Liu Siqi, Xu Yi-Jun
State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou, 350002, P. R. China.
College of Chemistry, New Campus, Fuzhou University, Fuzhou 350108, P. R. China.
Sci Rep. 2016 Mar 7;6:22742. doi: 10.1038/srep22742.
The recent thrust in utilizing atomically precise organic ligands protected gold clusters (Au clusters) as photosensitizer coupled with semiconductors for nano-catalysts has led to the claims of improved efficiency in photocatalysis. Nonetheless, the influence of photo-stability of organic ligands protected-Au clusters at the Au/semiconductor interface on the photocatalytic properties remains rather elusive. Taking Au clusters-TiO2 composites as a prototype, we for the first time demonstrate the photo-induced transformation of small molecular-like Au clusters to larger metallic Au nanoparticles under different illumination conditions, which leads to the diverse photocatalytic reaction mechanism. This transformation process undergoes a diffusion/aggregation mechanism accompanied with the onslaught of Au clusters by active oxygen species and holes resulting from photo-excited TiO2 and Au clusters. However, such Au clusters aggregation can be efficiently inhibited by tuning reaction conditions. This work would trigger rational structural design and fine condition control of organic ligands protected-metal clusters-semiconductor composites for diverse photocatalytic applications with long-term photo-stability.
最近,利用原子精确的有机配体保护金簇(Au簇)作为光敏剂与半导体耦合用于纳米催化剂的研究取得了进展,这使得人们声称光催化效率得到了提高。尽管如此,有机配体保护的Au簇在Au/半导体界面处的光稳定性对光催化性能的影响仍然相当难以捉摸。以Au簇-TiO2复合材料为原型,我们首次证明了在不同光照条件下,小分子状的Au簇会光诱导转变为更大的金属Au纳米颗粒,这导致了不同的光催化反应机制。这个转变过程经历了扩散/聚集机制,同时伴随着光激发的TiO2和Au簇产生的活性氧物种和空穴对Au簇的攻击。然而,通过调节反应条件可以有效抑制这种Au簇的聚集。这项工作将引发对有机配体保护的金属簇-半导体复合材料进行合理的结构设计和精细的条件控制,以实现具有长期光稳定性的各种光催化应用。