双金属
电子转移
活动中心
降级(电信)
碳纳米管
金属
碳纤维
材料科学
活动站点
激进的
化学工程
氧化还原
无机化学
化学
光化学
催化作用
纳米技术
物理化学
有机化学
计算机科学
复合数
复合材料
工程类
电信
作者
Qingqing Shi,Yaqi Hou,Qiting Zhu,Yongmei Hao
标识
DOI:10.1016/j.seppur.2024.129107
摘要
Due to the complex structure of metal–carbon-based catalysts derived from metal-organic frameworks (MOFs), it is difficult to clarify the active sites and catalytic mechanisms. Constructing of structure–activity relationship is conducive for identifying active center, but there is still a gap in the bimetal-carbon-based catalysts/PMS systems. Here, we report a highly efficient and stable CuCo bimetal-nitrogen doped carbon catalyst (CuCo@C-N) for the activation of PMS for efficient degradation of PNP. By manipulating the catalyst structure, establishing the structure–activity relationship and combining with DFT calculation, the non-metallic active centers were determined, including defects, C=O and graphite N. Co was the only metal active center, and the presence of Cu accelerated the redox cycle of the system. The degradation of PNP was dependent on electron transfer and ROS activation. The metal active center was used to generate sulfate radicals (SO4•−), and the non-metal active sites accelerated electron transfer and non-radical pathways to generate 1O2.
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