Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
We discover that large uniaxial magnetocrystalline anisotropy driven by the simultaneous presence of spin-orbit coupling and structural distortions is the origin of the giant coercivity observed experimentally in the double perovskite LuNiIrO. The magnetic easy axis turns out to be the monoclinic -axis with an anisotropy constant as high as 1.9 × 10 erg/cm. The predicted coercive field of 50 kOe and Curie temperature of 220 K agree with the experimentally observed values and point to potential of LuNiIrO in spintronics applications. We find that the spin-orbit coupling induces a rare Ir = 1/2 Mott insulating state, suggesting that LuNiIrO provides a playground to study the interplay between spin-orbit coupling and electronic correlations in a 5d transition metal oxide. The spin-orbit coupling also results in a direct band gap with the valence and conduction states localized on different transition metal sublattices, i.e., efficient electron-hole separation upon photoexcitation and low electron-hole recombination.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.nanolett.1c01450 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!