Controlled Substitution of Chlorine for Iodine in Single-Crystal Nanofibers of Mixed Perovskite MAPbI3-xClx

Abstract

Longer carrier diffusion length and improved power conversion efficiency have been reported for thin-film solar cell of organolead mixed-halide perovskite MAPbI_{3– x} Cl _x in comparison with MAPbI₃. Instead of substituting I in the MAPbI₃ lattice, Cl-incorporation has been shown to mainly improve the film morphology of perovskite absorber. Well-defined crystal structure, adjustable composition (x), and regular morphology, remains a formidable task. Herein, a facile solution-assembly method is reported for synthesizing single-crystalline nanofibers (NFs) of tetragonal-lattice MAPbI_{3– x} Cl _x with the Cl-content adjustable between 0 ≤ x ≤ 0.75, leading to a gradual blueshift of the absorption and photoluminescence maxima from x = 0 to 0.75. The photoresponsivity (R) of MAPbI₃ NFs keeps almost unchanging at a value independent of the white-light illumination intensity (P). In contrast, R of MAPbI_{3– x} Cl _x NFs decreases rapidly with increasing both the x and P values, indicating Cl-substitution increases the recombination traps of photogenerated free electrons and holes. This study provides a model system to examine the role of extrinsic Cl ions in both perovskite crystallography and optoelectronic properties.