Abstract <p>Cs<sub>3</sub>(HSO<sub>4</sub>)<sub>2</sub>(H<sub>2</sub>PO<sub>4</sub>) and Cs<sub>4</sub>(HSO<sub>4</sub>)<sub>3</sub>(H<sub>2</sub>PO<sub>4</sub>) superprotonic crystals have been investigated by conductive atomic force microscopy at increasing temperature. Local <i>I‒V</i> characteristics have been measured and an increase in the conductivity of the Cs<sub>3</sub>(HSO<sub>4</sub>)<sub>2</sub>(H<sub>2</sub>PO<sub>4</sub>) and Cs<sub>4</sub>(HSO<sub>4</sub>)<sub>3</sub>(H<sub>2</sub>PO<sub>4</sub>) crystals at 413‒453 K by two and three orders of magnitude, respectively, has been detected. Differences in the conductive characteristics of the crystals of different compositions in the vicinity of the phase transition are shown. Information on topographic and electrical features of the crystalline phases before and after exposure to temperature and electric fields has been obtained. The effect of external factors on the stability of the surface microstructure is evaluated. Possible mechanisms of the structure and phase transformations in the isostructural compounds with different ratios of sulfate and phosphate groups are discussed.</p>

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Cesium Hydrosulfate Phosphate Crystals: Conductivity and Real Structure at Increasing Temperature

  • R. V. Gainutdinov,
  • A. L. Tolstikhina,
  • I. P. Makarova,
  • S. Leesment,
  • V. A. Komornikov

摘要

Abstract

Cs3(HSO4)2(H2PO4) and Cs4(HSO4)3(H2PO4) superprotonic crystals have been investigated by conductive atomic force microscopy at increasing temperature. Local I‒V characteristics have been measured and an increase in the conductivity of the Cs3(HSO4)2(H2PO4) and Cs4(HSO4)3(H2PO4) crystals at 413‒453 K by two and three orders of magnitude, respectively, has been detected. Differences in the conductive characteristics of the crystals of different compositions in the vicinity of the phase transition are shown. Information on topographic and electrical features of the crystalline phases before and after exposure to temperature and electric fields has been obtained. The effect of external factors on the stability of the surface microstructure is evaluated. Possible mechanisms of the structure and phase transformations in the isostructural compounds with different ratios of sulfate and phosphate groups are discussed.