ACS Appl Mater Interfaces. 2018 Aug 29;10(34):28702-28708. doi: 10.1021/acsami.8b09634. Epub 2018 Aug 20.
Sub-nanometer silver clusters that exhibit discrete electronic structure with molecular-like properties are highly desirable in various technologies. However, the methods for their preparation suffer from limitations related with the reproducibility and particles uniformity and/or the possibility of the scale-up. Another critical drawback is that free sub-nanometer silver clusters tend to aggregate into larger particles. In this work, a new approach that successfully overcomes the above limitations is developed. It allows, for the first time, an ultrafast preparation of sub-nanometer silver particles with high abundance, uniformity (7 Å), and stability into the cages of nanosized zeolite crystals. The new method consists of UV excitation of a water suspension of nanozeolite containing photoactive vanadate clusters in the presence of ethanol (as an electron donor) and silver precursor. The characteristic features of sub-nanometer silver particles are presented, and the mechanism of their formation is discussed. Sub-nanometer Ag clusters exhibit exceptional photocatalytic activity and selectivity in the reforming of formic acid to H and CO under visible light.
具有分子特性的离散电子结构的亚纳米银团簇在各种技术中是非常需要的。然而,它们的制备方法受到与重现性和颗粒均匀性以及/或扩大规模的可能性相关的限制。另一个关键的缺点是,游离的亚纳米银团簇容易聚集成长颗粒。在这项工作中,开发了一种成功克服上述限制的新方法。它首次允许在纳米沸石晶体的笼中快速制备具有高丰度、均匀性(7 Å)和稳定性的亚纳米银颗粒。该新方法包括在存在乙醇(作为电子给体)和银前体的情况下,用纳米沸石水悬浮液中的光活性钒酸盐簇进行紫外线激发。介绍了亚纳米银颗粒的特征,并讨论了其形成机制。亚纳米 Ag 团簇在可见光下甲酸重整为 H 和 CO 的反应中表现出异常的光催化活性和选择性。