材料科学
非阻塞I/O
工作职能
佩多:嘘
有机太阳能电池
X射线光电子能谱
氧化铟锡
能量转换效率
太阳能电池
紫外光电子能谱
聚合物太阳能电池
化学工程
分析化学(期刊)
光电子学
图层(电子)
纳米技术
复合材料
有机化学
催化作用
化学
工程类
聚合物
作者
K. Xerxes Steirer,Paul F. Ndione,N. Edwin Widjonarko,Matthew T. Lloyd,Jens Meyer,Erin L. Ratcliff,Antoine Kahn,Neal R. Armstrong,Calvin J. Curtis,David S. Ginley,Joseph J. Berry,Dana C. Olson
标识
DOI:10.1002/aenm.201100234
摘要
Abstract We show enhanced efficiency and stability of a high performance organic solar cell (OPV) when the work‐function of the hole collecting indium‐tin oxide (ITO) contact, modified with a solution‐processed nickel oxide (NiO x ) hole‐transport layer (HTL), is matched to the ionization potential of the donor material in a bulk‐heterojunction solar cell. Addition of the NiO x HTL to the hole collecting contact results in a power conversion efficiency ( PCE ) of 6.7%, which is a 17.3% net increase in performance over the 5.7% PCE achieved with a poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) HTL on ITO. The impact of these NiO x films is evaluated through optical and electronic measurements as well as device modeling. The valence and conduction band energies for the NiO x HTL are characterized in detail through photoelectron spectroscopy studies while spectroscopic ellipsometry is used to characterize the optical properties. Oxygen plasma treatment of the NiO x HTL is shown to provide superior contact properties by increasing the ITO/NiO x contact work‐function by 500 meV. Enhancement of device performance is attributed to reduction of the band edge energy offset at the ITO/NiO x interface with the poly(N‐9′‐heptadecanyl‐2,7‐carbazole‐alt‐5,5‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothidiazole) (PCDTBT):[6,6]‐phenyl‐C61 butyric acid methyl ester PCBM and [6,6]‐phenyl‐C71 butyric acid methyl ester (PC 70 BM) active layer. A high work‐function hole collecting contact is therefore the appropriate choice for high ionization potential donor materials in order to maximize OPV performance.
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