双锰矿
绿脓素
光电流
电子转移
生物膜
循环伏安法
光化学
化学
材料科学
化学工程
纳米技术
电化学
光电子学
群体感应
细菌
生物
电极
有机化学
催化作用
物理化学
工程类
遗传学
氧化锰
作者
Guiping Ren,Yuan Sun,Yang Ding,Anhuai Lu,Yan Li,Changqiu Wang,Hongrui Ding
标识
DOI:10.1016/j.bioelechem.2018.06.003
摘要
Abstract In recent years, considerable research effort has explored the interaction between semiconducting minerals and microorganisms, such relationship is a promising way to increase the efficiency of bioelectrochemical systems. Herein, the enhancement of electron transfer between birnessite photoanodes and Pseudomonas aeruginosa PAO1 under visible light was investigated. Under light illumination and positive bias, the light–birnessite–PAO1 electrochemical system generated a photocurrent of 279.57 μA/cm 2 , which is 322% and 170% higher than those in the abiotic control and dead culture, suggesting photoenhanced electrochemical interaction between birnessite and Pseudomonas . The I-t curves presented repeatable responses to light on/off cycles, and multi-conditions analyses indicated that the enhanced photocurrent was attributed to the additional redox species associated with P. aeruginosa PAO1 and with the biofilm on birnessite. Electroconductibility analysis was conducted on the biofilm cellularly by conductive atomic force microscope. Pyocyanin was isolated as the biosynthesized extracellular shuttle and characterized by cyclic voltammetry and surface-enhanced Raman spectroscopy. Rapid bioelectron transfer driven by light was observed. The results suggest new opportunities for designing photo-bioelectronic devices and expanding our understanding of extracellular electron transfer with semiconducting minerals under light in nature environments.
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