4.6 Article

Bloch Surface Waves and Internal Optical Modes-Driven Photonic Crystal-Coupled Emission Platform for Femtomolar Detection of Aluminum Ions

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 124, Issue 13, Pages 7341-7352

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.9b11092

Keywords

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Funding

  1. Tata Education and Development Trust [TEDT/MUM/HEA/SSSIHL/2017-2018/0069-RM-db]
  2. Prasanthi Trust, Inc., United States [2206-2018]
  3. DST-Technology Development Program [IDP/MED/19/2016]
  4. DST-Inspire Fellowship, Govt. of India [IF180392]
  5. DST-Advanced Manufacturing Technology Program [DST/TDT/AMT/2017/050]

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The intrinsically lossy nature of plasmonic-based detection platforms necessitates the use of alternative nanophotonic platforms such as one-dimensional photonic crystals (1DPhCs) to exploit properties pertaining to photonic stop band (PSB), Bloch surface waves (BSWs), microcavity, and band-edge modes. We present a highly desirable confinement of internal optical modes (IOMs) and large surface electromagnetic (EM) field due to BSWs on a plasmon-free, metal template-free, photonic crystal-coupled emission (PCCE) platform ensuing 44-fold emission enhancements of the, otherwise, omnidirectionally emitting radiating dipoles. The effect of dielectric thickness in the PCCE platform has also been explored, and the optimized thicknesses for enhanced coupling of both BSWs and IOMs with the radiating dipoles have been obtained. Cavity engineering involving quantum emitters sandwiched in hot spots between 1DPhCs and Ag nanoparticles (AgNPs) has delivered similar to 200-fold emission enhancements on account of the improved local density of states (LDOS) via exceptional EM field trapping by BSWs, IOMs, and localized surface plasmon resonance (LSPR) of plasmonic nanoparticles. Experimental results that are in strong agreement with the numerically calculated data validate this augmentation in enhancements due to the amplified coupling between the radiating dipoles and modes supported by 1DPhCs. Moreover, the tightly entrapped optical energy within the hot spots between AgNPs and 1DPhCs was adopted for sensing environmentally hazardous Al3+ ions at a 0.21 parts per quadrillion (ppq) limit of detection in drinking water samples with reliable and reproducible results, opening new avenues for investigating distinctive photonic crystal nanoarchitectures as a robust, practical, and user-friendly technology for multiplexed diagnostic fluorescence assays.

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