Volume 17, Issue 27 2004836
Full Paper

Synthesis and Photophysical Properties of Light-Harvesting Gold Nanoclusters Fully Functionalized with Antenna Chromophores

Kyunglim Pyo

Kyunglim Pyo

Department of Chemistry, Yonsei University, Seoul, 03722 Republic of Korea

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Hongmei Xu

Hongmei Xu

Department of Chemistry, Yonsei University, Seoul, 03722 Republic of Korea

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Sang Myeong Han

Sang Myeong Han

Department of Chemistry, Yonsei University, Seoul, 03722 Republic of Korea

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Shivi Saxena

Shivi Saxena

Department of Chemistry, Western Michigan University, Kalamazoo, MI, 49008 USA

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Sook Young Yoon

Sook Young Yoon

Department of Chemistry, Yonsei University, Seoul, 03722 Republic of Korea

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Gary Wiederrecht

Gary Wiederrecht

Center for Nanoscale Materials, Argonne National Laboratory, Chicago, IL, 60439 USA

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Guda Ramakrishna

Corresponding Author

Guda Ramakrishna

Department of Chemistry, Western Michigan University, Kalamazoo, MI, 49008 USA

E-mail: [email protected], [email protected]

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Dongil Lee

Corresponding Author

Dongil Lee

Department of Chemistry, Yonsei University, Seoul, 03722 Republic of Korea

E-mail: [email protected], [email protected]

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First published: 09 February 2021
Citations: 11

Abstract

The development of efficient light-harvesting systems is important to understand the key aspects of solar-energy conversion processes and to utilize them in various photonic applications. Here, atomically well-defined gold nanoclusters are reported as a new platform to fabricate artificial light-harvesting systems. An efficient amide coupling method is developed to synthesize water-soluble Au22 clusters fully protected with pyrene chromophores by taking advantage of their facile phase-transfer reaction. The synthesized Au22 clusters with densely packed 18 pyrene chromophores (Au22–PyB18) exhibit triple-emission in blue, green, and red wavelength regions arising respectively from pyrene monomer, pyrene excimer, and Au22 emission, producing bright white light emission together. The photoluminescence of Au22 is enhanced by more than tenfold, demonstrating that pyrenes at the periphery efficiently channel the absorbed energy to the luminescent Au22 at the center. A combination of femtosecond transient absorption and anisotropy measurements of Au22–PyB18 explicitly reveals three main decay components of 220 fs, 3.5 ps, and 160 ps that can be assigned to energy migration between pyrenes and energy transfer processes from pyrene monomer and excimer to the central Au22, respectively.

Conflict of Interest

The authors declare no conflict of interest.

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