4.5 Article

Au/NiFe/M(Au, MoS2, graphene) trilayer magnetoplasmonics DNA-hybridized sensors with high record of sensitivity

Journal

JOURNAL OF BIOMEDICAL OPTICS
Volume 22, Issue 12, Pages -

Publisher

SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS
DOI: 10.1117/1.JBO.22.12.127001

Keywords

magnetoplasmonic; magneto-optical-biosensor; DNA; MoS2; graphene

Funding

  1. Alzahra University research deputy
  2. Iran Science Elites Federation (ISEF)
  3. Iran's National Elites Foundation (INEF)
  4. Iran's Cognitive Sciences and Technologies Council [2714]

Ask authors/readers for more resources

The demonstration of biosensors based on the surface plasmon effect holds promise for future high-sensitive electrodeless biodetection. The combination of magnetic effects with surface plasmon waves brings additional freedom to improve sensitivity and signal selectivity. Stacking biosensors with two-dimensional (2-D) materials, e.g., graphene (Gr) and MoS2, can influence plasmon waves and facilitate surface physiochemical properties as additional versatility aspects. We demonstrate magnetoplasmonic biosensors through the detuning of surface plasmon oscillation modes affected by magnetic effect via the presence of the NiFe (Py) layer and different light absorbers of Gr, MoS2, and Au ultrathin layers in three stacks of Au/Py/M(MoS2, Gr, Au) trilayers. We found minimum reflection, resonance angle shift, and transverse magneto-optical Kerr effect (TMOKE) responses of all sensors in the presence of the ss-DNA monolayer. Very few changes of similar to 5x 10(-7) in the ss-DNA's refractive index result in valuable TMOKE response. We found that the presence of three-layer Gr and two-layer MoS2 on top of the Au/Py bilayer can dramatically increase the sensitivity by nine and four times, respectively, than the conventional Au/Co/Au trilayer. Our results show the highest reported DNA sensitivity ased on the coupling of light with 2-D materials in magnetoplasmonic devices. (C) 2017 society of Photo-Optical Instrumentation Engineers (SPIE)

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