胞外聚合物
水溶液中的金属离子
银纳米粒子
透射电子显微镜
化学
氯化银
傅里叶变换红外光谱
化学工程
氯化物
金属
纳米颗粒
纳米晶
光化学
材料科学
纳米技术
生物膜
有机化学
电极
遗传学
细菌
物理化学
工程类
生物
作者
Sicheng Xiong,Xuesong Cao,Hao Fang,Huiyuan Guo,Baoshan Xing
标识
DOI:10.1016/j.scitotenv.2021.145867
摘要
Abstract Natural conversion of metal species is an important source for nanoscale metal particles in the aquatic environment, and it could affect their fate and toxicity. Extracellular polymeric substances (EPSs) are ubiquitous and abundant in the aquatic environment, thus likely can reduce metal ions to nanoscale particles. However, the effect of natural inorganic ligand and light on this process has not been well investigated. In this work, Ag+ was readily reduced to silver nanoparticles (AgNPs, around 15 nm in size) by the EPS collected from Chlorella pyrenoidosa. AgNPs could be generated in the dark environment but at a slow rate. Visible light accelerated the photoreduction. The reaction mechanism probed by Fourier transform infrared spectroscopy and three-dimensional excitation-emission matrix spectrometry demonstrated that the reduction in Ag+ was attributed to the protein and polysaccharides in the EPS. The presence of chloride ions (Cl−) largely shortened the duration of photoreduction. Scanning electron microscopy results indicated that with the aid of EPS, the AgCl nanocrystal was converted to core–shell structure, with dot-like nano Ag acting as the shell and the AgCl nanocrystal acting as the core. Size and morphological changes were observed on transmission electron microscopy. This study adds new knowledge of the joint effect of light exposure, Cl−, and EPS on the formation of AgNPs from Ag+ and advances the understanding of the natural formation mechanism of AgNPs.
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