SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4448-y
Zero-dimensional (0D) hybrid metal halides are promising for optoelectronic displays, bioimaging, and anti-counterfeiting due to strong exciton localization and self-trapped exciton (STE) emission. However, low-toxicity, biocompatible zinc halides with blue emission remain scarce, hindered by structural isolation of [ZnBr4]2− tetrahedra, electron-phonon coupling, lattice distortion, and nonradiative relaxation. Here, we synthesize MPAZnBr4 (MPA = N-(3-aminopropyl) morpholine), a 0D zinc bromide halide. Single-crystal X-ray diffraction reveals a monoclinic P21/c space group with a = 6.65190 Å, b = 16.11210 Å, c = 13.79640 Å, β = 94.5700°, Z = 4, and a calculated density of 2.394 g/cm3. The isolated [ZnBr4]2− tetrahedra are hydrogen-bonded to MPA cations, with the shortest Br···Br contact of 4.76 Å indicating weak inter-cluster electronic coupling. Upon photoexcitation, MPAZnBr4 exhibits bright blue emission centered at 450 nm with a full width at half maximum of 135 nm. Wavelength-dependent emission mapping confirms a single radiative pathway, while temperature-dependent photoluminescence identifies triplet STE emission with a thermal quenching activation energy of 55 meV. The extensive hydrogen-bonding network imparts remarkable structural stability, showing negligible photoluminescence decay under prolonged excitation or storage. As a proof-of-concept, we demonstrate switchable and rewritable information encryption and decryption, enabling complex luminescent patterns. These findings provide a strategy for constructing highly stable, low-toxicity blue-emissive Zn-based 0D metal halides for advanced photonic and information-security applications.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3648-2
Transient energy storage devices represent an emerging class of biodegradable power systems that provide temporary energy for implantable medical electronics before safely degrading in vivo. From early transient primary batteries to contemporary rechargeable batteries integrated with wireless charging systems, these devices have evolved to enable stable prolonged power supply. Through rational transient design and structural engineering, they achieve desirable electrochemical performance, tunable degradation rates, and mechanical compatibility with soft, irregular, and dynamic biological tissues. This work provides a critical review of state-of-the-art transient energy storage devices, including transient primary batteries, transient secondary batteries, and transient supercapacitors, with emphasis on their electrodes, electrolytes, encapsulation materials, fabrication processes, and applications. We critically analyze material selection strategies, transient design principles, and architecture design for various transient batteries and capacitors. Finally, we discuss existing challenges and outline future directions to guide the clinical translation of biodegradable power solutions for biomedical implants.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3777-0
Optically clear adhesives (OCAs) are critical for next-generation optoelectronic systems, yet their end-of-life management remains a sustainability challenge. Here, we report a debondable and robust polyurethane (PU)-based OCA that integrates both mechanical and chemical recyclability. The PU-based OCA exhibits high optical transparency (>90% transmittance from visible to near-infrared), strong adhesion to glass and polymeric substrates (bonding strength up to 5.0 MPa), and thermally sensitive H-bonding interactions that enable on-demand deadhesion at elevated temperatures. This capability facilitates non-destructive detachment of functional assemblies, promoting component reuse and material recycling. The adhesive demonstrates excellent mechanical properties, including ductility and strength, and outperforms several commercial optical adhesives in key performance metrics. Its straightforward synthesis and industrial scalability make it a promising solution for advancing circular economy principles in optoelectronic device manufacturing. The work addresses critical bottlenecks in balancing mechanical performance, adhesion/detachment, and recyclability, offering a transformative approach to sustainable advanced manufacturing.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202604025
To meet the minute-level early-warning requirements for odor and multi-pollutant emissions at waste treatment facilities, this study proposed a multivariate short-term time-series prediction framework applicable to multi-tier scenarios covering source and boundary points (i.e., workshops and plant boundaries). Based on continuous online monitoring data with a 5-second resolution, a long short-term memory (LSTM) model using a sliding-window and recursive multi-step prediction strategy was constructed to jointly model odor concentration (OU) and pollutants including VOCs, NH3, H2S, and CH3SH (mg/m³). An evaluation protocol aligned with environmental supervision practice was established, incorporating mean absolute error (MAE), root mean square error (RMSE), goodness-of-fit (R²), skill scores (SS) relative to a persistence baseline, and threshold-based error stratification to characterize uncertainty during peak emission periods. The results showed that at workshop monitoring sites with relatively stable operating conditions, VOCs, NH3, H2S, and CH3SH exhibited a high goodness of fit and low prediction errors. In contrast, at boundary sites affected by plume arrival delays and diffusion-dilution non-stationarity, OU and VOCs displayed significantly amplified errors during peak episodes, and the skill score advantage over the baseline became unstable at certain sites. Stratified analysis consistently revealed that non-peak periods outperformed peak periods, indicating that event-driven fluctuations were the main sources of error. Accordingly, this study suggested incorporating exogenous variables such as wind speed and direction, ventilation and gate access control, and operational rhythms, along with peak-sensitive loss functions, into the model to enhance its capacity to characterize and provide early warnings for transient emission pulses. Overall, this study established a reusable methodological baseline and evaluation paradigm for minute-scale multi-pollutant prediction, providing quantitative support for the operational management and source-to-boundary coordinated control of waste treatment facilities.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(25)60618-9
Aromatic hydrocarbons, essential chemical feedstocks for fuels, synthetic fibers, and pharmaceuticals, are predominantly derived from petroleum refining. The catalytic conversion of lignin, a major lignocellulosic component, offers a renewable route to these chemicals. This review systematically examines the influence of pyrolysis methods, catalysts, and reaction conditions on the catalytic pyrolysis of lignin to aromatic hydrocarbons. Key parameters include catalyst acidity and pore structure, which govern selectivity and yield. Reaction temperature, catalyst-to-lignin ratio, and residence time critically affect product distribution. The review outlines catalytic mechanisms, such as deoxygenation, cracking, and aromatization, and highlights the role of zeolite catalysts, particularly HZSM-5, in enhancing monocyclic aromatic hydrocarbon yields. Metal modification (e.g., Fe, Ni, Ga) and pretreatment strategies (e.g., torrefaction) are discussed for improving efficiency. Challenges remain in catalyst deactivation due to coking and the complexity of lignin structure. Future research directions include developing robust catalysts, optimizing reactor designs, and integrating processes for industrial viability. This review provides theoretical and technological guidance for advancing lignin-to-aromatics conversion.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3963-5
Metal additive manufacturing (MAM) enables integrated one-piece fabrication of parts, high material utilization efficiency, and unparalleled design freedom. However, problems such as low production efficiency, difficulties in ensuring quality stability and defect control limit the large-scale industrial application of AM. In-situ active modulation for AM enables dynamic regulation of parts during the fabrication process, thereby enhancing the quality of the final fabricated parts without introducing extra processing steps. In-situ active regulation enables direct intervention during defect nucleation, providing better effectiveness than post-printing repairs while avoiding performance degradation risks associated with post-processing. Based on the difference of core factors directly affected during regulation, in-situ active regulation is categorized into the following. (1) Process and path parameter optimization, where regulation directly impacts manufacturing-related procedural rules. It is the simplest method of control and the preferred approach, with widespread attention focused on its effects on microstructure and mechanical properties. (2) Laser beam shaping, where regulation directly influences the energy carrier morphology. To address issues such as edge over-melting and localized energy deficiency caused by non-uniform energy distribution, laser beam shaping should be employed. (3) Additional physical field modulation achieved by superimposing supplementary physical fields. When optimal process and path parameters still fail to obtain the desired microstructure and mechanical properties, additional physical field control may be considered. Meanwhile, this work summarized the effects of different additional physical fields on the mechanical properties of various metallic base materials. The future trends of in-situ modulation in additive manufacturing are also discussed.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202510060
Wastewater treatment plant (WWTP) effluent is a significant pathway for emerging contaminants (ECs) to enter natural water bodies. This study investigated the removal of ECs by two field-scale gravel-based constructed wetlands: a horizontal subsurface flow constructed wetland (QL-CW) and a surface flow constructed wetland (BL-CW), both treating actual WWTP effluent. The influence of operation mode and wetland plant type on EC removal was examined. Using liquid chromatography-mass spectrometry, principal component analysis, and ecological risk assessment, the removal efficiencies and mechanisms for various ECs were explored. In QL-CW, biodegradation was more pronounced, particularly via ammonia-oxidizing bacteria co-metabolism, favoring ECs with benzyl, secondary amine, secondary amide, tertiary amide, halogenated, and carboxyl functional groups. In BL-CW, electrostatic attraction and hydrophobic interactions were more significant, with plant and root-microorganism uptake and adsorption playing key roles. Surface flow mode achieved significantly higher removal of antibiotics (45.3% vs. 34.1%) compared to horizontal subsurface flow, while no significant differences were observed for non-antibiotic pharmaceuticals (66.6% vs. 64.4%) and pesticides (49.8% vs. 34.2%). Planting Cyperus alternifolius (windmill grass) was more beneficial for antibiotic removal (43.6% vs. 30.1%) than planting Ipomoea aquatica (water spinach). The wetlands effectively reduced the ecological risks of most ECs to marginal levels. This study provides insights into the deep treatment of ECs in WWTP effluent by constructed wetlands.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025040102
Calcium peroxide (CaO2) with a rich porous structure was synthesized via chemical precipitation for efficient fluoride removal from aqueous solutions. The adsorbent was characterized by SEM, BET, LPSA, and XRD, revealing a mesoporous material with a total pore volume of 0.51 cm3·g−1. Batch experiments investigated the effects of adsorbent dosage, initial fluoride concentration, reaction time, pH, and coexisting anions. Adsorption kinetics followed a fractal-like pseudo-first-order model, with intraparticle diffusion as the rate-limiting step. Equilibrium data were well described by the Sips isotherm, predicting a maximum adsorption capacity of 479.8 mg·g−1. Site energy distribution analysis indicated a normal distribution with an average energy of 13.36 kJ·mol−1. Mechanistic studies using FTIR and XPS revealed that fluoride removal proceeds via surface precipitation, ligand exchange, and electrostatic attraction. The high density of active sites contributes to the exceptional defluoridation performance, positioning CaO2 as a promising adsorbent for fluoride-contaminated water treatment.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4030-y
In the era of artificial intelligence, efficient perception and processing of massive visual information demand advanced machine vision systems. Inspired by human visual adaptation, various optoelectronic devices have been developed, yet most rely on external gate voltages or complex circuits for dynamic sensitivity modulation. This work demonstrates an all-optically controlled biomimetic sensor based on a one-dimensional ZnO/MAPbBr3 heterojunction, achieving both positive and negative photoconductivity effects. By modulating oxygen vacancy states with ultraviolet light, the competition between intrinsic photoconduction and trap-mediated carrier capture is regulated, enabling dynamic control of visible-light photoresponse within a single device. This tunable behavior mimics scotopic adaptation (photopigment regeneration under weak illumination), photopic adaptation (photopigment bleaching in bright environments), and eyelid-like self-protection against intense light. The device operates without external gate bias or cascaded circuits, offering a promising strategy for next-generation intelligent biomimetic sensors in machine vision.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3643-8
Inverted perovskite solar cells (PSCs) suffer from defect-mediated nonradiative recombination and inefficient charge extraction, particularly at the buried interface and grain boundaries (GBs), which limit power conversion efficiency (PCE) and operational stability. This study introduces a multifunctional phosphonic acid molecule, (2-(3,6-bis(trifluoromethoxy)-9H-carbazol-9-yl)ethyl)phosphonic acid (M28), as an additive in the perovskite precursor solution. M28 spontaneously segregates toward the buried interface and GBs, fulfilling three roles: (1) slowing crystallization to enlarge grains and improve film quality, (2) passivating defects to suppress charge recombination, and (3) inducing p-type doping to create an extra electric field that promotes hole transport. Devices incorporating M28 achieve a champion PCE of 25.96% and retain 80% of initial efficiency after 1500 h of maximum power point tracking. This work demonstrates the efficacy of multifunctional phosphonic acid additives in addressing buried-interface and GB defects, offering a viable route to high-performance, stable inverted PSCs.