期刊
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 1, 期 17, 页码 2530-2535出版社
AMER CHEMICAL SOC
DOI: 10.1021/jz1008399
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资金
- NSF [CHE-0239688]
- NIRT [CTS-0608896]
Femtosecond transient absorption (TA) is used to investigate population dynamics of electronic states in CdTe/CdSe core/shell nanocrystals (NCs) with varying CdSe shell coverage. Upon CdSe shell growth, the CdTe/CdSe NCs show a gradual evolution of surface passivation toward a quasi-type-II charge separation regime. Our results indicate that ultrafast electron transfer (ET) through the interface of CdTe/CdSe NCs becomes measurable as the CdSe shell approaches the quasi-type-II regime which we experimentally determined to be at 0.4 nm (shell) for a 3.4 nm CdTe core. This work reports the first measurement using femtosecond TA to study the electronic states in CdTe/CdSe NCs and spectroscopically observe the evolution of an ultrafast charge transfer (CT) in such a core/shell system. Time-resolved photoluminescence (PL) spectroscopy is used to study the radiative lifetimes of the CdTe/CdSe NCs. One monolayer CdSe coverage leads to longer-lived PL, which is red-shifted by 140 nm compared to the CdTe core PL. It is concluded that this is due to greater electron hole separation providing a longer-lived CT state.
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