盐酸四环素
阳极
人体净化
对偶(语法数字)
机制(生物学)
四环素
盐酸盐
组合化学
化学
电化学
阴极
光化学
材料科学
化学工程
有机化学
电极
物理化学
废物管理
生物化学
艺术
哲学
文学类
认识论
工程类
抗生素
作者
Xin-yue Lan,Zhi Huang,Yanying Liu,Junming Hong,Qian Zhang
标识
DOI:10.1016/j.jece.2024.112928
摘要
MOF anodes were especially prepared with dual-ligand and S/N crosslinking atoms for tetracycline hydrochloride (TCH) electrocatalytic degradation. Results showed S(HTTP)-Ni-N(HAB) and N(HITP)-Ni-S(BHT) exhibited high electrocatalytic performance with 100% TCH degradation in 10 min, which were superior to that of S(HTTP)-Ni-S(BHT) and N(HITP)-Ni-N(HAB). The experimental and DFT calculation results jointly unraveled that the electron delocalization created by adjacent S/N crosslinking atoms facilitated the electron conduction and produced positive-charged Ni sites for the improved generation of ·O2− and ·OH radicals. The positive contributions of ·O2− and ·OH radicals then proved the degradation pathways of TCH. In addition, extended experiments on various conditions and pollutions highlighted the application potential of S/N hybrid MOF anodes. The final results provided new insight into MOF anode design and preparation via large cardinal ligand and crosslinking atom adjustment for environmental application.
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