Controlled aggregation of methylene blue in silica-methylene blue nanocomposite for enhanced 1O2 generation

被引:18
作者
Saita, Satoshi [1 ]
Anzai, Maho [1 ]
Mori, Nanase [1 ]
Kawasaki, Hideya [1 ]
机构
[1] Kansai Univ, Fac Chem Mat & Bioengn, Dept Chem & Mat Engn, Suita, Osaka 5648680, Japan
关键词
Silica nanoparticle; Methylene blue; Adsorption; Photosensitizer; Nanocomposite; PHOTODYNAMIC EFFICIENCY; SINGLET OXYGEN; ENCAPSULATION; OXIDATION; THERAPY;
D O I
10.1016/j.colsurfa.2021.126360
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Organic photosensitizers can facilitate photochemical singlet-oxygen (O-1(2)) production, providing a promising strategy for photocatalysis, photodynamic therapy, and environmental protection. Unfortunately, most organic photosensitizers tend to self-aggregate because of their hydrophobicity and conjugated pi-pi electronic structure, leading to the inactivation of their photosensitizing capabilities. Thus, the controlled aggregation of organic photosensitizers is critical for photosensitizer's applications. We report a nanocomposite of porous silica nanoaggregates and the organic photosensitizer methylene blue (P-SiOx NAs/MB) that allows the aggregation control of methylene blue (MB). This nanocomposite-photosensitizer consists of highly dispersed MB in P-SiOx NAs and enhances O-1(2) production under light irradiation without the inactivation of the photosensitizing ability of MB. The enhanced O-1(2) generation rate of P-SiOx NAs/MB is 1.36 times larger than that of free MB. This behavior is contrasted with the inactivation of the photosensitizing ability of MB-encapsulated organo-silica nanoparticles, due to MB self-aggregation within the particles. This study provides a strategy for creating an efficient photosensitizer via suppression of MB self-aggregation to enhance the generation of O-1(2).
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页数:9
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