RESUMO
An ordered germanium terminated (1 0 0) diamond surface has been formed and characterised using a combination of low energy electron diffraction and synchrotron-based core level photoemission spectroscopy. A number of preparation methods are explored, in each case inducing a two domain [Formula: see text] surface reconstruction. The surface becomes saturated with bonded germanium such that each [Formula: see text] unit cell hosts 1.26 Ge atoms on average, and possesses a negative electron affinity of -0.71 eV.
RESUMO
Hydrogen-terminated diamond possesses due to transfer doping a quasi-two-dimensional (2D) hole accumulation layer at the surface with a strong, Rashba-type spin-orbit coupling that arises from the highly asymmetric confinement potential. By modulating the hole concentration and thus the potential using an electrostatic gate with an ionic-liquid dielectric architecture the spin-orbit splitting can be tuned from 4.6-24.5 meV with a concurrent spin relaxation length of 33-16 nm and hole sheet densities of up to 7.23 × 10(13) cm(-2). This demonstrates a spin-orbit interaction of unprecedented strength and tunability for a 2D hole system at the surface of a wide band gap semiconductor. With a spin relaxation length that is experimentally accessible using existing nanofabrication techniques, this result suggests that hydrogen-terminated diamond has great potential for the study and application of spin transport phenomena.