Neutron-diffraction study of RNiO3 (R=La,Pr,Nd,Sm): Electronically induced structural changes across the metal-insulator transition

Abstract

In the RNiO3 series (R=La,Pr,Nd,Sm), the metal-insulator (M-I) transition temperature rises systematically as the size of the rare earth decreases and as the subsequent distortion from the ideal cubic perovskite increases. For R=La the system keeps its metallic character down to 1.5 K, while for R=Pr, Nd, and Sm electronic localization occurs at 135, 200, and 400 K, respectively. High-resolution neutron-powder-diffraction experiments have been performed to investigate the structural anomalies across the first-order M-I transition in the orthorhombic PrNiO3 and NdNiO3 compounds. The cell volume undergoes a subtle increase when the compounds become insulating, due to a slight increase of the Ni-O distances. This effect is accompanied by coupled tilts of NiO6 octahedra, which imply changes in the Ni-O-Ni angles (ΔΘO-Ni-O-0.5°) governing the transfer integral between Ni eg and O 2p orbitals. These changes are sterically driven by the observed increase of the nickel-oxygen distances (ΔdNi-O+0.004) in the insulating (low-temperature) phase. The results of valence-bond calculations suggest the existence of Ni3+(d7) and R3+ states for nickel and rare earth. © 1992 The American Physical Society.