Metal-Halide-Ligated Cadmium Selenide Quantum Belts by Facile Surface Exchange
Yuewei Yao, Yang Zhou, William M. Sanderson, Richard A. Loomis, William E. Buhro
Index: 10.1021/acs.chemmater.8b01294
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Abstract
Amine-ligated {CdSe[n-octylamine]0.53±0.06} quantum belts undergo instantaneous, reversible exchange of the L-type amine ligation for Z-type ligation provided by the neutral metal halides MX2 (M = Cd, Zn; X = Cl, Br, I). The CdX2-ligated quantum belts are determined to have the compositions {CdSe[CdCl2]1.23}, {CdSe[CdBr2]1.03}, and {CdSe[CdI2]0.42}, corresponding to two, two, and one CdX2 monolayer shells, respectively. Exchange from L-type to Z-type MX2 ligation results in large shifts of the quantum-belt absorption (extinction) features to lower energy, which are 252, 151, and 157 meV for CdCl2, CdBr2, and CdI2 ligation, respectively. These spectral shifts, which are due to changes in the strain states of the quantum belts (QBs), and extension of the CdSe crystal lattice by surface coordination of the ligand Cd atoms, are rapidly and completely reversed by back exchange to n-octylamine ligation. Similar, reversible spectral shifts are observed upon L-type to Z-type exchange with ZnX2 ligation, although the shifts are smaller in magnitude. The results demonstrate the facility, reversibility, and generality of L-type for Z-type surface exchanges in wurtzite CdSe quantum belts, and that neutral metal halides may function as Z-type ligands in semiconductor nanocrystals.