Pressure dependence of spin canting in ammonium metal formate antiferromagnets. Issue 37 (17th September 2018)
- Record Type:
- Journal Article
- Title:
- Pressure dependence of spin canting in ammonium metal formate antiferromagnets. Issue 37 (17th September 2018)
- Main Title:
- Pressure dependence of spin canting in ammonium metal formate antiferromagnets
- Authors:
- Collings, Ines E.
Manna, Rudra Sekhar
Tsirlin, Alexander A.
Bykov, Maxim
Bykova, Elena
Hanfland, Michael
Gegenwart, Philipp
van Smaalen, Sander
Dubrovinsky, Leonid
Dubrovinskaia, Natalia - Abstract:
- Abstract : Compression of ammonium metal formates enhances spin canting, with up to a twenty-fold increase when the metal is Fe 2+ . Abstract : High-pressure single-crystal X-ray diffraction at ambient temperature and high-pressure SQUID measurements down to 2 K were performed up to ∼2.5 GPa on ammonium metal formates, [NH4 ][M(HCOO)3 ] where M = Mn 2+, Fe 2+, and Ni 2+, in order to correlate structural variations to magnetic behaviour. Similar structural distortions and phase transitions were observed for all compounds, although the transition pressures varied with the size of the metal cation. The antiferromagnetic ordering in [NH4 ][M(HCOO)3 ] compounds was maintained as a function of pressure, and the magnetic ordering transition temperature changed within a few kelvins depending on the structural distortion and the metal cation involved. These compounds, in particular [NH4 ][Fe(HCOO)3 ], showed greatest sensitivity to the degree of spin canting upon compression, clearly visible from the twenty-fold increase in the low-temperature magnetisation for [NH4 ][Fe(HCOO)3 ] at 1.4 GPa, and the change from purely antiferromagnetic to weakly ferromagnetic ordering in [NH4 ][Mn(HCOO)3 ] at 1 GPa. The variation in the exchange couplings and spin canting was checked with density-functional calculations that reproduce well the increase in canted moment within [NH4 ][Fe(HCOO)3 ] upon compression, and suggest that the Dzyaloshinskii–Moriya (DM) interaction is evolving as a function ofAbstract : Compression of ammonium metal formates enhances spin canting, with up to a twenty-fold increase when the metal is Fe 2+ . Abstract : High-pressure single-crystal X-ray diffraction at ambient temperature and high-pressure SQUID measurements down to 2 K were performed up to ∼2.5 GPa on ammonium metal formates, [NH4 ][M(HCOO)3 ] where M = Mn 2+, Fe 2+, and Ni 2+, in order to correlate structural variations to magnetic behaviour. Similar structural distortions and phase transitions were observed for all compounds, although the transition pressures varied with the size of the metal cation. The antiferromagnetic ordering in [NH4 ][M(HCOO)3 ] compounds was maintained as a function of pressure, and the magnetic ordering transition temperature changed within a few kelvins depending on the structural distortion and the metal cation involved. These compounds, in particular [NH4 ][Fe(HCOO)3 ], showed greatest sensitivity to the degree of spin canting upon compression, clearly visible from the twenty-fold increase in the low-temperature magnetisation for [NH4 ][Fe(HCOO)3 ] at 1.4 GPa, and the change from purely antiferromagnetic to weakly ferromagnetic ordering in [NH4 ][Mn(HCOO)3 ] at 1 GPa. The variation in the exchange couplings and spin canting was checked with density-functional calculations that reproduce well the increase in canted moment within [NH4 ][Fe(HCOO)3 ] upon compression, and suggest that the Dzyaloshinskii–Moriya (DM) interaction is evolving as a function of pressure. The pressure dependence of spin canting is found to be highly dependent on the metal cation, as magnetisation magnitudes did not change significantly for when M = Ni 2+ or Mn 2+ . These results demonstrate that the overall magnetic behaviour of each phase upon compression was not only dependent on the structural distortions but also on the electronic configuration of the metal cation. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 20:Issue 37(2018)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 20:Issue 37(2018)
- Issue Display:
- Volume 20, Issue 37 (2018)
- Year:
- 2018
- Volume:
- 20
- Issue:
- 37
- Issue Sort Value:
- 2018-0020-0037-0000
- Page Start:
- 24465
- Page End:
- 24476
- Publication Date:
- 2018-09-17
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8cp03761b ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8448.xml