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| Identifiers | |||
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3D model (JSmol) | |||
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| Properties | |||
| CsHO4S | |||
| Molar mass | 229.97 g·mol−1 | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
Caesium bisulfate or cesium hydrogen sulfate is an inorganic compound with the formula CsHSO4. The caesium salt of bisulfate, it is a colorless solid obtained by combining Cs2SO4 and H2SO4. [1]
Above 141 °C, CsHSO4 is a superionic conductor. [1] The rapid ionic conductivity arise especially in the range of these temperatures due to the high activity of protons. [2]
Based on the results of X-ray crystallography, the structure consists of tetrahedral sulfate centers that bridge caesium ions. The proton is associated with the oxygen on sulfate. [3]
CsHSO4 goes through three crystalline phases that are referred to as phase III, II, and I. [4] CsHSO4 is initially existing in phase III at a room temperature of 21 °C. Phase III ranges from 21 °C to 90 °C with a transition temperature of 90 °C to 100 °C between phase III and phase II. Phase II ranges from 90 °C to 140 °C. At 140 °C, CsHSO4 undergoes a phase shift from phase II to phase I. [5]
Phase III (21 °C to 90 °C) and Phase II (90 °C to 140 °C) are referred to as the monoclinic phases, in which CsHSO4 exhibits its lowest proton conductivity. As the crystalline structure's temperature is raised, it will show variations in the unit cell volume and the arrangement of its hydrogen bonds, which will alter the ability of a CsHSO4 crystalline structure to allow the displacement of protons.
At 141 °C, the CsHSO4 crystal structure experiences a structural change from monoclinic phase II to a tetragonal phase, becoming phase I. Phase I has more elevated crystal symmetry and widened lattice dimensions. Phase I is noted as the superprotonic phase (strong conducting phase), which triggers an extreme growth in proton conductivity by four orders of magnitude, reaching 10 mS/cm. This makes the conductivity of CsHSO4 ten-fold stronger than the conductivity of a sodium chloride aqueous solution. In the superprotonic phase, the movement of an SO4 tetrahedron generates a disruption of the hydrogen bond network, which accelerates proton transfer. [5] The tetragonal anions available in the structure are accountable for the arrangement of the hydrogen bonds with the moving protons. [6]
The maximum conductivity of pure CsHSO4 is 10 mS/cm, which is too low for practical applications. In composites with SiO2, TiO2, and Al2O3), the proton conductivity below the phase transition temperature is enhanced by a few orders of magnitude. [7]
Unlike hydrated protonic conductors, the absence of water in CsHSO4 provides thermal and electrochemical stability. Electromotive force (EMF) measurements in a humidified oxygen concentration cell verified the high ionic nature of CsHSO4 in its superprotonic phase. [8] Based on heat rotation, the voltage stayed the same for over 85 hours during the measurement, particularly at the high temperature. [8] These results, demonstrate the thermal independence from humidity-type environments. Additionally, the crystal structure of CsHSO4 allows for quick transport of smaller charged ions, resulting in efficient energy transfer in electrochemical devices.
In chemistry, a salt or ionic compound is a chemical compound consisting of an ionic assembly of positively charged cations and negatively charged anions, which results in a neutral compound with no net electric charge. The constituent ions are held together by electrostatic forces termed ionic bonds.
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Ionic conductivity is a measure of a substance's tendency towards ionic conduction. Ionic conduction is the movement of ions. The phenomenon is observed in solids and solutions. Ionic conduction is one mechanism of current.
Rubidium silver iodide is a ternary inorganic compound with the formula RbAg4I5. Its conductivity involves the movement of silver ions within the crystal lattice. It was discovered while searching for chemicals which had the ionic conductivity properties of alpha-phase silver iodide at temperatures below 146 °C for AgI.
Yttria-stabilized zirconia (YSZ) is a ceramic in which the cubic crystal structure of zirconium dioxide is made stable at room temperature by an addition of yttrium oxide. These oxides are commonly called "zirconia" (ZrO2) and "yttria" (Y2O3), hence the name.
Solid-state ionics is the study of ionic-electronic mixed conductor and fully ionic conductors and their uses. Some materials that fall into this category include inorganic crystalline and polycrystalline solids, ceramics, glasses, polymers, and composites. Solid-state ionic devices, such as solid oxide fuel cells, can be much more reliable and long-lasting, especially under harsh conditions, than comparable devices with fluid electrolytes.
Sossina M. Haile is an American chemist, known for developing the first solid acid fuel cells. She is a professor of materials science and engineering at Northwestern University, Illinois, US.
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Lithium lanthanum zirconium oxide (LLZO, Li7La3Zr2O12) or lithium lanthanum zirconate is a lithium-stuffed garnet material that is under investigation for its use in solid-state electrolytes in lithium-based battery technologies. LLZO has a high ionic conductivity and thermal and chemical stability against reactions with prospective electrode materials, mainly lithium metal, giving it an advantage for use as an electrolyte in solid-state batteries. LLZO exhibits favorable characteristics, including the accessibility of starting materials, cost-effectiveness, and straightforward preparation and densification processes. These attributes position this zirconium-containing lithium garnet as a promising solid electrolyte for all-solid-state lithium-ion rechargeable batteries.
Lithium aluminium germanium phosphate, typically known with the acronyms LAGP or LAGPO, is an inorganic ceramic solid material whose general formula is Li
1+xAl
xGe
2-x(PO
4)
3. LAGP belongs to the NASICON family of solid conductors and has been applied as a solid electrolyte in all-solid-state lithium-ion batteries. Typical values of ionic conductivity in LAGP at room temperature are in the range of 10–5 - 10–4 S/cm, even if the actual value of conductivity is strongly affected by stoichiometry, microstructure, and synthesis conditions. Compared to lithium aluminium titanium phosphate (LATP), which is another phosphate-based lithium solid conductor, the absence of titanium in LAGP improves its stability towards lithium metal. In addition, phosphate-based solid electrolytes have superior stability against moisture and oxygen compared to sulfide-based electrolytes like Li
10GeP
2S
12 (LGPS) and can be handled safely in air, thus simplifying the manufacture process. Since the best performances are encountered when the stoichiometric value of x is 0.5, the acronym LAGP usually indicates the particular composition of Li
1.5Al
0.5Ge
1.5(PO
4)
3, which is also the typically used material in battery applications.
The phosphate sulfates are mixed anion compounds containing both phosphate and sulfate ions. Related compounds include the arsenate sulfates, phosphate selenates, and arsenate selenates.
