Ruthenium(platinum)-doped tin dioxide inverted opals for gas sensors: Synthesis, electron paramagnetic resonance, Mossbauer, and electrical investigation
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作者:
Acciarri, M
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Acciarri, M
Barberini, R
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Barberini, R
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Canevali, C
Mattoni, M
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Mattoni, M
Mari, CM
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Mari, CM
Morazzoni, F
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Morazzoni, F
Nodari, L
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Nodari, L
Polizzi, S
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Polizzi, S
Ruffo, R
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Ruffo, R
Russo, U
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Russo, U
Sala, M
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Sala, M
Scotti, R
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机构:Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
Scotti, R
机构:
[1] Univ Milan, INSTM, Dipartimento Sci Mat, I-20125 Milan, Italy
[2] Univ Padua, Dipartimento Sci Chim, I-35131 Padua, Italy
[3] Univ Venice, Dipartimento Chim Fis, INSTM, I-30172 Venice, Italy
Tin dioxide and ruthenium(platinum)-doped tin dioxide were synthesized in the form of inverted opals, aiming to investigate the interaction of these materials with CO reducing gas. The results of electron paramagnetic resonance (EPR) investigation allowed us to conclude that CO interaction causes the formation of singly ionized oxygen vacancies located in the subsurface region. These ones transfer their electrons to transition metal centers, Ru or Pt, enhancing the SnO2 surface reactivity toward CO. The reduction of Ru4+ and Pt4+ was assessed both by EPR and Mossbauer spectroscopy. Resistance measurements showed that the materials are well-suitable for use in CO sensor devices because of their reproducible and fast electrical response; this was related to the homogeneous and high dispersion of Ru and Pt centers in the oxide matrix and to the subsurface location of the species active in the electron-transfer processes.