Year: 2026
Type: article
Abstract: Resonant inelastic X‐ray scattering (RIXS) is an indispensable tool that can selectively probe the electronic structure of active sites in energy conversion systems, for example, iridium oxides. However, decoding the RIXS spectra remains challenging due to its inherently complex many‐body interactions. Here, we analyze Ir L 3 edge RIXS spectra of Ir, IrCl 3 , and IrO 2 , employing the joint density of states (JDOS) calculated directly from electronic band‐structure calculations. The overall energy‐loss features in the RIXS spectra are well reproduced by the JDOS, reaffirming the close correspondence between electron–hole excitations and RIXS spectra observed in prior studies. Intriguingly, the RIXS spectra above ∼4 eV in metallic Ir and IrO 2 follow a power‐law behavior, , where Δ is the energy loss and p is the associated power‐law exponent. This is consistent with edge‐singularity behavior commonly found in resonant X‐ray scattering from metallic samples. Furthermore, orbital‐projected JDOS enables a decomposition of the IrO 2 spectrum into specific dd transitions, providing a clear interpretation of orbital excitations and an efficient strategy for decoding RIXS spectra in iridium‐based energy conversion systems.
Authors: Kyeong Jun Lee, Seo Hyoung Chang, Jungho Kim
Language: English
Subfield: Radiation
Field: Physics and Astronomy
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,430
OpenAlex ID: W7130337578