767
Near Surface Structures and the Electronic States of Polar InN

Monday, 1 October 2018: 10:40
Universal 12 (Expo Center)
Y. Yamashita, A. Yang (National Institute for Materials Science), and K. Kobayashi (Japan Atomic Energy Agency)
InN has received great research attention because of the small band-gap (~ 0.7 eV) and superior electrical transport properties. As a wurtzite crystal lacks inversion symmetry along c-axis direction, In-polar and N-polar InN exhibit different properties. Therefore, investigation of near-surface structure and electronic states of polar InN films are important to fully realize their potential. Due to the element and chemical state specificity and the larger probing depth, hard X-ray photoelectron diffraction (HXPD) was used to investigate the near-surface structures of polar InN films [1].
The HXPD system consists of a monochromatic Cr Kα source (5414.7 eV), a high energy version of the VG SCIENTA R4000 10 kV analyzer with wide acceptance objective lens.The angle acceptance of the combined objective lens and the analyzer is ±35° with an angular resolution of 0.5°. The total energy resolution was 1 eV. In this study, the polar angle θ is defined to be zero for the photoemission direction normal to a sample surface. The θ-dependent sensitivity of the analyzer, was calibrated using an amorphous GeSbTe sample.
Figure 1 shows the HXPD patterns from In 3d5/2 and N 1s core levels of In-polar and N-polar InN. The patterns were different from each other and then they were compared with the simulation results using a multiple-scattering cluster model[2], which is shown in Fig.1. It was found that the near-surface structure of the In-polar InN film was close to the ideal wurtzite structure. On the other hand, on the N-polar InN film, defects-rich surface was formed. In addition, the existence of the In-polar domains was observed in the HXPD patterns.

References:
[1] A. Yang, Y. Yamashita, et al., Appl. Phys. Lett. 102, 031914 (2013).
[2] T. Matsushita, et a., J. Electron Spectrosc. Relat. Phenom. 178, 195 (2010).