A Wide-Bandgap Molecular Ferroelectric Semiconductor with a Two-Step Wide-Temperature Second Harmonic Generation Response: [FMeQ] <sub>2</sub> ZnI <sub>4</sub>
Wide-bandgap molecular ferroelectric semiconductors are emerging as critical candidates for next-generation multifunctional optoelectronics, yet integrating robust ferroelectricity with a wide optical bandgap remains a formidable challenge. Herein, we report a zero-dimensional organic-inorganic hybrid ferroelectric semiconductor, [FMeQ]<sub>2</sub>ZnI<sub>4</sub> (FMeQ = <i>N</i>-fluoromethyl-quinuclidine), constructed via a targeted cation fluorination strategy. This compound crystallizes in the polar orthorhombic space group <i>Pna</i>2<sub>1</sub> and exhibits a wide indirect bandgap of approximately 3.65 eV, comparable to traditional inorganic semiconductors like GaN. Remarkably, [FMeQ]<sub>2</sub>ZnI<sub>4</sub> undergoes two sequential reversible order-disorder phase transitions at 306 and 336 K, endowing the material with a unique two-step switchable second harmonic generation (SHG) response over a wide temperature range. Electronic structure analysis reveals an effective decoupling mechanism where the inorganic [ZnI<sub>4</sub>]<sup>2-</sup> anion dominates the wide bandgap, while the dynamic organic cation dictates the ferroelectricity. This discovery provides an alternative approach to explore wide-bandgap molecular ferroelectrics, especially ferroelectric semiconductors with high-performance multistate optical switching capabilities.
Authors
- L. Chen
- Zhong Ni (ORCID: https://orcid.org/0000-0001-6080-0286)
- Chen Zhang (ORCID: https://orcid.org/0000-0002-4589-7742)
- Wenhe Zhong (ORCID: https://orcid.org/0000-0002-7617-8345)
- Lin-Na Tian
- Rui-Si Yu
- Jia-Jia Zhao
Institutions
- Jiangsu University of Science and Technology (CN)
Publication Details
- Journal
- Inorganic Chemistry
- Published
- 2026-03-15
- DOI
- https://doi.org/10.1021/acs.inorgchem.6c00486
- Primary Topic
- Perovskite Materials and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00