Operando electrochemical SERS monitors nanoparticle reactions by capping agent fingerprints

Nano Research(2022)

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摘要
Nanomaterials are frequently employed in daily life goods, including health, textile, and food industry. A comprehensive picture is lacking on the role of the capping agents, added ligand molecules, in case of nanoparticle reactions and degradation in aqueous solutions, like surface waters or biofluids. Here, we aim to elucidate the capping agent influence on nanoparticle reactivity probing two commonly employed capping agents citrate and polyvinylpyrrolidone (PVP). Their influence on silver nanoparticle (AgNP) transformation is studied, which is particularly important due to its application as an antimicrobial agent. We induce oxidation and reduction processes of AgNPs in halide solutions and we monitor the associated transformations of particles and capping agents by spectro-electrochemical surface-enhanced Raman spectroscopy (SERS). Raman bands of the capping agents are used here to track chemical changes of the nanoparticles under operando conditions. The sparingly soluble and non-plasmon active silver salts (AgBr and AgCl) are formed under potential bias. In addition, we spectroscopically observe plasmon-mediated structural changes of citrate to cis- or trans-aconitate, while PVP is unaltered. The different behavior of the capping agents implies a change in the physical properties on the surface of AgNPs, in particular with respect to the surface accessibility. Moreover, we showcase that reactions of the capping agents induced by different external stimuli, such as applied bias or laser irradiation, can be assessed. Our results demonstrate how SERS of capping agents can be exploited to operando track nanoparticle conversions in liquid media. This approach is envisaged to provide a more comprehensive understanding of nanoparticle fates in complex liquid environments and varied redox conditions.
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关键词
capping agent,electrochemical surface-enhanced Raman spectroscopy,silver nanoparticle,nanoparticle reaction
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