Low-temperature heat-capacity studies of R2Ni3Si5 (R = Pr, Nd, Sm, Gd, Tb, Dy, Ho)
DSpace at IIT Bombay
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Title |
Low-temperature heat-capacity studies of R2Ni3Si5 (R = Pr, Nd, Sm, Gd, Tb, Dy, Ho)
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Creator |
MAZUMDAR, C
GHOSH, K NAGARAJAN, R RAMAKRISHNAN, S PADALIA, BD GUPTA, LC |
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Subject |
earth iron silicides
rare-earth magnetic-properties anomalous magnetoresistance gadolinium compounds superconductivity ce2ni3si5 |
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Description |
We report here our low temperature (2-30 K) hear capacity, C-p measurements of R2N3Si5 (R = Pr, Nd, Sm, Gd-Ho). Large peaks in heat capacity data at magnetic transition temperatures (T-N) confirm the bulk nature of magnetic order in these compounds. In Nd2Ni3Si5, Gd2Ni3Si5, and Dy2Ni3Si5, magnetization studies indicated only one magnetic transition, whereas, hear-capacity data show two transitions. T-N of the heavier rare-earth member, Tb2Ni3Si5, showing significant deviation from de Gennes scaling is notable. Magnetic entropy, Delta S, estimated from heat-capacity data suggest that the magnetic ground state is a doublet in R2Ni3Si5 (R = Pr, Nd, Sm, Dy, Ho) and a quartet in Tb2Ni3Si5. In all the cases, Delta S, at T-N is slightly less than that expected due to the suggested states, which we attribute to the occurrence of precursor effects of magnetic order above T-N. Except for Gd2Ni3Si5,, Delta S of the compounds does not reach the saturation limit of R ln(2J+1) even at 30 K, indicating the presence of crystalline electric field (CEF) effects. A hump in C-p is observed below T-N in Gd2Ni3Si5 which is interpreted in terms of a possible amplitude-modulated magnetic spin structure. [S0163-1829(99)12605-5].
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Publisher |
AMERICAN PHYSICAL SOC
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Date |
2011-07-17T16:06:09Z
2011-12-26T12:50:23Z 2011-12-27T05:53:40Z 2011-07-17T16:06:09Z 2011-12-26T12:50:23Z 2011-12-27T05:53:40Z 1999 |
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Type |
Article
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Identifier |
PHYSICAL REVIEW B, 59(6), 4215-4220
0163-1829 http://dx.doi.org/10.1103/PhysRevB.59.4215 http://dspace.library.iitb.ac.in/xmlui/handle/10054/4777 http://hdl.handle.net/10054/4777 |
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Language |
en
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