Synthesis and Surface Chemistry of Cadmium Carboxylate Passivated CdTe Nanocrystals from Cadmium bis(Phenyltellurolate)
Source abstract
Abstract
We report the synthesis of cadmium telluride nanocrystals from cadmium bis (phenyltellurolate) (Cd(TePh) 2 ) and cadmium alkylcarboxylates (Cd(O 2 CR) 2, O 2 CR = oleate, tetradecanoate). Cd(TePh) 2 reacts quantitatively with Cd(O 2 CR) 2 at 220 °C over 1 h with the concomitant elimination of diphenyl telluride (Ph 2 Te) and CdTe nanocrystals. The nanocrystal diameter approaches 3.0–3.2 nm at full conversion regardless of changes to the solvent, carboxylate chain length, heating conditions, and reaction concentration. Larger nanocrystals may be grown by slow addition of additional precursors to the crude product mixture. Isolated nanocrystals have carboxylate ligands (2.1–4.7 nm –2 ) that can be displaced along with excess cadmium ions using low concentrations of N,N,N′,N′-tetramethylethylenediamine (TMEDA) (1.5–280 mM). Using 1 H NMR spectroscopy, we measure the extent of the displacement and show that the binding of Cd(O 2 CR) 2 to CdTe is weaker than to CdSe nanocrystals of similar size. The weaker binding is proposed to arise from a lower polarity and greater stability of reconstructed CdTe surfaces.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Columbia University, New York, New York 10027, United States
Funding
Basic Energy Sciences · U.S. Department of Energy
References (40)
Show source-provided references
1. 10.1021/cm303564210.1021/cm3035642 ↗
2. 10.1126/science.aaa295110.1126/science.aaa2951 ↗
3. 10.1021/nn204008q10.1021/nn204008q ↗
4. 10.1021/nn305916810.1021/nn3059168 ↗
5. 10.1021/nn301182h10.1021/nn301182h ↗
6. 10.1021/nn400596e10.1021/nn400596e ↗
7. Krum S. · First Solar · 2015 · 1
8. 10.1021/nn502442g10.1021/nn502442g ↗
9. 10.1021/nl403912w10.1021/nl403912w ↗
10. 10.1116/1.356975710.1116/1.3569757 ↗
11. 10.1103/PhysRevLett.112.15610310.1103/PhysRevLett.112.156103 ↗
12. 10.1021/ja00257a05510.1021/ja00257a055 ↗
13. 10.1021/cm00010a01710.1021/cm00010a017 ↗
14. 10.1021/ja00193a07910.1021/ja00193a079 ↗
15. 10.1039/b910466f10.1039/b910466f ↗
16. 10.1039/b008376n10.1039/b008376n ↗
17. 10.1002/anie.19860165210.1002/anie.198601652 ↗
18. 10.1021/ja00530a02310.1021/ja00530a023 ↗
19. 10.1021/ic050517h10.1021/ic050517h ↗
20. 10.1021/ja411018210.1021/ja4110182 ↗
21. 10.1071/CH982046910.1071/CH9820469 ↗
22. 10.1021/jp212281m10.1021/jp212281m ↗
23. 10.1021/cm034081k10.1021/cm034081k ↗
24. 10.1021/cm034729t10.1021/cm034729t ↗
25. 10.1002/anie.20050227910.1002/anie.200502279 ↗
26. 10.1021/nn303769h10.1021/nn303769h ↗
27. 10.1016/S0927-7757(99)00366-010.1016/S0927-7757(99)00366-0 ↗
28. 10.1021/ja106777j10.1021/ja106777j ↗
29. 10.1021/ja408675810.1021/ja4086758 ↗
30. 10.1021/nn300046610.1021/nn3000466 ↗
31. 10.1126/science.125272710.1126/science.1252727 ↗
32. 10.1021/cr950212s10.1021/cr950212s ↗
33. 10.1021/jp044557310.1021/jp0445573 ↗
34. 10.1021/ja503590h10.1021/ja503590h ↗
35. 10.1021/jz100224q10.1021/jz100224q ↗
36. 10.1002/anie.20080426610.1002/anie.200804266 ↗
37. 10.1021/cm303219a10.1021/cm303219a ↗
38. 10.1021/cm302695710.1021/cm3026957 ↗
39. Badiello R. · 1986 · 1
40. Yamago, S.; Yoshida, J.Organic Tellurium Compound, Process for Producing the Same, Living Radical Polymerization Initiator, Process for Producing Polymer with the Same, and Polymer. Patent Application EP1541550, June 15, 2005.