Quantum Yield Regeneration: Influence of Neutral Ligand Binding on Photophysical Properties in Colloidal Core/Shell Quantum Dots
Source abstract
Abstract
This article describes an experiment designed to identify the role of specific molecular ligands in maintaining the high photoluminescence (PL) quantum yield (QY) observed in as-synthesized CdSe/CdZnS and CdSe/CdS quantum dots (QDs). Although it has been possible for many years to prepare core/shell quantum dots with near-unity quantum yield through high-temperature colloidal synthesis, purification of such colloidal particles is frequently accompanied by a reduction in quantum yield. Here, a recently established gel permeation chromatography (GPC) technique is used to remove weakly associated ligands without a change in solvent: a decrease in ensemble QY and average PL lifetime is observed. Minor components of the initial mixture that were removed by GPC are then added separately to purified QD samples to determine whether reintroduction of these components can restore the photophysical properties of the initial sample. We show that among these putative ligands trioctylphosphine and cadmium oleate can regenerate the initial high QY of all samples, but only the "L-type" ligands (trioctyphosphine and oleylamine) can restore the QY without changing the shapes of the optical spectra. On the basis of the PL decay analysis, we confirm that quenching in GPC-purified samples and regeneration in ligand-introduced samples are associated chiefly with changes in the relative population fraction of QDs with different decay rates. The reversibility of the QY regeneration process has also been studied; the introduction and removal of trioctylphosphine and oleylamine tend to be reversible, while cadmium oleate is not. Finally, isothermal titration calorimetry has been used to study the relationship between the binding strength of the neutral ligands to the surface and photophysical property changes in QD samples to which they are added.
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 and Biochemistry and ‡USC Nanocenter, University of South Carolina, Columbia, South Carolina 29208, United States
Funding
Office of Experimental Program to Stimulate Competitive Research
References (97)
Show source-provided references
1. Smith A. M. · Acc. Chem. Res. · 2010 · 43 · 19010.1021/ar9001069 ↗
2. Leatherdale C. A. · J. Phys. Chem. B · 2002 · 106 · 761910.1021/jp025698c ↗
3. Jasieniak J. · J. Phys. Chem. C · 2009 · 113 · 1946810.1021/jp906827m ↗
4. Blanton S. A. · J. Lumin. · 1996 · 70 · 25310.1016/0022-2313(96)00059-2 ↗
5. Larson D. R. · Science · 2003 · 300 · 143410.1126/science.1083780 ↗
6. Wu X. · Nat. Biotechnol. · 2003 · 21 · 4110.1038/nbt764 ↗
7. Medintz I. L. · Nat. Mater. · 2005 · 4 · 43510.1038/nmat1390 ↗
8. Erathodiyil N. · Acc. Chem. Res. · 2011 · 44 · 92510.1021/ar2000327 ↗
9. Lemon C. M. · Inorg. Chem. · 2014 · 53 · 190010.1021/ic401587r ↗
10. Zhang B. · RSC Adv. · 2014 · 4 · 1380510.1039/C4RA00288A ↗
11. Anikeeva P. O. · Nano Lett. · 2009 · 9 · 253210.1021/nl9002969 ↗
12. Talapin D. V. · Chem. Rev. · 2010 · 110 · 38910.1021/cr900137k ↗
13. Panthani M. G. · Nano Lett. · 2014 · 14 · 67010.1021/nl403912w ↗
14. Zhang J. · ACS Nano · 2014 · 8 · 61410.1021/nn405236k ↗
15. Zhitomirsky D. · Nat. Commun. · 2014 · 5 · 380310.1038/ncomms4803 ↗
16. Meinardi F. · Nat. Photonics · 2014 · 8 · 39210.1038/nphoton.2014.54 ↗
17. Erickson C. S. · ACS Nano · 2014 · 8 · 346110.1021/nn406360w ↗
18. Geyer S. M. · ACS Nano · 2011 · 5 · 556610.1021/nn2010238 ↗
19. Zhu H. · Acc. Chem. Res. · 2013 · 46 · 127010.1021/ar300202d ↗
20. Efros A. L. · Phys. Rev. Lett. · 1997 · 78 · 111010.1103/PhysRevLett.78.1110 ↗
21. Frantsuzov P. A. · Phys. Rev. Lett. · 2009 · 103 · 20740210.1103/PhysRevLett.103.207402 ↗
22. Chen Y. · J. Am. Chem. Soc. · 2008 · 130 · 502610.1021/ja711379k ↗
23. Mahler B. · Nat. Mater. · 2008 · 7 · 65910.1038/nmat2222 ↗
24. Spinicelli P. · Phys. Rev. Lett. · 2009 · 102 · 13680110.1103/PhysRevLett.102.136801 ↗
25. Efros A. L. · Phys. Rev. B · 1996 · 54 · 484310.1103/PhysRevB.54.4843 ↗
26. Schlegel G. · Phys. Rev. Lett. · 2002 · 88 · 13740110.1103/PhysRevLett.88.137401 ↗
27. Fisher B. R. · J. Phys. Chem. B · 2004 · 108 · 14310.1021/jp035756+ ↗
28. Kuno M. · J. Chem. Phys. · 1997 · 106 · 986910.1063/1.473875 ↗
29. Mooney J. · J. Chem. Phys. · 2013 · 138 · 20470510.1063/1.4807054 ↗
30. Kalyuzhny G. · J. Phys. Chem. B · 2005 · 109 · 701210.1021/jp045352x ↗
31. Bullen C. · Langmuir · 2006 · 22 · 300710.1021/la051898e ↗
32. Munro A. M. · Nano Lett. · 2008 · 8 · 258510.1021/nl801132t ↗
33. Greytak A. B. · Chem. Sci. · 2012 · 3 · 202810.1039/c2sc00561a ↗
34. Anderson N. C. · Chem. Mater. · 2013 · 25 · 6910.1021/cm303219a ↗
35. Peterson M. D. · Annu. Rev. Phys. Chem. · 2014 · 65 · 31710.1146/annurev-physchem-040513-103649 ↗
36. Hines M. A. · J. Phys. Chem. · 1996 · 100 · 46810.1021/jp9530562 ↗
37. Qin H. · J. Am. Chem. Soc. · 2013 · 136 · 17910.1021/ja4078528 ↗
38. Morris-Cohen A. J. · Chem. Mater. · 2013 · 25 · 115510.1021/cm302108j ↗
39. Liu W. · J. Am. Chem. Soc. · 2008 · 130 · 127410.1021/ja076069p ↗
40. Shen Y. · Chem. Mater. · 2013 · 25 · 283810.1021/cm4012734 ↗
41. Morris-Cohen A. J. · J. Phys. Chem. C · 2010 · 114 · 89710.1021/jp909492w ↗
42. Hassinen A. · J. Am. Chem. Soc. · 2012 · 134 · 2070510.1021/ja308861d ↗
43. Owen J. · Science · 2015 · 347 · 61510.1126/science.1259924 ↗
44. Guyot-Sionnest P. · J. Chem. Phys. · 2005 · 123 · 07470910.1063/1.2004818 ↗
45. McArthur E. A. · J. Phys. Chem. B · 2009 · 114 · 1451410.1021/jp102101f ↗
46. Kilina S. · ACS Nano · 2012 · 6 · 651510.1021/nn302371q ↗
47. Munro A. M. · J. Phys. Chem. C · 2007 · 111 · 622010.1021/jp068733e ↗
48. Knowles K. E. · J. Am. Chem. Soc. · 2009 · 132 · 104110.1021/ja907253s ↗
49. Morris-Cohen A. J. · ACS Nano · 2012 · 6 · 55710.1021/nn203950s ↗
50. Zhu H. · J. Am. Chem. Soc. · 2011 · 133 · 876210.1021/ja202752s ↗
51. Zhao H. · Phys. Chem. Chem. Phys. · 2010 · 12 · 1475410.1039/c0cp01305f ↗
52. Lee J. R. I. · Nano Lett. · 2012 · 12 · 276310.1021/nl300886h ↗
53. Anderson N. C. · J. Am. Chem. Soc. · 2013 · 135 · 1853610.1021/ja4086758 ↗
54. Ji X. · J. Am. Chem. Soc. · 2008 · 130 · 572610.1021/ja710909f ↗
55. Williams E. S. · J. Phys. Chem. C · 2013 · 117 · 422710.1021/jp309896e ↗
56. Yang J. · J. Nanosci. Nanotechnol. · 2012 · 12 · 732210.1166/jnn.2012.6493 ↗
57. Park C. · Colloids Surf. B Biointerfaces · 2010 · 75 · 47210.1016/j.colsurfb.2009.09.021 ↗
58. Chen C.-J. · RSC Adv. · 2015 · 5 · 981910.1039/C4RA14280B ↗
59. Wang M. · Langmuir · 2009 · 25 · 1173210.1021/la900614e ↗
60. Oszajca M. · Eur. J. Inorg. Chem. · 2013 · 2013 · 355010.1002/ejic.201300331 ↗
61. Sharma S. N. · J. Phys. Chem. B · 2003 · 107 · 1008810.1021/jp034109f ↗
62. Burda C. · J. Phys. Chem. B · 2001 · 105 · 1228610.1021/jp0124589 ↗
63. Kern S. J. · Nano Lett. · 2011 · 11 · 349310.1021/nl202086b ↗
64. Jones M. · Proc. Natl. Acad. Sci. U.S.A. · 2009 · 106 · 301110.1073/pnas.0809316106 ↗
65. Zhao J. · Phys. Rev. Lett. · 2010 · 104 · 15740310.1103/PhysRevLett.104.157403 ↗
66. Hens Z. · Chem. Mater. · 2013 · 25 · 121110.1021/cm303361s ↗
67. Freyer M. W. · Methods Cell Biol. · 2008 · 84 · 7910.1016/S0091-679X(07)84004-0 ↗
68. Grossoehme N. · J. Biol. Inorg. Chem. · 2010 · 15 · 118310.1007/s00775-010-0693-3 ↗
69. Ravi V. · Nano Lett. · 2013 · 13 · 444210.1021/nl402315z ↗
70. Lindman S. · Nano Lett. · 2007 · 7 · 91410.1021/nl062743+ ↗
71. Mondal S. · J. Phys. Chem. C · 2012 · 116 · 977410.1021/jp210528n ↗
72. Tan R. · Chem. Mater. · 2013 · 25 · 372410.1021/cm402148s ↗
73. Li J. J. · J. Am. Chem. Soc. · 2003 · 125 · 1256710.1021/ja0363563 ↗
74. Davis K. · Langmuir · 2014 · 30 · 1091810.1021/la502204g ↗
75. Owen J. S. · J. Am. Chem. Soc. · 2008 · 130 · 1227910.1021/ja804414f ↗
76. Kopping J. T. · J. Am. Chem. Soc. · 2008 · 130 · 568910.1021/ja077414d ↗
77. Beaumont P. C. · J. Chem. Soc. Faraday Trans. · 1993 · 89 · 418510.1039/ft9938904185 ↗
78. Gomes R. · J. Phys. Chem. Lett. · 2011 · 2 · 14510.1021/jz1016729 ↗
79. Knowles K. E. · J. Phys. Chem. Lett. · 2012 · 3 · 1810.1021/jz2013775 ↗
80. Ning Z. · Phys. Chem. Chem. Phys. · 2011 · 13 · 584810.1039/c0cp02688c ↗
81. Jasieniak J. · J. Am. Chem. Soc. · 2007 · 129 · 284110.1021/ja066205a ↗
82. Minotto A. · J. Phys. Chem. C · 2014 · 118 · 2411710.1021/jp506778n ↗
83. Lakowicz J. R. · 200610.1007/978-0-387-46312-4 ↗
84. Sillen A. · Photochem. Photobiol. · 1998 · 67 · 47510.1111/j.1751-1097.1998.tb09082.x ↗
85. Galland C. · Nature · 2011 · 479 · 20310.1038/nature10569 ↗
86. Orfield N. J. · ACS Nano · 2014 · 9 · 83110.1021/nn506420w ↗
87. Tyagi P. · J. Chem. Phys. · 2011 · 134 · 09470610.1063/1.3561063 ↗
88. Singh G. · J. Phys. Chem. C · 2014 · 118 · 1469210.1021/jp5043766 ↗
89. Son D. H. · Science · 2004 · 306 · 100910.1126/science.1103755 ↗
90. Lambert K. · Chem. Mater. · 2009 · 21 · 77810.1021/cm8029399 ↗
91. Li H. · Nano Lett. · 2011 · 11 · 496410.1021/nl202927a ↗
92. Ren L. · Macromolecules · 2010 · 43 · 930410.1021/ma101935a ↗
93. Hassinen A. · J. Phys. Chem. Lett. · 2010 · 1 · 257710.1021/jz100781h ↗
94. Fleischer C. C. · J. Phys. Chem. B · 2014 · 118 · 1401710.1021/jp502624n ↗
95. Rempel J. Y. · J. Phys. Chem. B · 2006 · 110 · 1800710.1021/jp064051f ↗
96. Shanavas K. V. · J. Phys. Chem. C · 2012 · 116 · 650710.1021/jp2079428 ↗
97. Grabolle M. · Anal. Chem. · 2009 · 81 · 628510.1021/ac900308v ↗