Bal?i?nas SPavlovaite DKinka MYeh J.-YHan P.-CShieh F.-KWu K.C.-W?imenas MGrigalaitis RBanys J.KEVIN CHIA-WEN WU2021-09-022021-09-02202014203049https://www.scopus.com/inward/record.uri?eid=2-s2.0-85083803773&doi=10.3390%2fmolecules25081962&partnerID=40&md5=b1ab213fecbf01faad7e61ad202acfc6https://scholars.lib.ntu.edu.tw/handle/123456789/581582We present a dielectric spectroscopy study of dipolar dynamics in the hydrated UiO-66(Zr) type metal-organic frameworks (MOFs) functionalized with ?NH2 and ?F groups. Experiments are performed in a broad temperature and frequency ranges allowing us to probe several dipolar relaxations. For both samples at temperature below 220 K, we observe confined supercooled water dynamics, which can be described by the Arrhenius law. At slightly higher temperature, a second less pronounced dipolar relaxation is identified, and its origin is discussed. At even higher temperature, the dielectric permittivity exhibits anomalous increase with increasing temperature due to the proton conductivity. Upon further heating, the permittivity shows a sudden decrease indicating a reversible removal of water molecules. Measurements of the dehydrated samples reveal absence of all three dipolar processes. ? 2020 by the authors.metal organic framework; organometallic compound; phthalic acid derivative; UiO-66; water; algorithm; chemical model; chemical structure; chemistry; impedance spectroscopy; temperature; Algorithms; Dielectric Spectroscopy; Metal-Organic Frameworks; Models, Chemical; Molecular Structure; Organometallic Compounds; Phthalic Acids; Temperature; Waterjournal article10.3390/molecules25081962