Transition from dense Kondo to the intermediate-valence regime in the Ce (Pt1-xNix)2Si2 alloys

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dc.contributor.author Ragel, F. C.
dc.contributor.author P de V du Plessis
dc.date.accessioned 2019-08-07T06:18:04Z
dc.date.available 2019-08-07T06:18:04Z
dc.date.issued 2004
dc.identifier.issn 0953-8984
dc.identifier.uri http://www.digital.lib.esn.ac.lk/handle/123456789/3934
dc.description.abstract Electrical resistivity ρ(T) measurements on polycrystalline samples of the Ce (Pt1−xNix)2Si2 system exhibit dense Kondo behaviour for alloys with . The temperature at which a maximum appears in ρ(T) shifts from Tmax = 65 K for x = 0 to Tmax = 290 K for x = 0.6 as the system evolves towards the intermediate-valence regime for the CeNi2Si2 compound. At low temperatures the Ce (Pt1−xNix)2Si2 alloys show a Fermi liquid T2 contribution to ρ(T) below the coherence temperature Tcoh. It is observed that , with a transition that takes place from a dense Kondo regime of TK< TCF () to a regime of TK> TCF (). TK () and TCF denote the Kondo and crystalline electric field splitting, EF and ER are the Fermi and the Abrikosov–Suhl resonance energies and j denotes the total angular momentum. An electronic Grüneisen parameter value of 19 has been obtained for the alloy system which is in reasonable agreement with Ω = 28 found from pressure studies on CePt2Si2. It is argued that volume effects are mainly responsible for the hybridization in the Ce (Pt1−xNix)2Si2 system and application of the compressible Kondo lattice model to Tmax data yields |JN(EF)| = 0.309 ± 0.008, where J is the on-site exchange interaction between conduction electrons and the localized 4f spin and N(EF) is the density of states at EF. https://iopscience.iop.org/article/10.1088/0953-8984/16/15/016 en_US
dc.language.iso en en_US
dc.publisher Journal of Physics: Condensed Matter en_US
dc.title Transition from dense Kondo to the intermediate-valence regime in the Ce (Pt1-xNix)2Si2 alloys en_US
dc.type Article en_US
dc.identifier.sslno 16 en_US
dc.identifier.doi https://iopscience.iop.org/article/10.1088/0953-8984/16/15/016 en_US


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