Current rectification via Photosystem I monolayers induced by their orientation on hydrophilic self-assembled monolayers on titanium nitride

Jonathan Rojas, Zhe Wang, Feng Liu, Jerry A. Fereiro, Domenikos Chryssikos, Thomas Dittrich, Dario Leister, David Cahen, Marc Tornow
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Abstract

Photosystem I (PSI) is a photosynthetic protein which evolved to efficiently transfer electrons through the thylakoid membrane. This remarkable process attracted the attention of the biomolecular electronics community, which aims to study and understand the underlying electronic transport through these proteins by contacting ensembles of PSI with solid-state metallic contacts. This paper extends published work of immobilizing monolayers of PSI with a specific orientation, by using organophosphonate self-assembled molecules with hydrophilic heads on ultra-flat titanium nitride. Electrical measurements carried out with eutectic GaIn top contacts showed current rectification ratios of up to ~200. The previously proposed rectification mechanism, relying on the protein's internal electric dipole, was inquired by measuring shifts in the work function. Our straightforward bottom-up fabrication method may allow for further experimental studies on PSI molecules, such as embedding them in solid-state, transparent top contact schemes for optoelectronic measurements.
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氮化钛上亲水自组装单层的取向诱导光系统 I 单层实现电流整流
光系统 I(PSI)是一种光合作用蛋白质,其进化过程是通过类囊体膜高效传输电子。这一非凡的过程吸引了生物分子电子学界的关注,他们的目标是通过将 PSI 组合与固态金属触头接触,研究和了解通过这些蛋白质进行电子传输的基本原理。本文利用有机膦酸盐自组装分子在超平氮化钛上的亲水头,扩展了已发表的固定 PSI 单层特定取向的工作。使用共晶铟镓顶触点进行的电学测量显示,电流整流比高达 ~200。之前提出的整流机制依赖于蛋白质的内部电偶极子,我们通过测量工作函数的偏移对这一机制进行了探究。我们这种自下而上的直接制备方法可用于对 PSI 分子进行进一步的实验研究,例如将它们嵌入固态透明顶面接触方案中进行光电测量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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