Effect of oxygen and water on the lifetime of organic solar cells

M. Chakaroun, R. Fawaz, B. Ratier
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Abstract

Ageing of organic solar cells is still a problem to resolve before these devices can reach the market. This question can be addressed using different strategies including encapsulating materials, device design and buffer layers, with the latter being addressed in this paper. The shelf life of un-encapsulated small-molecule organic solar cells, (ITO/PEDOT-PSS/CuPC/C60/buffer layer/Al), have been studied under 100 mW/cm2 continuous illumination in open air with different thin buffer layers of bathocuproine (BCP), tris-8-hydroxy-quiolinato-aluminum (Alq3), 1,3,5-tris(2-N-phenylbenzimidazolyl) benzene (TPBI) and lithium fluoride (LiF). Changes in the main photovoltaic parameters upon ageing (power conversion efficiency, fill factor, open circuit voltage, short circuit current density, series and shunt resistances) have been monitored. In all cases two ageing mechanisms with two different time constants have been demonstrated and attributed to a rapid degradation of cathode contact followed by contamination of the active layer.
氧和水对有机太阳能电池寿命的影响
在这些设备进入市场之前,有机太阳能电池的老化仍然是一个需要解决的问题。这个问题可以通过不同的策略来解决,包括封装材料、器件设计和缓冲层,本文将讨论缓冲层。在100 mW/cm2的露天连续照明下,研究了未封装的小分子有机太阳能电池(ITO/PEDOT-PSS/CuPC/C60/缓冲层/Al)在不同薄缓冲层(BCP)、三羟基喹啉铝(Alq3)、1,3,5-三(2- n-苯基苯并咪唑)苯(TPBI)和氟化锂(liff)下的保质期。监测了老化后光伏主要参数(功率转换效率、填充系数、开路电压、短路电流密度、串联和分流电阻)的变化情况。在所有情况下,具有两个不同时间常数的两种老化机制已被证明,并归因于阴极接触的快速退化,随后是活性层的污染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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