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In Situ Investigation of Dynamic Silver Crystallization Driven by Chemical Reaction and Diffusion

机译:化学反应和扩散驱动的动态银结晶的原位研究

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摘要

Rational synthesis of materials is a long-term challenging issue due to the poor understanding on the formation mechanism of material structure and the limited capability in controlling nanoscale crystallization. The emergent in situ electron microscope provides an insight to this issue. By employing an in situ scanning electron microscope, silver crystallization is investigated in real time, in which a reversible crystallization is observed. To disclose this reversible crystallization, the radicals generated by the irradiation of electron beam are calculated. It is found that the concentrations of radicals are spatiotemporally variable in the liquid cell due to the diffusion and reaction of radicals. The fluctuation of the reductive hydrated electrons and the oxidative hydroxyl radicals in the cell leads to the alternative dominance of the reduction and oxidation reactions. The reduction leads to the growth of silver crystals while the oxidation leads to their dissolution, which results in the reversible silver crystallization. A regulation of radical distribution by electron dose rates leads to the formation of diverse silver structures, confirming the dominant role of local chemical concentration in the structure evolution of materials.
机译:由于对材料结构的形成机理了解甚少,并且控制纳米级结晶的能力有限,因此材料的合理合成是一个长期的挑战性问题。新兴的原位电子显微镜为这一问题提供了见识。通过使用原位扫描电子显微镜,实时研究了银的结晶,其中观察到可逆的结晶。为了公开这种可逆结晶,计算了通过电子束照射产生的自由基。已经发现,由于自由基的扩散和反应,在液体池中自由基的浓度在时空上是可变的。电池中还原性水合电子和氧化性羟基自由基的波动导致还原和氧化反应的替代优势。还原导致银晶体的生长,而氧化导致它们的溶解,从而导致可逆的银结晶。电子剂量率对自由基分布的调节导致形成各种银结构,从而证实了局部化学浓度在材料结构演变中的主导作用。

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