Single-molecule imaging and kinetic analysis of intermolecular polyoxometalate reactions
Jack W. Jordan, Kayleigh L. Y. Fung, Stephen T. Skowron, Christopher S. Allen, Johannes Biskupek, Graham N. Newton, Ute Kaiser, Andrei N. Khlobystov
Abstract
an intermediate state of an oxide nanowire. Kinetic analysis enabled by controlled variation of the electron flux in TEM revealed the reaction to be highly flux-dependent, which leads to reaction rates too fast to follow under the standard TEM imaging conditions. Although this presents a challenge for traditional structural characterisation of POM molecules, we harness this effect by controlling the conditions around the molecules and tuning the imaging parameters in TEM, which combined with theoretical modelling and image simulation, can shed light on the atomistic mechanisms of the reactions of POMs. This approach, based on the direct space and real time chemical reaction analysis by TEM, adds a new method to the arsenal of single-molecule kinetics techniques.