J. Mater. Sci. Technol. ›› 2021, Vol. 67: 70-79.DOI: 10.1016/j.jmst.2020.04.084
• Research article • Previous Articles Next Articles
Qian Wua, Xiangmei Liua,*(), Bo Lib, Lei Tana, Yong Hanb,*(), Zhaoyang Lib, Yanqin Liangb, Zhenduo Cuib, Shengli Zhub, Shuilin Wuc,*(), Yufeng Zhengd
Received:
2020-02-07
Revised:
2020-04-04
Accepted:
2020-04-13
Published:
2021-03-20
Online:
2021-04-15
Contact:
Xiangmei Liu,Yong Han,Shuilin Wu
About author:
shuilinwu@tju.edu.cn (S. Wu).Qian Wu, Xiangmei Liu, Bo Li, Lei Tan, Yong Han, Zhaoyang Li, Yanqin Liang, Zhenduo Cui, Shengli Zhu, Shuilin Wu, Yufeng Zheng. Eco-friendly and degradable red phosphorus nanoparticles for rapid microbial sterilization under visible light[J]. J. Mater. Sci. Technol., 2021, 67: 70-79.
Fig. 1. (a) Preparation process of the RPNPs; (b) optical image of RP and RPNP powder samples and their aqueous dispersion; (c) TEM image of the RPNPs; (d) Raman spectra of the RP and RPNPs; (e) UV-vis absorption spectra of different concentrations (200 and 400 μg/mL) of RP and RPNPs, as determined by a microplate reader.
Fig. 2. (a) The samples’ UV-vis-NIR diffuse reflectance spectra (DRS) of RPNPs and RP; (b) The corresponding tauc plots derived from DRS which the RPNPs and RP are regarded as a direct bandgap semiconductor; UPS measurement with a monochromatic He I light source (21.22 eV) of: (c) RP, and (d) RPNPs.
Fig. 3. Photoelectrochemical and photocatalytic characterization of the RP and RPNPs: (a) photoluminescence spectra of the RP and RPNPs; (b) transient photocurrent response curves of the samples; (c) electrochemical impedance spectroscopy of the samples; (d) ESR signal detection of the RP and RPNPs.
Fig. 5. Photothermal response of the samples: (a) schematic photothermal mechanism of the samples; (b) photothermal heating curves of different concentrations of RPNPs (100, 200, and 400 μg/mL) and RP (200 μg/mL); (c) real-time image each sample’s temperature of during the heating process shown in Fig. 5(b); (d) photothermal cycle curve of the RPNPs (400 μg/mL).
Fig. 6. Degradation experiment of deionized water dispersion with RPNPs at 200 μg/mL at 37 ℃: (a) optical image of RPNP dispersion at different time points (0, 1, 5, and 8 weeks); (b) changes in UV-vis absorption intensity of the solution during RPNP degradation; (c) TEM image of the morphology of RPNPs corresponding to the solution shown in Fig. 6(a); (d) ion chromatography showing the phosphate concentration in the solution after degradation for 8 weeks.
Fig. 7. Spread plate and corresponding antibacterial efficiency under different antibacterial conditions: (a) antibacterial rate analysis of RPNPs co-cultured with bacteria for 20 min; (b) photocatalytic antibacterial rate analysis; (c) photothermal + photocatalytic antibacterial rate analysis. The error bars (n = 3) represent means ± standard deviations. * P < 0.05, ** P < 0.01.
Fig. 8. (a) Detection of protein leakage during the bactericidal process of photoexcited RPNPs; (b) determination of bacterial membrane permeability after light sterilization; (c) bacterial morphology revealed by SEM (scale bar: 500 nm); (d) sterilization mechanism of the RPNPs under simulated sunlight. The error bars (n = 3) represent means ± standard deviations. *** P < 0.001.
Fig. 9. (a) MTT detection of different concentrations of RPNPs co-cultured with NIH/3T3 cells for 1 day; (b) MTT assay of the supernatant performed after 8 weeks of degradation of the RPNP aqueous dispersion; (c) MTT assay of the mixed solution performed after 8 weeks of degradation of the RPNP aqueous dispersion. (d) cell fluorescence image (scale bar: 50 μm) corresponding to the MTT detection shown in Fig. 9(a). The error bars (n = 3) represent means ± standard deviations. * P < 0.05.
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