Intraband quantum dots are degenerately doped semiconductor nanomaterials
that exhibit unique optical properties in mid- to long-wavelength
infrared. To date, these quantum dots have been only studied as lateral
photoconductive devices, while transitioning toward a vertically stacked
structure can open diverse opportunities for investigating advanced
device designs. Here, we report the first vertical intraband quantum
dot heterojunction devices composed of Ag2Se/PbS/Ag2Se quantum dot stacks that bring the advantage of reduced
dark conductivity with a simplified device fabrication procedure.
We discuss the improvement in the colloidal synthesis of Ag2Se quantum dots that are critical for vertical device fabrication,
identify an important process that determines the mid-wavelength infrared
responsivity of the quantum dot film, and analyze the basic device
characteristics and key detector performance parameters. Compared
to the previous generation of Ag2Se quantum dot-based photoconductive
devices, approximately 70 times increase in the mid-wavelength responsivity,
at room temperature, is observed.
In recent years, there has been increasing interest in leveraging two-dimensional (2D) van der Waals (vdW) crystals for infrared (IR) photodetection, exploiting their unusual optoelectrical properties. Some 2D vdW materials with small band gap energies such as graphene and black phosphorus have been explored as stand-alone IR responsive layers in photodetectors. However, the devices incorporating these IR-sensitive 2D layers often exhibited poor performances owing to their preparation issues such as limited scalability and air instability. Herein, we explored wafer-scale 2D platinum ditelluride (PtTe 2 ) layers for near-to-mid IR photodetection by directly growing them onto silicon (Si) wafers. 2D PtTe 2 /Si heterojunctions exhibited wavelengthand intensity-dependent high photocurrents in a spectral range of ∼1−7 μm, significantly outperforming stand-alone 2D PtTe 2 layers. The observed superiority is attributed to their excellent Schottky junction characteristics accompanying suppressed carrier recombination as well as optical absorbance competition between 2D PtTe 2 layers and Si. The direct and scalable growth of 2D PtTe 2 layers was further extended to demonstrate mechanically flexible IR photodetectors.
As an emerging member of the colloidal
semiconductor quantum dot
materials family, intraband quantum dots are being extensively studied
for thermal infrared sensing applications. High-performance detectors
can be realized using a traditional p–n junction device design;
however, the heavily doped nature of intraband quantum dots presents
a new challenge in realizing diode devices. In this work, we utilize
a trait uniquely available in a colloidal quantum dot material system
to overcome this challenge: the ability to blend two different types
of quantum dots to control the electrical property of the resulting
film. We report on the preparation of binary mixture films containing
midwavelength infrared Ag2Se intraband quantum dots and
the fabrication of p–n heterojunction diodes with strong rectifying
characteristics. The peak specific detectivity at 4.5 μm was
measured to be 107 Jones at room temperature, which is
an orders of magnitude improvement compared to the previous generation
of intraband quantum dot detectors.
Various near-atom-thickness two-dimensional
(2D) van der Waals
(vdW) crystals with unparalleled electromechanical properties have
been explored for transformative devices. Currently, the availability
of 2D vdW crystals is rather limited in nature as they are only obtained
from certain mother crystals with intrinsically possessed layered
crystallinity and anisotropic molecular bonding. Recent efforts to
transform conventionally non-vdW three-dimensional (3D) crystals into
ultrathin 2D-like structures have seen rapid developments to explore
device building blocks of unique form factors. Herein, we explore
a “peel-and-stick” approach, where a nonlayered 3D platinum
sulfide (PtS) crystal, traditionally known as a cooperate mineral
material, is transformed into a freestanding 2D-like membrane for
electromechanical applications. The ultrathin (∼10 nm) 3D PtS
films grown on large-area (>cm2) silicon dioxide/silicon
(SiO2/Si) wafers are precisely “peeled” inside
water retaining desired geometries via a capillary-force-driven surface
wettability control. Subsequently, they are “sticked”
on strain-engineered patterned substrates presenting prominent semiconducting
properties, i.e., p-type transport with an optical
band gap of ∼1.24 eV. A variety of mechanically deformable
strain-invariant electronic devices have been demonstrated by this
peel-and-stick method, including biaxially stretchable photodetectors
and respiratory sensing face masks. This study offers new opportunities
of 2D-like nonlayered semiconducting crystals for emerging mechanically
reconfigurable and stretchable device technologies.
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