Exciton dissociation mechanism and exciton density in organic semiconductors by modulated-photocurrent spectroscopy

被引:1
|
作者
Kounavis, P. [1 ]
Symeonidis, I. [1 ]
机构
[1] Univ Patras, Dept Elect & Comp Engn, Patras 26504, Greece
来源
PHYSICAL REVIEW MATERIALS | 2024年 / 8卷 / 11期
关键词
FIELD-EFFECT TRANSISTORS; PHASE-SHIFT ANALYSIS; PENTACENE; STATES; PHOTORESPONSE; TRANSPORT; DYNAMICS; FISSION; HOLES;
D O I
10.1103/PhysRevMaterials.8.113807
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Light excitation in organic semiconductors produces excitons, which are tightly bound electron-hole pairs that must be separated into mobile charge carriers to produce photocurrent in organic optoelectronic devices. The details of the exciton dissociation mechanism are required to control and improve the performance of these devices. Here it is demonstrated that modulated photocurrent spectrofscopy is sensitive to elucidating this mechanism. In this technique, a probe light beam of modulated intensity and a bias light beam of fixed intensity are combined to excite a two-terminal organic semiconductor device. The resulting modulated photocurrent is measured by a lock-in amplifier. In order to analyze the modulated photocurrent spectra, a model analysis is developed that incorporates in the photogeneration process different possible exciton disassociation mechanisms. Analytical expressions are derived which reveal the essential key spectral features that are the signature of each different exciton dissociation mechanism. Among the investigated mechanisms, exciton dissociation through electron transfer to donorlike traps in the lower part of the energy gap that creates single-type carriers (holes) photocurrent was found to dominate in the pristine small molecule organic semiconductors studied here. This process becomes evident by affecting the dynamics of the interactions of holes with the above traps which are captured by the modulated photocurrent spectroscopy, highlighting its sensitivity to this mechanism. Moreover, a very useful method is proposed to extract the steady-state exciton density.
引用
收藏
页数:17
相关论文
共 50 条
  • [31] Ultrafast Hot Exciton Dissociation at Organic Interfaces
    Maiuri, Margherita
    Grancini, Giulia
    Fazzi, Daniele
    Petrozza, Anna Maria
    Brida, Daniele
    Cerullo, Giulio
    Lanzani, Guglielmo
    2013 CONFERENCE ON LASERS AND ELECTRO-OPTICS EUROPE AND INTERNATIONAL QUANTUM ELECTRONICS CONFERENCE (CLEO EUROPE/IQEC), 2013,
  • [32] Exciton dissociation mediated by phonons in organic photovoltaics
    Fomichev, Stepan
    Ruocco, Leonard
    Tully, Alexandra
    Berciu, Mona
    PHYSICAL REVIEW B, 2023, 107 (19)
  • [33] LASER SPECTROSCOPY OF ADMIXED AND EXCITON-STATES IN SEMICONDUCTORS
    KYAZYMZADE, AG
    ABUTALYBOV, GI
    DZHAKHANGIROVA, SA
    ZHURNAL TEKHNICHESKOI FIZIKI, 1992, 62 (05): : 169 - 171
  • [34] OPTICAL PROPERTIES OF SEMICONDUCTORS HAVING A HIGH EXCITON DENSITY
    GERGEL, VA
    SOVIET PHYSICS SOLID STATE,USSR, 1970, 11 (12): : 2962 - +
  • [35] Simulations of singlet exciton diffusion in organic semiconductors: a review
    Bjorgaard, Josiah A.
    Kose, Muhammet Erkan
    RSC ADVANCES, 2015, 5 (11) : 8432 - 8445
  • [36] Spin injection effects on exciton formation in organic semiconductors
    Yunus, M.
    Ruden, P. P.
    Smith, D. L.
    APPLIED PHYSICS LETTERS, 2008, 93 (12)
  • [37] What controls triplet exciton transfer in organic semiconductors?
    Koehler, Anna
    Baessler, Heinz
    JOURNAL OF MATERIALS CHEMISTRY, 2011, 21 (12) : 4003 - 4011
  • [38] Singlet fission and triplet exciton dynamics in organic semiconductors
    Bardeen, Chris
    Burdett, Jon
    Dillon, Robert
    Piland, Geoff
    Nichols, Valerie
    Lee, Jiun-Haw
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2013, 246
  • [39] Effect of hyperfine interactions on exciton formation in organic semiconductors
    Kersten, S. P.
    Schellekens, A. J.
    Koopmans, B.
    Bobbert, P. A.
    SYNTHETIC METALS, 2011, 161 (7-8) : 613 - 616
  • [40] Exciton dynamics in 2D organic semiconductors
    Sharma, Ankur
    Hasan, Md Mehedi
    Lu, Yuerui
    MATERIALS FUTURES, 2022, 1 (04):