The disordered high-temperature structure of (NH4)3H(SO4)2 and its relationship to the room-temperature phase

被引:24
作者
Friese, K
Aroyo, MI
Schwalowsky, L
Adiwidjaja, G
Bismayer, U
机构
[1] Univ Hamburg, Mineral Petrog Inst, D-20146 Hamburg, Germany
[2] Univ Basque Country, Dept Fis Mat Condensada, E-48080 Bilbao, Spain
关键词
letovicite; (NH4)(3)H(SO4)(2); high-temperature phase; disorder; symmetry mode analysis;
D O I
10.1006/jssc.2002.9516
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The structure of letovicite, (NH4)(3)H(SO4)(2) has been redetermined at 293 and 420K. At room temperature the structure crystallizes monoclinic, space group C12/c1 (no. 15), with lattice parameters a = 15.418(5) Angstrom, b = 5.905(5) Angstrom, c = 10.223(5) Angstrom and beta = 102.806(5)degrees. The structure is composed of two symmetrically independent isolated NH4+ tetrahedra and [SO4-H-SO4](3-) dimers with a symmetrical hydrogen bond connecting the two sulfate tetrahedra. At 420 K the structure is rhombohedral, space group R (3) over barm (no. 166) with lattice parameters a = 5.9039(5) and c = 22.5360(6) Angstrom. While the low-temperature phase is completely ordered, this does not hold for the high-temperature phase: the hydrogen and oxygen atoms which constitute the hydrogen bond are disordered with the consequence that the hydrogen bond is now strongly asymmetric. Furthermore, the hydrogen atoms in one of the two symmetrically independent NH4+ tetrahedra are disordered and have probably some share in the high protonic conductivity which has so far been attributed mainly to the hydrogen atom of the hydrogen bond. (C) 2002 Elsevier Science (USA).
引用
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页码:136 / 147
页数:12
相关论文
共 18 条
[1]   Symmetry-mode analysis of displacive phase transitions using International Tables for Crystallography [J].
Aroyo, MI ;
Perez-Mato, JM .
ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 1998, 54 :19-30
[2]   A HEATING DEVICE FOR 4-CIRCLE DIFFRACTOMETERS [J].
BOHM, H .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1995, 28 :357-357
[3]   X-RAY STUDY ON THE PHASE-TRANSITIONS IN TRIAMMONIUM HYDROGEN DISULFATE CRYSTALS AND DEUTERATED CRYSTALS [J].
CHEN, RH ;
WANG, LM ;
YANG, SC .
PHASE TRANSITIONS, 1992, 37 (2-3) :141-147
[4]  
Cracknell A.P., 1979, Kronecker product tables. Vol. 1, V1
[5]   Proton dynamics in letovicite, (NH4)3H(SO4)2:: A 1H and 14N NMR spectroscopic study [J].
Fechtelkord, M ;
Engelhardt, A ;
Buhl, JC ;
Schwalowsky, L ;
Bismayer, U .
SOLID STATE NUCLEAR MAGNETIC RESONANCE, 2000, 17 (1-4) :76-88
[6]   A NEW PHASE-TRANSITION OF (NH4)3H(SO4)2 AT 190-DEGREES-C [J].
FUKAMI, T ;
TOBARU, K ;
KANEDA, K ;
NAKASONE, K ;
FURUKAWA, K .
JOURNAL OF THE PHYSICAL SOCIETY OF JAPAN, 1994, 63 (05) :2006-2007
[7]   Crystal structure of (NH4)(3)H(SO4)(2) in phase I [J].
Fukami, T ;
Horiuchi, K ;
Nakasone, K ;
Furukawa, K .
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS SHORT NOTES & REVIEW PAPERS, 1996, 35 (4A) :2253-2254
[8]   DIELECTRIC STUDY ON PHASE-TRANSITIONS IN TRIAMMONIUM HYDROGEN DISULFATE (NH-4)3H(SO-4)2 [J].
GESI, K .
PHYSICA STATUS SOLIDI A-APPLIED RESEARCH, 1976, 33 (02) :479-482
[9]   PRESSURE-INDUCED FERROELECTRICITY IN (NH4)H(SO4)2-H-3 [J].
GESI, K .
JOURNAL OF THE PHYSICAL SOCIETY OF JAPAN, 1977, 43 (06) :1941-1948
[10]  
KAMOUNI M, 1987, PHASE TRANSITION, V9, P147