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In the realm of NH gas-sensing applications, the electrically conductive nature of TiCT MXene, adorned with surface terminations such as -O and -OH groups, renders it a compelling material. However, the inherent challenges of atmospheric instability and selectivity in the presence of gas mixtures have prompted the exploration of innovative solutions. This work introduces a strategic solution through the deposition of a mixed-matrix membrane (MMM) composed of poly(vinylidene fluoride) (PVDF) as the matrix and zeolitic imidazolate framework-67 (ZIF-67) as the filler. This composite membrane acts as a selective filter, permitting the passage of a specific gas, namely NH. Leveraging the hydrophobic and chemically inert nature of PVDF, the MMM enhances the atmospheric stability of TiCT by impeding water molecules from interacting with the MXene. Furthermore, ZIF-67 is selective to NH gas via acid-base interactions within the zeolite group and selective pore size. The TiCT sensor embedded in the MMM filter exhibits a modest 1.3% change in the sensing response to 25 ppm of NH gas compared to the response without the filter. This result underscores the filter's effectiveness in conferring selectivity and diffusivity, particularly at 35% relative humidity (RH) and 25 °C. Crucially, the hydrophobic attributes of PVDF impart heightened stability to the TiCT sensor even amidst varying RH conditions. These results not only demonstrate effective NH detection but also highlight the sensor's adaptability to diverse environmental conditions, offering promising prospects for practical applications.
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http://dx.doi.org/10.1021/acssensors.3c02551 | DOI Listing |
RSC Adv
August 2025
School of Physics and Information Engineering, Shanxi Normal University Taiyuan 030031 China
Twisted intramolecular charge transfer (TICT) is a critical mechanism influencing the emission efficiency and stability of fluorescent materials, thereby playing a pivotal role in the design of highly fluorescent and stable dyes. Although substantial research has concentrated on the role of intermolecular hydrogen bonding in excited-state dynamics, the impact of intramolecular hydrogen bonding has not been thoroughly investigated. To elucidate the solvent polarity dependence of C7 and C30, we employed the Kamlet-Taft and Catalán 4P models in conjunction with steady-state and transient absorption spectroscopy, complemented by time-dependent density functional theory (TDDFT) calculations.
View Article and Find Full Text PDFSci Bull (Beijing)
July 2025
Hainan Institute of East China Normal University, State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Process, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China; School of Chemist
Arynes are straightforward and effective synthons for π-extension accompanying by vicinal difunctionalization simultaneously, thereby being ideal building blocks for polycyclic aromatic hydrocarbons (PAHs) construction. However, CC triple bond in an aromatic system, with the distorted bond angle and shortened bond distance, arouses tremendous challenges for thermodynamic stability and kinetically reactive selectivity, especially for heteroarynes. Herein, controllable aryne generation was achieved for nitrogen-doped polycyclic aromatic hydrocarbons via designed cyclic pyridine-benzene λ-iodanes, in which the iodine ensured the thermodynamic stability and kinetic site-selectivity via p→π* interaction with aryne for chemo- and regio-selectivity.
View Article and Find Full Text PDFAnal Methods
May 2025
Institute of Optical Materials and Chemical Biology, Guangxi Key Laboratory of Electrochemical Energy Materials, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P. R. China.
Viscosity, as a fundamental biophysical parameter of cellular microenvironments, critically regulates physiological processes, including molecular transport and signal transduction. Lysosomes, functioning as pivotal organelles, orchestrate essential biological activities such as macromolecular degradation and autophagic flux. Aberrant viscosity fluctuations disrupt the substrate delivery within lysosomal enzymatic activation zones, precipitating accumulation of undegraded metabolites and subsequent release of inflammatory mediators, ultimately contributing to chronic inflammatory diseases.
View Article and Find Full Text PDFJ Phys Chem B
March 2025
Department of Complex Systems Science, Graduate School of Informatics, Nagoya University, Nagoya 464-8601, Japan.
Photoresponsive molecules that respond to the surrounding environment are expected to be utilized as optical functional materials, such as sensors. Recently reported 2-aryl-3H-1,3-benzazaphosphole oxide with a diphenylamino group (ABPO) is one such molecule having interesting solvent-dependent properties. The absorption spectra of ABPO in nonpolar and polar solvents are almost identical in shape and excitation energy, whereas the fluorescence spectrum is red-shifted as the solvent polarity increases.
View Article and Find Full Text PDFBioorg Chem
February 2025
Key Laboratory for Tibet Plateau Phytochemistry of Qinghai Province, College of Pharmacy, Qinghai Minzu University, Xining 810007 Qinghai, China; State Key Laboratory of Applied Organic Chemistry and College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China. Electronic
Viscosity is a fundamental property in biological systems, influencing organelle function and molecular diffusion. Abnormal viscosity is associated with diseases such as metabolic disorders, neurodegeneration, and cancer. Lysosomes, central to cellular degradation and recycling, are sensitive to viscosity changes, which can disrupt enzymatic activity and cellular homeostasis.
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