Abstract:Polar materials display a series of interesting and widely exploited properties owing to the inherent coupling between their fixed electric dipole and any action that involves a change in their charge distribution. Among these properties are piezoelectricity, ferroelectricity, pyroelectricity, and the bulk photovoltaic effect. Here we report the observation of a related property in this series, where an external electric field applied parallel or anti-parallel to the polar axis of a crystal leads to an increas… Show more
“…The angle‐dependent SHG intensity of OH1 is different from other nanowires previously reported, such as Te, ZnO, GaAs, and DPFO, which show appreciable SHG signals when the polarization of FW laser is parallel or perpendicular to the microwires. [ 37–40 ] As for DAT2, polarization‐resolved SHG exhibits a fourfold rotational symmetry, and the SHG intensity reaches its maximum when the polarization direction is ±45 degrees to the microwires (Figure 4f). Calculating the polarization ratio ρ = ( I max − I min ) / ( I max + I min ) helps to provide a value of virtual unity.…”
Organic nonlinear optical (NLO) crystals play an indispensable role in high‐performance photonic devices due to their large nonlinear coefficient, fast response time, and low dielectric constant. However, in contrast to the strides of bulk crystals, researches on the next generation of nanophotonic devices are ignored to some extent. One of the bottlenecks is the controllable manufacturing and patterning of high‐quality organic NLO crystals with the nanometer‐scale thickness. Herein, a confined assembly method for fabricating the microwire arrays of organic NLO crystal OH1 and DAT2 with precise position, flat morphology, high crystallinity, and consistent crystallographic orientation is reported. Two strong NLO effects observed in the experiments are comprehensively studied, including second harmonic generation (SHG) and two‐photon excited fluorescence. Furthermore, it is demonstrated that the anisotropic SHG effect depends on both the polarization of incident light and the crystallographic orientation of microwire arrays. Microwire arrays can exhibit large in‐plane anisotropy with the polarization ratio up to 0.95 and second‐order nonlinear coefficient up to 55.1 pm V−1. This work provides new insights into the potential applications of organic NLO crystals in integrated optical devices.
“…The angle‐dependent SHG intensity of OH1 is different from other nanowires previously reported, such as Te, ZnO, GaAs, and DPFO, which show appreciable SHG signals when the polarization of FW laser is parallel or perpendicular to the microwires. [ 37–40 ] As for DAT2, polarization‐resolved SHG exhibits a fourfold rotational symmetry, and the SHG intensity reaches its maximum when the polarization direction is ±45 degrees to the microwires (Figure 4f). Calculating the polarization ratio ρ = ( I max − I min ) / ( I max + I min ) helps to provide a value of virtual unity.…”
Organic nonlinear optical (NLO) crystals play an indispensable role in high‐performance photonic devices due to their large nonlinear coefficient, fast response time, and low dielectric constant. However, in contrast to the strides of bulk crystals, researches on the next generation of nanophotonic devices are ignored to some extent. One of the bottlenecks is the controllable manufacturing and patterning of high‐quality organic NLO crystals with the nanometer‐scale thickness. Herein, a confined assembly method for fabricating the microwire arrays of organic NLO crystal OH1 and DAT2 with precise position, flat morphology, high crystallinity, and consistent crystallographic orientation is reported. Two strong NLO effects observed in the experiments are comprehensively studied, including second harmonic generation (SHG) and two‐photon excited fluorescence. Furthermore, it is demonstrated that the anisotropic SHG effect depends on both the polarization of incident light and the crystallographic orientation of microwire arrays. Microwire arrays can exhibit large in‐plane anisotropy with the polarization ratio up to 0.95 and second‐order nonlinear coefficient up to 55.1 pm V−1. This work provides new insights into the potential applications of organic NLO crystals in integrated optical devices.
“…Although there has yet no systematic mathematical description for dipole moment structure as the description for electron structure, two key strategies still can be found from our study to arrive at a large macroscopic SHG response. First, it is necessary that large magnitude of instantaneous dipole moments could be generated by electron transition from anion unit to cation unit, [32] here from the BO/AlO anion group to Ba cation. This requires an appropriate anion unit and cation, and an appropriate interaction between the anion unit and the cation.…”
A deep understanding on the crucial factors of the enhanced macroscopic second harmonic generation (SHG) in some deep-ultraviolet nonlinear optical (NLO) materials is needed to design new NLO materials. Since an optical process relates to the electron excitation and polarization simultaneously, the instantaneous dipole moments and their structures in excitation should be seriously taken account to seek the principal factor in SHG response. In this work, we study the Ba 4 B 11 O 20 F (BBOF), a NLO material, by using the orbital projection technique. From the projected SHG of our theoretic calculation, we recognize the principal dipole moment of the dominant influence on SHG and the relevant atom groups between which the dipole moment is accommodated. With the conclusion that the dipole moment with the most significant influence on SHG is the one between the oxygen-boron polyhedral anion group and barium cation, we predict that Ba 4 Al 11 O 20 F (BAOF) has a comparable SHG response.
“…The buildup of these free charges on the crystal's relative surface causes surface redox reactions, which allow the transformation of mechanical energy into chemical energy. [1,[28][29][30][31] Significant advancements in this field of study have been accomplished recently, resulting in the exploitation of various piezoelectric material-based catalysts, such as ZnO, [32][33][34] BaTiO 3 , [32][33][34] NaNbO 3 , [35,36] and KNbO 3 , [37] C 3 N 4 , [38] CdS, [39] and MoS 2 . [40]…”
Section: Piezoelectric Effect and Piezoelectric Catalysismentioning
Piezoelectric, pyroelectric, and ferroelectric materials are considered unique biomedical materials due to their dielectric crystals and asymmetric centers that allow them to directly convert various primary forms of energy in the environment, such as sunlight, mechanical energy, and thermal energy, into secondary energy, such as electricity and chemical energy. These materials possess exceptional energy conversion ability and excellent catalytic properties, which have led to their widespread usage within biomedical fields. Numerous biomedical applications have demonstrated great potential with these materials, including disease treatment, biosensors, and tissue engineering. For example, piezoelectric materials have been used to stimulate cell growth in bone regeneration, while pyroelectric materials have been applied in skin cancer detection and imaging. Ferroelectric materials have even found use in neural implants that record and stimulate electrical activity in the brain. This paper reviews the relationship between ferroelectric, piezoelectric, and pyroelectric effects and the fundamental principles of different catalytic reactions. It also highlights the preparation methods of these three materials and the significant progress made in their biomedical applications. The review concludes by presenting key challenges and future prospects for efficient catalysts based on piezoelectric, pyroelectric, and ferroelectric nanomaterials for biomedical applications.This article is protected by copyright. All rights reserved
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