Bright and Water-Soluble Near IR-Emitting CdSe/CdTe/ZnSe Type-II/Type-I Nanocrystals, Tuning the Efficiency and Stability by Growth
Source abstract
Abstract
Highly photoluminescent CdSe/CdTe/ZnSe type-II/type-I composite nanocrystals, both dot- and peanut-shaped, were prepared via the modified successive ionic layer adsorption and reaction (SILAR) techniques, straight SILAR for peanut-shaped ones and SILAR coupled with thermal-cycling (SILAR-TC) for dot-shaped ones. The CdSe/CdTe type-II heterojunction offered the nanocrystals with near-infrared emission and the CdTe/ZnSe type-I heterojunction helped to confine the photogenerated charges away from the ligands and solution environment. This structural feature makes the photoluminescence quantum yield of the CdSe/CdTe/ZnSe core/shell/shell type-II/type-I dots that have a uniformly grown ZnSe shell retain as high as 60% after replacing the original amine ligands with mercaptopropionic acid (MPA). Conversely, the emission of the corresponding CdSe/CdTe core/shell dots (CdSe/CdTe/ZnSe composite peanuts) was completely (almost completely) quenched by the same ligand treatment. The emission properties of the MPA-coated CdSe/CdTe/ZnSe core/shell/shell dots were stable in water in the buffer solutions with their pH in a range between about 5 and 9.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry & Biochemistry, University of Arkansas, Fayetteville, Arkansas 72701, and NN-Laboratories LLC, Fayetteville, Arkansas 72703
References (21)
Show source-provided references
1. Bruchez M. · Science · 1998 · 281 · 201310.1126/science.281.5385.2013 ↗
2. Chan W. C. W. · Science · 1998 · 281 · 201610.1126/science.281.5385.2016 ↗
3. Klimov V. I. · Science · 2000 · 290 · 31410.1126/science.290.5490.314 ↗
4. Colvin V. L. · Nature · 1994 · 370 · 35410.1038/370354a0 ↗
5. Michalet X. · Science · 2005 · 307 · 53810.1126/science.1104274 ↗
6. Kim S. · Nat. Biotechnol. · 2004 · 22 · 9310.1038/nbt920 ↗
7. Blackman B. · Chem. Mater. · 2007 · 19 · 381510.1021/cm0704682 ↗
8. Kim S. · J. Am. Chem. Soc. · 2003 · 125 · 1146610.1021/ja0361749 ↗
9. Balet L. P. · Nano Lett. · 2004 · 4 · 148510.1021/nl049146c ↗
10. Li J. J. · Chem. Phys. · 2005 · 318 · 8210.1016/j.chemphys.2005.04.029 ↗
11. Yu K.;. · Small · 2005 · 1 · 33210.1002/smll.200400069 ↗
12. Halpert J. E. · J. Am. Chem. Soc. · 2006 · 128 · 1259010.1021/ja0616534 ↗
13. Wang C. H. · J. Appl. Phys. · 2006 · 99 · 123521/1
14. Li J. J. · J. Am. Chem. Soc. · 2003 · 125 · 1256710.1021/ja0363563 ↗
15. Qu L. · J. Am. Chem. Soc. · 2002 · 124 · 204910.1021/ja017002j ↗
16. Pradhan N. · Nano Lett. · 2007 · 7 · 31210.1021/nl062336y ↗
17. Battaglia D. · J. Am. Chem. Soc. · 2005 · 127 · 1088910.1021/ja0437297 ↗
18. Aldana J. · J. Am. Chem. Soc. · 2001 · 123 · 884410.1021/ja016424q ↗
19. Murray C. B. · J. Am. Chem. Soc. · 1993 · 115 · 870610.1021/ja00072a025 ↗
20. Peng X. · Struct. Bonding · 2005 · 118 · 7910.1007/b137472 ↗
21. Ivanov S. A. · J. Am. Chem. Soc. · 2007 · 129 · 1170810.1021/ja068351m ↗