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Scalable routes to gold nanoshells with tunable sizes and their response to near infrared pulsed laser irradiation

机译:尺寸可变的金纳米壳的可扩展路线及其对近红外脉冲激光辐照的响应

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摘要

We present a simplified synthesis of hollow gold nanoshells 20-50 nm in diameter via the well-established templated galvanic replacement reaction of silver for gold. The surface plasmon resonance absorbance of nanoshells made in this fashion can be tuned using basic colloid chemistry to control the size of the silver templates. The gold nanoshells can be varied in size and shell thickness depending on silver/gold reagent ratios and have an aqueous core. The template replacement chemistry is rapid, highly scalable, uses minimal amounts of toxic reagents, and in many cases is a true `one pot' synthesis. The smallest nanoshells (20 nm diameter, 7 nm wall thickness) reach the highest temperature on irradiation with femtosecond light pulses in the near infrared and anneal to form spherical nanoparticles fastest, even though their plasmon resonance does not overlap as well as the larger nanoshells (50 nm diameter, 7 nm wall thickness) with the 800 nm wavelength excitation. Optimizing a nanoshell structure to reach the highest nanoshell temperature is not the same as optimizing the structure for maximum energy absorbance.
机译:我们提出了一种通过完善的银模板化电化金置换反应,直径为20-50 nm的空心金纳米壳的简化合成方法。可以使用基本的胶体化学来控制以这种方式制备的纳米壳的表面等离子体共振吸收,以控制银模板的大小。金纳米壳的大小和壳厚度可以根据银/金试剂的比例而变化,并具有水核。模板替代化学反应快速,高度可扩展,使用最少的有毒试剂,并且在许多情况下是真正的“一锅法”合成。最小的纳米壳(直径20 nm,壁厚7 nm)在飞秒的近红外飞秒光脉冲辐照下达到最高温度并退火,以最快的速度形成球形纳米颗粒,即使它们的等离子体激元共振不会像较大的纳米壳一样重叠(直径为50 nm,壁厚为7 nm)受800 nm波长激发。优化纳米壳结构以达到最高的纳米壳温度与优化结构以最大程度地吸收能量不同。

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