The Modification of Indium Tin Oxide with Phosphonic Acids: Mechanism of Binding, Tuning of Surface Properties, and Potential for Use in Organic Electronic Applications

被引:349
作者
Hotchkiss, Peter J. [1 ]
Jones, Simon C. [1 ]
Paniagua, Sergio A. [1 ]
Sharma, Asha [2 ]
Kippelen, Bernard [2 ]
Armstrong, Neal R. [3 ]
Marder, Seth R. [1 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Ctr Organ Photon & Elect, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Sch Elect & Comp Engn, Ctr Organ Photon & Elect, Atlanta, GA USA
[3] Univ Arizona, Dept Chem & Biochem, Tucson, AZ 85721 USA
基金
美国国家科学基金会;
关键词
SELF-ASSEMBLED MONOLAYERS; LIGHT-EMITTING DIODE; COUPLING MOLECULES; HOLE-INJECTION; CHARGE INJECTION; ITO; ADSORPTION; STABILITY; CHEMISTRY; KINETICS;
D O I
10.1021/ar200119g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transparent metal oxides, In particular, indium tin oxide (ITO), are I critical transparent contact materials for applications in next-generation organic electronics, including organic light emitting diodes (OLEDs) and organic photovoltaics (OPVs). Understanding and controlling the surface properties of ITO allows for the molecular engineering of the ITO organic interface, resulting in fine control of the interfacial chemistries and electronics. In particular, both surface energy matching and work function compatibility at material interfaces can result in marked improvement in OLED and OPV performance. Although there are numerous ways to change the surface properties of ITO, one of the more successful surface modifications is the use of monolayers based on organic molecules with widely variable end functional groups. Phosphonic acids (PAs) are known to bind strongly to metal oxides and form robust monolayers on many different metal oxide materials. They also demonstrate several advantages over other functionalizing moieties such as silanes or carboxylic acids. Most notably, PAs can be stored in ambient conditions without degradation, and the surface modification procedures This Account focuses on our research studying PA binding to ITO, are typically robust and easy to employ. the tunable properties of the resulting surfaces, and subsequent effects on the performance of organic electronic devices. We have used surface characterization techniques such as X-ray photoelectron spectroscopy (XPS) and infrared reflection adsorption spectroscopy (IRRAS) to determine that PAs bind to ITO in a predominantly bidentate fashion (where two of three oxygen atoms from the PA are involved in surface binding). Modification of the functional R-groups on PAs allows us to control and tune the surface energy and work function of the ITO surface. In one study using fluorinated benzyl PM, we can keep the surface energy of ITO relatively low and constant but tune the surface work function. PA modification of ITO has resulted in materials that are more stable and more compatible with subsequently deposited organic materials, an effective work function that can be tuned by over 1 eV, and energy barriers to hole injection (OLED) or hole-harvesting (OPV) that can be well matched to the frontier orbital energies of the organic active layers, leading to better overall device properties.
引用
收藏
页码:337 / 346
页数:10
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