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链烷硫醇引起的颗粒间间距变化对纳米晶金膜表面等离子体带及其他性质的影响。

Effects of changes in the interparticle separation induced by alkanethiols on the surface plasmon band and other properties of nanocrystalline gold films.

作者信息

Agrawal Ved Varun, Varghese Neenu, Kulkarni G U, Rao C N R

机构信息

Chemistry and Physics of Material Unit and DST Unit on Nanoscience, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur P.O., Bangalore 560064, India.

出版信息

Langmuir. 2008 Mar 18;24(6):2494-500. doi: 10.1021/la703237m. Epub 2008 Feb 16.

Abstract

Effects of changing the interparticle separation on the surface plasmon bands of ultrathin films of gold nanoparticles have been investigated by examining the interaction of alkanethiols of varying chain length on nanocrystalline gold films generated at the organic-aqueous interface. Adsorption of alkanethiols causes blue-shifts of the surface plasmon adsorption band, the magnitude of the shift being proportional to the chain length. The disordered nanocrystals thus created (lambdamax, 530 m) are in equilibrium with the ordered nanocrystals in the film (lambdamax, 700 m) as indicated by an isosbestic point around 600 nm. Long chain thiols disintegrate or disorder the gold films more effectively, as demonstrated by the increased population of the thiol-capped gold nanocrystals in solution. The rate of interaction of the thiols with the film decreases with the decreasing chain length. The effect of an alkanethiol on the spectrum of the gold film is specific, in that the effects with long and short chains are reversible. The changes in the plasmon band of gold due to interparticle separation can be satisfactorily modeled on the basis of the Maxwell-Garnett formalism. Spectroscopic studies, augmented by calorimetric measurements, suggest that the interaction of alkanethiols involves two steps, the first step being the exothermic gold film-thiol interaction and the second step includes the endothermic disordering process followed by further thiol capping of isolated gold particles.

摘要

通过研究不同链长的链烷硫醇在有机 - 水界面生成的纳米晶金膜上的相互作用,考察了改变颗粒间间距对金纳米颗粒超薄膜表面等离子体带的影响。链烷硫醇的吸附导致表面等离子体吸附带发生蓝移,蓝移的幅度与链长成正比。由此产生的无序纳米晶体(λmax,530nm)与膜中的有序纳米晶体(λmax,700nm)处于平衡状态,这由600nm左右的等吸收点表明。长链硫醇能更有效地使金膜分解或无序化,溶液中硫醇封端的金纳米晶体数量增加就证明了这一点。硫醇与膜的相互作用速率随链长的减小而降低。链烷硫醇对金膜光谱的影响是特定的,即长链和短链的影响是可逆的。基于麦克斯韦 - 加尼特形式理论,可以令人满意地模拟由于颗粒间间距导致的金等离子体带的变化。光谱研究结合量热测量表明,链烷硫醇的相互作用涉及两个步骤,第一步是放热的金膜 - 硫醇相互作用,第二步包括吸热的无序化过程,随后是孤立金颗粒的进一步硫醇封端。

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