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Formation mechanism of nanopores in dense films of anodic alumina
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作者 Peng-ze LI Yu ZHANG +5 位作者 Jia-zheng ZHANG Lin LIU Shi-yi WANG Rui LIU Ye SONG Xu-fei ZHU 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2024年第9期2918-2927,共10页
Constant-current anodization of pure aluminum was carried out in non-corrosive capacitor working electrolytes to study the formation mechanism of nanopores in the anodic oxide films.Through comparative experiments,nan... Constant-current anodization of pure aluminum was carried out in non-corrosive capacitor working electrolytes to study the formation mechanism of nanopores in the anodic oxide films.Through comparative experiments,nanopores are found in the anodic films formed in the electrolytes after high-temperature storage(HTS)at 130°C for 240 h.A comparison of the voltage-time curves suggests that the formation of nanopores results from the decrease in formation efficiency of anodic oxide films rather than the corrosion of the electrolytes.FT-IR and UV spectra analysis shows that carboxylate and ethylene glycol in electrolytes can easily react by esterification at high temperatures.Combining the electronic current theory and oxygen bubble mold effect,the change in electrolyte composition could increase the electronic current in the anodizing process.The electronic current decreases the formation efficiency of anodic oxide films,and oxygen bubbles accompanying electronic current lead to the formation of nanopores in the dense films.The continuous electronic current and oxygen bubbles are the prerequisites for the formation of porous anodic oxides rather than the traditional field-assisted dissolution model. 展开更多
关键词 anodic alumina formation mechanism NANOPORES formation efficiency electronic current oxygen bubble
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多联吡啶铱(Ⅲ)配合物的合成、发光及DNA/BSA结合活性
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作者 顾顺心 姜琴 施鹏飞 《江苏海洋大学学报(自然科学版)》 CAS 2022年第1期70-78,共9页
多联吡啶环金属铱(Ⅲ)配合物具有优异的发光和抗肿瘤性能。设计合成了一种N^N^C型多联吡啶配体PhbpyOH,利用该配体制备了铱(Ⅲ)配合物Ir-NNC,采用核磁共振氢谱、质谱、X-ray单晶衍射法对配体和配合物进行了结构表征。配合物在415 nm呈... 多联吡啶环金属铱(Ⅲ)配合物具有优异的发光和抗肿瘤性能。设计合成了一种N^N^C型多联吡啶配体PhbpyOH,利用该配体制备了铱(Ⅲ)配合物Ir-NNC,采用核磁共振氢谱、质谱、X-ray单晶衍射法对配体和配合物进行了结构表征。配合物在415 nm呈现出强MLCT吸收峰,Gaussian计算结果显示配合物激发态电子云由PhbpyOH跃迁到辅助配体苯基吡啶上。Ir-NNC的单、双光子发光性能均弱于PhbpyOH,配合物还能在光激发下诱导生成单线态氧(量子产率约为0.1)。紫外滴定实验和分子对接模拟结果表明,配合物Ir-NNC能进入DNA的小沟区,配合物可与BSA的ⅠB亚结构域内的谷氨酸和天冬氨酸发生氢键结合。 展开更多
关键词 多联吡啶铱(Ⅲ)配合物 发光性能 DNA/BSA结合 抗肿瘤
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