Self-cleaning electrode for stable synthesis of alkaline-earth metal peroxides

被引:0
|
作者
Wang, Minli [1 ,2 ]
Cheng, Jinhuan [3 ]
Xu, Wenwen [1 ,2 ]
Zhu, Dandan [3 ]
Zhang, Wuyong [1 ]
Wen, Yingjie [1 ]
Guan, Wanbing [1 ,2 ]
Jia, Jinping [3 ]
Lu, Zhiyi [1 ,2 ]
机构
[1] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Key Lab Marine Mat & Related Technol, Zhejiang Key Lab Adv Fuel Cells & Electrolyzers Te, Ningbo, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, Beijing, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Environm Sci & Engn, Shanghai, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
CALCIUM PEROXIDE; HYDROGEN-PEROXIDE; ELECTROCHEMICAL SYNTHESIS; OXYGEN REDUCTION; WATER; PERFORMANCE; H2O2;
D O I
10.1038/s41565-024-01815-x
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Alkaline-earth metal peroxides (MO2, M = Ca, Sr, Ba) represent a category of versatile and clean solid oxidizers, while the synthesis process usually consumes excessive hydrogen peroxide (H2O2). Here we discover that H2O2 synthesized via two-electron electrochemical oxygen reduction (2e(-) ORR) on the electrode surface can be efficiently and durably consumed to produce high-purity MO2 in an alkaline environment. The crucial factor lies in the in-time detachment of in situ-generated MO2 from the self-cleaning electrode, where the solid products spontaneously detach from the electrode to solve the block issue. The self-cleaning electrode is achieved by constructing micro-/nanostructure of a highly active catalyst with appropriate surface modification. In experiments, an unprecedented accumulated selectivity (similar to 99%) and durability (>1,000 h, 50 mA cm(-2)) are achieved for electrochemical synthesis of MO2. Moreover, the comparability of CaO2 and H2O2 for tetracycline degradation with hydrodynamic cavitation is validated in terms of their close efficacies (degradation efficiency of 87.9% and 93.6% for H2O2 and CaO2, respectively).
引用
收藏
页码:67 / 74
页数:11
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