Predicting and Probing the Local Temperature Rise Around Plasmonic Core–Shell Nanoparticles to Study Thermally Activated Processes

Ultrafast spectroscopy can be used to study dynamic processes on femtosecond to nanosecond timescales, but is typically used for photoinduced processes. Several materials can induce ultrafast temperature rises upon absorption of femtosecond laser pulses, in principle allowing to study thermally activated processes, such as (catalytic) reactions, phase transitions, and conformational changes. Gold–silica core–shell nanoparticles are particularly interesting for this, as they can be used in a wide range of media and are chemically inert. Here we computationally model the temporal and spatial temperature profiles of gold nanoparticles with and without silica shell in liquid and gas media. Fast rises in temperature within tens of picoseconds are always observed. This is fast enough to study many of the aforementioned processes. We also validate our results experimentally using a poly(urethane‐urea) exhibiting a temperature‐dependent hydrogen bonding network, which shows local temperatures above 90 °C are reached on this timescale. Moreover, this experiment shows the hydrogen bond breaking in such polymers occurs within tens of picoseconds. Gold–silica core–shell nanoparticles can transform light into ultrafast temperature rises. We show computationally that they can heat the environment in tens of picoseconds in different media and we also show experimentally that high local temperatures can be reached on this timescale. This shows the potential of these nanoparticles as chemically inert nanoheaters to study thermally activated processes using pump–probe spectroscopy.