4.8 Article

Crystal-Field Splitting and Correlation Effect on the Electronic Structure of A2IrO3

Journal

PHYSICAL REVIEW LETTERS
Volume 110, Issue 7, Pages -

Publisher

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.110.076402

Keywords

-

Funding

  1. NSERC
  2. CFI
  3. OMRI
  4. Computational Materials and Chemical Sciences Network (CMCSN) Program of the Division of Materials Science and Engineering, U.S. Department of Energy [DE-SC0007091]
  5. U.S. DOE Office of Science [DE-AC02-06CH11357]
  6. DOE, Office of Science, Division of Materials Science [DE-AC02-98CH10886]
  7. KOFST through the Brainpool Program
  8. NRF through the ARP [R17-2008-033-01000-0]
  9. KISTI Supercomputing Center through the strategic support program for supercomputing application research [KSC-2010-S00-0005]
  10. Erasmus Mundus Eurindia Project
  11. National Research Foundation of Korea [2008-0060612] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

The electronic structure of the honeycomb lattice iridates Na2IrO3 and Li2IrO3 has been investigated using resonant inelastic x-ray scattering (RIXS). Crystal-field-split d-d excitations are resolved in the high-resolution RIXS spectra. In particular, the splitting due to noncubic crystal fields, derived from the splitting of j(eff) = 3/2 states, is much smaller than the typical spin-orbit energy scale in iridates, validating the applicability of jeff physics in A(2)IrO(3). We also find excitonic enhancement of the particle-hole excitation gap around 0.4 eV, indicating that the nearest-neighbor Coulomb interaction could be large. These findings suggest that both Na2IrO3 and Li2IrO3 can be described as spin-orbit Mott insulators, similar to the square lattice iridate Sr2IrO4. DOI: 10.1103/PhysRevLett.110.076402

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available