Electrochemical Charging of CdSe Quantum Dot Films: Dependence on Void Size and Counterion Proximity

被引:61
作者
Boehme, Simon C. [1 ]
Wang, Hai [1 ]
Siebbeles, Laurens D. A. [1 ]
Vanmaekelbergh, Daniel [2 ]
Houtepen, Arjan J. [1 ]
机构
[1] Delft Univ Technol, NL-2628 BL Delft, Netherlands
[2] Univ Utrecht, Debye Inst Condensed Matter & Interfaces, NL-3508 TA Utrecht, Netherlands
关键词
spectroelectrochemistry; electrochemical charging; quantum dot; surface functionalization; layer by layer; ligand; energy level; ELECTRICAL-PROPERTIES; NANOCRYSTALS; TRANSPORT; SEMICONDUCTORS; INTERCALATION; RECOMBINATION; PHOTOVOLTAICS; ACCUMULATION; ACETONITRILE; ELECTROLYTE;
D O I
10.1021/nn3058455
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Films of colloidal quantum dots (QDs) show great promise for application in optoelectronic devices. Great advances have been made in recent years in designing efficient QD solar cells and LEDs. A very important aspect in the design of devices based on QD films is the knowledge of their absolute energy levels. Unfortunately, reported energy levels vary markedly depending on the employed measurement technique and the environment of the sample. In this report, we determine absolute energy levels of QD films by electrochemical charge Injection. The concomitant change in optical absorption of the film allows quantification of the number of charges in quantum-confined levels and thereby their energetic position. We show here that the size of voids in the QD films (le., the space between the quantum dots) determines the amount of charges that may be Injected into the films. This effect is attributed to size exclusion of countercharges from the electrolyte solution. Further, the energy of the QD levels depends on subtle changes in the QD film and the supporting electrolyte: the size of the cation and the QD ligand length. These nontrivial effects can be explained by the proximity of the cation to the QD surface and a concomitant lowering of the electrochemical potential. Our findings help explain the wide range of reported values for QD energy levels and redefine the limit of applicability of electrochemical measurements on QD films. Finally, the finding that the energy of QD levels depends on ligand length and counterion size may be exploited in optimized designs of QD sensitized solar cells.
引用
收藏
页码:2500 / 2508
页数:9
相关论文
共 60 条
[1]   Quantum Dot Light-Emitting Devices with Electroluminescence Tunable over the Entire Visible Spectrum [J].
Anikeeva, Polina O. ;
Halpert, Jonathan E. ;
Bawendi, Moungi G. ;
Bulovic, Vladimir .
NANO LETTERS, 2009, 9 (07) :2532-2536
[2]   Photodriven heterogeneous charge transfer with transition-metal compounds anchored to TiO2 semiconductor surfaces [J].
Ardo, Shane ;
Meyer, Gerald J. .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (01) :115-164
[3]   A review of recent results on electrochemical determination of the density of electronic states of nanostructured metal-oxide semiconductors and organic hole conductors [J].
Bisquert, Juan ;
Fabregat-Santiago, Francisco ;
Mora-Sero, Ivan ;
Garcia-Belmonte, Germa ;
Barea, Eva M. ;
Palomares, Emilio .
INORGANICA CHIMICA ACTA, 2008, 361 (03) :684-698
[4]   Electron accumulation in nanostructured TiO2 (anatase) electrodes [J].
Boschloo, G ;
Fitzmaurice, D .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (37) :7860-7868
[5]   Photogenerated Exciton Dissociation in Highly Coupled Lead Salt Nanocrystal Assemblies [J].
Choi, Joshua J. ;
Luria, Justin ;
Hyun, Byung-Ryool ;
Bartnik, Adam C. ;
Sun, Liangfeng ;
Lim, Yee-Fun ;
Marohn, John A. ;
Wise, Frank W. ;
Hanrath, Tobias .
NANO LETTERS, 2010, 10 (05) :1805-1811
[6]   Laser Scribing of High-Performance and Flexible Graphene-Based Electrochemical Capacitors [J].
El-Kady, Maher F. ;
Strong, Veronica ;
Dubin, Sergey ;
Kaner, Richard B. .
SCIENCE, 2012, 335 (6074) :1326-1330
[7]   Influence of electrolyte in transport and recombination in dye-sensitized solar cells studied by impedance spectroscopy [J].
Fabregat-Santiago, F ;
Bisquert, J ;
Garcia-Belmonte, G ;
Boschloo, G ;
Hagfeldt, A .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2005, 87 (1-4) :117-131
[8]   Two types of luminescence blinking revealed by spectroelectrochemistry of single quantum dots [J].
Galland, Christophe ;
Ghosh, Yagnaseni ;
Steinbrueck, Andrea ;
Sykora, Milan ;
Hollingsworth, Jennifer A. ;
Klimov, Victor I. ;
Htoon, Han .
NATURE, 2011, 479 (7372) :203-U75
[9]   Quantum Dot Size Dependent J-V Characteristics in Heterojunction ZnO/PbS Quantum Dot Solar Cells [J].
Gao, Jianbo ;
Luther, Joseph M. ;
Semonin, Octavi E. ;
Ellingson, Randy J. ;
Nozik, Arthur J. ;
Beard, Matthew C. .
NANO LETTERS, 2011, 11 (03) :1002-1008
[10]   Photoconductivity of PbSe Quantum-Dot Solids: Dependence on Ligand Anchor Group and Length [J].
Gao, Yunan ;
Aerts, Michiel ;
Sandeep, C. S. Suchand ;
Talgorn, Elise ;
Savenije, Tom J. ;
Kinge, Sachin ;
Siebbeles, Laurens D. A. ;
Houtepen, Arjan J. .
ACS NANO, 2012, 6 (11) :9606-9614