PK Shukla
Address: Noida, Uttar Pradesh, India
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Papers by PK Shukla
graphene oxide (TR) composites synthesized by a facile and ecological route, for enhanced visible light
(470 nm) photocatalytic degradation of Methylene Blue (MB) (99% efficiency), with high rate constant
values (1800% over bare TiO2). TG couples TiO2 nanopowder with Graphene Oxide (GO) while TR
couples it with reduced graphene oxide (RGO). The present study, unlike previous reports, discusses
never-before-reported double absorption edges obtained for both TG (3.51 eV and 2.51 eV) and TR
(3.42 eV and 2.39 eV) composites, which represents the reason behind feasible visible light (2.56 eV)
induced photocatalysis. TiO2 domains in the composites dominate the higher band edge, while GO/RGO
domains explain the lower band edge. Formation of Ti–O–C bonds in both TG and TR drives the shifting
upwards of the valence band edge and reduction in band gap. Further, these bonds provide a conductive
pathway for charge carriers from TiO2 nanopowder to the degraded species via the GO/RGO matrix,
resulting in decreased charge carrier recombination in TiO2 and enhanced efficiency. To attest that the
developed theory is correct, density function theory (DFT) calculations were performed. DFT obtained
energetics and electronic structures support experimental findings by demonstrating the role of the
Ti–O–C bond, which results in double band edge phenomenon in composites. Finally, the mechanism
behind MB degradation is discussed comprehensively and the effect of the weight percent of GO/RGO
in the composite on the rate constant and photodegradation efficiency has been studied experimentally
and explained by developing analytical equations.
were characterized using XRD, UV-VIS absorbance spectroscopy, FT-IR and SEM. PbS nanoparticles serve as surface state depressors, which reduces the surface states of TiO2 films. This further reduces recombination rate and increases the conversion efficiency of DSSC. The mechanism of charge transport on photovoltaic response and other parameters of the DSSC using PbS–TiO2 nanocomposite are also presented in detail.
polymer electrolyte - (PVAx:NH4SCN)y:PVAc system. Complexation and morphology of
the composite electrolyte films are discussed on the basis of X-ray diffraction and differential
scanning calorimetry data. Coulometry and transient ionic current measurements revealed charge
transport through protons. The maximum ion conductivity was found to be 7.4.10 -4 S.cm -1 for the
composition: x = 0.15, y = 0.12. The observed conductivity behaviour is correlated to the morphology
of the films. The temperature dependence of the electrical conductivity exhibits Arrhenius
characteristics in two different temperature ranges separated by a plateau region related to morphological
changes occurring in the electrolyte.
(NH4SCN) have been investigated at various frequencies (from 100 Hz to 10 kHz) in the temperature
range from 303 to 383 K. The relative permittivity (e0), loss tangent (tan d) and relaxation
time (t) were found to be temperature and dopant concentration dependent. The experimental results
reveal a, ab and b-types of relaxation processes for PVA±NH4SCN complexes.
the conductivity response of PVA-based composite polymer electrolytes following the Effective
Medium Theory (EMT) approach. In the present investigation, the variation in the thickness
of the highly amorphous space charge layer (responsible for enhancement in conductivity),
covering the dispersed grains, has been taken into account while interpreting the conductivity
data. During the estimation of the surface layer conductivity the role of glass transition temperature
and degree of crystallinity were also considered. The simulated conductivity data incorporating
these parameters in the EMT model show a better fit to the experimental conductivity
response.
area for modular design of photoelectrolysis cell. This was done for determining the electrode area for optimum electrical
output and hydrogen production rate. The nanostructured TiO2 has been formed by hydrolysis of titanium tetraisopropoxide
Ti[OCH(CH3)2]4 followed by the deposition with spin on technique. The photoelectrochemical cell having nanostructured
TiO2 photoanode of several geometricareas, namely, 0.21, 0.50, 0.72, 1.47 and 1:85 cm2, were fabricated and characterized. It
has been found that the photoanode area corresponding to optimum electrical output and hydrogen production rate corresponds
to ∼ 0:5 c m2.
oxidation of titanium sheet. The microstructural characterization revealed the porous nature of the 3lm consisting of randomly
oriented microcrystals. The photoelectrochemical (PEC) characterization of TiO2 3lms has been carried out by employing
standard electrochemical techniques. The investigations being reported involve I–V and C–V measurements, besides the use
of PEC cell for hydrogen production by employing photovoltaic power as external biasing source. The open circuit voltage
and short circuit current for the cell were found to be 780 mV and 9:27 mA cm−2, respectively. The observed frequency
dispersion in Mott–Schottky plots was related to the presence of interface states participating in the charge exchange with bulk
electrolyte. The hydrogen production rates were found to be 37.4 and 24:6 l h−1 m−2, respectively, for PV biased PEC and
PV (stand-alone) driven electrolysis modes. ? 2001 International Association for Hydrogen Energy. Published by Elsevier
Science Ltd. All rights reserved.
graphene oxide (TR) composites synthesized by a facile and ecological route, for enhanced visible light
(470 nm) photocatalytic degradation of Methylene Blue (MB) (99% efficiency), with high rate constant
values (1800% over bare TiO2). TG couples TiO2 nanopowder with Graphene Oxide (GO) while TR
couples it with reduced graphene oxide (RGO). The present study, unlike previous reports, discusses
never-before-reported double absorption edges obtained for both TG (3.51 eV and 2.51 eV) and TR
(3.42 eV and 2.39 eV) composites, which represents the reason behind feasible visible light (2.56 eV)
induced photocatalysis. TiO2 domains in the composites dominate the higher band edge, while GO/RGO
domains explain the lower band edge. Formation of Ti–O–C bonds in both TG and TR drives the shifting
upwards of the valence band edge and reduction in band gap. Further, these bonds provide a conductive
pathway for charge carriers from TiO2 nanopowder to the degraded species via the GO/RGO matrix,
resulting in decreased charge carrier recombination in TiO2 and enhanced efficiency. To attest that the
developed theory is correct, density function theory (DFT) calculations were performed. DFT obtained
energetics and electronic structures support experimental findings by demonstrating the role of the
Ti–O–C bond, which results in double band edge phenomenon in composites. Finally, the mechanism
behind MB degradation is discussed comprehensively and the effect of the weight percent of GO/RGO
in the composite on the rate constant and photodegradation efficiency has been studied experimentally
and explained by developing analytical equations.
were characterized using XRD, UV-VIS absorbance spectroscopy, FT-IR and SEM. PbS nanoparticles serve as surface state depressors, which reduces the surface states of TiO2 films. This further reduces recombination rate and increases the conversion efficiency of DSSC. The mechanism of charge transport on photovoltaic response and other parameters of the DSSC using PbS–TiO2 nanocomposite are also presented in detail.
polymer electrolyte - (PVAx:NH4SCN)y:PVAc system. Complexation and morphology of
the composite electrolyte films are discussed on the basis of X-ray diffraction and differential
scanning calorimetry data. Coulometry and transient ionic current measurements revealed charge
transport through protons. The maximum ion conductivity was found to be 7.4.10 -4 S.cm -1 for the
composition: x = 0.15, y = 0.12. The observed conductivity behaviour is correlated to the morphology
of the films. The temperature dependence of the electrical conductivity exhibits Arrhenius
characteristics in two different temperature ranges separated by a plateau region related to morphological
changes occurring in the electrolyte.
(NH4SCN) have been investigated at various frequencies (from 100 Hz to 10 kHz) in the temperature
range from 303 to 383 K. The relative permittivity (e0), loss tangent (tan d) and relaxation
time (t) were found to be temperature and dopant concentration dependent. The experimental results
reveal a, ab and b-types of relaxation processes for PVA±NH4SCN complexes.
the conductivity response of PVA-based composite polymer electrolytes following the Effective
Medium Theory (EMT) approach. In the present investigation, the variation in the thickness
of the highly amorphous space charge layer (responsible for enhancement in conductivity),
covering the dispersed grains, has been taken into account while interpreting the conductivity
data. During the estimation of the surface layer conductivity the role of glass transition temperature
and degree of crystallinity were also considered. The simulated conductivity data incorporating
these parameters in the EMT model show a better fit to the experimental conductivity
response.
area for modular design of photoelectrolysis cell. This was done for determining the electrode area for optimum electrical
output and hydrogen production rate. The nanostructured TiO2 has been formed by hydrolysis of titanium tetraisopropoxide
Ti[OCH(CH3)2]4 followed by the deposition with spin on technique. The photoelectrochemical cell having nanostructured
TiO2 photoanode of several geometricareas, namely, 0.21, 0.50, 0.72, 1.47 and 1:85 cm2, were fabricated and characterized. It
has been found that the photoanode area corresponding to optimum electrical output and hydrogen production rate corresponds
to ∼ 0:5 c m2.
oxidation of titanium sheet. The microstructural characterization revealed the porous nature of the 3lm consisting of randomly
oriented microcrystals. The photoelectrochemical (PEC) characterization of TiO2 3lms has been carried out by employing
standard electrochemical techniques. The investigations being reported involve I–V and C–V measurements, besides the use
of PEC cell for hydrogen production by employing photovoltaic power as external biasing source. The open circuit voltage
and short circuit current for the cell were found to be 780 mV and 9:27 mA cm−2, respectively. The observed frequency
dispersion in Mott–Schottky plots was related to the presence of interface states participating in the charge exchange with bulk
electrolyte. The hydrogen production rates were found to be 37.4 and 24:6 l h−1 m−2, respectively, for PV biased PEC and
PV (stand-alone) driven electrolysis modes. ? 2001 International Association for Hydrogen Energy. Published by Elsevier
Science Ltd. All rights reserved.