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Measuring Magnetically-Tuned Ferroelectric Polarization in Liquid Crystals
Published on: August 15, 2018
二次非线性光学的横向桥式h形铁电二次物质:铁电和第二波生成
Yongqiang Zhang1, Josu Martinez-Perdiguero, Ute Baumeister
1Displaytech Inc., 2602 Clover Basin Drive, Longmont, Colorado 80503, USA. yqzhang@micron.com
Journal of the American Chemical Society
|November 26, 2009
概括
研究人员开发了具有稳定的铁电性的新型H形铁电液晶 (FLC). 由于具有创纪录的非线性系数,这些材料显示出非线性光学应用的潜力.
科学领域:
- 材料科学 材料科学 材料科学
- 有机化学 有机化学
- 凝聚物质物理学 凝聚物质物理学
背景情况:
- 铁电液晶 (FLC) 对于光电子设备至关重要.
- H 形的 FLC 具有独特的结构特性.
- 在H形FLC中实现稳定,地面状态的铁电是具有挑战性的.
研究的目的:
- 为了合成和表征新的H形FLCs.
- 为了研究它们的铁电特性.
- 探索它们在非线性光学中的潜力.
主要方法:
- 用阿佐和分散红色1 (DR-1) 染色体合成以阿佐桥为桥梁的H形FLC.
- 使用偏光显微镜,差分扫描热量计和二维X射线衍射进行了表征.
- 电光检测和第二波生成 (SHG) 测量.
主要成果:
- 成功合成了两个类型的H形FLCs.
- 展示了第一个具有基态,热力学稳定的反热性SmC*阶段 (基态铁电) 的H形FLC.
- 对于含有DR-1的化合物,达到了非线性系数d(22) = 17pm/V,这对于性FLC来说是最大的.
结论:
- 开发的H形FLC表现出稳定的铁电.
- 这些材料对非线性光学应用具有前景.
- 创纪录的非线性系数为先进的光子设备开辟了道路.
相关概念视频
Stereoisomerism
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para position.

