Insights into O2 Activation via MnIIIOOH Species on Mn-Rich Biochar

作者:Fang, Yanfen; Ying, Dengyu; Niu, Huibin; Xu, Yan; Wang, Shaobin; Duan, Ran; Zhu, Huaiyong; Deng, Chaoyuan; Chen, Chuncheng; Huang, Yingping*
来源:ACS Catalysis, 2023, 13(21): 13955-13967.
DOI:10.1021/acscatal.3c02265

摘要

Although metal-rich biochar (M-BC) is widely used in soil remediation and pollution control, the activation mechanism of molecular oxygen (O-2) by M-BC still needs to be clarified due to the low metal loading. In this study, we enhanced the manganese content of low-temperature manganese-rich biochar (Mn-BC) by treating it with hydrogen peroxide (H2O2), resulting in the formation of MnBC-Hx (where x represents the volume of H2O2 used in mL). MnBC-H5 was particularly effective in activating O-2, leading to the successful degradation of phenol and dyes. Characterizations showed that the Mn-II in the outer layer of MnC2O4<middle dot>2H(2)O nanoparticles evenly dispersed over Mn-BC was oxidized to Mn-III by H2O2. This process was accompanied by the removal of coordinated H2O, resulting in the formation of (MnC2O4)-C-III on MnBC-H5. Under visible light irradiation, Mn-III can bind to O-2 to form (MnOOH)-O-III species, which facilitates the transfer of charges and generates superoxide radicals (O-<middle dot>(2)-) that effectively degrade organics. Notably, Mn-III of MnBC-H5 remains stable after the organic degradation reaction. This study will not only provide a theoretical basis for developing environmentally friendly biochar-based catalysts but also promote the study of the environmental effects of biochar.

  • 单位
    中国科学院

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