Hybrid organic–inorganic perovskites
(HOIPs) with chiral
organic ligands exhibit highly spin-dependent transport and strong
natural optical activity (NOA). Here we show that these remarkable
features can be traced to a chirality-induced spin–orbit coupling
(SOC), Hso = ατkzσz, which connects the carrier’s spin (σz), its wave vector (kz), and the material’s helicity (τ) along the screw
direction with strength α controlled by the geometry of the
organic ligands. This SOC leads to a macroscopic spin polarization
in the presence of an electrical current and is responsible for the
observed spin-selective transport. NOA originates from a coupling
between the exciton’s center-of-mass wave vector Kz and its circular polarization jzex, Hso′ = α′τKzjzex, contributed
jointly from the electron’s and the hole’s SOCs in an
exciton. Our model provides a roadmap to achieve a strong and tunable
chirality in HOIPs for novel applications utilizing carrier spin and
photon polarization.