A macrocycle-assisted nanoparticlization process for bulk Ag2S12. Issue 1 (26th September 2014)

• Record Type: Journal Article
• Authors: He, Xin; Wang, Yuechao; Gao, Cai-Yan; Jiang, Hong; Zhao, Liang
• Is Part Of: Chemical science. Volume 6:Issue 1(2015:Jan.)
• Page Start: 654
• Page End: 658
• Publication Date: 2014-09-26
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c4sc01884b
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : A new nanoparticlization process for the bulk-to-nano transformation of Ag2 S by incorporating both top-down and bottom-up approaches is reported. Abstract : We report herein a new nanoparticlization process for the bulk-to-nano transformation of Ag2 S by incorporating both top-down and bottom-up approaches. Bulk Ag2 S was dissolved in solution with the assistance of a macrocyclic ligand, hexamethylazacalix[6]pyridine (Py[6] ), to produce polynuclear silver sulfide cluster aggregates. All Ag–S cluster aggregates obtained in three crystalline complexes were protected byPy[6] macrocycles. Removing the protectivePy[6] macrocycles by protonation led to the generation of unconventional Ag–S nanoparticles with a large energy gap. Theoretical calculations by a hybrid DFT method demonstrated that the silver sulfide clusters with high Ag/S ratio exhibited more localized HOMO–LUMO orbitals, which consequently enlarged their band gap energies. These experimental and theoretical studies broaden our understanding of the fabrication of nanomaterials by virtue of the advantages of both bottom-up and top-down methods and meanwhile provide a viable means of adjusting the band gap of binary nanomaterials independent of their size.