Efficient Solar Driven Upgrading of N2 to Urea Through Photoredox Reactions on Pt Cluster/TiO2

尿素 催化作用 光催化 材料科学 星团(航天器) 氮气 人口 甲醇 光化学 无机化学 化学 有机化学 人口学 社会学 计算机科学 程序设计语言
作者
Weiping Yang,Lei Xiao,Weidong Dai,Shiyong Mou,Fan Dong
出处
期刊:Advanced Energy Materials [Wiley]
卷期号:14 (28) 被引量:38
标识
DOI:10.1002/aenm.202303806
摘要

Abstract Synthetic nitrogen fertilizers, such as urea, are instrumental in augmenting agricultural output and addressing the demands of a growing population. Nevertheless, conventional urea production heavily relies on energy‐intensive processes. In this study, an environmentally friendly photocatalytic method is proposed for directly and selectively synthesizing urea from nitrogen (N 2 ) and methanol (CH 3 OH using a Pt cluster‐decorated TiO 2 catalyst (Pt cluster/TiO 2 ). Remarkably, the Pt cluster/TiO 2 exhibits outstanding urea synthesis performance with a rate of 105.68 µmol g −1 h −1 and N‐selectivity of 97.29 ± 0.79%, representing the highest level of photocatalytic urea synthesis from N 2 . Further analysis with density functional theory (DFT) calculation reveals that the “ σ–π *” donor–acceptor interaction occurred between Pt clusters and N 2 , efficiently reducing the N 2 hydrogenation barrier. EPR experiments demonstrate that photogenerated electrons (e − ) and hole (h + ) are synchronously consumed through N 2 reduction and CH 3 OH oxidation, thereby accelerating urea synthesis. The crucial step of C─N coupling is initiated by the reaction between *NH─NH and *CHO intermediate, facilitated by the low energy barrier on Pt cluster/TiO 2 . This work suggests an mild route of urea production and provides profound insights into the underlying chemistry of the C─N coupling reaction, which can guide the sustainable synthesis of essential indispensable chemicals.
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