Issue 32, 2025

Guided mode resonance-driven photoluminescence enhancement and angular emission control in a 2D dielectric photonic lattice

Abstract

Utilizing fluorescent emitters with precisely designed nanostructures regulates their emission characteristics, which has great potential in light-emitting devices, biosensing, and quantum technologies. In this context, we propose a large area nanostructured design on a flexible polyethylene terephthalate (PET) substrate by patterning it in a square periodic symmetry and coating it with a TiO2 thin layer to demonstrate cost-effective photoluminescence enhancement and directionality. The proposed design enables a controlled light emission enhancement of about 110 times from the emitter layer over the array through resonance-mediated light confinement. Such mode confinement leads to an increase in the local density of states, which leads to a 100-fold increase in the Purcell factor. Beyond amplification, the polarization-dependent excitation of GMR modes enables directional coupling of photoluminescence into the radiative zeroth-order channel, resulting in well-defined angular emission profiles, as validated by angle-resolved spectroscopy and back focal plane imaging for both transverse electric and transverse magnetic polarization of incident light. The proposed large-area photonic array on a PET substrate offers potential for incorporation into advanced light-emitting optical devices, owing to its scalability and adaptability for practical applications.

Graphical abstract: Guided mode resonance-driven photoluminescence enhancement and angular emission control in a 2D dielectric photonic lattice

Supplementary files

Article information

Article type
Communication
Submitted
21 May 2025
Accepted
21 Jul 2025
First published
30 Jul 2025

Nanoscale, 2025,17, 18560-18570

Guided mode resonance-driven photoluminescence enhancement and angular emission control in a 2D dielectric photonic lattice

J. Ahuja, S. Pandey, S. Devinder, J. Sardana, A. Tiwari, N. Subramaniyam and J. Joseph, Nanoscale, 2025, 17, 18560 DOI: 10.1039/D5NR02160J

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