TY - JOUR
T1 - Visualizing Ultrafast Electron Transfer Processes in Semiconductor-Metal Hybrid Nanoparticles
T2 - Toward Excitonic-Plasmonic Light Harvesting
AU - Camargo, Franco V.A.
AU - Ben-Shahar, Yuval
AU - Nagahara, Tetsuhiko
AU - Panfil, Yossef E.
AU - Russo, Mattia
AU - Banin, Uri
AU - Cerullo, Giulio
N1 - Publisher Copyright:
© 2021 The Authors. Published by American Chemical Society.
PY - 2021/2/10
Y1 - 2021/2/10
N2 - Recently, it was demonstrated that charge separation in hybrid metal-semiconductor nanoparticles (HNPs) can be obtained following photoexcitation of either the semiconductor or of the localized surface plasmon resonance (LSPR) of the metal. This suggests the intriguing possibility of photocatalytic systems benefiting from both plasmon and exciton excitation, the main challenge being to outcompete other ultrafast relaxation processes. Here we study CdSe-Au HNPs using ultrafast spectroscopy with high temporal resolution. We describe the complete pathways of electron transfer for both semiconductor and LSPR excitation. In the former, we distinguish hot and band gap electron transfer processes in the first few hundred fs. Excitation of the LSPR reveals an ultrafast (<30 fs) electron transfer to CdSe, followed by back-transfer from the semiconductor to the metal within 210 fs. This study establishes the requirements for utilization of the combined excitonic-plasmonic contribution in HNPs for diverse photocatalytic applications.
AB - Recently, it was demonstrated that charge separation in hybrid metal-semiconductor nanoparticles (HNPs) can be obtained following photoexcitation of either the semiconductor or of the localized surface plasmon resonance (LSPR) of the metal. This suggests the intriguing possibility of photocatalytic systems benefiting from both plasmon and exciton excitation, the main challenge being to outcompete other ultrafast relaxation processes. Here we study CdSe-Au HNPs using ultrafast spectroscopy with high temporal resolution. We describe the complete pathways of electron transfer for both semiconductor and LSPR excitation. In the former, we distinguish hot and band gap electron transfer processes in the first few hundred fs. Excitation of the LSPR reveals an ultrafast (<30 fs) electron transfer to CdSe, followed by back-transfer from the semiconductor to the metal within 210 fs. This study establishes the requirements for utilization of the combined excitonic-plasmonic contribution in HNPs for diverse photocatalytic applications.
KW - hot-electron transfer
KW - localized surface plasmon resonances
KW - photocatalysis
KW - semiconductor nanoparticles
KW - ultrafast optical spectroscopy
UR - http://www.scopus.com/inward/record.url?scp=85100278100&partnerID=8YFLogxK
U2 - 10.1021/acs.nanolett.0c04614
DO - 10.1021/acs.nanolett.0c04614
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C2 - 33481610
AN - SCOPUS:85100278100
SN - 1530-6984
VL - 21
SP - 1461
EP - 1468
JO - Nano Letters
JF - Nano Letters
IS - 3
ER -