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Dimensionality-Controlled Insulator-Metal Transition and Correlated Metallic State in 5d Transition Metal Oxides Srn+1IrnO3n+1 ( n=1 , 2, and ∞ )

S. J. Moon, Hyo‐Eon Jin, Kyung Wan Kim, Woo Seok Choi, Y. S. Lee, Jaejun Yu, Gang Cao, Akihiro Sumi, Hiroshi Funakubo, Christian Bernhard, Tae Won Noh

📄 Abstract

We investigated the electronic structures of the 5d Ruddlesden-Popper series Sr n+1Ir nO3n+1 (n=1, 2, and infinity) using optical spectroscopy and first-principles calculations. As 5d orbitals are spatially more extended than 3d or 4d orbitals, it has been widely accepted that correlation effects are minimal in 5d compounds. However, we observed a Mott insulator-metal transition with a change of bandwidth as we increased n. In addition, the artificially synthesized perovskite SrIrO3 showed a very large mass enhancement of about 6, indicating that it was in a correlated metallic state.

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