期刊
ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 54, 期 1, 页码 537-549出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.est.9b05627
关键词
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资金
- National Natural Science Foundation of China [21706224]
- Science and Technology Innovation Commission of Shenzhen Municipality [JCYJ20180307123906004]
- Research Grants Council of Hong Kong [CityU 21301817, CityU 11215518, GRF14100115]
A novel and efficient 3D biohybrid photocatalyst, defective MoS2 nanosheets encapsulated carbonized rape pollen, was fabricated and applied to water disinfection. The rape pollen-MoS2 (PM) biohybrid showed excellent dispersibility, high stability, and efficient charge-carrier separation and migration ability, resulting in the highly enhanced photocatalytic inactivation performance toward various waterborne bacteria under different light sources. The inactivation mechanisms were systematically investigated. Reactive species (RSs), including electrons, holes, and reactive oxygen species (center dot O-2(-) and center dot OH), played major roles in inactivating bacteria. The antioxidant system of bacteria exhibited a self-protection capacity by eliminating the photogenerated RSs from PM biohybrid at the early stage of inactivation. With the accumulation of RSs, the cell membrane and membrane-associated functions were destroyed, as suggested by the collapse of cell envelope and subsequent loss of cell respiration and ATP synthesis capacity. The microscopic images further confirmed the destruction of the bacterial membrane. After losing the membrane barrier, the oxidation of cytoplasmic proteins and lipids caused by invaded RSs occurred readily. Finally, the leakage of DNA and RNA announced the irreversible death of bacteria. These results indicated that the bacterial inactivation began with the membrane rupture, followed by the oxidation and leakage of intracellular substances. This work not only provided a new insight into the combination of semiconductors with earth-abundant biomaterials for fabricating high-performance photocatalysts, but also revealed the underlying mechanisms of photocatalytic bacterial inactivation in depth.
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