Theoretical modeling demonstrates full conversion to spin-polarized photocurrent in vacancy-engineered gallium selenide, indicating design principles for low-energy optoelectronics.
Spin-polarized photocurrent generation enables ultrafast optical manipulation and energy-efficient spin transport, offering a promising route to overcome the speed and energy limitations of conventional electronics, although suitable half-metallic materials remain exceptionally rare. Herein, we demonstrate versatile functionalities in ε-GaSe photonics by engineering vacancies to break parity-time symmetry. Previous theoretical and experimental studies highlight the exceptional performance of ε-GaSe-based photonic systems. Material-level vacancy engineering enables controlled transitions between semiconductor/metal, nonmagnetic/half-metallic, and weak/strong ferroelectric states. Device-level implementations achieve polarization switching and full conversion of charge current to a completely spin-polarized photocurrent. These findings provide critical design principles for developing tunable, energy-efficient, and multifunctional optoelectronic devices.
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Xie et al. (2025) studied this question.
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