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Revisiting Tungsten Trioxide Hydrates (TTHs) Synthesis - Is There Anything New?
We report a very simple precipitation route to prepare a layered perovskite-type structure, tungsten trioxide hydrate (TTH), with the nominal chemical formula of WO3·1.3H2O (≡ 1/2H2W2O7·1.6H2O), using aqueous Na2WO4 and SrCl2. Our investigation shows that the concentration of HCl used to dissolve th...
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Published in: | Inorganic chemistry 2009-07, Vol.48 (14), p.6804-6811 |
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description | We report a very simple precipitation route to prepare a layered perovskite-type structure, tungsten trioxide hydrate (TTH), with the nominal chemical formula of WO3·1.3H2O (≡ 1/2H2W2O7·1.6H2O), using aqueous Na2WO4 and SrCl2. Our investigation shows that the concentration of HCl used to dissolve the SrCl2 plays a crucial role in the stabilization of different structure types of layered TTHs. Highly acidic SrCl2 (dissolved in 9 M HCl) solution yields an orthorhombic layered TTH of WO3·2H2O, while SrCl2 dissolved in 3 M HCl appears to give an A-site-deficient Ruddlesdon−Popper (RP) related double-perovskite-type layered structure (DOLS-TTH). A well-known scheelite-type structure is obtained under weakly basic conditions (pH = 10.3 for Na2WO4(aq), 7.0 for SrCl2(aq)). Previously, RP-type a DOLS of H2W2O7·0.58H2O was prepared, using an acid-leaching method, from the corresponding n = 2 member of the layered Aurivillius phase (AP) Bi2W2O9. Powder X-ray diffraction showed the formation of layered RP DOLS with a large d spacing ∼12.5 Å, which is consistent with acid-leaching (Kuto et al. Inorg. Chem. 2003, 42, 4479−4484; Wang et al. J. Solid State Chem. 2007, 180, 1125−1129) and exfoliation (Schaak et al. Chem. Commun. 2002, 706−707) methods for synthesized TTHs. The proposed DOLS-TTH structure of newly prepared TTHs was further confirmed by an intercalation reaction using n-octylamine (C8A). A transmission electron microscopy study showed the formation of nanosized particles, and scanning electron microscopy coupled with energy dispersive X-ray analysis showed the absence of Na and Sr in the air-dried, as-precipitated products under acidic conditions. The bulk electrical (proton) conductivity of presently prepared TTHs was found to be on the order of 10−4−10−3 S/cm at room temperature in wet N2. |
doi_str_mv | 10.1021/ic900738m |
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Our investigation shows that the concentration of HCl used to dissolve the SrCl2 plays a crucial role in the stabilization of different structure types of layered TTHs. Highly acidic SrCl2 (dissolved in 9 M HCl) solution yields an orthorhombic layered TTH of WO3·2H2O, while SrCl2 dissolved in 3 M HCl appears to give an A-site-deficient Ruddlesdon−Popper (RP) related double-perovskite-type layered structure (DOLS-TTH). A well-known scheelite-type structure is obtained under weakly basic conditions (pH = 10.3 for Na2WO4(aq), 7.0 for SrCl2(aq)). Previously, RP-type a DOLS of H2W2O7·0.58H2O was prepared, using an acid-leaching method, from the corresponding n = 2 member of the layered Aurivillius phase (AP) Bi2W2O9. Powder X-ray diffraction showed the formation of layered RP DOLS with a large d spacing ∼12.5 Å, which is consistent with acid-leaching (Kuto et al. Inorg. Chem. 2003, 42, 4479−4484; Wang et al. J. Solid State Chem. 2007, 180, 1125−1129) and exfoliation (Schaak et al. Chem. Commun. 2002, 706−707) methods for synthesized TTHs. The proposed DOLS-TTH structure of newly prepared TTHs was further confirmed by an intercalation reaction using n-octylamine (C8A). A transmission electron microscopy study showed the formation of nanosized particles, and scanning electron microscopy coupled with energy dispersive X-ray analysis showed the absence of Na and Sr in the air-dried, as-precipitated products under acidic conditions. 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Chem</addtitle><description>We report a very simple precipitation route to prepare a layered perovskite-type structure, tungsten trioxide hydrate (TTH), with the nominal chemical formula of WO3·1.3H2O (≡ 1/2H2W2O7·1.6H2O), using aqueous Na2WO4 and SrCl2. Our investigation shows that the concentration of HCl used to dissolve the SrCl2 plays a crucial role in the stabilization of different structure types of layered TTHs. Highly acidic SrCl2 (dissolved in 9 M HCl) solution yields an orthorhombic layered TTH of WO3·2H2O, while SrCl2 dissolved in 3 M HCl appears to give an A-site-deficient Ruddlesdon−Popper (RP) related double-perovskite-type layered structure (DOLS-TTH). A well-known scheelite-type structure is obtained under weakly basic conditions (pH = 10.3 for Na2WO4(aq), 7.0 for SrCl2(aq)). Previously, RP-type a DOLS of H2W2O7·0.58H2O was prepared, using an acid-leaching method, from the corresponding n = 2 member of the layered Aurivillius phase (AP) Bi2W2O9. Powder X-ray diffraction showed the formation of layered RP DOLS with a large d spacing ∼12.5 Å, which is consistent with acid-leaching (Kuto et al. Inorg. Chem. 2003, 42, 4479−4484; Wang et al. J. Solid State Chem. 2007, 180, 1125−1129) and exfoliation (Schaak et al. Chem. Commun. 2002, 706−707) methods for synthesized TTHs. The proposed DOLS-TTH structure of newly prepared TTHs was further confirmed by an intercalation reaction using n-octylamine (C8A). A transmission electron microscopy study showed the formation of nanosized particles, and scanning electron microscopy coupled with energy dispersive X-ray analysis showed the absence of Na and Sr in the air-dried, as-precipitated products under acidic conditions. The bulk electrical (proton) conductivity of presently prepared TTHs was found to be on the order of 10−4−10−3 S/cm at room temperature in wet N2.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNptkMFKw0AQhhdRbK0efAHZi2gP0dlsdrM5SSlqhWJBI3gLm2TSbmmTupuoeXtTWvTiaebw_R8zPyHnDG4Y-OzWZBFAyNX6gPSZ8METDN4PSR-g25mUUY-cOLcEgIgH8pj0WBRw5Qu_T2Yv-GmcqU05p3FTzl2NJY2tqb5NjnTS5lbX6Oh1HE_ckL62Zb1AZxz16JOj8QIt0lHZ1ott_hm_7k7JUaFXDs_2c0DeHu7j8cSbzh6fxqOppzkLai9iWinNfJ1GIWCqi1AKlHkmBQephQoLhO7IUIa6yHUqskimWjEhgyzQSgAfkKudd2OrjwZdnayNy3C10iVWjUtCzhmoUMmOHO7IzFbOWSySjTVrbduEQbKtL_mtr2Mv9tYmXWP-R-776oDLHaAzlyyrxpbdk_-IfgCOZ3Ux</recordid><startdate>20090720</startdate><enddate>20090720</enddate><creator>Kuti, Lisa M</creator><creator>Bhella, Surinderjit Singh</creator><creator>Thangadurai, Venkataraman</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090720</creationdate><title>Revisiting Tungsten Trioxide Hydrates (TTHs) Synthesis - Is There Anything New?</title><author>Kuti, Lisa M ; Bhella, Surinderjit Singh ; Thangadurai, Venkataraman</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a314t-91a88a12ab970ebaf765e6dc65306a587fe0194767afdab5c96ba81564c4a8503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuti, Lisa M</creatorcontrib><creatorcontrib>Bhella, Surinderjit Singh</creatorcontrib><creatorcontrib>Thangadurai, Venkataraman</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuti, Lisa M</au><au>Bhella, Surinderjit Singh</au><au>Thangadurai, Venkataraman</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Revisiting Tungsten Trioxide Hydrates (TTHs) Synthesis - Is There Anything New?</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2009-07-20</date><risdate>2009</risdate><volume>48</volume><issue>14</issue><spage>6804</spage><epage>6811</epage><pages>6804-6811</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>We report a very simple precipitation route to prepare a layered perovskite-type structure, tungsten trioxide hydrate (TTH), with the nominal chemical formula of WO3·1.3H2O (≡ 1/2H2W2O7·1.6H2O), using aqueous Na2WO4 and SrCl2. Our investigation shows that the concentration of HCl used to dissolve the SrCl2 plays a crucial role in the stabilization of different structure types of layered TTHs. Highly acidic SrCl2 (dissolved in 9 M HCl) solution yields an orthorhombic layered TTH of WO3·2H2O, while SrCl2 dissolved in 3 M HCl appears to give an A-site-deficient Ruddlesdon−Popper (RP) related double-perovskite-type layered structure (DOLS-TTH). A well-known scheelite-type structure is obtained under weakly basic conditions (pH = 10.3 for Na2WO4(aq), 7.0 for SrCl2(aq)). Previously, RP-type a DOLS of H2W2O7·0.58H2O was prepared, using an acid-leaching method, from the corresponding n = 2 member of the layered Aurivillius phase (AP) Bi2W2O9. Powder X-ray diffraction showed the formation of layered RP DOLS with a large d spacing ∼12.5 Å, which is consistent with acid-leaching (Kuto et al. Inorg. Chem. 2003, 42, 4479−4484; Wang et al. J. Solid State Chem. 2007, 180, 1125−1129) and exfoliation (Schaak et al. Chem. Commun. 2002, 706−707) methods for synthesized TTHs. The proposed DOLS-TTH structure of newly prepared TTHs was further confirmed by an intercalation reaction using n-octylamine (C8A). A transmission electron microscopy study showed the formation of nanosized particles, and scanning electron microscopy coupled with energy dispersive X-ray analysis showed the absence of Na and Sr in the air-dried, as-precipitated products under acidic conditions. The bulk electrical (proton) conductivity of presently prepared TTHs was found to be on the order of 10−4−10−3 S/cm at room temperature in wet N2.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>19438252</pmid><doi>10.1021/ic900738m</doi><tpages>8</tpages></addata></record> |
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title | Revisiting Tungsten Trioxide Hydrates (TTHs) Synthesis - Is There Anything New? |
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