Suppr超能文献

通过飞秒时间分辨X射线光电子能谱直接观察有机光捕获系统中的电荷分离。

Direct observation of charge separation in an organic light harvesting system by femtosecond time-resolved XPS.

作者信息

Roth Friedrich, Borgwardt Mario, Wenthaus Lukas, Mahl Johannes, Palutke Steffen, Brenner Günter, Mercurio Giuseppe, Molodtsov Serguei, Wurth Wilfried, Gessner Oliver, Eberhardt Wolfgang

机构信息

Institute of Experimental Physics, TU Bergakademie Freiberg, Freiberg, Germany.

Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.

出版信息

Nat Commun. 2021 Feb 19;12(1):1196. doi: 10.1038/s41467-021-21454-3.

Abstract

The ultrafast dynamics of photon-to-charge conversion in an organic light-harvesting system is studied by femtosecond time-resolved X-ray photoemission spectroscopy (TR-XPS) at the free-electron laser FLASH. This novel experimental technique provides site-specific information about charge separation and enables the monitoring of free charge carrier generation dynamics on their natural timescale, here applied to the model donor-acceptor system CuPc:C. A previously unobserved channel for exciton dissociation into mobile charge carriers is identified, providing the first direct, real-time characterization of the timescale and efficiency of charge generation from low-energy charge-transfer states in an organic heterojunction. The findings give strong support to the emerging realization that charge separation even from energetically disfavored excitonic states is contributing significantly, indicating new options for light harvesting in organic heterojunctions.

摘要

利用自由电子激光FLASH的飞秒时间分辨X射线光电子能谱(TR-XPS)研究了有机光捕获系统中光子到电荷转换的超快动力学。这种新颖的实验技术提供了关于电荷分离的位点特异性信息,并能够在其自然时间尺度上监测自由电荷载流子的产生动力学,这里应用于模型供体-受体系统CuPc:C。确定了一个以前未观察到的激子解离成移动电荷载流子的通道,首次直接实时表征了有机异质结中低能电荷转移态产生电荷的时间尺度和效率。这些发现有力地支持了新出现的认识,即即使是能量上不利的激子态的电荷分离也有显著贡献,这为有机异质结中的光捕获指明了新的方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5967/7895929/ff4aad295459/41467_2021_21454_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验