多金属氧酸盐
材料科学
石墨氮化碳
共价键
电催化剂
共价有机骨架
电子转移
氮化碳
电化学
化学工程
X射线光电子能谱
光化学
光催化
催化作用
电极
物理化学
有机化学
化学
工程类
作者
Shen Zhao,Xu Zhao,Shouxin Zhang,Jiang Li,Yongfa Zhu
出处
期刊:Nano Energy
[Elsevier]
日期:2017-04-08
卷期号:35: 405-414
被引量:174
标识
DOI:10.1016/j.nanoen.2017.04.017
摘要
The polyoxometalate (POM) cluster of [PW11O39]7- (PW11) has been successfully covalent combined with the three dimensionally ordered macroporous graphitic carbon nitride (3DOM g-C3N4) through the organic linker strategy. The characterization such as solid-state NMR and XPS results confirm the organosilicon agent of (triethoxysilyl)-propyl isocyanate can act as the linker to covalent combine the PW11 cluster with 3DOM g-C3N4. The hybrid catalyst of 3DOM g-C3N4-PW11 exhibits efficient catalytic performance (2.4 μmol h−1) for light-driven H2O2 production from H2O and O2 in the absence of organic electron donors. The ESR results suggest that one-electron reduction of O2 to •OOH is indeed suppressed over 3DOM g-C3N4-PW11. Furthermore, the Koutecky-Levich plot obtained from electrochemical rotating disk electrode (RDE) analysis of oxygen reduction reaction (ORR) for 3DOM g-C3N4-PW11 reveals the value of electron transfer during the ORR process is 2.30, indicating the covalent combination can promote the two-electron O2 reduction. In addition, the recycle experiment results reveal that the heterogeneous 3DOM g-C3N4-PW11 is catalytic stable.
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