单线态氧
催化作用
吸附
选择性
离解(化学)
掺杂剂
环境友好型
化学
分子
光化学
氧气
材料科学
无机化学
兴奋剂
物理化学
光电子学
有机化学
生物
生态学
作者
Liangbo Xie,Pengfei Wang,Yi Li,Dongpeng Zhang,Denghui Shang,Wenwen Zheng,Yuguo Xia,Sihui Zhan,Wenping Hu
标识
DOI:10.1038/s41467-022-33149-4
摘要
Due to environmentally friendly operation and on-site productivity, electrocatalytic singlet oxygen (1O2) production via O2 gas is of immense interest in environment purification. However, the side-on configuration of O2 on the catalysts surface will lead to the formation of H2O, which seriously limits the selectivity and activity of 1O2 production. Herein, we show a robust N-doped CuO (N-CuO) with Pauling-type (end-on) adsorption of O2 at the N-Cu-O3 sites for the selective generation of 1O2 under direct-current electric field. We propose that Pauling-type configuration of O2 not only lowers the overall activation energy barrier, but also alters the reaction pathway to form 1O2 instead of H2O, which is the key feature determining selectivity for the dissociation of Cu-O bonds rather than the O-O bonds. The proposed N dopant strategy is applicable to a series of transition metal oxides, providing a universal electrocatalysts design scheme for existing high-performance electrocatalytic 1O2 production.
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