Electronic structure and luminescence assets in white-light emitting Ca2V2O7, Sr2V2O7 and Ba2V2O7 pyro-vanadates: X-ray absorption spectroscopy investigations. Issue 46 (24th July 2018)
- Record Type:
- Journal Article
- Title:
- Electronic structure and luminescence assets in white-light emitting Ca2V2O7, Sr2V2O7 and Ba2V2O7 pyro-vanadates: X-ray absorption spectroscopy investigations. Issue 46 (24th July 2018)
- Main Title:
- Electronic structure and luminescence assets in white-light emitting Ca2V2O7, Sr2V2O7 and Ba2V2O7 pyro-vanadates: X-ray absorption spectroscopy investigations
- Authors:
- Sharma, Aditya
Varshney, Mayora
Chae, Keun-Hwa
Won, Sung Ok - Abstract:
- Abstract : Chemically synthesized pyro-vanadates exhibit sub-pentavalent V ions and white-light emission via charge transfer transitions of VO4 tetrahedra. Abstract : Ca2 V2 O7, Sr2 V2 O7, and Ba2 V2 O7 pyro-vanadates were synthesized using a modified chemical precipitation method and annealing. Detailed crystal structure, morphology, electronic structure and optical properties were investigated by XRD, UV-visible absorption, FTIR, Raman, FE-SEM, XANES, and photoluminescence spectroscopy. Rietveld refinement on the XRD patterns of Ca2 V2 O7, Sr2 V2 O7, and Ba2 V2 O7 has confirmed the triclinic structure (space group; P 1̄(2)) of the pyro-vanadates. The band gap energy of Ca2 V2 O7, Sr2 V2 O7, and Ba2 V2 O7 is estimated to be ∼2.67 eV, ∼2.97 eV and ∼3.09 eV, respectively. XANES spectra at the Ca L-edge, Sr K-edge and Ba L-edge have confirmed the Ca 2+, Sr 2+ and Ba 2+ ions in the Ca2 V2 O7, Sr2 V2 O7 and Ba2 V2 O7 compounds, respectively. V K-edge XANES spectra have strengthened the presence of sub-pentavalent V ions in all of the pyro-vanadates. O K-edge XANES spectra of Ca2 V2 O7, Sr2 V2 O7 and Ba2 V2 O7 have shown dominating tetrahedral symmetry of the V ions which is also corroborated with the V K-edge XANES. Broad-band emission spectra, ranging from 400 nm to 700 nm, have been observed from the charge-transfer transitions of VO4 tetrahedra. 3 T1 → 1 A1 and 3 T2 → 1 A1 transitions, from the VO4 tetrahedra, have provided two distinct emission peaks from the compounds whichAbstract : Chemically synthesized pyro-vanadates exhibit sub-pentavalent V ions and white-light emission via charge transfer transitions of VO4 tetrahedra. Abstract : Ca2 V2 O7, Sr2 V2 O7, and Ba2 V2 O7 pyro-vanadates were synthesized using a modified chemical precipitation method and annealing. Detailed crystal structure, morphology, electronic structure and optical properties were investigated by XRD, UV-visible absorption, FTIR, Raman, FE-SEM, XANES, and photoluminescence spectroscopy. Rietveld refinement on the XRD patterns of Ca2 V2 O7, Sr2 V2 O7, and Ba2 V2 O7 has confirmed the triclinic structure (space group; P 1̄(2)) of the pyro-vanadates. The band gap energy of Ca2 V2 O7, Sr2 V2 O7, and Ba2 V2 O7 is estimated to be ∼2.67 eV, ∼2.97 eV and ∼3.09 eV, respectively. XANES spectra at the Ca L-edge, Sr K-edge and Ba L-edge have confirmed the Ca 2+, Sr 2+ and Ba 2+ ions in the Ca2 V2 O7, Sr2 V2 O7 and Ba2 V2 O7 compounds, respectively. V K-edge XANES spectra have strengthened the presence of sub-pentavalent V ions in all of the pyro-vanadates. O K-edge XANES spectra of Ca2 V2 O7, Sr2 V2 O7 and Ba2 V2 O7 have shown dominating tetrahedral symmetry of the V ions which is also corroborated with the V K-edge XANES. Broad-band emission spectra, ranging from 400 nm to 700 nm, have been observed from the charge-transfer transitions of VO4 tetrahedra. 3 T1 → 1 A1 and 3 T2 → 1 A1 transitions, from the VO4 tetrahedra, have provided two distinct emission peaks from the compounds which exhibit a red-shift with the decreasing ionic-radii of alkali-earth metal ions. The mixed compounds, with equal weight proportions, have shown remarkable emission characteristics towards the realization of rare-earth element free white-light-emitting devices. … (more)
- Is Part Of:
- RSC advances. Volume 8:Issue 46(2018)
- Journal:
- RSC advances
- Issue:
- Volume 8:Issue 46(2018)
- Issue Display:
- Volume 8, Issue 46 (2018)
- Year:
- 2018
- Volume:
- 8
- Issue:
- 46
- Issue Sort Value:
- 2018-0008-0046-0000
- Page Start:
- 26423
- Page End:
- 26431
- Publication Date:
- 2018-07-24
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/RA ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8ra03347a ↗
- Languages:
- English
- ISSNs:
- 2046-2069
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8036.750300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 7059.xml