Abstract
Silver represents, by and large, the best plasmonic metal available, due to its very low optical losses in a broad photon-energy range encompassing all the visible optical spectrum. Its performances are, more often than not, severely hampered by the presence of a few-nanometer thick surface-tarnish layer; thermal annealing under high-vacuum (HV) conditions may however lead to its decomposition, thereby allowing to attain the clean-metal response. Here, we report an experimental investigation of the temperature dependence of the plasmonic response of Ag nanoparticles, either clean or tarnished, by means of in situ optical spectroscopies under HV conditions. For tarnished nanoparticles, we observed the temperature dynamics of thermal decomposition of the contamination layer in real time and compared it with the corresponding behavior of spatially extended, flat surfaces. For clean Ag nanoparticles we witness instead a remarkable temperature invariance of the localized-plasmon response, indicating Ag as a potential candidate for temperature-invariant thermoplasmonics applications.
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