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The fourth crystallographic closest packing unveiled in the gold nanocluster crystal

Metal nanoclusters have recently attracted extensive interest not only for fundamental scientific research, but also for practical applications. For fundamental scientific research, it is of major importance to explore the internal structure and crystallographic arrangement. Herein, we synthesize a...

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Detalles Bibliográficos
Autores principales: Gan, Zibao, Chen, Jishi, Wang, Juan, Wang, Chengming, Li, Man-Bo, Yao, Chuanhao, Zhuang, Shengli, Xu, An, Li, Lingling, Wu, Zhikun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376665/
https://www.ncbi.nlm.nih.gov/pubmed/28337982
http://dx.doi.org/10.1038/ncomms14739
Descripción
Sumario:Metal nanoclusters have recently attracted extensive interest not only for fundamental scientific research, but also for practical applications. For fundamental scientific research, it is of major importance to explore the internal structure and crystallographic arrangement. Herein, we synthesize a gold nanocluster whose composition is determined to be Au(60)S(6)(SCH(2)Ph)(36) by using electrospray ionization mass spectrometry and single crystal X-ray crystallography (SCXC). SCXC also reveals that Au(60)S(6)(SCH(2)Ph)(36) consists of a fcc-like Au(20) kernel protected by a pair of giant Au(20)S(3)(SCH(2)Ph)(18) staple motifs, which contain 6 tetrahedral-coordinate μ(4)-S atoms not previously reported in the Au–S interface. Importantly, the fourth crystallographic closest-packed pattern, termed 6H left-handed helical (6HLH) arrangement, which results in the distinct loss of solid photoluminescence of amorphous Au(60)S(6)(SCH(2)Ph)(36), is found in the crystals of Au(60)S(6)(SCH(2)Ph)(36). The solvent-polarity-dependent solution photoluminescence is also demonstrated. Overall, this work provides important insights about the structure, Au–S bonding and solid photoluminescence of gold nanoclusters.