| Literature DB >> 25376748 |
Qiaofeng Yao1, Yue Yu, Xun Yuan, Yong Yu, Dan Zhao, Jianping Xie, Jim Yang Lee.
Abstract
Ag44 (p-MBA)30 (4-) (p-MBA=para-mercaptobenzoic acid) nanocluster (NC) supracrystals (SCs) with customizable shapes can be obtained by simply altering the type and concentration of the counterions of the p-MBA ligands in the dimethylsulfoxide (DMSO)/water crystallization system. Changing the counterion of the p-MBA ligand from H(+) to Cs(+) eliminates the directional hydrogen bonds in the SCs, resulting in the packing of deprotonated Ag44 (p-MBA)30 (4-) NCs into octahedral SCs, which is in stark contrast to the rhombohedral SCs that were formed by the packing of protonated Ag44 (p-MBA)30 (4-) NCs in previous studies. Furthermore, the double layer of deprotonated Ag44 (p-MBA)30 (4-) NCs is sensitive to charge screening induced by increasing the Cs(+) concentration, thereby providing a means to regulate the precipitation kinetics of the Ag44 (p-MBA)30 (4-) NCs for SC shape engineering. Slow precipitation kinetics was found to favor over-growth at the corners and edges of the octahedral SC nuclei, shaping the SCs into concave octahedra.Entities:
Keywords: nanoclusters; noble metals; self-assembly; shape control; supracrystals
Year: 2014 PMID: 25376748 DOI: 10.1002/anie.201408675
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336