New correlated electronic states arising from strong spin-orbit coupling
Lead Research Organisation:
University College London
Department Name: London Centre for Nanotechnology
Abstract
Abstracts are not currently available in GtR for all funded research. This is normally because the abstract was not required at the time of proposal submission, but may be because it included sensitive information such as personal details.
Organisations
Publications
Alexeev P
(2019)
Nuclear resonant scattering from 193Ir as a probe of the electronic and magnetic properties of iridates.
in Scientific reports
Calder S
(2016)
Spin-orbit-driven magnetic structure and excitation in the 5d pyrochlore Cd2Os2O7.
in Nature communications
Calder S
(2017)
Strongly gapped spin-wave excitation in the insulating phase of NaOsO 3
in Physical Review B
Carneiro F
(2020)
Unveiling charge density wave quantum phase transitions by x-ray diffraction
in Physical Review B
Dashwood C
(2019)
Momentum-resolved lattice dynamics of parent and electron-doped Sr 2 IrO 4
in Physical Review B
Description | The key findings are well documented in the numerous publications which have arisen from the award, all in internationally leading journals. The overarching theme is that the combination of strong spin-orbit coupling and electron correlations can lead to novel electronic and magnetic states of matter. Revealing and understanding these states of matter using experimental techniques based on the exploitation and development of facilities for neutron and X-ray scattering has been a key objective of the grant. For example, Ca2RuO4 has attracted considerable attention in recent years as the Mott-insulating analogue of the unconventional superconductor Sr2RuO4. Using a combination of X-ray and neutron scattering we have revealed how the magnetic and electronic structures evolve as a function of doping, thus allowing us to understand the origin of the metal insulating transition it displays. This work alone led to three papers - two in PRB and one in Nature Communications. |
Exploitation Route | Our work arising from this funding is beginning to attract considerable interest in the academic community, facilitating progress on the development and exploitation of novel electronic materials. |
Sectors | Other |
Title | Data for "Spontaneous cycloidal order mediating a spin-reorientation transition in a polar metal" |
Description | Data for the manuscript "Spontaneous cycloidal order mediating a spin-reorientation transition in a polar metal" by C. D. Dashwood, L. S. I. Veiga, Q. Faure, J. G. Vale, D. G. Porter, S. P. Collins, P. Manuel, D. D. Khalyavin, F. Orlandi, R. S. Perry, R. D. Johnson, and D. F. McMorrow, Phys. Rev. B 102, 180410(R) (2020).All the data is provided in text files, each containing a single header line followed by the data. All temperatures are in Kelvin, magnetic field strengths in Tesla, angles in degrees, and resistances in Ohms.The parent folder contains the in-plane resistivity and powder XRD data.Neutron scattering data is contained in the "Neutron" folder, with each file labelled by the magnetic field strength and Bragg peak (commensurate peak "001" or incommensurate satellite peak "d01").Resonant x-ray scattering data is contained in the "X-ray" folder, under four subfolders for the azimuthal dependences ("Azi_deps"), energy dependences ("E_deps"), reciprocal space scans ("H_scans") and theta scans ("Th_scans"). Files in all the subfolders are labelled by the temperature and Bragg peak (commensurate peak "005" or incommensurate satellite peak "d05"), followed by further labels for the x-ray polarisation ("sig-sig" or "sig-pi"), azimuthal angle ("psi90" or "psi180") and absorption edge ("L2" or "L3"). The azimuthal dependences folder also contains a file "Parameters" with the fitted values of Ma and Mb (defined in the manuscript) and their errors. |
Type Of Material | Database/Collection of data |
Year Produced | 2021 |
Provided To Others? | Yes |
URL | https://rdr.ucl.ac.uk/articles/dataset/Data_for_Spontaneous_cycloidal_order_mediating_a_spin-reorien... |