Camargo Franco V A, Ben-Shahar Yuval, Nagahara Tetsuhiko, Panfil Yossef E, Russo Mattia, Banin Uri, Cerullo Giulio
Dipartimento di Fisica, IFN-CNR, Politecnico di Milano, Piazza Leonardo da Vinci 32, Milan 20133, Italy.
Institute of Chemistry and Center for Nanoscience & Nanotechnology, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.
Nano Lett. 2021 Feb 10;21(3):1461-1468. doi: 10.1021/acs.nanolett.0c04614. Epub 2021 Jan 22.
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.
最近的研究表明,在混合金属 - 半导体纳米颗粒(HNP)中,通过光激发半导体或金属的局域表面等离子体共振(LSPR)都可以实现电荷分离。这暗示了光催化系统同时受益于等离子体和激子激发的有趣可能性,而主要挑战在于战胜其他超快弛豫过程。在此,我们使用具有高时间分辨率的超快光谱技术研究了CdSe - Au HNP。我们描述了半导体和LSPR激发下电子转移的完整路径。在前者中,我们区分了最初几百飞秒内的热电子转移和带隙电子转移过程。LSPR的激发揭示了向CdSe的超快(<30飞秒)电子转移,随后在210飞秒内从半导体反向转移回金属。这项研究确定了在各种光催化应用中利用HNP中激子 - 等离子体联合作用的要求。