SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4249-2
Underwater bubble manipulation is critical for water electrolysis, heat transfer, and mineral flotation, yet existing strategies relying on buoyancy or Laplace gradient forces from asymmetric surface geometries suffer from limited flexibility and narrow applicability. This work introduces a temperature-responsive anisotropic cilia surface (TRAS) that achieves bidirectional long-range bubble transport by modulating elastic modulus and stiffness. The TRAS enables precise control over the asymmetric three-phase contact line and viscous resistance, facilitating reversible bubble motion. Experimental validation using aqueous ethanol droplets with varying surface tensions (73.16 mN/m for 0 vol% to 22.27 mN/m for 100 vol%) on cilia with center-to-center spacings of 0.2–1.0 mm reveals that transport direction depends on both cilia spacing and liquid surface tension. Droplets of 0 vol% and 20 vol% ethanol exhibit sustained reverse transport on hard cilia, while 60 vol%, 80 vol%, and 100 vol% solutions show sustained forward transport. Notably, 40 vol% ethanol droplets display bidirectional transport at 0.6 mm spacing, reverse transport at 0.8 and 1.0 mm, and forward transport at 0.2 and 0.4 mm. These results demonstrate that tuning surface tension and cilia spacing provides a versatile platform for directional bubble manipulation, with promising applications in heat transfer, electrochemistry, and gas handling systems.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4313-7
Liquid-to-vapor mass transfer is central to energy and environmental processes. Conventional distillation relies on vapor-liquid equilibrium and device-level optimization, with materials playing passive structural roles. Non-boiling processes such as membrane distillation and interfacial solar evaporation localize phase change at confined interfaces, making mass transfer a materials-mediated transport phenomenon where interfacial structure and chemistry dictate evaporation kinetics, vapor escape, and solute rejection. Janus interface materials, featuring spatially separated hydrophilic and hydrophobic domains, introduce architectural asymmetry to regulate liquid-to-vapor mass transfer. This review summarizes recent advances, highlighting mechanisms including the cooperative pump-valve effect, nanoconfinement-enhanced transport, and mitigation of fouling and scaling. Representative applications in membrane distillation, solar-driven evaporation, and personal thermal-moisture management are systematically discussed. Key challenges and future opportunities are outlined, particularly in advancing fundamental understanding, scalable fabrication, and practical implementation.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4493-8
Metal halide perovskite photovoltaics have achieved power conversion efficiencies rivaling crystalline silicon, yet their transition from laboratory-scale devices to commercial deployment requires a paradigm shift toward application-specific engineering and macroscopic system integration. This review systematically evaluates the customized deployment of perovskite solar cells (PSCs) across diverse operational theaters, including building-integrated photovoltaics (BIPV), portable Internet of Things (IoT) systems, agricultural photovoltaics (Agri-PV), vehicle-integrated photovoltaics (VIPV), utility-scale tandems, and extreme space environments. Despite these opportunities, critical challenges persist in translating laboratory achievements into industrial-scale production. We critically evaluate primary bottlenecks hindering gigawatt-scale commercialization, focusing on the performance gap inherent in large-area manufacturing. Additionally, we analyze intrinsic material instabilities driven by dynamic ion migration and multi-scale lattice strain under realistic outdoor conditions. To conclude, we outline a strategic roadmap for overcoming these barriers, emphasizing lattice strain regulation, rigorous dynamic environmental testing protocols, and comprehensive sustainable lifecycle management. By synergizing mechanistic insights with scalable manufacturing and ecological assessments, this review provides a holistic framework to accelerate the ubiquitous commercialization of customizable, stable, and high-efficiency perovskite energy systems.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4179-x
Perylene diimide (PDI) radical anions exhibit poor environmental stability, restricting their generation efficiency and practical application. Here, a PDI-functionalized bispillar[5]arene (PDI-P5) was designed to construct stable and high-efficiency photothermal radicals. Intramolecular charge transfer (ICT) between PDI and bispillar[5]arene narrows the energy gap. Under 455 nm ultraviolet light irradiation and diethylamine (DEA) vapor exposure, photoinduced electron transfer (PET) efficiently generates PDI-P5·− radicals, which possess broad near-infrared (NIR) absorption, enhanced non-radiative transitions, and excellent stability. Notably, PDI-P5·− can rapidly reach 90 °C under 0.20 W cm−2 simulated sunlight irradiation. Moreover, it exhibits superior multi-step photothermal anti-counterfeiting performance. This work provides a novel strategy for the development of stable radical-based photothermal materials, which holds great potential for anti-counterfeiting and bioimaging applications.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202508004
Industrial processes generate substantial low-grade waste heat and cold, which can be harnessed via thermoelectric generators (TEGs) based on the Seebeck effect. However, the low-voltage output of TEGs poses application challenges. This study investigates a TEG-driven electrodeposition system for efficient treatment of low-concentration copper-containing wastewater from electroplating, integrated circuit, and energy industries. The TEG system, comprising two series-connected semiconductor modules, achieved a maximum power of 0.36 W at a temperature difference (ΔT) of 130 °C. Optimal operating parameters for the coupled system were determined: ΔT = 90 °C, counter-current flow (two-side inlet), flow rate of 20 mL·min⁻¹, initial Cu²⁺ concentration of 500 mg·L⁻¹, and electrode gap of 0.7 cm. Under these conditions, after 60 min of electrodeposition, copper removal efficiency reached 99.42%, current efficiency was 67.93%, and the energy conversion efficiency of the TEG-electrodeposition system was 36.96%. The system also treated real copper-containing wastewater, achieving 95.83% removal within 100 min. Characterization via SEM, XRD, and XPS revealed that the electrodeposited product consisted of metallic copper and cuprous oxide, with metallic copper accounting for approximately 60%. This work provides a promising approach for utilizing industrial waste heat and cold to achieve low-energy, high-efficiency treatment of heavy metal wastewater.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2024102303
Fluoride-containing wastewater treatment typically relies on calcium-based precipitation and flocculation, which suffer from low compliance rates and difficult valorization of fluoride-laden sludge. This study introduces a novel bismuth upconversion luminescent glass (BULG) synthesized from Bi2O3, SiO2, Yb2O3, and Er2O3, designed for efficient fluoride removal and subsequent photocatalytic application. By varying the Bi2O3:SiO2 molar ratio, a series of BULGs with superior upconversion luminescence were obtained. Under optimal conditions (Bi3+:F− molar ratio = 1:1, pH = 2), fluoride removal efficiencies exceeded 97% for all compositions, with the 0.7:0.3 Bi2O3:SiO2 formulation achieving 99.9% removal and rapid settling of the precipitate. The fluoride removal products retained upconversion luminescence and exhibited semiconductor heterojunctions, enabling complete photocatalytic degradation of ciprofloxacin (100% within 60 min). This approach not only efficiently removes fluoride ions but also valorizes the waste into a functional photocatalyst, offering a promising strategy for fluoride-containing wastewater treatment.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202511002
To treat large-air-volume, low-concentration volatile organic compounds (VOCs) containing tetrachloroethylene (PCE) generated from rubber-metal bonding, this study systematically investigated the adsorption-desorption behavior and interaction mechanisms of PCE, toluene, and methyl isobutyl ketone (MIBK) on granular activated carbon (GAC). Static adsorption experiments showed that PCE adsorption capacity reached 556.6 mg·g−1, while dynamic multi-component adsorption capacity was 179.6 mg·g−1. Kinetic analysis indicated that PCE adsorption was controlled by both intraparticle diffusion and external surface adsorption, whereas toluene and MIBK were primarily intraparticle diffusion-limited. During high-temperature nitrogen desorption, PCE underwent dechlorination, hydrogenation, and recombination, producing trichloroethylene, 1,2-dichloroethane, 1,2-dichloropropane, and HCl, with HCl accounting for 3.61% of the chlorine molar content in adsorbed PCE. After four adsorption-desorption cycles, the iodine value of GAC dropped below the industry standard of 600 mg·g−1; however, water washing and alkali immersion extended the cycle life to 8 and 9 cycles, respectively. The HCl generation pattern in co-adsorption systems was consistent with single-PCE systems. A regeneration process combining alkali immersion and water washing was proposed and integrated into an engineering strategy. Compared to conventional activated carbon adsorption coupled with RTO incineration, the proposed classification strategy reduced annual costs by 49.5×10⁴ CNY. This work provides a cost-effective and safe solution for Cl-VOCs treatment.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025040401
Conventional zero-valent iron (ZVI) suffers from limited electron transfer due to its dense surface oxide layer. This study introduces a mechanochemical ball-milling strategy incorporating sodium chloride (NaCl) with ZVI to fabricate chloride-modified ZVI (Cl-ZVIbm). Using hexavalent chromium (Cr(VI)) as a model pollutant, Cl-ZVIbm exhibited a 76.5-fold enhancement in removal kinetics (0.0306 min−1 vs. 0.0004 min−1) compared to ball-milled ZVI (ZVIbm), achieving complete removal of 2 mg·L−1 Cr(VI) within 120 min. Spectroscopic characterization and density functional theory (DFT) calculations revealed dual regulation mechanisms: (1) Cl− substitution of surface hydroxyl groups alters coordination environments, enabling Cr(VI) adsorption via a bidentate binuclear configuration with adsorption energy reduced from –0.28 eV to –1.64 eV; (2) The strong electron-withdrawing effect of Cl− drives directional electron migration from the iron core to the surface, increasing surface Fe(II) content by 26.9% (67.5% vs. 53.2%) and facilitating direct electron transfer to reduce 99.5% of Cr(VI) into low-toxicity Cr(III). Notably, chloride leaching during reactions was only 0.0126 mmol·L−1, far below industrial wastewater discharge standards, confirming environmental compatibility. This work provides atomic-scale insights into chloride-mediated electronic modulation on ZVI surfaces, offering novel principles for interfacial engineering of environmental functional materials and a theoretical basis for heavy metal remediation technologies.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(26)60665-2
Levulinic acid (LA) is a promising platform product with wide industrial applications. Efficient conversion of cellulose into LA has become a research hotspot, yet traditional experimental optimization is time-consuming and inefficient. This study integrates multidimensional data—reaction conditions, solvent properties, and physicochemical characteristics of metal salts—to construct a systematic dataset. Six machine learning models (decision tree, gradient boosting regression, K-nearest neighbors, multilayer perceptron, random forest, and support vector machine) were developed to predict LA yield. The gradient boosting regression (GBR) model achieved the best performance, with a test-set determination coefficient (R²) of 0.94 and the lowest root-mean-square error (RMSE). SHapley Additive exPlanations (SHAP) and partial dependence analysis identified water fraction, catalyst dosage, and reaction temperature as the key factors influencing LA formation. By integrating the GBR model with particle swarm optimization (PSO), RuCl₃ was identified as an efficient catalyst under high-temperature and short-reaction-time conditions. This study demonstrates the potential of machine learning in cellulose conversion research, providing a data-driven strategy and theoretical guidance for efficient and green LA production.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025051701
This study investigated the effects of selenium nanoparticles (SeNPs) on the growth, mycelium morphology, copper (Cu2+) removal rate, extracellular polymeric substances (EPS), and intracellular enzyme activity of Aspergillus flavus TL-F3 (A. flavus TL-F3) under Cu2+ stress. Results showed that different concentrations of Cu2+ inhibited the growth of A. flavus TL-F3. The highest Cu2+ removal rate of 56.32% was observed at a Cu2+ concentration of 50 mg·L−1. Under 50 mg·L−1 Cu2+ stress, 0.25 mg·L−1 SeNPs promoted the growth of A. flavus TL-F3, increasing its biomass by 2.71%, and significantly enhanced the fluorescence intensity of EPS, Na+/K+-ATPase activity, and decreased malondialdehyde (MDA) content, reduced superoxide dismutase (SOD) and catalase (CAT) enzyme activities. Additionally, SeNPs stimulated the glutathione (GSH-GSSG) cycle in A. flavus TL-F3, elevating glutathione peroxidase (GPX) and glutathione reductase (GR) activity by 17.2% and 23.94%, respectively, and increasing reduced glutathione (GSH) content by 18.59%, and decreasing the GSH/GSSG ratio, thereby effectively alleviating Cu2+ toxicity. Fourier transform infrared spectroscopy indicated that surface functional groups of A. flavus TL-F3, including carboxylic acid, alcohol, phenol, and phosphate/sulfate functional groups, might bind with Cu2+, enhancing its tolerance to Cu2+. This study enriches the theoretical knowledge of microorganism-heavy metal interactions and provides deeper insights into microbial heavy metal resistance mechanisms.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4026-0
Copper-based synergistic therapy integrating chemodynamic therapy (CDT) and cuproptosis holds promise for tumor treatment but faces clinical translation hurdles including long-term toxicity, low catalytic efficiency, off-target effects, and copper ion efflux. Here, we developed metabolizable ultrasmall benzothiazole-based covalent organic framework nanodots (COF NDs) via click condensation followed by liquid exfoliation. The dense donor-acceptor configurations confer a high photothermal conversion efficiency of 51.16%, while bisthiazole motifs enable specific Cu2+/Cu+ chelation (0.56:0.44), facile PEGylation, and mitochondrial targeting. These features enhance physiological stability and enable tumor-specific photothermal-catalytic synergy. Mitochondrial accumulation elevates intracellular copper to a critical threshold, inducing cuproptosis and suppressing tumor growth and metastasis. The NDs are efficiently excreted via renal and fecal pathways, demonstrating favorable biocompatibility and clinical potential as copper-based nanotherapeutics.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3294-1
Flexible thermoelectric power generation offers a route to self-powered wearable electronics, but n-type flexible thin films have lagged in performance. This work reports n-type Ag2Se thin films fabricated by thermal evaporation with Se precursor strategies, yielding a (201)-textured orientation. The optimized S-AF films exhibit a dense microstructure with trace nanopores and achieve a power factor of 2.14 mW m−1 K−2 at 300 K, the highest reported for thermally evaporated Ag2Se films. First-principles calculations confirm that the (201) orientation enhances carrier mobility, while Se nano-inclusions and Ag2Se/Se and Ag2Se/Ag heterointerfaces contribute to a high Seebeck coefficient via energy filtering. The inherent low thermal conductivity of Ag2Se is further reduced by nanopores, random in-plane orientation, and heterogeneous interfaces, which scatter phonons across a broad wavelength spectrum. Consequently, an optimal ZT of 0.73 at 363 K is obtained. This study demonstrates that crystallographic texture engineering is a viable strategy to decouple electrical and thermal transport in flexible thermoelectric films, providing a pathway for high-performance wearable energy harvesters.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3299-x
Aqueous zinc ion batteries (ZIBs) offer intrinsic safety and cost advantages for grid-scale energy storage, yet their practical deployment is constrained by parasitic reactions, poor anode stability, and dendritic zinc growth. This study introduces a ternary aqueous eutectic electrolyte composed of N-ethylacetamide (Nea), H2O, and Zn(OTf)2 to mitigate these failure modes. The Nea molecules preferentially adsorb on the zinc anode, establishing a uniform interfacial electric field and a de-watering shielding layer that suppresses side reactions. Concurrently, an organic/inorganic hybrid solid electrolyte interphase (SEI) forms in situ, inhibiting the tip effect and promoting homogeneous Zn2+ diffusion and deposition. The Zn//Zn symmetric cell achieves 4590 h cycling at 0.5 mA cm−2/0.5 mAh cm−2 and a depth of discharge of 85.4% at 1.0 mA cm−2/5.0 mAh cm−2. Full cells with a V2O5·1.6H2O cathode deliver over 5000 cycles with Coulombic efficiency near 100% at 1.0 and 2.0 A g−1. These results demonstrate that eutectic electrolyte engineering can simultaneously address dendrite formation and interfacial side reactions, providing a viable pathway for long-life aqueous ZIBs.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3446-2
Mn-doped GeTe dilute magnetic semiconductors exhibit potential for mid-temperature thermoelectric applications, yet the mechanistic role of Mn in transport remains unresolved. This study characterizes the transport, magnetic, and lattice vibrational properties of Ge1−xMnxTe (x = 0–0.1) across 50–300 K. Mn incorporation reduces carrier concentration from ~1.2 × 10^21 cm−3 (x = 0) to ~4.5 × 10^20 cm−3 (x = 0.05) and amplifies electron scattering, yielding a two-fold increase in power factor to ~28 μW cm−1 K−2 at 300 K. Concurrently, Mn doping softens optical phonons and reduces phonon group velocity, suppressing lattice thermal conductivity to ~0.65 W m−1 K−1 at 300 K. Ferromagnetic ordering below ~120 K further depresses magnetic excitation phonon modes, contributing to the overall thermoelectric performance. These findings establish a dual electronic–thermal optimization pathway for GeTe-based dilute magnetic semiconductors.
SCIENCE CHINA Materials•2025•DOI: 10.1007/s40843-025-3540-y
Polymeric multicolor afterglow materials with tunable phosphorescence and environmental adaptability remain a bottleneck in optical anti-counterfeiting. This work integrates triplet-to-singlet Förster resonance energy transfer (TS-FRET) with ultraviolet (UV) laser direct writing to fabricate phosphorescent anti-counterfeiting labels. Using poly(acrylamide-co-4'-vinyl-[1,1'-biphenyl]-3,5-dicarboxylic acid) (BCA2PAM) as the donor and rhodamine 6G (R6G) as the acceptor, precise color tuning is achieved. Time-resolved multicolor displays are realized by loading afterglow materials onto filter paper, while luminescent elastomers are synthesized via integration with polydimethylsiloxane (PDMS). Laser inscription of 'disappear' on R6G-doped BCA2PAM films at varying laser powers yields exclusive visibility of 'appear' under UV irradiation; upon UV off, 'disappear' emerges, followed by reappearance of 'appear' after 1 s, demonstrating encryption efficacy. High-power laser-inscribed QR codes remain imperceptible under UV but become visible after simulated breath exposure and subsequent UV activation. Integrated with polyethylene terephthalate (PET) adhesive tapes, the films form tamper-evident labels with customizable branding. Laser-written patterns visible under UV can be erased under ambient humidity and re-encrypted with new motifs, exhibiting rewritable capability. These results provide a new method based on ultraviolet light and multicolor time-resolved coupling in optical encryption, demonstrating industrial production potential for high-end anti-counterfeiting labels.
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.