Low-temperature optical absorption of nickel fluosilicate crystals
The vibronic absorption spectrum of the Ni ++ ion in an electric field of trigonal (nearly cubic) symmetry at temperatures down to 4°K is reported and analysed in terms of ligand field and vibronic theory. The positions, widths, shapes and strengths of the bands are satisfactorily explained, togethe...
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Veröffentlicht in: | Philosophical magazine (London, England : 1945) England : 1945), 1964-09, Vol.10 (105), p.477-496 |
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creator | Pryce, M. H. L. Agnetta, G. Garofano, T. Palma-Vittorelli, M. B. Palma, M. U. |
description | The vibronic absorption spectrum of the Ni
++
ion in an electric field of trigonal (nearly cubic) symmetry at temperatures down to 4°K is reported and analysed in terms of ligand field and vibronic theory. The positions, widths, shapes and strengths of the bands are satisfactorily explained, together with their associated fine structures. In particular, the complex structure of the red band is well explained in detail as a consequence of the mutual perturbation of the
1
E and
3
T
4
levels, which strongly modifies the vibronic coupling and results in two fairly narrow bands, each showing resolved vibrational structure, superposed on a broad band.
A Trees correction term, αL(L+1), helps the agreement between observed and calculated electronic levels. The following parameters are found to give good agreement: Δ = 9100 cm
−1
, B=955 cm
−1
, C=3750 cm
−1
, α=80 cm
−1
, ζ = 600 cm
−1
. |
doi_str_mv | 10.1080/14786436408224225 |
format | Article |
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++
ion in an electric field of trigonal (nearly cubic) symmetry at temperatures down to 4°K is reported and analysed in terms of ligand field and vibronic theory. The positions, widths, shapes and strengths of the bands are satisfactorily explained, together with their associated fine structures. In particular, the complex structure of the red band is well explained in detail as a consequence of the mutual perturbation of the
1
E and
3
T
4
levels, which strongly modifies the vibronic coupling and results in two fairly narrow bands, each showing resolved vibrational structure, superposed on a broad band.
A Trees correction term, αL(L+1), helps the agreement between observed and calculated electronic levels. The following parameters are found to give good agreement: Δ = 9100 cm
−1
, B=955 cm
−1
, C=3750 cm
−1
, α=80 cm
−1
, ζ = 600 cm
−1
.</description><identifier>ISSN: 0031-8086</identifier><identifier>DOI: 10.1080/14786436408224225</identifier><language>eng</language><publisher>London: Taylor & Francis Group</publisher><ispartof>Philosophical magazine (London, England : 1945), 1964-09, Vol.10 (105), p.477-496</ispartof><rights>Copyright Taylor & Francis Group, LLC 1964</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c326t-114ff94da0ff1948438b3617c6bac283ee43188cb6961f404727282067e93d163</citedby><cites>FETCH-LOGICAL-c326t-114ff94da0ff1948438b3617c6bac283ee43188cb6961f404727282067e93d163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27848,27903,27904</link.rule.ids></links><search><creatorcontrib>Pryce, M. H. L.</creatorcontrib><creatorcontrib>Agnetta, G.</creatorcontrib><creatorcontrib>Garofano, T.</creatorcontrib><creatorcontrib>Palma-Vittorelli, M. B.</creatorcontrib><creatorcontrib>Palma, M. U.</creatorcontrib><title>Low-temperature optical absorption of nickel fluosilicate crystals</title><title>Philosophical magazine (London, England : 1945)</title><description>The vibronic absorption spectrum of the Ni
++
ion in an electric field of trigonal (nearly cubic) symmetry at temperatures down to 4°K is reported and analysed in terms of ligand field and vibronic theory. The positions, widths, shapes and strengths of the bands are satisfactorily explained, together with their associated fine structures. In particular, the complex structure of the red band is well explained in detail as a consequence of the mutual perturbation of the
1
E and
3
T
4
levels, which strongly modifies the vibronic coupling and results in two fairly narrow bands, each showing resolved vibrational structure, superposed on a broad band.
A Trees correction term, αL(L+1), helps the agreement between observed and calculated electronic levels. The following parameters are found to give good agreement: Δ = 9100 cm
−1
, B=955 cm
−1
, C=3750 cm
−1
, α=80 cm
−1
, ζ = 600 cm
−1
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H. L.</au><au>Agnetta, G.</au><au>Garofano, T.</au><au>Palma-Vittorelli, M. B.</au><au>Palma, M. U.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low-temperature optical absorption of nickel fluosilicate crystals</atitle><jtitle>Philosophical magazine (London, England : 1945)</jtitle><date>1964-09-01</date><risdate>1964</risdate><volume>10</volume><issue>105</issue><spage>477</spage><epage>496</epage><pages>477-496</pages><issn>0031-8086</issn><abstract>The vibronic absorption spectrum of the Ni
++
ion in an electric field of trigonal (nearly cubic) symmetry at temperatures down to 4°K is reported and analysed in terms of ligand field and vibronic theory. The positions, widths, shapes and strengths of the bands are satisfactorily explained, together with their associated fine structures. In particular, the complex structure of the red band is well explained in detail as a consequence of the mutual perturbation of the
1
E and
3
T
4
levels, which strongly modifies the vibronic coupling and results in two fairly narrow bands, each showing resolved vibrational structure, superposed on a broad band.
A Trees correction term, αL(L+1), helps the agreement between observed and calculated electronic levels. The following parameters are found to give good agreement: Δ = 9100 cm
−1
, B=955 cm
−1
, C=3750 cm
−1
, α=80 cm
−1
, ζ = 600 cm
−1
.</abstract><cop>London</cop><pub>Taylor & Francis Group</pub><doi>10.1080/14786436408224225</doi><tpages>20</tpages></addata></record> |
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title | Low-temperature optical absorption of nickel fluosilicate crystals |
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