Deciphering the Metal-C60 Interface in Optoelectronic Devices: Evidence for C60 Reduction by Vapor Deposited Al

被引:22
作者
Matz, Dallas L. [1 ]
Ratcliff, Erin L. [1 ]
Meyer, Jens [2 ]
Kahn, Antoine [2 ]
Pemberton, Jeanne E. [1 ]
机构
[1] Univ Arizona, Dept Chem & Biochem, Tucson, AZ 85721 USA
[2] Princeton Univ, Dept Elect Engn, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
fullerene; charge transfer; charge displacement; organic photovoltaic; Raman spectroscopy; electron spectroscopy; OPEN-CIRCUIT VOLTAGE; ENERGY-LEVEL ALIGNMENT; SURFACE RAMAN-SPECTROSCOPY; SOLID-STATE BENZENE; TRIS-(8-HYDROXYQUINOLINE) ALUMINUM; PHOTOELECTRON-SPECTROSCOPY; ELECTRONIC-STRUCTURES; CHARGE-TRANSFER; THIN-FILMS; SPECTRA;
D O I
10.1021/am400640x
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The formation of interfacial midgap states due to the reduction of bucluninsterfullerene (C-60) to amorphous carbon upon subsequent vapor deposition of Al is confirmed using Raman spectroscopy and X-ray, ultraviolet, and inverse photoemission spectroscopies. We demonstrate that vapor deposition of Al results in n-type doping of C-60 due to an electron transfer from Al to the LUMO of C-60, resulting in the formation of midgap states near the C-60 Fermi level. Raman spectroscopy in ultrahigh vacuum clearly identifies the presence of the C-60 anion radical (C-60(center dot-)) as well as amorphous carbon created by further degradation of C-60(center dot-). In contrast, the interface formed by vapor deposition of Ag shows only a slight Ag/C-60 interfacial charge displacement with no evidence for complete metal-to-C-60 electron transfer to form the anion radical or its further degradation products. These results confirm previous speculations of metal-induced chemical damage of C-60 films after Al deposition, which is widely suspected of decreasing charge collection efficiency in OPVs, and provide key insight into charge collection at metal/organic interfaces in such devices.
引用
收藏
页码:6001 / 6008
页数:8
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