Organic−inorganic hybrid ferroelectrics have attracted considerable attention due to their outstanding piezoelectricity, mechanical flexibility, and robust nonlinear optical properties. But the species with above room-temperature (RT) ferroelectricity, visible-light bandgap, and high photoelectric performance are still scarce. Herein, a novel organic−inorganic hybrid ferroelectric [C 4 N 2 H 14 ] 2 [Sb 2 I 10 ] has been synthesized hydrothermally and employed as a light-absorbing layer in organic−inorganic hybrid solar cells. A polar monoclinic structure with a space group of Pn was resolved by single-crystal XRD. A direct band gap of 1.89 eV was revealed in [C 4 N 2 H 14 ] 2 [Sb 2 I 10 ] by UV−vis spectroscopy and density functional theory (DFT) studies. A dramatic enhancement in photoelectric performance has been achieved by turning the ferroelectric polarization, leading to a maximum V oc ∼ 0.52 V and J sc ∼ 15.52 μA/cm 2 , which are 15-fold and 29-fold higher than those of the unpoled sample, respectively. This work may open new avenues for the application of molecular ferroelectrics in optoelectronic devices.