In Situ Surface-Enhanced Raman Spectroscopy on Organic Mixed Ionic-Electronic Conductors: Tracking Dynamic Doping in Light-Emitting Electrochemical Cells

被引:2
作者
Jafari, Mohammad Javad [1 ]
Pedersen, Jonas Oshaug [1 ]
Barhemat, Samira [2 ]
Ederth, Thomas [1 ]
机构
[1] Linkoping Univ, Div Biophys & Bioengn, IFM, S-58183 Linkoping, Sweden
[2] Mabema AB, Dept Vis Inspect, S-58422 Linkoping, Sweden
关键词
light-emitting electrochemicalcell; surface-enhancedRaman spectroscopy; electrochemical doping; time-resolved; MEH-PPV; RESONANT RAMAN; SERS; PROFILES; OXYGEN;
D O I
10.1021/acsami.4c00684
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In the domain of organic mixed ionic-electronic conductors (OMIECs), simultaneous transport and coupling of ionic and electronic charges are crucial for the function of electrochemical devices in organic electronics. Understanding conduction mechanisms and chemical reactions in operational devices is pivotal for performance enhancement and is necessary for the informed and systematic development of more promising materials. Surface-enhanced Raman spectroscopy (SERS) is a potent tool for monitoring electrochemical evolution and dynamic doping in operational devices, offering enhanced sensitivity to subtle spectral changes. We demonstrate the utility of SERS for in situ tracking of doping in OMIECs in an organic light-emitting electrochemical cell (LEC) containing a conjugated polymer (poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene]; MEH-PPV), a molecular anion (lithium triflate), and an electrolyte network (poly(ethylene oxide); PEO). SERS enhancement is achieved via an interleaved layer of gold particles formed by spontaneous breakup of a deposited thin gold film. The results successfully highlight the ability of SERS to unveil time-resolved MEH-PPV doping and polaron formation, elucidating the effects of triflate ion transfer in the operating device and validating the electrochemical doping model in LECs.
引用
收藏
页码:28938 / 28948
页数:11
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