Organic phototransistors (OPTs) have
attracted enormous attention
because of their promising applications in sensing, communication,
and imaging. Currently, most OPTs reported utilize field-effect transistors
(FETs) with relative long channel length which usually has undesired
amplification because of their inherent low transconductance originated
from their low channel capacitance, limiting the further improvement
of performance. Herein, a vertical channel hybrid electrochemical
phototransistor with a nanoscale channel and large transconductance
(VECPT) is invented for the first time to achieve ultrahigh photoresponsivity
along with a fast response speed. Benefiting from the nanoscale channel
length and large transconductance, the photo-generated carriers in
channel can be efficiently dissociated, transported, and amplified
into the enlarged photocurrent output. Therefore, the devices deliver
substantially improved optoelectronic performances with a photoresponsivity
as high as ≈2.99 × 107 A/W, detectivity of
≈1.49 × 1013 Jones, and fast-speed response
of ≈73 μs under a low voltage of 1 V, which are superior
to those of the reported OPTs based on FETs. Moreover, the in situ
Kelvin probe microscopy is performed to characterize the surface potential
of device systems for better elucidating the photosensing mechanism.
Furthermore, taking advantage of its excellent optoelectronic performance,
an ultraviolet light monitoring system is constructed by integrating
VECPT with a light-emitting diode, which also shows the real-time,
high-sensitive, and controllable photoresponse threshold properties.
All these results demonstrate the great potential of these electrochemical
phototransistors and provide valuable insights into the design of
the nanoscale channel length device system for high-performance photodetection.