The exchange kinetics of octylamine between a free state and a state bound to the surface of CdSe quantum dots is analyzed using nuclear magnetic resonance (NMR) spectroscopy in solution. On the basis of 1D 1 H and DOSY and NOESY spectroscopy, we find that all octylamine molecules present interact with the CdSe quantum dot surface, although the octylamine resonances and diffusion coefficient resemble those of free octylamine. This indicates that these NMR observables are a weighted average of a free and a bound state, implying that the overall octylamine exchange rate is fast as compared to the intrinsic NMR time scale. A lower limit on the first-order desorption rate constant of 50 s -1 follows from DOSY measurements as a function of the diffusion delay. This result is compared with literature data based on the quenching of the CdSe photoluminescence upon alkylamine desorption.
SECTION Nanoparticles and NanostructuresL igands provide physicochemical functionality to colloidal nanoparticles (NPs). Used during synthesis to control nucleation and growth, they end up as a monolayer covering the NP surface and stabilizing the NP colloidal dispersion. After synthesis, they can be exchanged by others, and this has proven to be a powerful method to functionalize colloidal NPs, with the aim of, for example, raising their photoluminescence quantum yield, 1 rendering them biocompatible and bioselective 2,3 or enhancing their conductivity for applications in electronics 4,5 and photovoltaics. 6 In line with the increasing importance of NP ligands, a number of studies have addressed the interaction between ligands and NPs, and at the same time, a number of experimental techniques like nuclear magnetic resonance spectroscopy (NMR), 7-10 infrared spectroscopy, 11 or photoluminescence spectroscopy 1,12-14 were developed to investigate ligands bound to colloidal NPs.An interesting model system in this respect is CdSe quantum dots (Q-CdSe) stabilized by alkylamines. It has been shown by a number of authors that alkylamines strongly enhance the Q-CdSe photoluminescence (PL). 1,12,15 On the basis of this, the increase or decrease of the Q-CdSe PL intensity has been interpreted in terms of an increased or reduced surface coverage by alkylamines, which means that the PL quantum yield is used as an indirect probe of the ligand surface coverage. 12 As a result, a number of adsorption isotherms and rate constants for desorption have been published. With desorption rates ranging from 0.01 to 1.5 Â 10 -4 s -1 , 1,12 all of these studies point toward a dynamic yet relatively strong binding of alkylamines to Q-CdSe. This contrasts with the fast exchange rates determined in a NMR spectroscopy study on Q-CdTe stabilized by dodecylamine (DDA) and on Q-ZnO stabilized by octylamine (OctA). 16 In both cases, the QDs are observed to be dynamically stabilized by alkylamines, with an overall exchange rate exceeding 100 s -1 for Q-CdTe. In contrast to PL spectroscopy, NMR can directly address the ligands. Apart from simply identifying and q...