scholarly journals A Facile Synthesis of Visible-Light Driven Rod-on-Rod like α-FeOOH/α-AgVO3 Nanocomposite as Greatly Enhanced Photocatalyst for Degradation of Rhodamine B

Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 392 ◽  
Author(s):  
Meng Sun ◽  
Raja Senthil ◽  
Junqing Pan ◽  
Sedahmed Osman ◽  
Abrar Khan
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Rhodamine B ◽  
Diffuse Reflectance Spectroscopy ◽  
Hole Pair ◽  
Precipitation Method ◽  
Aqueous Environment ◽  
Electron Hole ◽  
X Ray ◽  
Electron Hole Pair

In this work, we have synthesized the rod-on-rod–like α-FeOOH/α-AgVO3 nanocomposite photocatalysts with the different amounts of solvothermally synthesized α-FeOOH nanorods via a simple co-precipitation method. The as-synthesized photocatalysts were characterized by X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy, UV−Visible diffuse reflectance spectroscopy, scanning electron microscopy (SEM), element mapping, high-resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS) analysis. The observed SEM images show that both α-AgVO3 and α-FeOOH exhibits the rod-shaped morphology with nano size. Furthermore, the photocatalytic activities of the obtained photocatalysts were evaluated towards the degradation of Rhodamine B (RhB) under visible-light irradiation. It is demonstrated that the 3 mg α-FeOOH added to the α-FeOOH/α-AgVO3 nanocomposite exhibited an enhanced photocatalytic performance as compared with the pure α-AgVO3 and α-FeOOH. This significant improvement can be attributed to the increased photo-excited electron-hole pair separation efficiency, large portion of visible-light absorption ability and the reduced recombination of the electron-hole pair. The recycling test revealed that the optimized nanocomposite exhibited good photostability and reusability properties. In addition, the believable photodegradation mechanism of RhB using α-FeOOH/α-AgVO3 nanocomposite is proposed. Hence, the developed α-FeOOH/α-AgVO3 nanocomposite is a promising material for the degradation of organic pollutants in an aqueous environment.

Few-Layered MoS2 Nanostructures for Highly Efficient Visible Light Photocatalysis

NANO ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. 1650114 ◽  
Author(s):  
Dan Li ◽  
Jianwei Li ◽  
Caiqin Han ◽  
Xinsheng Zhao ◽  
Haipeng Chu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Electrochemical Impedance ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
Electrochemical Impedance Spectra ◽  
X Ray ◽  
Transmission Electron ◽  
Electron Hole Pair

Few-layered MoS2 nanostructures were successfully synthesized by a simple hydrothermal method without the addition of any catalysts or surfactants. Their morphology, structure and photocatalytic activity were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy, electrochemical impedance spectra and UV-Vis absorption spectroscopy, respectively. These results show that the MoS2 nanostructures synthesized at 180[Formula: see text]C exhibit an optimal visible light photocatalytic activity (99%) in the degradation of Rhodamine B owing to the relatively easier adsorption of pollutants, higher visible light absorption and lower electron–hole pair recombination.

scholarly journals Visible Light-Driven Mn-MoS2/rGO Composite Photocatalysts for the Photocatalytic Degradation of Rhodamine B

2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Thi Thuy Trang Phan ◽  
Thanh Tam Truong ◽  
Ha Tran Huu ◽  
Le Tuan Nguyen ◽  
Van Thang Nguyen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Rhodamine B ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Electron Paramagnetic Resonance Spectroscopy ◽  
Resonance Spectroscopy ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Composite Photocatalysts

The n%Mn-MoS2/rGO (labeled as n%MMS/rGO, where n% = Mn/(Mn + Mo) in mol) composites were successfully prepared by a facile hydrothermal method from the Mn-MoS2 (MMS) and rGO precursors, in which the MMS was obtained by a facile one-step calcination of (NH4)6Mo7O24·4H2O, (NH2)2CS, and Mn(CH3COO)2·4H2O as precursors in N2 gas at 650°C. The samples were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), electron paramagnetic resonance spectroscopy (EPR), UV-visible diffuse reflectance spectroscopy (UV-Vis DRS), and X-ray photoelectron spectroscopy (XPS), which indicates the composites containing nanosheets of Mn-MoS2 and rGO components. The photocatalytic activities of the n%MMS/rGO composite photocatalysts were evaluated through the photodegradation of rhodamine B (RhB) under the visible light irradiation. The enhancement in the photocatalytic performance of the achieved composites was attributed to the synergic effect of Mn doping and rGO matrix. The investigation of photocatalytic mechanism was also conducted.

Enhanced visible-active photocatalytic behaviors observed in Mn-doped BiFeO3

2018 ◽  
Vol 32 (17) ◽  
pp. 1850185 ◽  
Author(s):  
Yun-Hui Si ◽  
Yu Xia ◽  
Ya-Yun Li ◽  
Shao-Ke Shang ◽  
Xin-Bo Xiong ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Band Gap ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
X Ray ◽  
Mn Doped ◽  
Hole Recombination ◽  
Narrow Band Gap Semiconductors

A series of BiFeO3 and BiFe[Formula: see text]Mn[Formula: see text]O3 (x = 0, 0.02, 0.04, 0.06, 0.08, 0.10) were synthesized by a hydrothermal method. The samples were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy (EDS) and UV–Vis diffuse reflectance spectroscopy, and their photocatalytic activity was studied by photocatalytic degradation of methylene blue in aqueous solution under visible light irradiation. The band gap of BiFeO3 was significantly decreased from 2.26 eV to 1.90 eV with the doping of Mn. Furthermore, the 6% Mn-doped BiFeO3 photocatalyst exhibited the best activity with a degradation rate of 94% after irradiation for 100 min. The enhanced photocatalytic activity with Mn doping could be attributed to the enhanced optical absorption, increment of surface reactive sites and reduction of electron–hole recombination. Our results may be conducive to design more efficient photocatalysts responsive to visible light among narrow band gap semiconductors.

Thermally driven characteristic and highly photocatalytic activity based on N-isopropyl acrylamide/high-substituted hydroxypropyl cellulose/g-C3N4 hydrogel by electron beam pre-radiation method

2020 ◽  
pp. 089270572094421
Author(s):  
Guo Liu ◽  
Ting-Ting Li ◽  
Xiao-Fang Song ◽  
Jin-Yu Yang ◽  
Jiang-Tao Qin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Electron Beam ◽  
Visible Light ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydroxypropyl Cellulose ◽  
Resonance Spectroscopy ◽  
X Ray ◽  
Isopropyl Acrylamide ◽  
Thermally Driven

A new type of N-isopropyl acrylamide/high-substituted hydroxypropyl cellulose/graphite carbon nitride (NIPAAm/HHPC/g-C3N4) smart hydrogel-based photocatalyst with thermally driven characteristic was successfully prepared by electron beam pre-radiation polymerization and radiation cross-linking methods. The agglomeration and loss of g-C3N4 nanosheets can be avoided effectively, and ensured high photocatalytic activity under visible light, once the g-C3N4 nanosheets are uniformly dispersed into the skeleton of a thermosensitive NIPAAm/HHPC hydrogel. NIPAAm/HHPC/g-C3N4 (NHC) hydrogel was characterized by nuclear magnetic resonance spectroscopy, Fourier-transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, X-ray diffraction, X-ray photoelectron spectroscopy, and diffuse reflectance spectroscopy. The microstructure of NHC was further characterized by scanning electron microscopy, transmission electron microscopy, and Brunauer–Emmett–Teller. The adsorption–photocatalytic removal rate of rhodamine B reached 71.4% at the mass ratio of g-C3N4 of 0.8% (NHC-0.8%) hydrogel in an aqueous medium under visible light. The thermal shrinkage ratio can reach 90.6% at 60°C after 5 min and could effectively achieve the function of recycling-free in a portable photocatalytic reaction device under the optimal conditions. Possible mechanism of adsorption–photocatalysis and thermally driven recycling-free on NHC hydrogel was also obtained. These thermally driven recycling-free characteristic and highly photocatalytic properties of the hybrid hydrogel-based photocatalyst show that it can be used as a promising new material with extensive applications in wastewater treatment.

scholarly journals Significantly Enhanced Aqueous Cr(VI) Removal Performance of Bi/ZnO Nanocomposites via Synergistic Effect of Adsorption and SPR-Promoted Visible Light Photoreduction

Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 426 ◽  
Author(s):  
Xiaoya Yuan ◽  
Zijuan Feng ◽  
Jianjun Zhao ◽  
Jiawei Niu ◽  
Jiasen Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Synergistic Effect ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray ◽  
Enhanced Absorption ◽  
Bismuth Nanoparticles ◽  
Effective Transfer

Bismuth nanoparticles (BiNPs) and Zinc Oxide photocatalysts (BiNPs/ZnO) with different Bi loadings were successfully prepared via a facile chemical method. Their morphology and structure were thoroughly characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-Vis (Ultraviolet-Visible) diffuse reflectance spectroscopy (DRS), photoluminescence spectra (PL), and electrochemical impedance spectroscopy (EIS). The results showed that a modification of hexagonal wurtzite-phase ZnO nanoparticles with Bi is achievable with an intimate interfacial interaction within its composites. The performance of the photocatalytic Cr(VI) removal under visible light irradiation indicated that BiNPs/ZnO exhibited a superior removal performance to bare ZnO, Bi, and the counterpart sample prepared using a physical mixing method. The excellent performance of the BiNPs/ZnO photocatalysts could be ascribed to the synergistic effect between the considerable physical Cr (VI) adsorption and enhanced absorption intensity in the visible light region, due to the surface plasmon resonance (SPR) as well as the effective transfer and separation of the photogenerated charge carriers at the interface.

scholarly journals Experimental Study of CO2 Conversion into Methanol by Synthesized Photocatalyst (ZnFe2O4/TiO2) Using Visible Light as an Energy Source

Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 163 ◽  
Author(s):  
Numair Manzoor ◽  
Muhammad Sadiq ◽  
Muhammad Naqvi ◽  
Umair Sikandar ◽  
Salman Raza Naqvi
Keyword(s):  
Titanium Dioxide ◽  
Global Warming ◽  
Visible Light ◽  
Band Gap ◽  
Zinc Ferrite ◽  
Maximum Yield ◽  
Hole Pair ◽  
Electron Hole ◽  
Bet Analysis ◽  
Electron Hole Pair

Ozone layer depletion is a serious threat due to the extensive release of greenhouse gases. The emission of carbon dioxide (CO2) from fossil fuel combustion is a major reason for global warming. Energy demands and climate change are coupled with each other. CO2is a major gas contributing to global warming; hence, the conversion of CO2 into useful products such as methanol, formic acid, formaldehyde, etc., under visible light is an attractive topic. Challenges associated with the current research include synthesizing a photocatalyst that is driven by visible light with a narrow band gap range between 2.5 and 3.0 eV, the separation of a mixed end product, and the two to three times faster recombination rate of an electron–hole pair compared with separation over yield. The purpose of the current research is to convert CO2 into useful fuel i.e., methanol; the current study focuses on the photocatalytic reduction of CO2into a useful product. This research is based on the profound analysis of published work, which allows the selection of appropriate methods and material for this research. In this study, zinc ferrite (ZnFe2O4) is synthesized via the modified sol–gel method and coupled with titanium dioxide (TiO2). Thereafter, the catalyst is characterized by Fourier transform infrared (FTIR), FE-SEM, UV–Vis, and XRD characterization techniques. UV–Vis illustrates that the synthesized catalyst has a low band gap and utilizes a major portion of visible light irradiation. The XRD pattern was confirmed by the formation of the desired catalyst. FE-SEM illustrated that the size of the catalyst ranges from 50 to 500 nm and BET analysis determined the surface area, which was 2.213 and 6.453 m2/g for ZnFe2O4 and ZnFe2O4/TiO2, respectively. The continuous gas flow photoreactor was used to study the activity of the synthesized catalyst, while titanium dioxide (TiO2) has been coupled with zinc ferrite (ZnFe2O4) under visible light in order to obtain the maximum yield of methanol as a single product and simultaneously avoid the conversion of CO2 into multiple products. The performance of ZnFe2O4/TiO2was mainly assessed through methanol yield with a variable amount of TiO2 over ZnFe2O4 (1:1, 1:2, 2:1, 1:3, and 3:1). The synthesized catalyst recycling ability has been tested up to five cycles. Finally, we concluded that the optimum conditions for maximum yield were found to be a calcination temperature of ZnFe2O4at 900 °C, and optimum yield was at a 1:1 w/w coupling ratio of ZnFe2O4/TiO2. It was observed that due to the enhancement in the electron–hole pair lifetime, the methanol yield at 141.22 μmol/gcat·h over ZnFe2O4/TiO2was found to be 7% higher than the earlier reported data.

Preparation and Characterization of Ag/TiO2-xNx Nanoparticles

2007 ◽  
Vol 534-536 ◽  
pp. 105-108
Author(s):  
Zhong Qing Liu ◽  
Zheng Hua Li ◽  
Yan Ping Zhou ◽  
Chang Chun Ge
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Ultraviolet Light ◽  
Hole Pair ◽  
Electron Hole ◽  
Photoexcited Electron ◽  
Photochemical Deposition ◽  
Electron Hole Pair

The Ag/TiO2-xNx nanoparticles were synthesized by photochemical deposition with irradiation of visible light in a TiO2-XNX suspension system. The prepared products were characterized by means of XRD, Uv-vis, and FEM. Its photocatalytic activity was investigated by the decomposition of methylene blue (MB) solution under illumination of visible and ultraviolet light, respectively. Compared to TiO2-xNx, the photocatalytic activity of as–prepared Ag/TiO2-xNx is obviously enhanced due to the decreasing recombination of a photoexcited electron-hole pair. The mechanism in which photocatalytic activity is enhanced is discussed in detail.

scholarly journals Synthesis of BiSI/Ag2CO3 Composite Material for Photocatalytic Degradation of Rhodamine B under Visible Light

2021 ◽  
Author(s):  
Rui Zhang ◽  
ziyin chen ◽  
Chen Zhao ◽  
Kunlin Zeng ◽  
Lu Cai ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Rhodamine B ◽  
Photocatalytic Performance ◽  
Electrochemical Impedance ◽  
Diffuse Reflectance Spectroscopy ◽  
Mass Ratio ◽  
X Ray ◽  
Visible Light Driven

Abstract A novel binary BiSI/Ag2CO3 photocatalyst with excellent visible light-driven photocatalytic performance was prepared. The products were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS) and electrochemical impedance spectroscopy (EIS). The photocatalytic activity of the samples were evaluated by photocatalytic degradation of rhodamine B(RhB) under the irradiation of visible light. The results showed that the BiSI improves the photocatalytic activity of BiSI/Ag2CO3. Moreover, when the mass ratio of BiSI in BiSI/Ag2CO3 composites was 40%, the as-prepared BiSI/Ag2CO3 composite exhibited the best photocatalytic activity for degrading RhB. Finally, the possible mechanism for photodegradation over the BiSI/Ag2CO3 composites is also proposed.

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