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Diffusion of Nanoparticles with Activated Hopping in Crowded Polymer Solutions

机译:纳米颗粒的扩散在拥挤的聚合物溶液中具有活性跳跃

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摘要

A long-distance hop of diffusive nanoparticles (NPs) in crowded environments was commonly considered unlikely, and its characteristics remain unclear. In this work, we experimentally identify the occurrence of the intermittent hops of large NPs in crowded entangled poly(ethylene oxide) (PEO) solutions, which are attributed to thermally induced activated hopping. We show that the diffusion of NPs in crowded solutions is considered as a superposition of the activated hopping and the reptation of the polymer solution. Such activated hopping becomes significant when either the PEO molecular weight is large enough or the NP size is relatively small. We reveal that the time-dependent non-Gaussianity of the NP diffusion is determined by the competition of the short-time relaxation of a polymer entanglement strand, the activated hopping, and the long-time reptation. We propose an exponential scaling law tau(hop)/tau(e) similar to exp(d/d(t)) to characterize the hopping time scale, suggesting a linear dependence of the activated hopping energy barrier on the dimensionless NP size. The activated hopping motion can only be observed between the onset time scale of the short-time relaxation of local entanglement strands and the termination time scale of the long-time relaxation. Our findings on activated hopping provide new insights into long-distance transportation of NPs in crowded biological environments, which is essential to the delivery and targeting of nanomedicines.
机译:在拥挤的环境中扩散纳米颗粒(NP)的长距离跳被普遍认为是不可能的,它的特点仍不清楚。在这项工作中,我们通过实验确定在拥挤缠结聚(环氧乙烷)大NP的间歇啤酒花的发生(PEO)的解决方案,这归因于热致活化的跳频。我们表明,纳米颗粒在拥挤的解决方案扩散被认为是激活跳跃的叠加,将聚合物溶液的爬行。时,无论是PEO分子量足够大或NP尺寸比较小这种活化跳频变得显著。我们揭示了NP扩散的依赖于时间的非高斯通过聚合物缠结链的短时松弛的竞争,活化跳频,并长时间蠕动确定。我们提出了一种指数比例法的tau(跳)/ tau蛋白(e)中类似EXP(d / d(t))的表征跳频时标,这表明在无量纲NP尺寸被激活的跳频能量势垒的线性依赖性。只能本地缠结股线的短松弛时间的开始时间和规模的长时间松弛的终止时间尺度之间观察到的激活跳跃运动。我们对激活跳跃发现提供了新的见解在拥挤的生物环境NP的长途运输,这是必不可少的交付和纳米医学的目标。

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