普鲁士蓝
光催化
材料科学
亚甲蓝
吸附
无机化学
罗丹明B
催化作用
阳离子聚合
选择性
铜
化学工程
核化学
扫描电子显微镜
氧化物
降级(电信)
拉曼光谱
纳米颗粒
氧化铜
罗丹明
光化学
化学
杂质
光降解
甲基蓝
罗丹明6G
选择性吸附
硝基苯胺
作者
Nikolay Sirotkin,Anna Khlyustova,Valeriya Aisina,Anton Kraev,Ruslan Kriukov,Alena Shkapina,Alexander Agafonov
摘要
This work presents a novel one-step plasma–solution synthesis of Prussian Blue (PB) and copper hexacyanoferrate (Cu-PBA) nanoparticles via underwater pulsed DC discharge. For the first time, the direct plasma-assisted formation of these coordination polymers is reported. The obtained materials were examined by X-ray diffraction, Fourier-transform infrared spectroscopy, Raman spectroscopy, and scanning electron microscopy (SEM). These analyses confirmed that the desired phases had formed, along with small amounts of oxide byproducts (α-Fe2O3, CuO) arising from the erosion of the electrodes. Photocatalytic activity was evaluated through the degradation of organic dyes (Reactive Red 6C, Rhodamine B, and Methylene Blue) under UV-light irradiation. Both catalysts achieved complete dye degradation within 90 min of UV irradiation (after an initial 30 min dark adsorption step, total experiment time 120 min). Notably, selective performance was observed: PB exhibited higher activity toward the cationic dye Methylene Blue, while Cu-PBA was more effective for the anionic dye Reactive Red 6C. This selectivity is attributed to the specific oxide impurities forming heterojunctions that facilitate charge separation and generate distinct reactive oxygen species. The plasma–liquid method offers a rapid and environmentally benign route to functional PBA-based composites, with potentially scalable characteristics pending further engineering optimization. These findings highlight the potential of utilizing synthesis-induced impurities to tailor photocatalytic selectivity for water purification applications.
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