SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3536-5
Nanomaterial-based optical biomedicine and devices have attracted significant attention for tumor diagnosis and treatment, yet their application in tumor ablation is often hindered by limited functional integration and concerns over excessive radiation exposure. In this study, we address these challenges by developing a multifunctional fiber probe based on lanthanide-doped nanoparticles, featuring decoupled modules for localized heating and optical thermometry. This design enables synergistic therapy under near-infrared (NIR) laser irradiation. Beyond achieving precise photothermal ablation and real-time temperature monitoring, we uncovered a unique phenomenon: the generation of reactive oxygen species (ROS) by these nanoparticles under NIR laser excitation, even in the absence of traditional photosensitizers. Through a combination of experimental and computational approaches, we elucidated the physical mechanisms underlying ROS generation in wide-bandgap lanthanide nanoparticles. Leveraging these insights, we constructed an all-optical fiber system capable of simultaneous precise thermal control and photodynamic therapy. Our findings offer valuable guidance for the development of advanced optical nanomaterials and devices for effective tumor treatment, both in vivo and in vitro.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-026-4054-x
The sluggish kinetics and high onset potentials of the oxygen evolution reaction (OER) at the anode of alkaline water/seawater electrolyzers limit overall energy efficiency. Noble-metal oxides like RuO2 are active but suffer from high cost, agglomeration, and dissolution under oxidizing potentials, especially in chloride-rich electrolytes where competing chloride oxidation reaction (ClOR) occurs. Here, we report a mild two-step dry-wet milling strategy to achieve throughout lattice doping of F− into MnO2 (F-MnO2) and subsequent anchoring of atomically dispersed Ru via Ru–O/F hybrid bonds. The strengthened Mn 3d–O/F 2p hybridization and negative charge shielding of surface F− enhance OER activity/selectivity relative to ClOR and impart superior Cl− tolerance and corrosion resistance. The resulting F-Ru-MnO2-TH electrocatalyst exhibits overpotentials of 280 mV and 200 mV at 10 mA cm−2 in alkaline water and simulated seawater, respectively. It retains ~100% of initial activity after 200 h continuous operation in alkaline media and >95% after 300 h in simulated seawater, significantly outperforming Ru-MnO2 and commercial RuO2. This work provides a scalable route to durable, high-performance OER catalysts for seawater electrolysis.
Journal of Fuel Chemistry and Technology•2026•DOI: 10.1016/S1872-5813(26)60680-9
Low-temperature chemical looping air separation (CLAS) is a promising technology for producing oxygen-enriched gas streams, utilizing the redox properties of solid oxygen carriers to selectively capture and release oxygen from air. Oxygen vacancy formation energy (Eovf) is a key descriptor for evaluating the ease of oxygen release. In this study, the applicable range of Eovf for CLAS oxygen carriers was determined to be <2.3 eV via thermodynamic calculations. A graph neural network (GNN) model, specifically the ALIGNN architecture, was trained to predict Eovf with a mean absolute error (MAE) of 0.26 eV on the test set. Using this model, a high-throughput screening of 3,649 compositions of SrxA1−xFeyB1−yO3 perovskites was conducted to identify promising CLAS oxygen carriers. The predictions revealed that doping with Ba and Ca at the A-site and Co at the B-site effectively reduces Eovf. The screening criterion of Eovf < 2.3 eV successfully rediscovered several previously reported low-temperature CLAS oxygen carriers, validating the approach. This work demonstrates that GNN-based Eovf prediction can significantly accelerate the discovery of CLAS materials, with broader implications for other chemical looping applications such as full oxidation and syngas production.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202608028
Ship loading operations emit multi-component volatile organic compounds (VOCs) with complex composition, including methanol, dichloromethane, trichloroethylene, p-xylene, acrylonitrile, benzene, and acetonitrile. Under high-humidity marine conditions, treatment is challenging. This study systematically screened three molecular sieves with distinct pore sizes—ZSM-5, β-type, and HY—for selective adsorption of these seven VOCs at moisture contents of 0%, 2.5%, and 5%. Competitive adsorption in acrylonitrile/p-xylene mixtures was examined on ZSM-5-all-silica and HY-100. Results showed: (1) saturated adsorption capacity decreased with increasing moisture content, confirming water-VOC competition; higher Si/Al ratios enhanced hydrophobicity, with all-silica ZSM-5 exhibiting superior water resistance. (2) Selective adsorption followed pore size matching: ZSM-5 (0.54–0.56 nm) suited C1–C3 small molecules (10–50 mg/g); β-type (1.1–1.2 nm) showed best universality for C3–C6; HY (2.16–2.76 nm) favored C8 molecules like p-xylene (100–120 mg/g). (3) Optimizing molecular sieve proportion and layered arrangement balanced adsorption capacities across components, significantly prolonging breakthrough time. The optimal configuration placed ZSM-5 in the upper layer and HY in the lower layer. Molecular sieves also exhibited good thermal stability and regenerability. This study provides technical support for efficient treatment of multi-component VOCs from ship loading operations.