主要结构单元"D+A-" 离子对主导近红外光热转换有机离子合晶体的近红外光热转换
Meng-Meng Zhang1, Shun-Li Chen1, Siya Huang1
1College of Chemistry and Chemical Engineering, and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou 515063, China.
"D+A-"离子对,而不是堆叠模式,主要决定有整数电荷转移的有机共晶体的特性. 这一发现为设计先进的光热转换材料提供了新的见解.
科学领域:
- 材料科学 材料科学 材料科学
- 超分子化学 超分子化学
- 摄影化学的使用.
背景情况:
- 同晶的特性通常与D/A块堆叠有关.
- 这种范式可能不适用于具有显著电荷转移的系统.
研究的目的:
- 研究整数电荷转移的F4TCNQ共晶体中的结构-属性相关性.
- 确定结构单元与堆叠模式在光热转换中的作用.
主要方法:
- 基于F4TCNQ的共晶体的合成和表征.
- 对电荷转移,吸收和兴奋状态动态的分析.
- 评估近红外光热转换 (NIR-PTC) 的效率.
主要成果:
- 有着多种堆叠模式的共晶体显示出类似的DA相互作用和广泛的红移吸收.
- 观察到超快的兴奋状态放松 (1-3 ps) 和优秀的NIR-PTC特性.
- 导致"D+A-"离子对的整数电荷转移被确定为主导因素.
结论:
- 由整数电荷转移形成的"D+A-"离子对是共晶性质的主要决定因素.
- 堆叠模式在这些系统中起到次要作用.
- 这项工作促进了对结构-动力学-属性关系的理解,用于设计用于光热应用的有机材料.
更多相关视频
12:51A 'Plug and Play' Method to Create Water-dispersible Nanoassemblies Containing an Amphiphilic Polymer, Organic Dyes and Upconverting Nanoparticles
Published on: November 14, 2015
06:08Time-resolved Photophysical Characterization of Triplet-harvesting Organic Compounds at an Oxygen-free Environment Using an iCCD Camera
Published on: December 27, 2018
相关概念视频
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Intermolecular Forces
