Hexagonal
boron nitride (h-BN), a two-dimensional-layered material,
exhibits the outstanding properties of ultrawide band gap, high absorption
coefficient, and high chemical and thermal stability. Because of these
appealing properties, h-BN has emerged as a suitable material for
the fabrication of deep-ultraviolet (UV) photodetectors (PDs). We
demonstrate plasmonic-enhanced deep-UV PDs based on h-BN nanosheets
by utilizing localized surface plasmon resonance in Al nanoparticles
(NPs) in the deep-UV region. Using a cost-effective and efficient
method of dewetting, different sizes of NPs are deposited on h-BN
layers, and their effect on PDs is investigated. Upon performing a
detailed set of photoelectrical measurements, we establish that the
presence of NPs leads to a significant enhancement in the illumination
current and related performance parameters of the PDs. By using an
extremely low value of the incident optical power density of 2.5 μW
cm–2, a significant enhancement by 5.5 times is
observed in the current at a deep-UV wavelength of 205 nm. Moreover,
at a low input voltage of 1 V, the responsivity improves by ∼60%,
without degrading the UV–visible rejection ratio of the PDs.
The mechanism behind the enhancement is investigated in detail by
numerical simulation of the absorbance spectra and electric field
intensity distributions of the Al NPs. Furthermore, even after surface
modification of h-BN, the speed of the PDs remains almost unaffected,
thereby establishing the effectiveness of the approach used to improve
the PDs.