The chirality-induced spin selectivity (CISS) effect
facilitates
a paradigm shift for controlling the outcome and efficiency of spin-dependent
chemical reactions, for example, photoinduced water splitting. While
the phenomenon is established in organic chiral molecules, its emergence
in chiral but inorganic, nonmolecular materials is not yet understood.
Nevertheless, inorganic spin-filtering materials offer favorable characteristics,
such as thermal and chemical stability, over organic, molecular spin
filters. Chiral cupric oxide (CuO) thin films can spin polarize (photo)electron
currents, and this capability is linked to the occurrence of the CISS
effect. In the present work, chiral CuO films, electrochemically deposited
on partially UV-transparent polycrystalline gold substrates, were
subjected to deep-UV laser pulses, and the average spin polarization
of photoelectrons was measured in a Mott scattering apparatus. By
energy resolving the photoelectrons and changing the photoexcitation
geometry, the energy distribution and spin polarization of the photoelectrons
originating from the Au substrate could be distinguished from those
arising from the CuO film. The findings reveal that the spin polarization
is energy dependent and, furthermore, indicate that the measured polarization
values can be rationalized as a sum of an intrinsic spin polarization
in the chiral oxide layer and a contribution via CISS-related spin
filtering of electrons from the Au substrate. The results support
efforts toward a rational design of further spin-selective catalytic
oxide materials.