SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3780-3
Real-time health monitoring and ongoing evaluation of physiological conditions are becoming increasingly vital for the advancement of future medical diagnostics and personalized healthcare solutions. Given that certain illnesses necessitate prompt and accessible detection methods, wearable chemical sensors have garnered considerable interest for their capability to monitor health through physiological signals and chemical indicators. This review delivers a thorough examination of recent developments in four primary categories of wearable chemical sensors: biosensors, humidity sensors, gas sensors, and ion sensors. We explore the representative materials, device structures, operating mechanisms, and various application scenarios for each type of sensor. By investigating the latest innovations in these technologies, we aim to provide a detailed overview of the current research landscape, highlight existing challenges, and present potential future directions of wearable chemical sensors in healthcare monitoring.
Journal of Environmental Engineering Technology•2026•DOI: 10.13205/j.hjgc.202605018
To address the inadequacy of existing temporal emission allocation coefficients for oil storage, transportation, and sales sources in regions with distinct seasonal temperature variations, this study focused on a large oil depot in Northwest China. A method for establishing temperature-dependent hourly allocation coefficients for VOCs emissions was proposed, revealing a positive correlation between ambient temperature and emission coefficients. The coefficient peaked at 0.068 when temperatures exceeded 14 °C and dropped to a minimum of 0.007 below 8.5 °C. Annual VOCs emissions totaled 256.13 t, with summer contributing 108.89 t (42.51% of annual total) and winter only 12.54 t (4.90%), making summer emissions approximately 8.68 times higher than winter. Using CALPUFF dispersion modeling, dynamic source strength scenarios produced a maximum hourly concentration of 2242.7 μg/m³, a 55.12% increase over the constant source strength scenario (1445.8 μg/m³). The area of exceedance increased by 0.03 km², and the atmospheric environmental protection distance extended by 450 m, from 0 m to 450 m. These results demonstrate that conventional constant emission assumptions underestimate peak concentrations and protection distances, posing health risks to nearby residents. The study provides a scientific basis for localized emission regulation and improved environmental protection distance calculations.
Chinese Journal of Environmental Engineering•2026•DOI: 10.12030/j.cjee.202509093
Amid intensifying global warming, carbon emission reduction and carbon dioxide removal (CDR) have become central to climate governance. In March 2023, the European Commission proposed the Green Claims Directive (GCD) to combat greenwashing and enhance the reliability, comparability, and verifiability of environmental claims. The GCD, together with the Empowering Consumers for the Green Transition Directive, the Carbon Removal Certification Framework, and the European Sustainability Reporting Standards, forms a policy cluster supporting the EU's green transition and CDR deployment. China, as a major greenhouse gas emitter, has made progress in renewable energy and national carbon market construction, yet its total emissions remain high, CDR technologies are nascent, and CCUS deployment is economically oriented, mainly in enhanced oil recovery. This study systematically reviews the legislative background, core objectives, and synergistic logic of the GCD and related policies, focusing on requirements for CDR certification, third-party verification, and carbon credit regulation. It compares Chinese and EU carbon markets in coverage, allowance allocation, and MRV systems. The analysis indicates that EU experience in policy integration, technical standardization, and market maturity can inform China's policy framework, technology pathways, and market efficiency, supporting large-scale CDR and the 'dual carbon' goals.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-3794-0
Luminescent transparent display technology is widely used in emerging fields such as augmented reality glass, head-up vehicle display, and commercial retail windows. While electroluminescent display is well established, the photoluminescent transparent screen of full-color rendering ability remains elusive due to the severe crosstalk between emitters. Herein, a full-color transparent screen of an orthogonal red/green/blue (R/G/B) luminescence is reported. Lanthanide fluoride nanocrystals are used as the emitters, where the color is tuned by a deliberate choice of doping activators including Tb3+, Eu3+, and Tm3+. Polyvinyl alcohol, with an identical refractive index to nanocrystals, is employed as the host matrix, enabling a high transparency up to 86% in the visible region upon a high loading content (~78 wt%) of nanocrystals. It should be noted that the nanocrystals are embedded in separate monolayers before integration by a UV-selective absorber, i.e., epoxy resin, which absorbs 254-nm UV to block cross-excitation between Tb3+ and Eu3+ layers, providing an asymmetric luminescent property from both sides of the screen. In a proof-of-concept experiment, a full-color prototype is showcased in real time for its potential applications in advanced displays of immersive experience.
Environmental Chemistry•2026•DOI: 10.7524/j.issn.0254-6108.2025040104
The oxidative transformation of 2,6-dichlorophenol (2,6-DCP) was investigated in three typical zonal soils: black soil, red soil, and brown soil. Results demonstrated that 2,6-DCP underwent oxidative coupling in all soils, yielding hydroxylated polychlorinated diphenyl ethers (OH-PCDEs) and hydroxylated polychlorinated biphenyls (OH-PCBs) as primary products. The highest oxidative efficiency occurred in black soil, with approximately 85.1% of 2,6-DCP transformed within three days. In contrast, red and brown soils exhibited lower efficiencies, indicating a strong dependence on soil properties. Thermodynamic analysis revealed that the oxidative coupling reaction is endothermic, with elevated temperatures favoring reaction progress. Furthermore, soil microorganisms and dissolved oxygen were identified as critical controlling factors, acting synergistically to drive the reaction. This study provides the first evidence of natural oxidative coupling of 2,6-DCP in soil, forming OH-PCDEs and OH-PCBs. These findings offer significant scientific insight into the environmental fate of halogenated phenolic pollutants in terrestrial systems.
SCIENCE CHINA Materials•2026•DOI: 10.1007/s40843-025-4025-y
Gd3+-sensitized Tb3+-based glasses are high light-yield scintillators. Energy transfer sensitization between Gd3+ and Tb3+ is well-recognized. Gd3+ ions are also found to typically modulate the interionic distances of Tb3+ ions; however, the mechanism why this effect enhances the latter’s photoluminescence still remains unclear. This work focuses on Gd3+, Tb3+ co-doped La2O3-B2O3-SiO2 (LBSO), first demonstrating Tb3+ clusters via spectroscopy. LBSO’s optimal Tb3+ single-doping concentration is 37%, rising to 50% with 20% Gd3+. The LBSO:20%Gd3+,50%Tb3+ sample exhibits a 542 nm emission intensity 2.22 times that of the 37%Tb3+ single-doped sample, 38% scintillation efficiency (vs. BGO), and >20 lp mm−1 X-ray resolution. The introduction of Gd3+ increases the interionic distance between Tb3+ ions within the clusters, thereby suppressing the concentration quenching effect and enhancing the fluorescence emission. We propose this mechanism as “cluster-dispersion sensitization effect”. This effect was further confirmed in other glass systems (LBSO:Lu3+, Tb3+, LBSO:Y3+, Tb3+, Bi-based:Lu3+, Tb3+, etc.). Spectroscopic analysis shows Gd3+-Tb3+ energy transfer efficiency up to 80%. In conclusion, Gd3+ synergistically enhances Tb3+ fluorescence via both effects. These findings not only fully elucidate the sensitization mechanism of Gd3+ ions in Gd3+, Tb3+ co-doped scintillating glasses but also provide new insights for researching the manipulation of activator ion clusters in luminescent materials. In search for novel scintillators, cluster-dispersion sensitization effect may greatly improve their spatial resolution via intrinsic architectures design in glasses, ceramics, thin films, and nanoparticles.