7 research outputs found
Influence of tin doped TiO2 nanorods on dye sensitized solar cells
The one-step hydrothermal method was used to synthesize Sn-doped TiO2 (Sn-TiO2) thin films, in which the variation in Sn content ranged from 0 to 7-wt % and, further, its influence on the performance of a dye-sensitized solar cell (DSSC) photoanode was studied. The deposited samples were analyzed by X-ray diffraction (XRD) and Raman spectroscopy, which confirmed the existence of the rutile phase of the synthesized samples with crystallite size ranges in between 20.1 to 22.3 nm. In addition, the bare and Sn-TiO2 thin films showed nanorod morphology. A reduction in the optical band gap from 2.78 to 2.62 eV was observed with increasing Sn content. The X-ray photoelectron spectroscopy (XPS) analysis confirmed Sn4+ was successfully replaced at the Ti4+ site. The 3-wt % Sn-TiO2 based DSSC showed the optimum efficiency of 4.01%, which was superior to 0.87% of bare and other doping concentrations of Sn-TiO2 based DSSCs. The present work reflects Sn-TiO2 as an advancing material with excellent capabilities, which can be used in photovoltaic energy conversion devices
Ion-by-Ion Adsorption Process and Reaction for the Synthesis of Hierarchical Manganese Tungstate (MnWO<sub>4</sub>) Microflowers as an Energy-Efficient Electrode for Supercapacitors
For the first time, manganese tungstate (MnWO4) electrodes
are successfully synthesized by the successive ionic layer adsorption
and reaction (SILAR) method. This study is mainly focused on synthesized
hierarchical MnWO4 microflowers (MFs) for electrochemical
supercapacitor application. The crystalline structure, morphology,
presence of functional groups, stretching and bending vibration, and
availability of chemical states present in the MnWO4 MFs
are investigated using X-ray diffraction (XRD), scanning electron
microscopy (SEM), Fourier transform infrared, Raman, and X-ray photoelectron
spectroscopy, respectively. In addition, the resultant materials undergo
electrochemical analysis using a three-electrode system. As a result,
the MnW-50 electrode reveals a maximum specific capacitance (Cs) and
capacity (Csp) of 698 F/g and 87 mAh/g at 5 mA/cm2 with
moderate energy density (ED) and power density (PD) of 19 Wh/kg and
700 W/kg, respectively. Furthermore, the aqueous hybrid device is
fabricated using MnWO4 MFs as a cathode and reduced graphene
oxide (rGO) as an anode material, which reveals the maximum performance
of the Cs and Csp of 206 F/g and 87 mAh/g at 5 mV/s and 185 F/g and
70 mAh/g with sufficient ED, and PD of 45 Wh/kg and 1960 W/kg at 5
mA/cm2, respectively. The aforementioned results indicate
the benefits and improved electrochemical efficiency of MnWO4 MFs as cathodes for hybrid supercapacitors
Influence of Tin Doped TiO2 Nanorods on Dye Sensitized Solar Cells
The one-step hydrothermal method was used to synthesize Sn-doped TiO2 (Sn-TiO2) thin films, in which the variation in Sn content ranged from 0 to 7-wt % and, further, its influence on the performance of a dye-sensitized solar cell (DSSC) photoanode was studied. The deposited samples were analyzed by X-ray diffraction (XRD) and Raman spectroscopy, which confirmed the existence of the rutile phase of the synthesized samples with crystallite size ranges in between 20.1 to 22.3 nm. In addition, the bare and Sn-TiO2 thin films showed nanorod morphology. A reduction in the optical band gap from 2.78 to 2.62 eV was observed with increasing Sn content. The X-ray photoelectron spectroscopy (XPS) analysis confirmed Sn4+ was successfully replaced at the Ti4+ site. The 3-wt % Sn-TiO2 based DSSC showed the optimum efficiency of 4.01%, which was superior to 0.87% of bare and other doping concentrations of Sn-TiO2 based DSSCs. The present work reflects Sn-TiO2 as an advancing material with excellent capabilities, which can be used in photovoltaic energy conversion devices
Square-Facet Nanobar MOF-Derived Co<sub>3</sub>O<sub>4</sub>@Co/N-doped CNT Core–Shell-based Nanocomposites as Cathode Materials for High-Performance Supercapacitor Studies
The binary as well as ternary nanocomposites of the square-facet
nanobar Co-MOF-derived Co3O4@Co/N-CNTs (N-CNTs:
nitrogen-doped carbon nanotubes) with Ag NPs and rGO have been synthesized
via an easy wet chemical route, and their supercapacitor behavior
was then studied. At a controlled pH of the precursor solution, square-facet
nanobars of Co-MOF were first synthesized by the solvothermal method
and then pyrolyzed under a controlled nitrogen atmosphere to get a
core–shell system of Co3O4@Co/N-CNTs.
In the second step, different compositions of Co3O4@Co/N-CNT core–shell structures were formed by an ex-situ method with Ag NPs and rGO moieties. Among several
bare, binary, and ternary compositions tested in 6 M aqueous KOH electrolyte,
a ternary nanocomposite having a 7.0:1.5:1.5 stoichiometric ratio
of Co3O4@Co/N-CNT, Ag NPs, and rGO, respectively,
reported the highest specific capacitance (3393.8 F g–1 at 5 mV s–1). The optimized nanocomposite showed
the energy density, power density, and Coulombic efficiency of 74.1
W h.kg–1, 443.7 W.kg–1, and 101.3%,
respectively, with excellent electrochemical stability. After testing
an asymmetrical supercapacitor with a Co3O4@Co/N-CNT/Ag
NPs/rGO/nickel foam cathode and an activated carbon/nickel foam anode,
it showed 4.9 W h.kg–1 of energy density and 5000.0
W.kg–1 of power density
A Simple Aqueous Precursor Solution Processing of Earth-Abundant Cu<sub>2</sub>SnS<sub>3</sub> Absorbers for Thin-Film Solar Cells
A simple and eco-friendly method
of solution processing of Cu<sub>2</sub>SnS<sub>3</sub> (CTS) absorbers
using an aqueous precursor solution is presented. The precursor solution
was prepared by mixing metal salts into a mixture of water and ethanol
(5:1) with monoethanolamine as an additive at room temperature. Nearly
carbon-free CTS films were formed by multispin coating the precursor
solution and heat treating in air followed by rapid thermal annealing
in S vapor atmosphere at various temperatures. Exploring the role
of the annealing temperature in the phase, composition, and morphological
evolution is essential for obtaining highly efficient CTS-based thin
film solar cells (TFSCs). Investigations of CTS absorber layers annealed
at various temperatures revealed that the annealing temperature plays
an important role in further improving device properties and efficiency.
A substantial improvement in device efficiency occurred only at the
critical annealing temperature, which produces a compact and void-free
microstructure with large grains and high crystallinity as a pure-phase
absorber layer. Finally, at an annealing temperature of 600 °C,
the CTS thin film exhibited structural, compositional, and microstructural
isotropy by yielding a reproducible power conversion efficiency of
1.80%. Interestingly, CTS TFSCs exhibited good stability when stored
in an air atmosphere without encapsulation at room temperature for
3 months, whereas the performance degraded slightly when subjected
to accelerated aging at 80 °C for 100 h under normal laboratory
conditions
Aqueous-Solution-Processed Cu<sub>2</sub>ZnSn(S,Se)<sub>4</sub> Thin-Film Solar Cells via an Improved Successive Ion-Layer-Adsorption–Reaction Sequence
A facile improved successive ionic-layer
adsorption and reaction
(SILAR) sequence is described for the fabrication of Cu<sub>2</sub>ZnSnÂ(S,Se)<sub>4</sub> (CZTSSe) thin-film solar cells (TFSCs) via
the selenization of a precursor film. The precursor films were fabricated
using a modified SILAR sequence to overcome compositional inhomogeneity
due to different adsorptivities of the cations (Cu<sup>+</sup>, Sn<sup>4+</sup>, and Zn<sup>2+</sup>) in a single cationic bath. Rapid thermal
annealing of the precursor films under S and Se vapor atmospheres
led to the formation of carbon-free Cu<sub>2</sub>ZnSnS<sub>4</sub> (CZTS) and CZTSSe absorber layers, respectively, with single large-grained
layers. The best devices based on CZTS and CZTSSe absorber layers
showed total area (∼0.30 cm<sup>2</sup>) power conversion efficiencies
(PCEs) of 1.96 and 3.74%, respectively, which are notably the first-demonstrated
efficiencies using a modified SILAR sequence. Detailed diode analyses
of these solar cells revealed that a high shunt conductance (<i>G</i><sub>sh</sub>), reverse saturation current density (<i>J</i><sub>o</sub>), and ideality factor (<i>n</i><sub>d</sub>) significantly affected the PCE, open-circuit voltage (<i>V</i><sub>oc</sub>), and fill factor (FF), whereas the short-circuit
current density (<i>J</i><sub>sc</sub>) was dominated by
the series resistance (<i>R</i><sub>s</sub>) and <i>G</i><sub>sh</sub>. However, the diode analyses combined with
the compositional and interface microstructural analyses shed light
on further improvements to the device efficiency. The facile layer-by-layer
growth of the kesterite CZTS-based thin films in aqueous solution
provides a great promise as an environmentally benign pathway to fabricate
a variety of multielement-component compounds with high compositional
homogeneities