Weak photon absorption and fast carrier kinetics in graphene restrict its applications in photosensitive reactions. Such restrictions/limitations can be overcome by covalent coupling of another photosensitive nanostructure to graphene, forming graphene-semiconductor nanocomposites. Herein, we report one-pot synthesis of RGO-Ag3 VO4 nanocomposites using various sacrificial agents like ethanol, methanol, propanol and ethylene glycol (EG) under visible light illumination. The Raman spectral analysis and (13) C MAS NMR suggest ethanol to be the best sacrificial agent among those studied. Thermal analysis studies, further, confirm the stability of the synthesized nanocomposite with ethanol as sacrificial agent. In view of this, the activity toward dye degradation was focused over the composites prepared via ethanol as sacrificial agent. It was observed and proved that cationic dyes could be degraded quantitatively and swiftly compared to anionic dyes (37.79%) in 1.5 h. This suggests that the surface of the nanocomposites is anionic as partial reduction takes place during synthesis process. In case of mixed dye degradation process, it was noticed that the presence of cationic dye doubles the degradation of anionic dye. The activity of these synthesized nanocomposites is more than five-fold toward the phototransformation of phenol and photodegradation of textile dyes under visible light illumination.
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http://dx.doi.org/10.1111/php.12172 | DOI Listing |
Dalton Trans
January 2025
College of Life Sciences, School of Chemical Engineering, Key Laboratory of Green Catalysis of Jiangxi Education Institutes, Jiangxi Normal University, Nanchang 330022, China.
The photocatalytic conversion of CO and HO into useful chemicals or fuels over semiconductor photocatalysts is regarded as a promising technology to address the problems of global warming and energy exhaustion. However, inefficient photo-absorption and slow charge dynamics limit the CO photoreduction efficiency. Here, a ternary heterojunction photocatalyst, CuCl(OH)/In/InO (Cu H IO), with an intimate interface is obtained a hydrogen chemical reduction approach followed by hydrolysis reaction, where In species can be produced on the surface of InO from the hydrogen chemical reaction with a calcining temperature of over 500 °C.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Tongji University, School of Chemical Science and Engineering, Chifeng Road No.67, Shanghai, CHINA.
The synthesis of crystalline covalent organic frameworks (COFs) has in principle relied on reversible dynamic chemistry. A general method to synthesize irreversibly bonded COFs is urgently demanded for driving the COF chemistry to a new era. Here we report a universal two-step method for the straightforward synthesis of irreversibly amide-linked COF (AmCOF) membranes by autocatalytic interfacial polymerization (AIP).
View Article and Find Full Text PDFLangmuir
January 2025
State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.
Oxygen and water generating hydrogen peroxide (HO) by optical drive is an extremely promising pathway, and the large amount of oxygen in air and natural sunlight illumination are excellent catalytic conditions. However, the separation efficiency of photogenerated electron-hole pairs greatly limits the photocatalytic efficiency, especially in the absence of sacrificial agents. Here, we report an InS nanosheet with an S vacancy (S-InS).
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China.
Silicon (Si) is regarded as a promising anode material owing to its high specific capacity and low lithiation potential. The large volume change and the pulverization of silicon during the lithiation/delithiation process hinder its direct energy storage application. This review focuses on the electrospun silicon/carbon (Si/C) nanofiber anode materials for lithium-ion batteries for long-term stable energy storage.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Chemistry and Pharmaceutical Science, Guangxi Normal University, Guilin 541004, China.
Imine-based covalent organic frameworks (COFs) have been widely applied in photocatalytic hydrogen peroxide (HO) production because of their highly crystalline properties and tunable chemical structures. However, the inherent polarization of C═N linkage brings a high energy barrier for π-electron delocalization, impeding the in-plane photoelectron transfer process, which leads to an inadequate efficiency of HO photosynthesis. In addition, the chemical stability of most imine-COFs remains insufficient due to the reversible nature of imine linkage.
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