光催化
硝酸
异质结
极性(国际关系)
氮气
化学
光化学
一氧化氮
材料科学
无机化学
光电子学
生物化学
催化作用
有机化学
细胞
作者
Xiaoxu Deng,Peng Chen,Ruirui Cui,Xingyong Gong,Xucheng Li,Xu Wang,Chaoyong Deng
摘要
Constructing heterojunctions has emerged as a widely embraced strategy for augmenting piezo-photocatalytic activities. However, the synergistic pressure response, the construction of charge transfer, polar direction sites and active site are often left in the basket. Here, the carboxylated C3N4 and Bi2MoO6 S-scheme heterostructure was elaborately designed for piezo-photocatalytic nitrogen oxidation towards nitric acid. Extensive research evidence proves that Bi-COOH interaction leads to the occurrence of polarity interaction and structural reconstruction. Those initiatives facilitate the efficient distribution of charges and acts as a pathway for carrier migration, thereby promoting charge transfer and the large intrinsic dipole moment. Furthermore, the combination of polarity interaction and structural reconstruction strengthens N2 polarization and electron transfer, facilitating the breaking of N≡N bonds and reducing activation energy. Consequently, the optimal BCO-3 catalyst revealed outstanding nitric acid production rates of 5930 μg g−1 h−1 , which is 3.66 times higher than that of C3N4-Bi2MoO6 heterostructure.
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