1 research outputs found
Charge Transport Across Au–P3HT–Graphene van der Waals Vertical Heterostructures
Hybrid van der Waals heterostructures based on 2D materials
and/or
organic thin films are being evaluated as potential functional devices
for a variety of applications. In this context, the graphene/organic
semiconductor (Gr/OSC) heterostructure could represent the core element
to build future vertical organic transistors based on two back-to-back
Gr/OSC diodes sharing a common graphene sheet, which functions as
the base electrode. However, the assessment of the Gr/OSC potential
still requires a deeper understanding of the charge carrier transport
across the interface as well as the development of wafer-scale fabrication
methods. This work investigates the charge injection and transport
across Au/OSC/Gr vertical heterostructures, focusing on poly(3-hexylthiophen-2,5-diyl)
as the OSC, where the PMMA-free graphene layer functions as the top
electrode. The structures are fabricated using a combination of processes
widely exploited in semiconductor manufacturing and therefore are
suited for industrial upscaling. Temperature-dependent current–voltage
measurements and impedance spectroscopy show that the charge transport
across both device interfaces is injection-limited by thermionic emission
at high bias, while it is space charge limited at low bias, and that
the P3HT can be assumed fully depleted in the high bias regime. From
the space charge limited model, the out-of-plane charge carrier mobility
in P3HT is found to be equal to μ ≈ 2.8 × 10–4 cm2 V–1 s–1, similar to the in-plane mobility reported in previous works, while
the charge carrier density is N0 ≈
1.16 × 1015 cm–3, also in agreement
with previously reported values. From the thermionic emission model,
the energy barriers at the Gr/P3HT and Au/P3HT interfaces result in
0.30 eV and 0.25 eV, respectively. Based on the measured barriers
heights, the energy band diagram of the vertical heterostructure is
proposed under the hypothesis that P3HT is fully depleted
