Atomically Thin Sheets of Lead-Free 1D Hybrid Perovskites Feature Tunable White-Light Emission from Self-Trapped Excitons.

Low-dimensional organic-inorganic perovskites synergize the virtues of two unique classes of materials featuring intriguing possibilities for next-generation optoelectronics: they offer tailorable building blocks for atomically thin, layered materials while providing the enhanced light-harvesting and emitting capabilities of hybrid perovskites. This work goes beyond the paradigm that atomically thin materials require in-plane covalent bonding and reports single layers of the 1D organic-inorganic perovskite [C H N] [BiCl ]Cl. Its unique 1D-2D structure enables single layers and the formation of self-trapped excitons, which show white-light emission.

Controlling the White-Light Generation of [(RSn) E ]: Effects of Substituent and Chalcogenide Variation.

Adamantane-type organotin chalcogenide clusters of the general composition [(RT) S ] (R=aromatic substituent, T=Si, Ge, Sn) have extreme non-linear optical properties that lead to highly directional white-light generation (WLG) upon irradiation with an IR laser diode. However, the mechanism is not yet understood. Now, a series of compounds [(RSn) E ] (R=phenyl, cyclopentadienyl, cyclohexyl, benzyl, CH CH (C H )CO Et; E=S, Se), were prepared, characterized, and investigated for their nonlinear optical properties.