arXiv · 1602.06692
Cage Electron-Hydroxyl Complex State as Electron Donor in Mayenite
Abstract
It is inferred from the chemical shift of muon spin rotation ($\mu$SR) spectra that muons implanted in pristine (fully oxidized) mayenite, [Ca$_{12}$Al$_{14}$O$_{32}]^{2+}$[$\square_5$O$^{2-}$] (C12A7, with $\square$ referring to the vacant cage), are bound to O$^{2-}$ at the cage center to form OMu$^-$ (where Mu represents muonium, a muonic analog of the H atom). However, an isolated negatively charged state (Mu$^-$, an analog of H$^-$) becomes dominant when the compound approaches the state of electride [Ca$_{12}$Al$_{14}$O$_{32}]^{2+}$[$\square_4$2e$^{-}$] as a result of the reduction process. Moreover, the OMu$^-$ state in the pristine specimen exhibits depolarization of paramagnetic origin at low temperatures (below $\sim$30~K), indicating that OMu$^-$ accompanies a loosely bound electron in the cage that can be thermally activated. This suggests that interstitial muons (and hence H) forming a "cage electron-hydroxyl" complex can serve as electron donors in C12A7.
Explore related subjects
Keep this discovery
M. Hiraishi, K. M. Kojima, M. Miyazaki, I. Yamauchi, H. Okabe, A. Koda, R. Kadono, S. Matsuishi, H. Hosono. 2016-02-22. Cage Electron-Hydroxyl Complex State as Electron Donor in Mayenite. https://doi.org/10.1103/physrevb.93.121201
Cite the original work for its findings. Save a collection to share your selection of sources.