In order to realize high efficiency visible-light absorption and electron-hole separation of bismuth vanadate (BVO), we synthesized carbon-doped BVO (C-BVO) with high visible-light absorption behavior. We used polyvinylpyrrolidone K-30 as a template and L-cysteine as the carbon source in a one-step hydrothermal synthesis method, and then obtained the carbon-doped BVO@multi-walled carbon nanotubes (C-BVO@MWCNT) by a two-step method. The carbon nanotubes were characterized by X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy, UV-vis diffuse reflectance spectroscopy, specific surface area, electron spin resonance, and transient photocurrent responses. The XRD analysis confirmed that all photocatalysts were in the same crystal form with a single monoclinic scheelite structure. Combining this with the other characterization results, we showed that the carbon element was successfully doped in BVO and the resulting C-BVO was successfully coupled with multi-walled carbon nanotubes. The removal ratio of rhodamine B by C-BVO@MWCNT was much higher than those by BVO and C-BVO under visible-light irradiation. Recycling experiments verified the stability of C-BVO@MWCNT, which was proved to offer excellent adsorption, strong visible-light absorption behavior, and high electronhole separation efficiency. Such properties are expected to be useful in practical applications.
The band gaps of bismuth vanadate (BiVO4) and bismuth sulfide (Bi2S3) are about 2.40 eV and 1.30 eV, respectively. Although both BiVO4 and Bi2S3 are capable of strong visible light absorption, electron–hole recombination occurs easily. To solve this problem, we designed a one-step hydrothermal method for synthesizing a Bismuth sulfide (Bi2S3)/Bismuth vanadate (BiVO4) heterojunction using polyvinylpyrrolidone K-30 (PVP) as a structure-directing agent, and 2-Amino-3-mercaptopropanoic acid (l-cysteine) as a sulfur source. The pH of the reaction solution was regulated to yield different products: when the pH was 7.5, only monoclinic BiVO4 was produced (sample 7.5); when the pH was 8.0 or 8.5, both Bi2S3 and BiVO4 were produced (samples 8.0 and 8.5); and when the pH was 9.0, only Bi2S3 was produced (sample 9.0). In sample 8.0, Bi2S3 and BiVO4 were closely integrated with each other, with Bi2S3 particles formed on the surface of concentric BiVO4 layers, but the two compounds grew separately in a pH solution of 8.5. Visible-light photocatalytic degradation experiments demonstrated that the degradation efficiency of the Bi2S3/BiVO4 heterojunction was highest when prepared under a pH of 8.0. The initial rhodamine B in the solution (5 mg/L) was completely degraded within three hours. Recycling experiments verified the high stability of Bi2S3/BiVO4. The synthesis method proposed in this paper is expected to enable large-scale and practical use of Bi2S3/BiVO4.
Microspherical bismuth oxychloride (BiOCl) can only utilize ultraviolet (UV) light to promote photocatalytic reactions. To overcome this limitation, a uniform and thin BiOCl nanosheet was synthesized with a particle size of about 200 nm. As results of UV-visible diffuse reflectance spectroscopy showed, the band gap of this nanostructure was reduced to 2.78 eV, indicating that the BiOCl nanosheet could absorb and utilize visible light. Furthermore, the upconversion material NaYF 4 doped with rare earth ions Yb 3+ and Er 3+ emitted visible light at 410 nm following excitation with near-infrared (NIR) light (980 nm), which could be utilized by BiOCl to produce a photocatalytic reaction. To produce a high-efficiency photocatalyst (NaYF 4 :Yb 3+ ,Er 3+ @BiOCl), BiOCl-loaded NaYF 4 :Yb 3+ ,Er 3+ was successfully synthesized via a simple twostep hydrothermal method. The as-synthesized material was confirmed using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy as well as other characterizations. The removal ratio of methylene blue by NaYF 4 :Yb 3+ ,Er 3+ @BiOCl was much higher than that of BiOCl alone.Recycling experiments verified the stability of NaYF 4 :Yb 3+ ,Er 3+ @BiOCl, which demonstrated excellent adsorption, strong visible-light absorption and high electron-hole separation efficiency. Such properties are expected to be useful in practical applications, and a further understanding of the NIR-light-responsive photocatalytic mechanism of this new catalytic material would be conducive to improving its structural design and function.
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