TY - JOUR
T1 - Microcavity-Mediated Spectrally Tunable Amplification of Absorption in Plasmonic Nanoantennas
AU - Huang, Qinglan
AU - Cunningham, Brian T.
N1 - Funding Information:
This work is supported by the National Science Foundation (Grant 1512043). Q.H. thanks the Sah Fellowship at the University of Illinois, Urbana–Champaign. The authors are grateful to Dr. Jui-Nung Liu for his participation in the design and implementation of instrument used to gather 1- R - T data and useful discussions. Dr. Liu declined to be listed as a coauthor for this paper. The authors would like to acknowledge Dr. Kathy Walsh and Dr. Jade Wang at the Materials Research Laboratory for assistance in material characterization.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/8/14
Y1 - 2019/8/14
N2 - Nanoantenna-microcavity hybrid systems offer unique platforms for the study and manipulation of light at the nanoscale, since their constituents have either low mode volume or long photon storage time. A nearby dielectric optical cavity can modify the photonic environment surrounding a plasmonic nanoantenna, presenting opportunities to sculpt its spectral response. However, matching the polar opposites for enhanced light-matter interactions remains challenging, as the antenna can be rendered transparent by the cavity through destructive Fano interferences. In this work, we tackle this issue by offering a new plasmonic-photonic interaction framework. By coupling to a photonic crystal guided resonance, a gold nanostar delivers 1 order of magnitude amplified absorption, and the ultrasharp Lorentzian-line-shaped hybrid resonance is continuously tunable over a broad spectral range by scanning of the incidence angle. Our intuitive coupled mode model reveals that a distinct optical pathway highlighting the cavity-mediated activation of nanoantennas is key for absorption enhancement. Moreover, we show that the line width of the enhancement can be widely tunable, and that the maximum power transferred to the antennas is attained under critical coupling. The cooperative hybrid system opens up new opportunities to boost a wealth of applications including ultrasensitive molecular spectroscopy, plasmonic hot carrier chemistry, thermoplasmonic, spontaneous emission enhancement, nanolasers, and many more.
AB - Nanoantenna-microcavity hybrid systems offer unique platforms for the study and manipulation of light at the nanoscale, since their constituents have either low mode volume or long photon storage time. A nearby dielectric optical cavity can modify the photonic environment surrounding a plasmonic nanoantenna, presenting opportunities to sculpt its spectral response. However, matching the polar opposites for enhanced light-matter interactions remains challenging, as the antenna can be rendered transparent by the cavity through destructive Fano interferences. In this work, we tackle this issue by offering a new plasmonic-photonic interaction framework. By coupling to a photonic crystal guided resonance, a gold nanostar delivers 1 order of magnitude amplified absorption, and the ultrasharp Lorentzian-line-shaped hybrid resonance is continuously tunable over a broad spectral range by scanning of the incidence angle. Our intuitive coupled mode model reveals that a distinct optical pathway highlighting the cavity-mediated activation of nanoantennas is key for absorption enhancement. Moreover, we show that the line width of the enhancement can be widely tunable, and that the maximum power transferred to the antennas is attained under critical coupling. The cooperative hybrid system opens up new opportunities to boost a wealth of applications including ultrasensitive molecular spectroscopy, plasmonic hot carrier chemistry, thermoplasmonic, spontaneous emission enhancement, nanolasers, and many more.
KW - Optical microcavity
KW - absorption enhancement
KW - coupling
KW - photonic crystal
KW - plasmonic nanoantenna
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U2 - 10.1021/acs.nanolett.9b01764
DO - 10.1021/acs.nanolett.9b01764
M3 - Article
C2 - 31315400
AN - SCOPUS:85070902357
SN - 1530-6984
VL - 19
SP - 5297
EP - 5303
JO - Nano Letters
JF - Nano Letters
IS - 8
ER -