Emergence of low-energy electronic states in oxygen-controlled Mott insulator Ca2RuO4+δ
Abstract
Insulator-to-metal transition in Ca2RuO4 has drawn keen attention because of its sensitivity to various stimulation and its potential controllability. Here, we report a direct observation of Fermi surface, which emerges upon introducing excess oxygen into an insulating Ca2RuO4, by using angle-resolved photoemission spectroscopy. Comparison between energy distribution curves shows that the Mott insulating gap is closed by eV-scale spectral-weight transfer with excess oxygen. Momentum-space mapping exhibits two square-shaped sheets of the Fermi surface. One is a hole-like α sheet around the corner of a tetragonal Brillouin zone, and the other is an electron-like β sheet around the point. The electron occupancies of the α and β bands are determined to be nα=1.6 and nβ=0.6, respectively. Our result indicates that the insulator-to-metal transition occurs selectively in dxz and dyz bands and not yet in dxy band. This orbital selectivity is most likely explained in terms of the energy level of dxy, which is deeper for Ca2RuO4+δ than for Ca1.8Sr0.2RuO4. Consequently, we found substantial differences from the Fermi surface of other ruthenates, shedding light on a unique role of excess oxygen among the metallization methods of Ca2RuO4.