Nano-photomechanical motion of small particles induced by switching photon force through photochemical processes

S. Ito, K. Setoura, H. Miyasaka
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Abstract

In the present study, we propose a combined (hybrid) approach of optical manipulation and photochemical reactions for achieving nano-photomechanical motions with small particles. Aa photochemical reactions, we have employed P-type and T-type photochromic reactions of diarylethene (DAE) and pyranoquinazoline (PQ) derivatives, respectively. Single polymer particle containing each of the photochromic compounds was optically trapped in water with a CW visible laser. At this stage, the particle experienced mainly gradient force and was trapped at the focal point of the CW laser. The absorption force was negligible because most of the photochromic molecules in the particle were in the colorless form. UV exposure induced the photoisomerization of the photochromic molecules, resulting in the increase in the number of colored forms. As a result, the absorption force acting on the particle increased and, the position of the particle shifted towards the light propagation direction depending on experimental condition. After turning the UV light off, the particle went back to the original position. The trapped particle thus underwent reciprocal motion synchronizing with the change of photo-response due to the photochromic reactions.
光化学过程中由光子力开关引起的小粒子的纳米光力学运动
在本研究中,我们提出了一种结合光学操作和光化学反应的方法来实现小颗粒的纳米光力学运动。在光化学反应中,我们分别采用了二乙烯(DAE)和吡喹唑啉(PQ)衍生物的p型和t型光致变色反应。用连续波可见激光将含有每种光致变色化合物的单个聚合物粒子捕获在水中。在这一阶段,粒子主要受到梯度力的作用,被困在连续激光的焦点处。吸收力可以忽略不计,因为粒子中的大部分光致变色分子都是无色的。紫外线照射诱导光致变色分子的光异构化,导致彩色形式的数量增加。因此,作用在粒子上的吸收力增大,粒子的位置根据实验条件向光传播方向偏移。关闭紫外线后,粒子又回到了原来的位置。捕获粒子的运动与光致变色反应引起的光响应变化同步。
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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