Crystalline Superlattices of Nanoscopic CdS Molecular Clusters: An X-ray Crystallography and 111Cd SSNMR Spectroscopy Study

被引:7
作者
Levchenko, Tetyana I. [1 ]
Lucier, Bryan E. G. [1 ]
Corrigan, John F. [1 ,2 ]
Huang, Yining [1 ,2 ]
机构
[1] Univ Western Ontario, Dept Chem, London, ON N6A 5B7, Canada
[2] Univ Western Ontario, Ctr Adv Mat & Biomat Res, London, ON N6A 5B7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
SOLID-STATE NMR; CHALCOGENIDE CLUSTERS; CHEMISTRY; SURFACE; SEMICONDUCTOR; COMPLEXES; SPECTRA; SIZE; NANOCRYSTALS; SELENOLATE;
D O I
10.1021/acs.inorgchem.7b02403
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Systematic Cd-111 solid-state (SS) NMR experiments were performed to correlate X-ray crystallographic data with SSNMR parameters for a set of CdS-based materials, varying from molecular crystals of small complexes [Cd(SPh)(4)](2-) and [Cd-4(SPh)(10)](2-) to superlattices of large monodisperse clusters [Cd54S32(SPh)(48)(dmf)(4)](4-) and 1.9 nm CdS. Methodical data analysis allowed for assigning individual resonances or resonance groups to particular types of cadmium sites residing in different chemical and/or crystallographic environments. For large CdS frameworks, Cd-111 resonances were found to form three groups. This result is noteworthy, since for related systems with size polydispersity and variations in composition, such as CdS or CdSe nanoparticles protected with an organic ligand shell, typically only two groups of resonances were observed. The generalized information obtained in this work can be used for the interpretation of Cd-111/113 SSNMR data for large CdS clusters and nanoparticles, for which crystal structure analysis remains inaccessible. Comparison of the powder X-ray diffraction patterns for freshly prepared and dried superlattices of large CdS clusters revealed an interesting superstructure rearrangement that was not observed for the smaller frameworks.
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页码:204 / 217
页数:14
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