Synthesis and Crystal Structure of Na 2 TiO 3



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27 卷 5 期 结 构 化 学 (JIEGOU HUAXUE) Vol. 27, No.5 2008. 5 Chinese J. Struct. Chem. 553~557 Synthesis and Crystal Structure of Na 2 TiO 3 MAO Shao-Yu 1 REN Xiao-Xia ZHOU Zhao-Hui (State Key Laboratory for Physical Chemistry of Solid Surfaces, Department of Chemistry, Xiamen University, Xiamen 361005, China) ABSTRACT The crystal structure of a sodium titanium oxide Na 2 TiO 3 obtained by high temperature solid state reaction method was determined from single-crystal X-ray diffraction study. The compound crystallizes in the monoclinic system, space group C2/c, M r = 141.88, a = 9.885(1), b = 6.4133(8), c = 5.5048(7) Å, β = 115.50(3)º, V = 314.99(7) Å 3, Z = 4, D c = 2.992 g/cm 3, λ = 0.71073 Å, µ = 27.80 cm 1, (000) = 272, T = 295 K, R = 0.0189 and wr = 0.0512 for 30 variables and 370 contributing unique reflections. The three-dimensional structure in Na 2 TiO 3 is constructed by the TiO(1) 4 O(2) and NaO(1) 3 O(2) 2 groups. The titanium atoms are grouped in the form of trigonal bipyramid and arranged along the c axis by sharing the edges. The structure is compared with other structures of related A 2 BO 3 compounds. Keywords: synthesis, crystal structure, X-ray diffraction 1 INTRODUCTION Titanates have received much attention because of their wide applications as ferroelectric materials [1]. Previous work on sodium titanates compounds has been focused on their synthesis and structural characterizations [2~4] due to their extensive applications in the synthesis of other titanates like BaTiO [5] 3. In previous reports, NaTiO 3 was synthesized normally by high temperature (T > 900 ) solid-state reaction [6, 7]. X-ray powder diffraction patterns of as-obtained products were indexed to several different symmetries. Nalbandyan has got Na 2 TiO 3 in rhombohedral symmetry R-3 (148) with a = 13.927 and c = 7.676 Å when prepared by solid-state synthesis at 900 [6]. Hill et al. have got two kinds of Na 2 TiO 3. One was prepared by annealing the high temperature phase α-na 2 O-TiO 2 or γ-na 2 O-TiO 2 for 3 h at 800. In this case, the crystal is of face-centered monoclinic with a = 13.021, b = 13.922, c = 9.526 Å and β = 95.539. As for the other kinds, a mixture of Na 2 CO 3 and TiO 2 (anatase) in molar proportion was heated in a P crucible in an electric furnace at 1200 for 1 h, and then cooled in air. In this method, the Na 2 TiO 3 belongs to the monoclinic system with a = 9.064, b = 6.457, c = 5.54 Ǻ, β = 97.923 [4]. However, the single-crystal structure determination of this compound has not been made yet. In this work, the system NaOH-TiO 2 is studied and single crystals of Na 2 TiO 3 as reported in JCPDS 37-0346 [7] have been obtained by the solid-state reaction at a lower temperature (T = 500 ). The crystal structure of Na 2 TiO 3 determined by singlecrystal X-ray diffraction is described, which is compared with other structures of related A 2 BO 3 compounds. 2 EXPERIMENTAL 2. 1 Synthesis of Na 2 TiO 3 A mixture of NaOH (96%, Sinopharm Chemical Received 23 January 2007; accepted 21 May 2007 (ICSD 419432) 1 Corresponding author. Mao Shao-Yu, born in 1963, professor, majoring in functional crystal materials. Tel: 86-592-2185667, E-mail: symao@xmu.edu.cn

554 MAO S.Y. et al.: Synthesis and Crystal Structure of Na 2 TiO 3 No. 5 Reagent Co., Ltd) and TiO 2 (98%, China Medicine (Group) Shanghai Chemical Reagent Corporation) in molar ratio of 3:1 was placed in an Al 2 O 3 crucible, heated for 12 h in an electric furnace at 500, and then slowly cooled to room temperature. Wellformed crystals were obtained by leaching and filtering the products. 2. 2 Structure determination X-ray powder diffraction pattern (Rigaku D/max- RC) of manually selected crystals agreed well with that calculated from the single-crystal data and also matched the data of Na 2 TiO 3 (JCPDS 37-0346), as shown in ig. 1. The chemical composition confirmed by a chemical semi-quantitative energy dispersive X-ray diffraction analysis (LEO1530, Oxford Instruments) showed the atomic ratio of Na/ Ti/O is approximately 1.04/1/4.39. ig. 1. Comparison of experimental X-ray powder diffraction pattern (upper) of Na 2 TiO 3 compound with the JCPDS card 37-0346 A single crystal with dimensions of 0.15mm 0.11mm 0.06mm was mounted on a Bruker Apex CCD diffractometer equipped with a graphite-monochromatic MoKα radiation at 295(2) K. Crystallographic data for the title compound are summarized in Table 1. A total of 892 reflections were taken from 3.91<θ<28.10º, yielding 370 unique reflections (R int = 0.0228) including 367 observed ones (I > 2σ(I)). The intensity data were corrected for Lp factors, and absorption correction was made in the final refinement (T min /T max =0.8747). The anomalous-dispersion coefficients were taken into account during the data processing. Systematic absence led to the space groups C2/c or Cc (International Tables for Crystallography, 1983, Vol. A). The structure was solved in space group C2/c and confirmed by the full-matrix least-squares refinement on 2 using SHELXL 97 [8]. 30 Variables including anisotropic displacement parameters were refined to R = 0.0187 and wr = 0.0512 (w = 1/[σ 2 ( 2 o ) + (0.0141P) 2 + 0.4656P], 2 where P = ( o + 2 2 c )/3) considering 370 contributing unique reflections with o > 4σ( o ), S = 1.180 and ( /σ) max = 0.000. The final residual electron density was +0.299 ( 0.317) e/å 3, 0.92(1.19) Å from the titanium atoms. The important bond distances are shown in Table 2. 1 2 2 2 2 ( ) o o c a b wr 2 = R1 = 4 wo w o c

2008 Vol. 27 结 构 化 学 (JIEGOU HUAXUE)Chinese J. Struct. Chem. 555 Table 1. Crystallographic Data for Na 2 TiO 3 ormula Na 2 TiO 3 ormula weight/amu 141.88 Space group C2/c Z 4 a/å 9.885(1) b/å 6.4133(8) c/å 5.5048(7) β 115.50(3) V/Å 3 314.99(7) D c /g cm 3 2.992 Linear absorption coefficient µ/cm 1 27.80 Temperature/K 293(2) Radiation, monochromator MoKα graphite Crystal shape, color Prism, colorless 2θ range/ 7.82~56.20 Total reflections 892 Unique reflections 370 ranges 13 h 12, 8 k 4, 7 l 7 Number of parameters 30 (000) 272 a R, b wr (I > 2σ(I)) 0.0187, 0.0512 a R, b wr (all data) 0.0187, 0.0512 Goodness-of-fit on 2 1.181 Residual peaks (hole)/e Å 3 0.299 (-0.317) Software Shelxl-97 [8] Table 2. Important Bond Distances of Na 2 TiO 3 Atom 1 Atom 2 Distance (Å) Ti(1) O(2) 1.7475(17) O(1) a 1.8797(13) O(1) b 1.8797(13) O(1) 2.0164(12) O(1) 2.0164(12) Na(2) O(1) c 2.3065(16) O(2) d 2.3090(14) O(2) e 2.3104(8) O(1) b 2.3643(14) O(1) e 2.3737(15) a: x, y+1, z +1/2; b: x +1, y +1, z; c: x +1, y, z +1/2; d: x +1/2, y +1/2, z; e: x 1/2, y +1/2, z 3 RESULTS AND DISCUSSION or the reaction between NaOH and TiO 2, when the molar ratio of NaOH and TiO 2 is not lower than 3, the following reactions may happen: 2NaOH+ TiO 2 = Na 2 TiO 3 + H 2 O 1) 2NaOH + 2TiO 2 = Na 2 Ti 2 O 5 + H 2 O 2) 2NaOH + 3TiO 2 = Na 2 Ti 3 O 7 + H 2 O 3) 4NaOH + TiO 2 = Na 4 TiO 4 + 2 H 2 O 4) At the temperature from 600 to 1200 K, all above reactions can take place automatically, but the thermodynamical tendency of reaction 1) is the biggest [5], and the system of NaOH-TiO 2 in our

556 MAO S.Y. et al.: Synthesis and Crystal Structure of Na 2 TiO 3 No. 5 synthesis favors the formation of Na 2 TiO 3 crystal. This is in agreement with the X-ray powder diffraction pattern of our product, a mixture of NaOH and Na 2 TiO 3. ig. 2. Three-dimensional network in the Na 2 TiO 3 structure presented in one unit cell The structure of Na 2 TiO 3 is displayed in ig. 2, which shows that the titanium atoms are bonded to five oxygen atoms grouped in the form of a trigonal bipyramid. They are arranged along the c direction by sharing edges (ig. 3). The sodium atoms are surrounded by five oxygen atoms, too. They serve as a bridge between TiO(1) 4 O(2) and NaO(1) 3 O(2) 2 groups thus developing a three-dimensional structure in Na 2 TiO 3 (ig. 2). In Na 2 TiO 3, the Na O bond distances are quite regular (from 2.31 to 2.37 Ǻ); however, the Ti O bond distances fall in a relatively wider range (1.75~2.02 Ǻ). Both titanium and sodium atoms have five coordination numbers. In the crystal structures of most sodium titanates elucidated, most Ti O units are in octahedral group [9~11]. In the crystal structures of compounds Li 2 TiO [12] 3 and Li 2 SnO [12] 3, the coordination number of Li + is six with average Li O bond distance of 2.13 (from 1.87 to 2.39 Ǻ) for Li 2 TiO 3 and 2.20 (in the range of 2.18 ~ 2.24 Ǻ) for Li 2 SnO 3. The coordination numbers of Ti or Sn atoms are also six, and the average Ti/Sn O bond distance is 1.95 (ranging from 1.91 to 1.99 Ǻ) for Li 2 TiO 3 and 2.07 (in the range of 2.06~2.08 Ǻ) for Li 2 SnO 3. The cell volumes of Li 2 TiO 3 and Li 2 SnO 3 are 425.22 and 480.24 Ǻ 3, respectively, consistent with the bigger radius of Sn 4+ than Ti 4+ and Na + than Li +. ig. 3. Structure of Na 2 TiO 3 viewed along <100> direction

2008 Vol. 27 结 构 化 学 (JIEGOU HUAXUE)Chinese J. Struct. Chem. 557 The crystal of compound Rb 2 TiO 3 belongs to orthorhombic symmetry, space group Cmca, with a = 6.0150, b = 11.9360, c = 13.3660 Ǻ, V = 959.61 Ǻ 3 and Z = 8. The titanium atoms are bonded to four oxygen atoms forming slightly distorted tetrahedra arranged along the c axis. As regards K 2 SnO 3, its crystal is of orthorhombic symmetry, space group Pnma, with a = 5.7400, b = 10.3400, c = 7.1400 Ǻ, V = 423.77 Ǻ 3 and Z = 4. The tin atom is bonded to five oxygen atoms. No connection between potassium and oxygen atoms is found due to the bigger cation radius of K + in K 2 SnO 3 than that of Na + in Na 2 TiO 3. ig. 4 is the schematic presentation of cell volume per unit formula for related A 2 BO 3 compounds (A: Li, Na, K Rb; B: Ti, Sn), showing the dependence of cell volume per unit formula on the radius of A + cation. ig. 4. Comparison of V/Z of some A 2 BO 3 compounds shown in histogram REERENCES (1) Hertling, G. H. J. Am. Ceram. Soc. 1999, 82, 797 817. (2) Andersson, S.; Wadsley, A. D. Acta Cryst. 1967, 23, 1948 1953 (3) Andersson, S.; Wadsley, A. D. Acta Cryst. 1962, 15, 194 201. (4) Werthmann, R.; Hoppe, R. Z. Anorg. Allg. Chem. 1984, 519, 117 133 (5) Sun, K.; Wu, J. H.; Ma, Y. Y.; Liang, L.. Mater. Rev. 2000, 14, 60 62. (6) Nalbandyan, V.; Shukaev, I. Russ. J. Inorg. Chem. (Engl. Transl.) 1990, 35, 613 615. (7) Hill, W.; Moon, A.; Higginbotham, G. J. Am. Ceram. Soc. 1985, 68, 266 268. (8) Sheldrick, G. M. SHELXS97 and SHELXL97. University of Göttingen, Germany 1997. (9) Akimoto, J.; Takei, H. J. Solid State Chem. 1989, 79, 212 217. (10) Akimoto, J.; Takei, H. J. Solid State Chem. 1990, 85, 8 14. (11) Akimoto, J.; Takei, H. J. Solid State Chem. 1991, 90, 147 154. (12) Dorrian, J..; Newnham, R. E. Mater. Res. Bull. 1969, 4, 179 184.