https://doi.org/10.1140/epjp/s13360-022-02402-6
Regular Article
Three orders of magnitude two-beam-coupling gain increase from Cu-doped (K0.5Na0.5)0.2(Sr0.75Ba0.25)0.9Nb2O6 crystal owing to huge depolarization field-induced surface metallization
1
School of Physics, Harbin Institute of Technology, 150001, Harbin, China
2
Key Laboratory of Micro-Optics and Photonics Technology of Heilongjiang Province, 150001, Harbin, China
3
Key Laboratory of Micro-Nano Optoelectronic Information System, Ministry of Industry and Information Technology, 150001, Harbin, China
Received:
3
June
2021
Accepted:
18
January
2022
Published online:
10
February
2022
Metallization at the nanoscale on ferroelectric-oxide surface was reported, stemming from depolarization of the huge self-spontaneous polarization. The striking metallization layer is found responsible for various exotic effects never seen in the bulk. Very encouragingly, by using density functional theory, along with the Thomas–Fermi semi-classic model, we have demonstrated the surface metallization in Cu-doped (K0.5Na0.5)0.2(Sr0.75Ba0.25)0.9Nb2O6 (Cu:KNSBN) crystal. The electron density in such a metallization layer is up to that in noble metals, making it possible in supporting visible surface plasmon polaritons. Since the very first specular reflection (VFSR) is dictated by the optical properties within the range of half a wavelength, we used it to probe experimentally the existence of the metallization layer. Indeed, as high as 5 × 104 cm−1 exponential gain coefficients were obtained by monitoring the marked increase and decrease of the VFSR on the ± C-face of a Cu:KNSBN crystal cuboid, which were three orders of magnitude higher than those of the previously reported results. Such high gains are beyond the limits of current theory, including the well-established photorefractive theory, yet can be explained well with phase grating mediated excitation of surface plasmon polaritons. This work expands, both experimentally and theoretically, the general picture regarding surface metallization in ferroelectric oxides.
© The Author(s), under exclusive licence to Società Italiana di Fisica and Springer-Verlag GmbH Germany, part of Springer Nature 2022