Journal Archive Collections

Permanent URI for this communityhttp://localhost:4000/handle/123456789/16937

Browse

Search Results

Now showing 1 - 2 of 2
  • Item
    Protonic Conductivity in Copper Formate Tetrahydrate
    (Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 73 (09), 1977) Murphy, Kathleen E.; Flanagan, Ted B.
    The conductivities of single crystals of copper formate tetrahydrate (CFT) have been determined along the three principal crystallographic axes with proton-injecting electrodes. The ohmic conductivities at 298 K are: 5.5 ± 1.6 × 10–7Ω–1 cm–1(along the b-axis), 8.5 ± 2.1 × 10–8Ω–1 cm–1(along the a-axis) and 7 ± 2 × 10–12Ω–1 cm–1(along the c axis). Since the H-bonded network lies in the ab-plane, the observed anisotropy of conduction suggests protonic conductivity. The Arrhenius plot of σ exhibits a change of slope and a transition to a lower conductivity at the paraelectric → antiferroelectric phase change (235 K). The energies of activation for conduction within the ab-plane are 0.56 eV above 235 K and 0.65 eV below 235 K. The tetradeuterate has an ohmic conductivity approximately an order of magnitude lower than the tetrahydrate (within the ab-plane). Space-charge-limited currents are observed at high fields. The CFT crystals behave as semipermeable membranes to protons and this supports the view that protons are mobile within CFT. If conduction is indeed protonic, CFT is a very ready hydrate protonic conductor exhibiting a conduction greater than ice.
  • Item
    Protonic Conductivity in Layered SnCl2 • 2H2O Single Crystal
    (Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (09-12), 1978) Mognaschi, Ezio R.; Chierico, Angelo; Parravicini, Gianbattista
    The electric conductivity of stannous chloride dihydrate single crystals, measured both with injecting and with metallic electrodes, shows two contributions: a critical, frequency dependent behaviour around the phase transition temperature and a temperature activated process, both in the disordered phase and in the ordered phase. This second process causes a very large conductivity which, along the c direction and at room temperature, results of the order of 10–6Ω–1 cm–1. The conduction shows ohmic behaviour at low fields and non-ohmic behaviour at higher fields (space–charge–limited current). Arguments in favour of protonic conduction are given and a model is proposed to interpret the conduction mechanism.