Organic
molecular monolayers (MoLs) have been used for improving the performance of various electronic device
structures. In this work, the concept of organic molecular surface
modification is applied for improving the performance of GaN-based
metal–semiconductor–metal (MSM) ultraviolet (UV) photodetectors
(PDs). Organic molecules of phenol-functionalized metallated porphyrin
(hydroxyl-phenyl-zinc-tetra-phenyl-porphyrin (Zn-TPPOH)) were adsorbed
on GaN, and Ni/Zn-TPPOH/GaN/Zn-TPPOH/Ni PD structures were fabricated.
This process was beneficial in two ways: first, the reverse-bias dark
current was reduced by 1000 times, and second, the photocurrent was
enhanced by ∼100 times, in comparison to the dark and photocurrent
values obtained for Ni/GaN/Ni MSM PDs, at high voltages of ±10
V. The responsivity of the devices was increased from 0.22 to 4.14
kA/W at 5 μW/cm2 optical power density at −10
V bias and at other voltages also. In addition to this, other PD parameters
such as photo-to-dark current ratio and UV-to-visible rejection ratio
were also enhanced. The spectral selectivity of the PDs was improved,
which means that the molecularly modified devices became more responsive
to UV spectral region and less responsive to visible spectral region,
in comparison to bare GaN-based devices. Photoluminescence measurements,
power-dependent photocurrent characteristics, and time-resolved photocurrent
measurements revealed that the MoL was passivating the defect-related
states on GaN. In addition, Kelvin probe force microscopy showed that
the MoL was also playing with the surface charge (due to surface states)
on GaN, leading to increased Schottky barrier height in dark conditions.
Resultant to both these phenomena, the reverse-bias dark current was
reduced for metal/MoL/GaN/MoL/metal PD structures. Further, the unusual
photoconductive gain in the molecularly modified devices has been
attributed to Schottky barrier lowering for UV-illuminated conditions,
leading to enhanced photocurrent.