File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.physb.2017.02.016
- Scopus: eid_2-s2.0-85013438982
- WOS: WOS:000398058500012
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Magnetic evolution of itinerant ferromagnetism and interlayer antiferromagnetism in cerium doped LaCo2 P2 crystals
Title | Magnetic evolution of itinerant ferromagnetism and interlayer antiferromagnetism in cerium doped LaCo<inf>2</inf>P<inf>2</inf>crystals |
---|---|
Authors | |
Keywords | ThCr2Si2-type phosphide Magnetic transition Rare earth doping, mixed valence state |
Issue Date | 2017 |
Citation | Physica B: Condensed Matter, 2017, v. 512, p. 75-80 How to Cite? |
Abstract | © 2017 Elsevier B.V. ThCr 2 Si 2 -type phosphide ACo 2 P 2 (A=Eu, La, Pr, Nd, Ce) has the same structure as iron arsenides, but their magnetic behaviors are quite distinct. In this paper, we grew a series of La 1−x Ce x Co 2 P 2 single crystals (x=0.0 to1.0), made structural and magnetic characterizations. We found the introduction of cerium induces a rapid decrease of c-axis and a change from ferromagnetic to antiferromagnetic states. Compared to other trivalent doped compounds, the enhancement of ferromagnetism with doping is suppressed and the transition from ferromagnetism to antiferromagnetism appear earlier. By employing first-principles band-structure calculations, we identify the increase of Ce valence suppress the itinerant ferromagnetism and leading to formation of P-P bonding with the shortening of c-axis. The bonding effectively drives an increase of interlayer antiferromagnetic interaction, eventually leads to antiferromagnetic ordering of cobalt in high-doping region. |
Persistent Identifier | http://hdl.handle.net/10722/254466 |
ISSN | 2023 Impact Factor: 2.8 2023 SCImago Journal Rankings: 0.492 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tian, Yong | - |
dc.contributor.author | Kong, Yixiu | - |
dc.contributor.author | Liu, Kai | - |
dc.contributor.author | Zhang, Anmin | - |
dc.contributor.author | He, Rui | - |
dc.contributor.author | Zhang, Qingming | - |
dc.date.accessioned | 2018-06-19T15:40:38Z | - |
dc.date.available | 2018-06-19T15:40:38Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Physica B: Condensed Matter, 2017, v. 512, p. 75-80 | - |
dc.identifier.issn | 0921-4526 | - |
dc.identifier.uri | http://hdl.handle.net/10722/254466 | - |
dc.description.abstract | © 2017 Elsevier B.V. ThCr 2 Si 2 -type phosphide ACo 2 P 2 (A=Eu, La, Pr, Nd, Ce) has the same structure as iron arsenides, but their magnetic behaviors are quite distinct. In this paper, we grew a series of La 1−x Ce x Co 2 P 2 single crystals (x=0.0 to1.0), made structural and magnetic characterizations. We found the introduction of cerium induces a rapid decrease of c-axis and a change from ferromagnetic to antiferromagnetic states. Compared to other trivalent doped compounds, the enhancement of ferromagnetism with doping is suppressed and the transition from ferromagnetism to antiferromagnetism appear earlier. By employing first-principles band-structure calculations, we identify the increase of Ce valence suppress the itinerant ferromagnetism and leading to formation of P-P bonding with the shortening of c-axis. The bonding effectively drives an increase of interlayer antiferromagnetic interaction, eventually leads to antiferromagnetic ordering of cobalt in high-doping region. | - |
dc.language | eng | - |
dc.relation.ispartof | Physica B: Condensed Matter | - |
dc.subject | ThCr2Si2-type phosphide | - |
dc.subject | Magnetic transition | - |
dc.subject | Rare earth doping, mixed valence state | - |
dc.title | Magnetic evolution of itinerant ferromagnetism and interlayer antiferromagnetism in cerium doped LaCo<inf>2</inf>P<inf>2</inf>crystals | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.physb.2017.02.016 | - |
dc.identifier.scopus | eid_2-s2.0-85013438982 | - |
dc.identifier.volume | 512 | - |
dc.identifier.spage | 75 | - |
dc.identifier.epage | 80 | - |
dc.identifier.isi | WOS:000398058500012 | - |
dc.identifier.issnl | 0921-4526 | - |