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Prominent Nonlinear Optical Absorption in SnS2‐Based Hybrid Inorganic–Organic Superlattice.
- Source :
- Advanced Functional Materials; 7/10/2024, Vol. 34 Issue 28, p1-11, 11p
- Publication Year :
- 2024
-
Abstract
- Nonlinear optical materials hold great promise for applications in advanced opto‐/opto‐electronic devices. However, achieving a substantial nonlinear absorption coefficient and modulation depth concurrently remains challenging. This study proposes an effective strategy for enhancing the nonlinear optical response of materials through the construction of hybrid inorganic–organic superlattices via convenient organic intercalation. Synthesizing SnS2 intercalated with various tetra‐alkylammonium cations, it is revealed that the optimized sample (SnS2/CTA: SnS2 intercalated with cetyltrimethylammonium, CTA+) exhibits a substantial enhancement of nonlinear absorption across a broad wavelength range (from 515 to 1550 nm) and for diverse nonlinear optical processes (saturable absorption, two‐photon absorption, and three‐photon absorption). Specifically, the SnS2/CTA demonstrates a third‐order nonlinear absorption coefficient of (9.847 ± 0.084) × 103 cm GW−1 and a 69% modulation depth under laser excitation at 800 nm. Under 1550 nm excitation, it displays a fifth‐order nonlinear absorption coefficient of (45.3 ± 1.2) cm3 GW−2 and a 62% modulation depth. Notably, these values surpass those of the majority of non‐exfoliated materials. Structural, spectral, and density functional theory calculations indicate no induced structure defects post‐organic intercalation. The observed bandgap reduction is attributed to the electron injection associated with the organic molecule intercalation. The calculated performance enhancement, based on dielectric enhancement and bandgap reduction, qualitatively aligns with experimental findings. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 1616301X
- Volume :
- 34
- Issue :
- 28
- Database :
- Complementary Index
- Journal :
- Advanced Functional Materials
- Publication Type :
- Academic Journal
- Accession number :
- 178355079
- Full Text :
- https://doi.org/10.1002/adfm.202400077