventionGraphical AbstractVerified
SCIENCE CHINA Materials2026

Tetrahedral Framework Nucleic Acid Loaded Celastrol Ameliorates Skin Fibrosis by Epithelial-Mesenchymal Transition Prevention

Progressive skin fibrosis ultimately results in irreversible contractures, causing both joint dysfunction and cosmetic deformity. The key pathological features of skin fibrosis include persistent inflammation and abnormal accumulation of the extracellular matrix (ECM), with epithelial-mesenchymal transition (EMT) playing a critical role in disease progression. However, current therapeutic strategies for cutaneous fibrosis are largely palliative and often require repeated interventions, with limited efficacy. Celastrol (Cel) exerts anti-inflammatory and anti-fibrotic effects in skin tissue, but its clinical application is limited by poor bioavailability and a narrow therapeutic window. Tetrahedral framework nucleic acid (tFNA), a novel nanocarrier system, exhibits multiple advantages, including enhanced cellular uptake, improved cell viability, and intrinsic anti-fibrotic and anti-inflammatory properties. Therefore, this study applied tFNA-Cel complex (TCC) as an advanced nanotherapeutic agent, designed to exert a synergistic anti-fibrotic effect. In this study, an in vitro model of skin fibrosis was established using human keratinocyte (HaCaT) cells treated with 5 ng mL−1 transforming growth factor beta (TGF-β) for 24 h. The results showed that TCC significantly inhibited EMT progression by reducing α-smooth muscle actin (α-SMA) levels and increasing E-cadherin level. Compared to tFNA or Cel alone, TCC exhibited superior anti-fibrotic effects in the fibrosis model, as evidenced by modulation of SMAD family member 2 (SMAD2) signaling and collagen I expression. Furthermore, the TCC group showed lower levels of nuclear factor κB p65 (NF-κB p65), BCL-2-associated X protein (Bax), and reactive oxygen species (ROS) compared to the Cel or tFNA groups. These findings highlight TCC as a promising treatment for skin fibrosis, with its synergistic anti-fibrotic effects providing new therapeutic avenues.

Read Full Abstract10.1007/s40843-025-3767-9
Lighting the Way: Precision Doping in Organic SemiconductorsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Lighting the Way: Precision Doping in Organic Semiconductors

Doping is essential for modulating semiconductor conductivity, forming p–n junctions, and reducing contact resistance. However, organic semiconductors (OSCs) face challenges in achieving precise regional doping due to uncontrollable dopant diffusion and poor process compatibility. This highlight discusses a breakthrough light-triggered strategy for spatially controlled n-type doping in OSCs, developed by Pei's Group. The method employs inert photoactivable dopants (iPADs) that are thermally stable but undergo rapid 6π-electrocyclization upon UV irradiation, transforming into potent n-dopants (PADs). These PADs irreversibly dope n-type OSCs via hydride transfer. With a high activation barrier (>28 kcal mol−1), the reaction is thermally suppressed even at 120°C, enabling orthogonal control: doping occurs only where and when light is applied. This approach achieves down to 1 μm spatial resolution, far surpassing physical masking methods. The method's universality accommodates diverse n-type OSCs (LUMO: −3.7 to −4.7 eV) with conductivity enhancements up to nine orders of magnitude (exceeding 30 S cm−1 in some systems). Doping levels, conductivity, and Fermi energy are tunable via UV dose and dopant concentration. The doped regions exhibit robust stability and withstand subsequent thermal processing, aligning with large-scale and flexible manufacturing. In organic field-effect transistors, precise spatial doping significantly enhances carrier mobility, reduces contact resistance to one-sixth of its original value, and effectively lowers surface trap density, providing critical support for device miniaturization and high-density integration.

Read Full Abstract10.1007/s40843-025-3692-9
Natural Material-Based Biodegradable Flexible Pressure Sensor for Fall Detection and Rehabilitation Monitoring in Elderly CareGraphical AbstractVerified
SCIENCE CHINA Materials2026

Natural Material-Based Biodegradable Flexible Pressure Sensor for Fall Detection and Rehabilitation Monitoring in Elderly Care

Flexible pressure sensors (FPSs) are pivotal for fall detection and rehabilitation training, yet conventional synthetic-based sensors suffer from resource-intensive manufacturing, high costs, and environmental pollution. This study introduces a sustainable fabrication strategy for FPSs using natural materials. Electrodes were fabricated by treating natural wood strips with a flame retardant, converting them into high-quality graphene via cost-effective infrared laser processing, and transferring onto starch-based substrates. The dielectric layer comprised an electrospun composite nanofiber membrane of cyclodextrin and carbon nanotubes. The resultant capacitive FPS exhibited high sensitivity (2.15 kPa⁻¹ within 0–10 kPa), a low detection limit (~6.5 Pa), rapid response and recovery times (29 ms and 39 ms), and excellent long-term stability exceeding 5000 cycles. Biocompatibility was outstanding (cell viability >98%), and the sensor fully degraded within 6 hours. Integrated with wireless technology, the sensor enabled a fall detection and rehabilitation monitoring system. Data processing utilized a Tiny Machine Learning module on a mobile platform, transmitting data to a cloud-based system. The system accurately identified five common fall postures and assisted clinicians in guiding rehabilitation exercises, achieving recognition accuracies of 99% and 100%, respectively. This work offers a sustainable healthcare solution for elderly care, addressing environmental and economic limitations of existing FPS technologies.

Read Full Abstract10.1007/s40843-025-3716-x
Solid-State Hot-Pressing Strategy Breaks Scalability and Monolithic Shaping Barriers for Covalent Organic FrameworksGraphical AbstractVerified
SCIENCE CHINA Materials2026

Solid-State Hot-Pressing Strategy Breaks Scalability and Monolithic Shaping Barriers for Covalent Organic Frameworks

Covalent organic frameworks (COFs) are porous crystalline materials assembled from organic building blocks via strong covalent bonds, offering well-defined pores, high surface area, and tunable properties for applications in gas storage, separation, catalysis, sensing, and energy conversion. However, conventional solvothermal synthesis requires high temperatures, long reaction times, and complex procedures, hindering scalability and increasing costs. Additionally, COFs are typically obtained as microcrystalline powders, limiting their direct use in flow processes. To overcome these barriers, a novel solid-state hot-pressing method was recently reported, enabling rapid synthesis of COF platelets with high crystallinity and porosity. This method involves applying pressure and heat simultaneously, reducing the energy barrier for monomer reactions and facilitating layer growth and stacking, as confirmed by density functional theory and molecular dynamics simulations. The approach demonstrated versatility by synthesizing 15 distinct COFs, including imine-, hydrazone-, β-ketoenamine-, and imide-linked frameworks, a three-dimensional COF (COF-300), and a mixed-monomer COF, all within 0.5–5 minutes. Notably, a free-standing COF platelet of 200 cm² was fabricated, showcasing scalability. This strategy addresses the trade-offs among synthetic convenience, product quality, environmental impact, and scalability, positioning COFs for commercial viability.

Read Full Abstract10.1007/s40843-025-3736-8
Cross-Flow Boosts Ultrafast-Charging Organic Cathodes via 2D Vertically Ladder-Like Polymer DesignGraphical AbstractVerified
SCIENCE CHINA Materials2026

Cross-Flow Boosts Ultrafast-Charging Organic Cathodes via 2D Vertically Ladder-Like Polymer Design

The escalating demand for energy storage systems capable of delivering high energy density alongside ultrafast charging and discharging has exposed the limitations of conventional lithium-ion batteries (LIBs), particularly in applications such as electric air vehicles, portable medical devices, and grid-scale storage. Organic cathode materials offer tunable molecular design but suffer from sluggish ion diffusion kinetics, especially under high-rate and low-temperature conditions. This study introduces a 2D vertically ladder-like polymer (2DVLP) synthesized from tribenzoquinoline tribenzoquinone (TTQ) via a 2D polymerization strategy. The polymer features a layered nanosheet structure with densely distributed carbonyl (C=O) redox-active sites serving as Li+ storage centers. Interlayer micropores (0.4–2.0 nm) and structural defects facilitate vertical Li+ diffusion, while weak van der Waals interlayer interactions (no π–π stacking) enable horizontal Li+ intercalation. Coin-type half-cells using 2DVLP cathodes demonstrated outstanding room-temperature performance: 2DVLP-1 and 2DVLP-2 achieved specific capacities of 302 and 291 mAh g−1 at low current densities, respectively. The cross-flow design—combining vertical and horizontal ion transport pathways—effectively mitigates concentration polarization, enabling ultrafast charging. This work provides a scalable strategy for developing high-power organic cathodes, addressing critical bottlenecks in fast-charging energy storage.

Read Full Abstract10.1007/s40843-025-3704-0
Organic Deep-Trap Fillers Enable 250 °C Polymer CapacitorsGraphical AbstractVerified
SCIENCE CHINA Materials2026

Organic Deep-Trap Fillers Enable 250 °C Polymer Capacitors

Polymer capacitors are essential for modern power electronics, but their operation is limited by poor energy density at elevated temperatures. Biaxially oriented polypropylene (BOPP), the industry standard, fails above ~105 °C. This highlight discusses a breakthrough by Yang et al. that uses a generative machine-learning pipeline to discover organic fillers with both wide bandgap (Eg) and high electron affinity (Ea), properties typically mutually exclusive. The model screened over fifty thousand structures to identify more than two hundred high-scoring candidates. Two representatives, 4,6-dinitrobenzene-1,3-dicarbonitrile and 2,4,6-tricyano-1,3,5-triazine, were synthesized, exhibiting Eg ≈ 5.5 eV and Ea ≈ 4.5 eV. Dispersed in a polyimide host, these fillers create deep electron traps that suppress leakage current and delay avalanche breakdown. Composite films achieved an energy density of 5.1 J cm−3 at 250 °C with 90% efficiency, outperforming conventional polymers. The team scaled production using a roll-to-roll line, producing kilometer-scale films with uniform dispersion. This work demonstrates a viable path to high-temperature polymer capacitors for traction inverters and DC-link applications.

Read Full Abstract10.1007/s40843-025-3729-9
Bias-free iontronic memory sensors realize adaptive chemotaxisGraphical AbstractVerified
SCIENCE CHINA Materials2026

Bias-free iontronic memory sensors realize adaptive chemotaxis

Biological intelligence achieves exceptional energy efficiency and environmental adaptability, exemplified by the human brain's ~20 W resting power consumption. A key strategy is the use of multi-ions as signal carriers for transduction and processing. Iontronics, employing ions instead of electrons, offer a promising route to low-energy, heat-dissipation-free devices for memory, sensing, and neuromorphic computing. However, conventional iontronics require external voltage bias to drive ion motion, complicating miniaturization and integration. Here, we highlight a recent breakthrough by Guo et al. reporting a bias-free iontronic memory sensor ('memsensor') that operates by controlling surface ion migration. The device couples vanadium dioxide (VO2) with a low-work-function indium (In) patch. Upon immersion in NaCl solution, In3+ ions generated electrochemically within the Debye length are driven by the intrinsic surface electric field to diffuse into the VO2 surface, inducing an insulator-to-metal phase transition and a measurable, non-volatile change in surface conductance. This conductance state correlates with NaCl concentration and can be reversibly restored by H2O2 treatment. The memsensor emulates the gustatory plasticity of C. elegans, mimicking the response dynamics of ASEL and ASER neurons. In a proof-of-concept, a model boat equipped with the memsensor exhibits adaptive chemotaxis: after 'starvation' training in high NaCl concentration, it avoids high-concentration zones; conversely, after training in low concentration, it migrates toward high-concentration zones. This work demonstrates a bias-free strategy for programmable memory and sensing, potentially advancing autonomous microsystems and bioinspired electronics.

Read Full Abstract10.1007/s40843-025-3728-5
A Drop-Printing Strategy for Low-Stress, Conformal BioelectronicsGraphical AbstractVerified
SCIENCE CHINA Materials2026

A Drop-Printing Strategy for Low-Stress, Conformal Bioelectronics

Conformal contact between functional electronic films and biological surfaces is critical for long-term device stability, high signal sensitivity, and favorable signal-to-noise ratio. Traditional transfer methods, such as soft stamps and pad printing, often involve mechanical pressing, leading to poor conformality, localized stress concentration, or structural failure. Alternative strategies, including geometric engineering of non-stretchable materials or using stretchable organic alternatives, mitigate these issues but increase design complexity and reduce fabrication efficiency. Here, we highlight a novel 'drop-printing' strategy introduced by Li et al. that leverages capillary force to manipulate a water droplet to pick up a thin film, transfer it to a target substrate, and print it onto the surface. As the droplet evaporates, the film conformally wraps the surface. The droplet acts as a lubricating layer, while interfacial liquid penetrating microstructures generates capillary pressure, facilitating shape-adaptive deformation and significantly reducing stress concentration. The final positioning and conformality are governed by droplet behavior on the target surface. This approach achieves positional deviation of less than 20 μm via regulation of three-phase contact lines. The strategy enables damage-free conformal wrapping of non-stretchable films onto three-dimensional biological surfaces, as demonstrated by drop-printed silicon microfilm conformally wrapping on a rat brain, with successful NIR laser stimulation triggering forelimb movement and synchronized brain electrophysiological signals. This gentle, high-precision method addresses the pressing need for low-stress conformal bioelectronics, offering a general solution for diverse biological interfaces.

Read Full Abstract10.1007/s40843-025-3772-y
Discontinuous ablation behavior of four-directional dual-matrix C/C composites under dual-pulse solid rocket motorsGraphical AbstractVerified
New Carbon Materials2026

Discontinuous ablation behavior of four-directional dual-matrix C/C composites under dual-pulse solid rocket motors

Four-directional dual-matrix C/C composites were fabricated from PAN-based carbon fibers using a combined approach of soft-hard hybrid weaving preform molding, chemical vapor infiltration (CVI) of pyrolytic carbon (PyC), and high-pressure impregnation and carbonization of pitch-derived carbon. The ablation resistance was evaluated in a dual-pulse solid rocket motor, and the ablation behavior was investigated. The carbon rods, formed by twisting and carbonizing fiber bundles, exhibited a hexagonal cross-section, surrounded by a dense PyC 'wall' structure. The linear ablation rates after pulse I and pulse II were 0.068 mm/s and 0.113 mm/s, respectively. A cellular-like PyC layer and nanowire structures were deposited on the surface of the throat convergent section during the post-combustion cooling phase, while cracks and delamination occurred on and within the divergent section. The ablation process involved ultra-high temperatures, high-speed gas scouring, oxygen-containing thermochemical ablation, and thermal shock. This work elucidates the ablation behaviors under dual-pulse conditions and provides technical guidance for designing C/C composites for extreme environments.

Read Full Abstract10.1016/S1872-5805(26)61069-4
Analysis of National and Local Policies for Medical Waste Treatment and Disposal in ChinaGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Analysis of National and Local Policies for Medical Waste Treatment and Disposal in China

The escalating generation of medical waste, driven by healthcare expansion and frequent medical activities, poses significant environmental and public health risks. Under the framework of ecological civilization, China is developing a comprehensive policy system for medical waste treatment and disposal, yet the current framework remains nascent and exhibits inconsistencies between national and local policies. This study systematically analyzes the status of national and local policies from 2003 to 2024, collecting 413 policy documents (166 from national ministries and 247 from provincial governments). The analysis examines temporal evolution, regional distribution, and policy focus, alongside the influence of medical waste output, treatment technologies, facility infrastructure, and major epidemic responses. Findings reveal distinct policy phases: initial self-disposal, exploratory management, foundational system building, and rapid development. Regional disparities are pronounced, with eastern coastal areas showing more advanced policies due to greater technical and financial resources. The surge in medical waste, particularly during the COVID-19 pandemic, underscores the need for enhanced regulatory guidance. Non-incineration technologies are gaining traction for their environmental and cost benefits, and facility coverage has improved but remains uneven. The study proposes five policy principles to foster technological innovation and industrial upgrading, ensuring safe medical waste management and environmental protection.

Read Full Abstract10.12030/j.cjee.202506005
Kinetic Analysis and Simulation of Pollutant Removal in Sewage NetworksGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Kinetic Analysis and Simulation of Pollutant Removal in Sewage Networks

This study investigates pollutant removal characteristics and kinetic behaviors in sewage networks, and analyzes their impact on the carbon-to-nitrogen ratio (C/N, as COD/TN) of influent to wastewater treatment plants. Source water quality sampling at drainage outlets revealed spatial and temporal variations in C/N, with domestic sewage exhibiting higher C/N than industrial sewage, and diurnal peaks reaching 6.92 versus 4.71 during off-peak hours. Using a pilot-scale adjustable sewage network system in Kunshan, experiments were conducted under high (0.491 m·s−1) and low (0.089 m·s−1) flow velocities, monitoring pollutant removal over 144 hours. Pseudo-first-order kinetics were applied to model COD and TN removal. Results showed that COD (including SCOD and PCOD), BOD5, and SS achieved approximately 80% removal within 144 h, with higher removal at low flow velocity. TN, NH3-N, and TP exhibited lower overall removal rates. Kinetic fitting revealed that COD removal rate constants (kCOD) were significantly higher than those for TN (kTN), and both decreased with increasing flow velocity: at low velocity, kCOD=0.0167 h−1 and kTN=0.0029 h−1; at high velocity, kCOD=0.0127 h−1 and kTN=0.0020 h−1. Simulations based on actual source pollutant concentrations indicated that the time for C/N to drop to the denitrification critical value of 4.50 was 12.24 h at high velocity, but shortened to 9.49 h at low velocity. These findings demonstrate that increasing flow velocity effectively retards the decline of C/N. Therefore, regulating network flow velocity to reduce hydraulic retention time is a key strategy for maintaining adequate C/N at the terminal and ensuring denitrification efficiency in wastewater treatment plants.

Read Full Abstract10.12030/j.cjee.202507064
Preparation of Trimetallic-Carbon Composite Catalysts and Their Application in Catalytic Ozonation of Industrial WastewaterGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Preparation of Trimetallic-Carbon Composite Catalysts and Their Application in Catalytic Ozonation of Industrial Wastewater

Advanced oxidation processes (AOPs) are promising for degrading organic pollutants in water treatment. Heterogeneous catalytic ozonation (HCO) has gained attention due to its high oxidation efficiency, strong interference resistance, and low secondary pollution. In this study, a series of trimetallic-carbon composite ozone catalysts were prepared via an organic precursor calcination method using γ-Al2O3 as support. This method enhanced catalytic activity and mechanical strength while overcoming the limitations of carbon materials (low mechanical strength) and metal-based materials (poor mass transfer). The optimized catalyst, CA-FeCoCu, comprising Fe, Co, Cu, carbon, and alumina, exhibited excellent performance in phenol degradation and real industrial wastewater treatment. Characterization revealed that the synergistic effect of trimetals and the introduction of multiple carbon types increased specific surface area and hydroxyl radical (·OH) generation. In a pilot-scale fixed-bed reactor, the CA-FeCoCu/O3 system reduced COD from 120 mg·L−1 to below 40 mg·L−1, with an O3 consumption ratio (O/C) of less than 1, effectively lowering operational costs. This work provides a new strategy for developing efficient and stable heterogeneous O3 catalysts and offers a reference for the practical application of HCO in industrial wastewater treatment.

Read Full Abstract10.12030/j.cjee.202506081
Differentiated Characteristics of Suspended Particulate Matter and Their Effects on Water Quality in the Middle and East Routes of the South-to-North Water Diversion ProjectGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Differentiated Characteristics of Suspended Particulate Matter and Their Effects on Water Quality in the Middle and East Routes of the South-to-North Water Diversion Project

This study investigates the spatiotemporal differentiation of suspended particulate matter (SPM) characteristics, sources, and their impacts on water quality between the Middle Route (closed artificial channel) and East Route (open natural water system) of the South-to-North Water Diversion Project. Thirty sampling sites (13 on the Middle Route, 17 on the East Route) were established, and samples were collected during dry and wet seasons. Water quality parameters and SPM characteristics were analyzed, including particle size distribution, total suspended solids (TSS), chlorophyll a, and stable carbon and nitrogen isotopes. Results show that the Middle Route maintains good and stable water quality, with SPM dominated by coarse particles (>63 μm, 61.43%–94.68%), total phosphorus (TP) <0.01 mg·L−1, and a significant positive correlation between chlorophyll a and coarse particles (r=0.60), indicating algal aggregation dominates particle formation. In contrast, the East Route exhibits high and fluctuating nitrogen and phosphorus concentrations, with SPM dominated by fine particles (<20 μm, 51.26%–88.61%), TP ranging from 0.03 to 1.11 mg·L−1, and a positive correlation with fine particles, suggesting significant external inputs. Carbon and nitrogen isotope analysis reveals that Middle Route SPM primarily originates from autochthonous algae (contribution >46.75%), while East Route SPM is influenced by both terrestrial C3 plants and algae. The distinct engineering and management approaches of the two routes lead to significant differences in SPM characteristics and sources, thereby affecting water quality dynamics. The Middle Route requires an 'algal reduction and hydrodynamic optimization' strategy to control algal-derived coarse particle deposition, whereas the East Route benefits from 'retention-sedimentation and wetland purification' to reduce external fine particles and pollutant inputs. This research provides theoretical support and practical guidance for differentiated SPM management in long-distance water diversion systems.

Read Full Abstract10.12030/j.cjee.202507085
Combined Ozone Micro-Nano Bubble Oxidation and Powdered Activated Carbon Adsorption for Removal of Taste and Odor Compounds from Drinking WaterGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Combined Ozone Micro-Nano Bubble Oxidation and Powdered Activated Carbon Adsorption for Removal of Taste and Odor Compounds from Drinking Water

Algal-derived taste and odor compounds (2-methylisoborneol, 2-MIB, and geosmin, GSM) in drinking water sources are poorly removed by conventional treatment. This study systematically evaluated the standalone and combined performance of ozone micro-nano bubbles (O3-MNBs) oxidation and powdered activated carbon (PAC) adsorption for removing 2-MIB, GSM, and algal cells from source water. Results showed that O3-MNBs pre-oxidation achieved >97.5% removal of odorants at 400 ng·L−1 and 67.2% algal cell removal within 30 min. When applied as a deep treatment stage, the degradation rate constant (k) was 10.1%–25.6% higher than in pre-oxidation due to lower background matrix interference. Both pre-oxidation and deep treatment reduced effluent concentrations of 2-MIB and GSM to below 10 ng·L−1, with oxidation kinetics fitting pseudo-first-order models (R²>0.95). PAC adsorption of both compounds followed pseudo-second-order kinetics (R²>0.99), with GSM equilibrium adsorption capacity approximately 20.0% higher than that of 2-MIB. In pure water, adsorption capacity increased by >10.0% compared to raw water. Based on kinetic models, a quantitative prediction method was established for O3-MNBs oxidation and PAC adsorption processes, aiming to achieve efficient odorant removal and cost optimization, providing theoretical support for advanced drinking water purification and smart water plant construction.

Read Full Abstract10.12030/j.cjee.202507110
Pulsed Electric Field Enhancement of Nitrogen Removal Performance and Microbial Community Structure Response in Anammox Granular SludgeGraphical AbstractVerified
Chinese Journal of Environmental Engineering2026

Pulsed Electric Field Enhancement of Nitrogen Removal Performance and Microbial Community Structure Response in Anammox Granular Sludge

This study investigated the effects of a ring-shaped pulsed electric field (PEF) (1.5 V, 4 h on-time per cycle) on nitrogen removal performance and microbial community structure of anammox granular sludge (AnGS). Two anaerobic sequencing batch reactors (R1 control, R2 with PEF) were operated under stepwise increasing nitrogen loading rates (NLR). At NLR below 1,155 mg·(L·d)−1, R2 exhibited total nitrogen removal efficiency (TRE) 7.5%–17.0% higher than R1, with biomass, specific anammox activity (SAA), and extracellular polymeric substances (EPS) increased by 5%–7%, 21%–71%, and 54%–77%, respectively. However, at NLR above 1,320 mg·(L·d)−1, the toxic effect of nitrite dominated, and PEF enhancement diminished or even reversed to inhibition. Microbial community analysis revealed that at low-to-moderate NLR, PEF increased the relative abundance of Planctomycetes and key anammox bacteria (Candidatus Brocadia and Candidatus Jettenia), along with enhanced community richness (Chao1) and diversity (Shannon/Simpson indices). At high NLR, PEF decreased microbial richness compared to R1. Principal component analysis and redundancy analysis indicated that PEF was the key factor driving community differences at low-to-moderate NLR, whereas nitrite concentration became the dominant factor at high NLR. This study provides theoretical support for enhancing the resilience and engineering application of anammox processes.

Read Full Abstract10.12030/j.cjee.202507111