Citation: Junyang FENG, Xiaoli HAN, Yongjie SONG, Gang LI. Proton conduction and fluorescence properties of an ionic hydrogen-bonded organic framework constructed from dibromophthalic acid[J]. Chinese Journal of Inorganic Chemistry, ;2026, 42(4): 693-702. doi: 10.11862/CJIC.20250350 shu

Proton conduction and fluorescence properties of an ionic hydrogen-bonded organic framework constructed from dibromophthalic acid

  • Corresponding author: Gang LI, gangli@zzu.edu.cn
  • Received Date: 24 November 2025
    Revised Date: 6 January 2026

Figures(8)

  • To address the pressing demand for proton-conducting materials with enhanced environmental adaptability and long-term stability, an ionic hydrogen-bonded organic framework (iHOF 1) was successfully constructed via a solvothermal method using 2, 5-dibromoterephthalic acid (H2BDC-Br2) as the building block. Its crystal structure, stability profiles, proton transport behavior, and photoluminescent properties were systematically investigated by a combination of characterization techniques, including single-crystal X-ray diffraction, powder X-ray diffraction, electrochemical impedance spectroscopy, solid-state fluorescence spectroscopy, etc. Structural analysis reveals that iHOF 1 crystallizes in the monoclinic space group C2/c, with its 3D framework stabilized by robust intermolecular H-bonds and electrostatic interactions between HBDC-Br2- anions and (Me2NH2)+ cations. Proton conductivity measurements demonstrate a distinct dependence on both temperature and relative humidity (RH), reaching a maximum value of 1.72×10-3 S·cm-1 at 100 ℃ and 98% of RH. Activation energy calculations yield values of 0.44 eV (at 68% of RH) and 0.41 eV (at 98% of RH), confirming that proton transport within the framework follows the Grotthuss hopping mechanism. This efficient proton conduction is facilitated by a contiguous H-bonded network formed by hydrophilic carboxyl groups, bromine atoms, and (Me2NH2)+ cations in the framework. Stability assessments indicated that iHOF 1 possessed excellent thermal stability (decomposition temperature: 230 ℃) and chemical stability, as evidenced by the retention of structural integrity after water immersion and prolonged electrochemical testing. Furthermore, upon excitation at 324 nm, the material exhibited a strong and monochromatic blue emission peak at 432 nm, which originates from the ππ* transition of the aromatic moieties and is significantly enhanced by the confinement effect of the rigid framework.
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