STRUCTURAL ORIGINS IN PHOTOSWITCHABLE ORGANIC FERROELECTRICITY USING TIME-RES
STRUCTURAL ORIGINS IN PHOTOSWITCHABLE ORGANIC FERROELECTRICITY USING TIME-RES
批准号:
8172008
负责人:
LIN CHEN
金额:
$1.7万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-08-01 至 2011-07-31
关键词:
ChemicalsComputer Retrieval of Information on Scientific Projects DatabaseFundingGrantHydrogen BondingInformation StorageInstitutionInterdisciplinary StudyMolecular MotorsPropertyResearchResearch PersonnelResourcesRotationSideSourceTechniquesTimeUnited States National Institutes of HealthUniversitiesWorkabsorptionbeamlinechemical synthesiselectron donoremission spectroscopyrepairedsuccesstime use
中文摘要
点击翻译按钮获取中文摘要
英文摘要
This subproject is one of many research subprojects utilizing the
resources provided by a Center grant funded by NIH/NCRR. The subproject and
investigator (PI) may have received primary funding from another NIH source,
and thus could be represented in other CRISP entries. The institution listed is
for the Center, which is not necessarily the institution for the investigator.
Organic ferroelectric materials are important for applications of information storage, molecular motors and actuators. The advantages of organic ferroelectric materials over their inorganic counter part are their chemical tunability, processibility and self-repair capability. Therefore, understanding the structural origins in organic ferroelectric materials and their connections to the properties of the materials is crucial in developing new materials with broad applications. The proposed work will investigate the structural origins of a group of photo-switchable organic ferroelectric materials made of small aromatic organic electron donors (D) and acceptors (A) self-assembled into alternating three dimensional DADA? arrays by steady-state and time-resolved x-ray diffraction techniques at Beamline 14ID of the APS. The structural origins for such photoswitchable ferroelectric materials are structural changes either due to change of the DA distances or rotation of the side groups that form or disrupt the hydrogen bonds. Using TR-XRD, Collet, Techert, et al. carried out pioneering studies on similar type of materials with power diffraction at ESRF. We are encouraged by their success and believe that our materials can be studied by the TR-XRD with Laue diffraction on single crystals at Beanline 14ID. We would like to capture the structural origins that enable the ferroelectricity and distinguish different types of the structural changes. The proposed structural studies will be combined with single crystal ultrafast transient absorption and emission spectroscopy conducted in our labs in Northwestern University. The structural information obtained at the APS and spectroscopic and theoretical as well as chemical synthesis will enable a productive interdisciplinary research to discover, character, and applying new materials.
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