2007
DOI: 10.1002/crat.200710961
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Synthesis and crystal structure of langbeinite related mixed‐metal phosphates K1.822Nd0.822Zr1.178(PO4)3 and K2LuZr(PO4)3

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Cited by 20 publications
(9 citation statements)
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“…In the last two decades, a large number of phosphates and sulfates with langbeinite structure have been developed for electro-optical and ferroelastic activity. Among them, KBaFe 2 (PO 4 ) 3 , KSrFe 2 (PO 4 ) 3 , KBaCr 2 (PO 4 ) 3 , Pb 1.5 V 2 (PO 4 ) 3 , K 2 M 3+ (M 4+ O 4 )­(PO 4 ) 2 (M 3+ = Fe, Sc; M 4+ = Mo, W), and K 2 M 0.5 Ti 1.5 (PO 4 ) 3 (M = Mn, Co) have been proposed as magnetic materials. , Rare earth ions doped K 2 GdZr­(PO 4 ) 3 , (Ce 3+ , Eu 2+ , Tb 3+ )/KMSc 2 (PO 4 ) 3 (M = Ba, Sr), (Eu, Cu)/K 2 Ca 2 (SO 4 ) 3 , K 2 Y 1– x Eu x Zr­(PO 4 ) 3 , and Nd 3+ :K 2 Mg 2 (SO 4 ) 3 are reported as luminescent materials. Recently, Ba 3 In 4 (PO 4 ) 6 and KBaIn 2 (PO 4 ) 3 are identified as excellent host materials for color tunable phosphors. , The physicochemical properties of langbeinites comprised with cesium and/or rubidium ions such as KCsFeZr­(PO 4 ) 3 , Cs 2 Ni 2 (MoO 4 ) 3 , Rb 3 Yb 2 (PO 4 ) 3 , Rb 2 YbTi­(PO 4 ) 3 , Rb 2 Cd 2 (SO 4 ) 3 , Rb 2 Yb 0.32 Ti 1.68 (PO 4 ) 3 , and Cs 1+ x Ln x Zr 2– x (PO 4 ) 3 (Ln = Sm–Lu), have also been investigated. , Since langbeinites exhibit different structural arrangements upon ionic substitutions and undergo phase transitions down to the temperature, the crystal chemistry of several langbeinite-type compounds has been extensively studied. For instance, crystal chemistry of K 2 FeZr­(PO 4 ) 3 , Pb 1.5 V 2 (PO 4 ) 3 , K 2 LnZr­(PO 4 ) 3 (Ln = Ce–Yb, Y), K 1.822 Nd 0.822 Zr 1.178 (PO 4 ) 3 , K 2 LuZr­(PO 4 ) 3 , K 2 MTi­(PO 4 ) 3 (M = Er, Yb or Y), Na 2 MTi­(PO 4 ) 3 (M = Fe, Cr), and titanium/lanthanide-mixed langbeinite phosphates with distinct structural relation between NZP and langbeinite structures have been reported. , Although the crystal structure investigation, luminescence, and magnetic properties of the above listed compounds are known, until now there are no reports available on KPbM 2 (PO 4 ) 3 (M = Cr, Fe) to the best of our knowledge. Therefore, in the current work we mainly focused on the structural elucidation of these two compounds, study of their thermal expansion, and magnetic behavior.…”
Section: Introductionmentioning
confidence: 99%
“…In the last two decades, a large number of phosphates and sulfates with langbeinite structure have been developed for electro-optical and ferroelastic activity. Among them, KBaFe 2 (PO 4 ) 3 , KSrFe 2 (PO 4 ) 3 , KBaCr 2 (PO 4 ) 3 , Pb 1.5 V 2 (PO 4 ) 3 , K 2 M 3+ (M 4+ O 4 )­(PO 4 ) 2 (M 3+ = Fe, Sc; M 4+ = Mo, W), and K 2 M 0.5 Ti 1.5 (PO 4 ) 3 (M = Mn, Co) have been proposed as magnetic materials. , Rare earth ions doped K 2 GdZr­(PO 4 ) 3 , (Ce 3+ , Eu 2+ , Tb 3+ )/KMSc 2 (PO 4 ) 3 (M = Ba, Sr), (Eu, Cu)/K 2 Ca 2 (SO 4 ) 3 , K 2 Y 1– x Eu x Zr­(PO 4 ) 3 , and Nd 3+ :K 2 Mg 2 (SO 4 ) 3 are reported as luminescent materials. Recently, Ba 3 In 4 (PO 4 ) 6 and KBaIn 2 (PO 4 ) 3 are identified as excellent host materials for color tunable phosphors. , The physicochemical properties of langbeinites comprised with cesium and/or rubidium ions such as KCsFeZr­(PO 4 ) 3 , Cs 2 Ni 2 (MoO 4 ) 3 , Rb 3 Yb 2 (PO 4 ) 3 , Rb 2 YbTi­(PO 4 ) 3 , Rb 2 Cd 2 (SO 4 ) 3 , Rb 2 Yb 0.32 Ti 1.68 (PO 4 ) 3 , and Cs 1+ x Ln x Zr 2– x (PO 4 ) 3 (Ln = Sm–Lu), have also been investigated. , Since langbeinites exhibit different structural arrangements upon ionic substitutions and undergo phase transitions down to the temperature, the crystal chemistry of several langbeinite-type compounds has been extensively studied. For instance, crystal chemistry of K 2 FeZr­(PO 4 ) 3 , Pb 1.5 V 2 (PO 4 ) 3 , K 2 LnZr­(PO 4 ) 3 (Ln = Ce–Yb, Y), K 1.822 Nd 0.822 Zr 1.178 (PO 4 ) 3 , K 2 LuZr­(PO 4 ) 3 , K 2 MTi­(PO 4 ) 3 (M = Er, Yb or Y), Na 2 MTi­(PO 4 ) 3 (M = Fe, Cr), and titanium/lanthanide-mixed langbeinite phosphates with distinct structural relation between NZP and langbeinite structures have been reported. , Although the crystal structure investigation, luminescence, and magnetic properties of the above listed compounds are known, until now there are no reports available on KPbM 2 (PO 4 ) 3 (M = Cr, Fe) to the best of our knowledge. Therefore, in the current work we mainly focused on the structural elucidation of these two compounds, study of their thermal expansion, and magnetic behavior.…”
Section: Introductionmentioning
confidence: 99%
“…In the case of phosphate K 0.10 Na 0.90 Ti 2 (PO 4 ) 3 such blocks are connected along axes c that is characteristic for sodium‐containing compounds with NASICON‐type structure (figure a). In the structure of K 0.877 Na 0.48 Ti ІІІ 0.357 Ti ІV 1.643 (PO 4 ) 3 the fragments [Ti 2 (PO 4 ) 3 ] run in four directions parallel to the cube diagonals (figure b) that is characteristic for complex substituted potassium or rubidium‐containing langbeinites .…”
Section: Resultsmentioning
confidence: 99%
“…They are: metal substitution in octahedra, element substitution in anion tetrahedra, and substitution of ions in cavities. Among these compounds, potassium-containing langbeinites are the most studied (Ogorodnyk et al, 2006(Ogorodnyk et al, , 2007bNorberg, 2002;Orlova et al, 2003). However, several reports concerning phosphate langbeinites with Rb + in the cavities of the framework are known: Rb 2 FeZr(PO 4 ) 3 (Trubach et al, 2004), Rb 2 YbTi(PO 4 ) 3 (Gustafsson et al, 2005) and Rb 2 TiY(PO 4 ) 3 (Gustafsson et al, 2006).…”
Section: Chemical Contextmentioning
confidence: 99%