Abstract:One of the most challenging issues in photocatalytic hydrogen evolution is to efficiently separate photocharge carriers. Although MoS2 loading could effectively improve the photoactivity of TiO2, a fundamental understanding of the charge transfer process between TiO2 and MoS2 is still lacking. Herein, TiO2 photocatalysts with different exposed facets were used to construct MoS2/TiO2 heterostructures. XPS, ESR, together with PL measurements evidenced the Type II electron transfer from MoS2 to {001}-TiO2. Differ… Show more
“…The presence of diffraction of anatase TiO 2 suggests that 2D-MoS 2 nanosheets loading does not change the crystal phase of TiO 2 . On the other hand, no apparent peaks for MoS 2 could be detected, due to its relatively lower amount along with its high dispersity and week intensity that is in well agreed with previous reports 37 , 38 . Further, no other impurity peaks are observed in the XRD patterns evidencing the single-phase formation of the samples.…”
Section: Resultssupporting
confidence: 92%
“…The shift of Ti2p peaks to higher binding energies indicates the functioning of Ti atom as an electron donor. The surface dependent interfacial electronic structure implies the exchange charge transfer behaviour between MoS 2 and TiO 2 heterostructures 37 .…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, the charge carriers in semiconductor photocatalyst strongly depends on the exposed facets and structural defects. Consider the example of (001) and (101) facets/phase of TiO 2 , two most common facets of anatase phase, usually exhibit different adsorption characteristics and redox abilities during the photocatalytic reaction 37 , 66 , 67 .…”
Current research is paying much attention to heterojunction nanostructures. Owing to its versatile characteristics such as stimulating morphology, affluent surface-oxygen-vacancies and chemical compositions for enhanced generation of reactive oxygen species. Herein, we report the hydrothermally synthesized TiO2@MoS2 heterojunction nanostructure for the effective production of photoinduced charge carriers to enhance the photocatalytic capability. XRD analysis illustrated the crystalline size of CTAB capped TiO2, MoS2@TiO2 and L-Cysteine capped MoS2@TiO2 as 12.6, 11.7 and 10.2 nm, respectively. The bandgap of the samples analyzed by UV–Visible spectroscopy are 3.57, 3.66 and 3.94 eV. PL spectra of anatase phase titania shows the peaks present at and above 400 nm are ascribed to the defects in the crystalline structure in the form of oxygen vacancies. HRTEM reveals the existence of hexagonal layered MoS2 formation on the spherical shaped TiO2 nanoparticles at the interface. X-ray photoelectron spectroscopy recommends the chemical interactions between MoS2 and TiO2, specifically, oxygen vacancies. In addition, the electrochemical impedance spectroscopy studies observed that L-MT sample performed low charge transfer resistance (336.7 Ω cm2) that promotes the migration of electrons and interfacial charge separation. The photocatalytic performance is evaluated by quantifying the rate of Congo red dye degradation under visible light irradiation, and the decomposition efficiency was found to be 97%. The electron trapping recombination and plausible photocatalytic mechanism are also explored, and the reported work could be an excellent complement for industrial wastewater treatment.
“…The presence of diffraction of anatase TiO 2 suggests that 2D-MoS 2 nanosheets loading does not change the crystal phase of TiO 2 . On the other hand, no apparent peaks for MoS 2 could be detected, due to its relatively lower amount along with its high dispersity and week intensity that is in well agreed with previous reports 37 , 38 . Further, no other impurity peaks are observed in the XRD patterns evidencing the single-phase formation of the samples.…”
Section: Resultssupporting
confidence: 92%
“…The shift of Ti2p peaks to higher binding energies indicates the functioning of Ti atom as an electron donor. The surface dependent interfacial electronic structure implies the exchange charge transfer behaviour between MoS 2 and TiO 2 heterostructures 37 .…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, the charge carriers in semiconductor photocatalyst strongly depends on the exposed facets and structural defects. Consider the example of (001) and (101) facets/phase of TiO 2 , two most common facets of anatase phase, usually exhibit different adsorption characteristics and redox abilities during the photocatalytic reaction 37 , 66 , 67 .…”
Current research is paying much attention to heterojunction nanostructures. Owing to its versatile characteristics such as stimulating morphology, affluent surface-oxygen-vacancies and chemical compositions for enhanced generation of reactive oxygen species. Herein, we report the hydrothermally synthesized TiO2@MoS2 heterojunction nanostructure for the effective production of photoinduced charge carriers to enhance the photocatalytic capability. XRD analysis illustrated the crystalline size of CTAB capped TiO2, MoS2@TiO2 and L-Cysteine capped MoS2@TiO2 as 12.6, 11.7 and 10.2 nm, respectively. The bandgap of the samples analyzed by UV–Visible spectroscopy are 3.57, 3.66 and 3.94 eV. PL spectra of anatase phase titania shows the peaks present at and above 400 nm are ascribed to the defects in the crystalline structure in the form of oxygen vacancies. HRTEM reveals the existence of hexagonal layered MoS2 formation on the spherical shaped TiO2 nanoparticles at the interface. X-ray photoelectron spectroscopy recommends the chemical interactions between MoS2 and TiO2, specifically, oxygen vacancies. In addition, the electrochemical impedance spectroscopy studies observed that L-MT sample performed low charge transfer resistance (336.7 Ω cm2) that promotes the migration of electrons and interfacial charge separation. The photocatalytic performance is evaluated by quantifying the rate of Congo red dye degradation under visible light irradiation, and the decomposition efficiency was found to be 97%. The electron trapping recombination and plausible photocatalytic mechanism are also explored, and the reported work could be an excellent complement for industrial wastewater treatment.
“…In particular, the large surface areas of 1-D structures and porous morphology are preferred in the design [ 5 , 6 ]. Moreover, composite films with a narrow band gap semiconductor are preferred, which can lead to superior performance of the pure TiO 2 films [ 7 , 8 , 9 ]. Both TiO2 and V 2 O 5 are two important materials due to their excellent electronic, chemical, and optical properties [ 10 , 11 ].…”
Porous V2O5/TiO2 nanoheterostructure films with different atomic ratios of Ti/V (4:1, 2:1, 1:1, and 1:2) were synthesized by a sparking method for the first time. The sparking method, which is a simple and cost-effective process, can synthesize highly porous and composite films in one step. Field-emission scanning electron microscope (FE-SEM) images revealed the porosity morphology of all prepared samples. V2O5/TiO2 nanoheterostructure films were confirmed by Raman spectroscopy, high-resolution transmission electron microscopy (HRTEM), and X-ray photoelectron spectroscopy (XPS). The secondary particle size and band gap of the samples were highly correlated to the V2O5 proportion, resulting in enhanced visible-light absorbance. V2O5/TiO2 nanoheterostructure films at an atomic ratio of 1:1 showed the highest photocatalytic performance, which improved the degradation rate up to 24% compared to pure TiO2 film. It is believed that the formed nanoheterostructure and greater portion of V4+ ions are reflected by this ratio.
“…Its layered structure is sandwiched together by Mo-S-Mo units with a weak van der Waals force [9], and the direct band gap is 1.82 eV [10]. This unique structure gives MoS 2 stable chemical properties, an adjustable band gap, a large specific surface area, and an abundant layered edge to provide a large number of unsaturated active sites [11]. Therefore, MoS 2 is expected to become a high-performance adsorbent.…”
It was found previously that neither monomer MoS 2 nor WO 3 is an ideal material for the adsorption of organic dyes, while MoS 2 /WO 3 composites synthesized by a two-step hydrothermal method have outstanding adsorption effects. In this work, the chemical state of each element was found to be changed after combination by X-ray photoelectron spectroscopy analysis, which lead to their differences in adsorption performance. Moreover, the adsorption test of methylene blue on MoS 2 /WO 3 composites was carried out under a series of temperatures, showing that the prepared composites also had appreciable adsorption rates at lower temperatures. The adsorption process could be well described by the Freundlich isothermal model and the pseudo-second order model. In addition, the particle-internal diffusion model simulation revealed that the internal diffusion of the particles played an important role in the whole adsorption process.
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