Abstract:The unique electronic structure of rare-earth elements
makes their
modified semiconductor photocatalysts show great advantages in solar
energy conversion. Herein, the pollen-like N, P self-doped biochar-based
rare-earth composite catalyst (Er/LP-C) has been successfully synthesized,
which combines the advantages of biochar and Er and is used for the
first time in the field of photocatalytic hydrogen production from
ethanol–water mixtures. Experimental results confirmed that
the performance of photocatalytic hy… Show more
“…The curve slopes of pure TNT and CeO 2 /TNT are positive, indicating their n-type semiconductor properties . The flat band potential can be regarded as the conduction band potential of n-type semiconductors, which is calculated using the Mott–Schottky equation by intercepting the slopes with the potential axis . The V fb values of pure TNT and CeO 2 /TNT are 0.0 and −0.30 V vs RHE, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…36 The flat band potential can be regarded as the conduction band potential of n-type semiconductors, which is calculated using the Mott−Schottky equation by intercepting the slopes with the potential axis. 37 The V fb values of pure TNT and CeO 2 /TNT are 0.0 and −0.30 V vs RHE, respectively. The negative shift in V fb of CeO 2 /TNT compared to pure TNT indicates a decrease in the transfer energy barrier of the interfacial electron and the charge transfer resistance.…”
Composite of rare earth oxides with
TiO2 nanotube arrays
can effectively modify the photoelectrochemical (PEC) behavior of
TiO2. A CeO2/TiO2 heterojunction
was prepared by loading CeO2 nanoparticles on anodized
TiO2 nanotube (TNT) arrays for PEC water splitting. The
CeO2/TNT electrode exhibited a high photocurrent density
of 2.11 mA·cm–2, 4.3 times that of pure TNT
(0.49 mA·cm–2) at 1.23 V vs RHE under AM 1.5G
light. And CeO2/TNT realized a high PEC H2 evolution
rate of 17.86 μmol/h, 4.5 times that of pure TNT at 1.55 V vs
RHE. The effective performance of the CeO2/TNT electrode
could be attributed to its reasonable band gap structure facilitating
visible light absorption and efficient charge transfer, inhibiting
the recombination of electron/hole pairs. This work confirms the successful
construction of CeO2/TiO2 heterojunction on
TNT arrays for improving the PEC performance of TiO2 for
H2 production.
“…The curve slopes of pure TNT and CeO 2 /TNT are positive, indicating their n-type semiconductor properties . The flat band potential can be regarded as the conduction band potential of n-type semiconductors, which is calculated using the Mott–Schottky equation by intercepting the slopes with the potential axis . The V fb values of pure TNT and CeO 2 /TNT are 0.0 and −0.30 V vs RHE, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…36 The flat band potential can be regarded as the conduction band potential of n-type semiconductors, which is calculated using the Mott−Schottky equation by intercepting the slopes with the potential axis. 37 The V fb values of pure TNT and CeO 2 /TNT are 0.0 and −0.30 V vs RHE, respectively. The negative shift in V fb of CeO 2 /TNT compared to pure TNT indicates a decrease in the transfer energy barrier of the interfacial electron and the charge transfer resistance.…”
Composite of rare earth oxides with
TiO2 nanotube arrays
can effectively modify the photoelectrochemical (PEC) behavior of
TiO2. A CeO2/TiO2 heterojunction
was prepared by loading CeO2 nanoparticles on anodized
TiO2 nanotube (TNT) arrays for PEC water splitting. The
CeO2/TNT electrode exhibited a high photocurrent density
of 2.11 mA·cm–2, 4.3 times that of pure TNT
(0.49 mA·cm–2) at 1.23 V vs RHE under AM 1.5G
light. And CeO2/TNT realized a high PEC H2 evolution
rate of 17.86 μmol/h, 4.5 times that of pure TNT at 1.55 V vs
RHE. The effective performance of the CeO2/TNT electrode
could be attributed to its reasonable band gap structure facilitating
visible light absorption and efficient charge transfer, inhibiting
the recombination of electron/hole pairs. This work confirms the successful
construction of CeO2/TiO2 heterojunction on
TNT arrays for improving the PEC performance of TiO2 for
H2 production.
“…The band gap energy Eg of these samples can be calculated from the IPCE spectra by a Tauc plot of (IPCE % × hv) 1/2 versus photon energy (hv) [ 16 , 33 , 34 , 35 ], as illustrated in Figure 8 a. The band gaps of the pure TiO 2 , CeO 2 -TiO 2 , and Ce/TiO 2 were 3.23, 3.24, and 2.73 eV, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…The curve slopes of the three samples are all positive, indicating their n-type semiconductor properties. The flat band potential can be regarded as the conduction band (CB) potential of n-type semiconductors, which is calculated by intercepting the slopes with the potential axis according to the M-S equation [ 25 , 34 ]. The values of V fb of pure TiO 2 , CeO 2 -TiO 2 , and Ce/TiO 2 are about 0.0, −0.13, and −0.16 V vs. RHE, respectively.…”
Cerium element with a unique electric structure can be used to modify semiconductor photocatalysts to enhance their photocatalytic performances. In this work, Ce-doped TiO2 (Ce/TiO2) was successfully achieved using the sol-gel method. The structural characterization methods confirm that Ce was doped in the lattice of anatase TiO2, which led to a smaller grain size. The performance test results show that the Ce doped in anatase TiO2 significantly enhances the charge transport efficiency and broadens the light absorption range, resulting in higher photocatalytic performance. The Ce/TiO2 exhibited a photocurrent density of 10.9 μA/cm2 at 1.0 V vs. Ag/AgCl, 2.5 times higher than that of pure TiO2 (4.3 μA/cm2) under AM 1.5 G light. The hydrogen (H2) production rate of the Ce/TiO2 was approximately 0.33 μmol/h/g, which is more than twice as much as that of the pure anatase TiO2 (0.12 μmol/h/g). This work demonstrates the effect of Ce doping in the lattice of TiO2 for enhanced photocatalytic hydrogen production.
“…The grating monochromator was equipped with a filter to eliminate higher-order diffraction for measuring the incident photon-to-current efficiency (IPCE). The IPCE value was determined using the formula provided (Equation ( 4)) [6,10,11,15,43,45].…”
This study details the rational design and synthesis of Cu2ZnSnS4 (CZTS)-doped anatase (A) heterostructures, utilizing earth-abundant elements to enhance the efficiency of solar-driven water splitting. A one-step hydrothermal method was employed to fabricate a series of CZTS–A heterojunctions. As the concentration of titanium dioxide (TiO2) varied, the morphology of CZTS shifted from floral patterns to sheet-like structures. The resulting CZTS–A heterostructures underwent comprehensive characterization through photoelectrochemical response assessments, optical measurements, and electrochemical impedance spectroscopy analyses. Detailed photoelectrochemical (PEC) investigations demonstrated notable enhancements in photocurrent density and incident photon-to-electron conversion efficiency (IPCE). Compared to pure anatase electrodes, the optimized CZTS–A heterostructures exhibited a seven-fold increase in photocurrent density and reached a hydrogen production efficiency of 1.1%. Additionally, the maximum H2 production rate from these heterostructures was 11-times greater than that of pure anatase and 250-times higher than the original CZTS after 2 h of irradiation. These results underscore the enhanced PEC performance of CZTS–A heterostructures, highlighting their potential as highly efficient materials for solar water splitting. Integrating Cu2ZnSnS4 nanoparticles (NPs) within TiO2 (anatase) heterostructures implied new avenues for developing earth-abundant and cost-effective photocatalytic systems for renewable energy applications.
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