Abstract

Four sizes of water-soluble thiol-capped CdTe quantum dots (QDs) have been synthesized and used to investigate the photoluminescence (PL) responses to Ag + ions. For small particles, the CdTe QDs exhibit PL enhancement in the presence of lower concentration of Ag + but show obvious quenching with the further increase of Ag +; for larger particles, however, PL of CdTe QDs is quenched all the time with the Ag + addition, no PL enhancement is observed. Mechanism study shows that small QDs with more traps on the particle surface are effectively passivated by initial adsorbed Ag +, which accounts for the PL enhancement observed; after the initial traps are saturated, the excess Ag + facilitates nonradiative recombination, resulting in PL quenching. For larger particles, the nonradiative recombination dominates the whole process even for the lower concentration of Ag +, due to the fewer traps on the QD surface. Compared with larger particles, the small CdTe QDs are more suitable for sensing Ag + because of the more sensitive and selective PL response. To our best knowledge, this is the first systematical study on the interaction of Ag + with different-sized CdTe QDs.

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