As an alternative buffer material to CdS, Zn
x
Cd1–x
S buffer
layers for
vapor transport-deposited SnS thin-film solar cells (TFSCs) were fabricated
using the successive ionic layer adsorption and reaction (SILAR) method.
Varying the Zn-to-Cd ratio resulted in a series of Zn
x
Cd1–x
S thin films
with controllable band gaps in the range of 2.40–3.65 eV. The
influence of the Zn-to-Cd ratio on the cell performance was investigated
in detail. The Zn0.34Cd0.66S buffer layer was
found to be the optimal composition for SnS TFSCs, and a record open-circuit
voltage (V
oc) of 0.405 V was achieved
with an efficiency of 3.72%, whereas the SILAR-CdS buffer layer rendered
a V
oc of 0.324 V. The improvement in V
oc when using the Zn0.34Cd0.66S buffer layer was corroborated by the spike-type conduction band
offset of 0.35 eV with the SnS absorber, as revealed by the X-ray
photoelectron spectroscopy analysis. In addition, minimized interfacial
recombination at the SnS/Zn0.34Cd0.66S heterojunction
was confirmed by the temperature-dependent V
oc analysis under illuminated conditions.
In the present investigation, we have fabricated copper oxide (CuO) thin film memristor by employing a hydrothermal method for neuromorphic application. The X-ray diffraction pattern confirms the films are polycrystalline in nature with the monoclinic crystal structure. The developed devices show analog memory and synaptic property similar to biological neuron. The size dependent synaptic behavior is investigated for as-prepared and annealed CuO memristor. The results suggested that the magnitude of synaptic weights and resistive switching voltages are dependent on the thickness of the active layer. Synaptic weights are improved in the case of the as-prepared device whereas they are inferior for annealed CuO memristor. The rectifying property similar to a biological neuron is observed only for the as-prepared device, which suggested that as-prepared devices have better computational and learning capabilities than annealed CuO memristor. Moreover, the retention loss of the CuO memristor is in good agreement with the forgetting curve of human memory. The results suggested that hydrothermally grown CuO thin film memristor is a potential candidate for the neuromorphic device development.
The replacement of CdS buffer layer is desirable for the development of nontoxic, environmentally friendly kesterite thin-film solar cells (TFSCs). Recently, several ternary compound semiconductors have been extensively investigated as an alternative buffer layer for Cd-free TFSCs. Herein, the effectiveness of (NH 4 ) 2 S treatment on the surface properties of the absorber, as well as the device performance of atomic layer deposited (ALD) Zn(O,S) buffer-based CZTSSe solar cells, has been investigated. X-ray photoelectron spectroscopy (XPS) results showed that the elemental compositions of CZTSSe surface were significantly influenced by (NH 4 ) 2 S treatment, whereas the surface morphologies of the CZTSSe-absorber layers remained unaffected. The XPS results further suggested that the (NH 4 ) 2 S solution treatment substantially removed the native oxide layer from the CTZSSe absorber surface. The fabricated CZTSSe/Zn(O,S) device without (NH 4 ) 2 S treatment displayed an initial cell efficiency of 7.46%. The energy conversion efficiency increased significantly to 9.82% after the (NH 4 ) 2 S treatment of absorber layers for an optimum duration of 1 min; to the best of our knowledge, this is the highest efficiency achieved to date for Zn(O,S) bufferbased kesterite solar cells. The improved device performance is predominantly attributed to the pronounced increase in the fill factor (FF) of TFSCs resulting from the removal of oxides/hydroxides from the CZTSSe surface and passivation of absorber surface with sulfur species. However, increasing the treatment duration to 3 or 5 min resulted in the deterioration of cell efficiency, primarily due to the progressive degradation in the FF of the device. This study demonstrates a plausible route to improve the performance of Zn(O,S) buffer layer-based kesterite solar cells through a simple surface treatment of the absorber layers using (NH 4 ) 2 S solution.
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