journal article·2018-01

How accurate are energies of HOMO and LUMO levels in small-molecule organic semiconductors determined from cyclic voltammetry or optical spectroscopy?

Juliusz Sworakowski

Synthetic Metals· Volume 235
Publisher page

Abstract

Abstract Examined are relations between the energies of the transport gaps (i.e., the gaps determined by UPS/IPES measurements and taken for ‘true’ HOMO-LUMO gaps), and the electrochemical gaps (determined from CV experiments) and optical gaps (determined from UV-VIS optical spectroscopy). The statistics, based on literature data for several small (non-polymeric) molecules, shows that, on average, the electrochemical measurements underestimate the gap energies by ca. 16%, and the optical gap is smaller than the transport gap by ca. 37%. These differences seriously affect the accuracy of determination of energies of HOMO and LUMO levels by indirect methods. The concordance with the results obtained from the UPS/IPES measurements can be improved by using correction factors put forward in the present paper.
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Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Molecular Junctions and Nanostructures

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References (50)

Show source-provided references
1. Fundamental electronic structure of organic solids and their interfaces by photoemission spectroscopy and related methods, Ch. 7
2. Experimental characterization of interfaces of relevance to organic electronics, Ch. 6
3. Principle and application of low energy inverse photoemission spectroscopy: a new method for measuring unoccupied states of organic semiconductors10.1016/j.elspec.2015.07.003 ↗
4. The transport gap of organic semiconductors studied using the combination of direct and inverse photoemission10.1016/j.chemphys.2006.02.003 ↗
5. Determination of transport levels of organic semiconductors by UPS and IPS10.1088/1367-2630/10/8/085001 ↗
6. Cyclic voltammetry − electrochemical spectroscopy10.1002/anie.198408313 ↗
7. Bard · 2001
8. Chain-length dependence of electronic and electrochemical properties of conjugated systems: polyacetylene, polyphenylene, polythiophene, and polypyrrole10.1021/ja00360a004 ↗
9. Relationship between the ionization and oxidation potentials of molecular organic semiconductors10.1016/j.orgel.2005.01.002 ↗
10. Measurement of the lowest unoccupied molecular orbital energies of molecular organic semiconductors10.1016/j.orgel.2008.12.011 ↗
11. On the reliability of determination of energies of HOMO and LUMO levels in organic semiconductors from electrochemical measurements. A simple picture based on the electrostatic model10.1016/j.orgel.2016.03.031 ↗
12. Recommendations on reporting electrode potentials in nonaqueous solvents10.1351/pac198456040461 ↗
13. On the reliability of determination of energies of HOMO levels in organic semiconducting polymers from electrochemical measurements10.1016/j.orgel.2017.05.031 ↗
14. Electronic properties and optical studies of luminescent polythiophene derivatives10.1016/S0379-6779(00)00368-4 ↗
15. Conjugated polymer energy level shifts in Lithium-ion battery electrolytes10.1021/am505416m ↗
16. Electrochemically-reversible, single-electron oxidation of C60 and C7010.1021/ja00074a066 ↗
17. Substituent effects in pentacenes: gaining control over HOMO-LUMO gaps and photooxidative resistances10.1021/ja804515y ↗
18. Electronic structure of small band gap oligomers based on cyclopentadithiophenes and acceptor units10.1039/b901374a ↗
19. Hydrazones containing electron-accepting and electron-donating moieties10.1016/j.dyepig.2011.02.002 ↗
20. Arylene bisimides with triarylamine N-substituents as new solution processable organic semiconductors: synthesis, spectroscopic, electrochemical and electronic properties10.1016/j.synthmet.2011.05.025 ↗
21. Substituent effect of ancillary ligands on the luminescence of bis[4,6-(di-fluorophenyl)-pyridinato-N,C2']iridium(III) complexes10.1039/c2dt30695f ↗
22. Symmetrically disubstituted bithiophene derivatives of 1,3,4-oxadiazole, 1,3,4-thiadiazole, and 1,2,4-triazole – spectroscopic, electrochemical, and spectroelectrochemical properties10.1021/jp507838c ↗
23. Optical properties and electronic structure of amorphous Germanium10.1002/pssb.19660150224 ↗
24. On determining the optical gap associated with an amorphous semiconductor: a generalization of the Tauc model10.1016/S0038-1098(97)00268-8 ↗
25. The dependence of the Tauc and Cody optical gaps associated with hydrogenated amorphous silicon on the film thickness: αl experimental limitations and the impact of curvature in the Tauc and Cody plots10.1063/1.2817822 ↗
26. Determination of the optical gap in thin films of amorphous dilithium phthalocyanine using the Tauc and Cody models10.3390/molecules170910000 ↗
27. Photo- and semi-conductance in organic crystals. Part V: ionized states in molecular crystals10.1039/jr9570005001 ↗
28. Gutmann · 1967
29. Polarization energies of organic solids determined by ultraviolet photoelectron spectroscopy10.1039/f29817701621 ↗
30. Ionization energies of free molecules and molecular solids
31. Volumen und Hydratationswärme der Ionen10.1007/BF01881023 ↗
32. Diffusion and electrolytic conduction in crystals (ionic semiconductors)10.1063/1.1749319 ↗
33. Polarization energy of a localized charge in a molecular crystal. V. Effect of vacancies10.1016/0301-0104(83)85064-2 ↗
34. Quadrupolar traps for charge carriers in the vicinity of lattice vacancies in pentacene crystals10.1016/0009-2614(84)85668-7 ↗
35. Reevaluation of electronic polarization energies in organic molecular crystals10.1016/0301-0104(87)80041-1 ↗
36. Electronic polarization effects upon charge injection in oligoacene molecular crystals: description via a polarizable force field10.1021/jp402991z ↗
37. Charge-separation energy in films of π-conjugated organic molecules10.1016/S0009-2614(00)00882-4 ↗
38. Mind the gap!10.1039/C3MH00098B ↗
39. Exciton binding energy in small organic conjugated molecule10.1016/j.synthmet.2013.04.010 ↗
40. Location of charge transfer states in a-sexithienyl determined by the electroabsorption technique10.1016/0009-2614(94)01368-6 ↗
41. Electron-hole interaction energy in the organic molecular semiconductor PTCDA10.1016/S0009-2614(97)00481-8 ↗
42. Excitons in conjugated polymers10.1016/S0379-6779(99)00187-3 ↗
43. T. Schwieger Band-gap and correlation effects in the organic semiconductor Alq310.1103/PhysRevB.65.033204 ↗
44. Exciton binding energies in organic semiconductors10.1007/s00339-003-2182-9 ↗
45. Calculation of electron affinity ionization potential, transport gap, optical band gap and exciton binding energy of organic solids using ‘solvation’ model and DFT10.1016/j.orgel.2009.06.011 ↗
46. Transport and optical gaps and energy band alignment at organic-inorganic interfaces10.1063/1.4823518 ↗
47. Effect of N-substituents on redox, optical, and electronic properties of naphthalene bisimides used for field-effect transistors fabrication10.1021/jp908931w ↗
48. Impact of linking topology on the properties of carbazole trimers and dimers10.1021/jp111333v ↗
49. Structure–properties relationship of carbazole and fluorene hybrid trimers: experimental and theoretical approaches10.1039/c4cp00302k ↗
50. Linearly π-conjugated oligothiophenes as simple metal-free sensitizers for dye-sensitized solar cells10.1039/C5TC01183C ↗