4.6 Article

Effect of loading rate of nano-silver on degradation of methyl orange by AgNPs@SBPN composite catalyst

期刊

MATERIALS CHEMISTRY AND PHYSICS
卷 279, 期 -, 页码 -

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ELSEVIER SCIENCE SA
DOI: 10.1016/j.matchemphys.2022.125761

关键词

Photocatalytic; Black phosphorus nanosheet; Nano silver; Loading rate

资金

  1. National Key R&D Program of China [2019YFC1803802]

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The influence of loading rate of nano-silver on the degradation of pollutants was investigated. The results showed that the loaded nano-silver increased the absorption of visible light and separation efficiency of charges, leading to enhanced degradation performance. Optimal degradation was achieved at an appropriate loading rate.
To determine the influence of loading rate of nano-silver on the degradation of pollutants, AgNPs were immobilized on the surface of small black phosphorus nanosheet (SBPN) with different loadings (2.5 wt%, 5 wt%, 7.5 wt% and 10 wt%) and constructed a series of composite photocatalysts, namely AgNPs@SBPN. The structure, size and morphological properties of AgNPs@SBPN were investigated. The photocatalytic performance of bare BP and AgNPs@SBPN was compared. The results confirmed that the surface plasmon resonance effect of loaded AgNPs increased the absorption of visible light and separation efficiency of charges of AgNPs@SBPN. The photocatalytic degradation performance of AgNPs@SBPN was AgNPs loading rate dependent. Compared with the pure BP, degradation rate of methyl orange (MO) increased by 35.3%-187.7% as the loading increased from 2.5 wt% to 7.5 wt%. The findings indicated that too much (10 wt%) or little nano silver (<2.5 wt%) was not conducive to the rapid transfer of electrons, resulting in low degradation efficiency. Under the optimal condition of AgNPs loading rate (7.5 wt%), the average particle size of AgNPs was 34 nm. About 72.0% MO was degraded within 120 min by 7.5 wt%-AgNPs@SBPN with the photocurrent density of 15.3 mu A cm(-2). Through liquid chromatography-mass spectrometry analysis, MO may be mineralized into CO2, H2O and NO3- under the oxidation of center dot OH and center dot O-2(-).

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