光催化
催化作用
电子转移
选择性
可见光谱
材料科学
光化学
兴奋剂
吸收(声学)
吸收边
纳米技术
化学
光电子学
带隙
有机化学
复合材料
作者
Baolin Yan,Shen Hu,Chunyan Bu,Yi'an Peng,Huaize Han,Xinghang Xu,Yihan Liu,Jianxiang Yu,Yuhua Dai
标识
DOI:10.1002/cnma.202300079
摘要
Abstract Despite the direct utilizing metal‐organic frameworks (MOFs) as promising photocatalysts for H 2 O 2 production, their activity and selectivity are still undesirable owing to the insufficient active centers, weak visible‐light absorption, and limited charge transfer. Herein, the Ce‐doped Ti‐based MOFs MIL‐125‐NH 2 photocatalysts (Ce/TiMOFs) were synthesized by a facile impregnation‐coordination method, during which the doped Ce species could not only extend the visible‐light absorption edge but also provide new reactive sites for promoting the charge transfer and selectivity of two‐electron O 2 reduction. Interestingly, the optimal Ce/TiMOFs‐0.010 achieved a rate of H 2 O 2 yield of 2464 μM h −1 g −1 with ∼3.4‐fold improvement compared to TiMOFs, attributed to the faster conversion rate of the main reactive oxygen intermediates (⋅O 2 − ) and improved average transfer electron number. This work provides an effective strategy to optimize the photocatalytic performances of MOFs and expands the application of MOFs in the sustainable energy production field.
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