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Volatile organic compounds (VOCs) serve as critical biomarkers in exhaled breath for early-stage cancer patients, and their rapid, trace-level detection holds marked implications for cancer screening. Surface-enhanced Raman scattering (SERS) technology demonstrates strong potential for trace VOC gas detection due to its ultra-high sensitivity and immunity to water interference. However, while surface plasmon resonance (SPR)-free semiconductor substrates offer superior spectral stability and selectivity, their sensitivity toward VOC detection remains suboptimal. This study introduces a novel semiconductor-based SERS substrate composed of copper single atoms anchored on UiO-66 (Cu/UiO-66), achieving a record-low detection limit of 10 parts per billion for VOC gases with a rapid 2-min response time, thereby elevating the gas-sensing performance of SPR-free substrates to unprecedented levels. The exceptional SERS activity originates from the highly delocalized electron properties of single-atomic copper, which effectively facilitates single-atom charge transfer processes. Concurrently, the incorporation of copper single atoms modulates the band structure of UiO-66, substantially enhancing the coupling resonance between the substrate and target molecules. In simulated breath tests mimicking lung cancer patients' exhalations, Cu/UiO-66 exhibits remarkable VOC recognition capability and robust anti-interference performance. This work pioneers a new paradigm for ultra-sensitive, rapid detection of trace VOCs in exhaled breath, holding substantial promise for early cancer diagnostics and clinical translation.
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http://dx.doi.org/10.34133/research.0841 | DOI Listing |
Int J Biol Macromol
August 2025
School of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, Jiangsu Province 212013, China. Electronic address:
Efficiently enhancing hydrogen peroxide (HO) production via photocatalysis remains challenging. This study employed genetic engineering to express His-tagged superoxide dismutase (His-SOD), which was selectively anchored onto the coordinatively unsaturated metal sites of etched UIO-66-NH₂ (UIO-66-NH) through coordination-driven assembly. The synergistic effect between His-SOD and UIO-66-NH significantly enhanced both the stability and substrate affinity of the enzyme, while simultaneously boosting the photocatalytic activity of the MOF.
View Article and Find Full Text PDFResearch (Wash D C)
August 2025
Laboratory of Advanced Theranostic Materials and Technology, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, China.
Volatile organic compounds (VOCs) serve as critical biomarkers in exhaled breath for early-stage cancer patients, and their rapid, trace-level detection holds marked implications for cancer screening. Surface-enhanced Raman scattering (SERS) technology demonstrates strong potential for trace VOC gas detection due to its ultra-high sensitivity and immunity to water interference. However, while surface plasmon resonance (SPR)-free semiconductor substrates offer superior spectral stability and selectivity, their sensitivity toward VOC detection remains suboptimal.
View Article and Find Full Text PDFJ Colloid Interface Sci
November 2025
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002 Jiangsu, PR China; State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing, Jiangsu 210023, PR China. Electronic address:
Lithium-sulfur batteries (LSBs) are recognized for their high energy density; however, challenges such as the lithium polysulfide (LiPS) shuttle effect and sluggish reaction kinetics remain unresolved. To mitigate these issues, a dual-functional metal-organic framework material integrated with graphene (UIO-66-NH-HSO@rGO) has been developed, with its Li transport and LiPS anchoring capabilities systematically investigated. Through density functional theory (DFT) calculations, it was demonstrated that the -HSO group in UIO-66-NH-HSO facilitates LiPS adsorption via strong electrostatic interactions while repelling polysulfide anions, whereas the -NH group chemically anchors these anions, thereby enhancing Li transport and LiPS trapping.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
July 2025
Guangdong Provincial Key Laboratory of Fuel Cell Technology, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510640, China.
Exploring an efficient catalytic system for tandem upcycling of CO and polyethylene terephthalate (PET) is highly desirable for achieving efficient resource utilization of wastes. However, the high activation energy for C═O bonds (in both PET and CO) and the difficulty in regulating the reaction pathways restricted PET recovery efficiency. Here, we demonstrated the rational design of a single-atom Cu catalyst for precisely catalyzing the hydrogenation of CO to methanol and tandem PET upcycling to ethylene glycol (EG) and p-xylene (PX).
View Article and Find Full Text PDFACS Mater Au
May 2025
Laboratory of Molecular Simulation (LSMO), Institut des Sciences et Ingénierie Chimiques, Valais École Polytechnique Fédérale de Lausanne (EPFL), Rue de l'Industrie 17, Sion, Valais CH-1951, Switzerland.
Homochiral metal-organic frameworks (MOFs) are exceptional media for heterogeneous enantiodifferentiation processes. Modifying available achiral structure-bearing MOF scaffolds is a preferred method to extend this class of materials. Reported postsynthetic covalent chiralizations generally lead to uniform, site-specific modifications.
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