1999
DOI: 10.1039/a805662e
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On the synthesis of monovalent, divalent and trivalent element vanadates

Abstract: A chimie douce method has been used to prepare vanadates ( V5+) of various elements, trivalent (Al, Cr, Fe, In, Y, Bi), divalent (Co, Ni), monovalent (Li, Tl ), and a combination of nickel and lithium. By varying several parameters, especially the pH during the synthesis, several types of vanadates have been obtained ranging from orthovanadates ( VO 4 3−) to decavanadates ( V 10 O 28 6−). The pH conditions required to prepare the various vanadates fall nicely within the expectations of the previously reported … Show more

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Cited by 41 publications
(28 citation statements)
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“…35,36 In the breadth of this band for 10V12CrAl and 12Cr10VAl and in the absence of CrVO 4 , diffraction lines for these samples suggest that the CrVO 4 domains are disordered and highly dispersed. 27,[37][38][39] The 820 cm -1 band may reflect the presence of polychromates, polyvanadates, or mixed V-O-Cr oligomers, but its specific origin remains unclear. Figure 2 shows X-ray absorption near-edge spectroscopy (XANES) spectra for 10VAl, 12CrAl, 10V12CrAl, and 12Cr10VAl after treatment at 773 K for 2 h in flowing dry air and for three crystalline compounds V 2 O 5 , CrO 3 , Cr 2 O 3 .…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…35,36 In the breadth of this band for 10V12CrAl and 12Cr10VAl and in the absence of CrVO 4 , diffraction lines for these samples suggest that the CrVO 4 domains are disordered and highly dispersed. 27,[37][38][39] The 820 cm -1 band may reflect the presence of polychromates, polyvanadates, or mixed V-O-Cr oligomers, but its specific origin remains unclear. Figure 2 shows X-ray absorption near-edge spectroscopy (XANES) spectra for 10VAl, 12CrAl, 10V12CrAl, and 12Cr10VAl after treatment at 773 K for 2 h in flowing dry air and for three crystalline compounds V 2 O 5 , CrO 3 , Cr 2 O 3 .…”
Section: Resultsmentioning
confidence: 99%
“…Crystalline bulk CrVO 4 was prepared using the method proposed by Touboul and co-workers. 28, 29 Nitric acid (3N, EM Science, GR) was added to an aqueous solution of Cr(NO 3 ) 3 and NH 4 VO 3 to give a pH of 1 and then was refluxed at 333 K for 6 h. The precipitate was filtered and washed with 300 mL of deionized water, dried at 393 K overnight in ambient air, and then treated in flowing dry air (Airgas, zero grade, 1.67 cm 3 s -1 ) at 1073 K for 6 h. The X-ray diffraction (XRD) pattern of the as-synthesized sample was measured with a Siemens D5000 unit at ambient temperature using CuKR radiation, an X-ray tube operating at 45 kV and 35 mA, and a scan rate of 1.2°min -1 . Crystalline CrVO 4 -I was identified by comparison with literature XRD patterns.…”
Section: Introductionmentioning
confidence: 99%
“…These results stimulated our interest in the search for new electrode materials among the divalent-element vanadates. The synthesis process was adapted (8) and led to a substantial number of compounds giving electroactive vanadates, either new or previously prepared by other methods (9,10). Some of the new materials were obtained as single crystals.…”
Section: Introductionmentioning
confidence: 99%
“…This dissolution-reprecipitation process can be applied to synthesizing a large variety of monovalent, divalent and trivalent vanadates. 10 Although all the above methods facilitate the synthesis of pure and different phases of InVO 4 , the products are in powder form. substrates were boiled in water for a few hours to ensure a hydrophilic surface.…”
Section: Introductionmentioning
confidence: 99%