具有中间1,1-二[(二-4-甲苯胺)苯基]环己烷层的有机/硅-纳米线杂化异质结太阳能电池效率为11%

Chia-Ying Tsai, Po-Han Chen, Yang-Yue Huang, Huai-Te Pen, P. Yu, H. Meng
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引用次数: 3

摘要

基于硅纳米线(SiNWs)的有机-无机异质结杂化太阳能电池具有低制造成本和高效率的潜力,是下一代光伏电池的理想选择。通过简单的金属辅助湿化学蚀刻方法制造的SiNW阵列产生了大的表面积与体积比,因此可以通过形成核心-鞘层p-n结来实现高效的光收集和电荷收集。然而,先前报道的功率转换效率(pce)大约限制在10%,这主要是由限制开路电压(Voc)和填充因子(FF)的界面缺陷密度所描述的。在这项工作中,我们引入了一种溶液处理的中间1,1-二[(二-4-甲苯胺)苯基]环己烷(TAPC)层,以减轻由SiNWs和共轭聚合物聚(3,4-乙烯二氧基噻吩):聚苯乙烯磺酸盐(PEDOT:PSS)组成的杂化异质结太阳能电池的界面重组损失。PCE达到创纪录的11.0%,相比之下,没有TAPC的参考产品的PCE为9.6%,这代表了14.2%的增强因子,归因于Voc和FF的显著改善。通过对暗饱和电流的抑制和对少数载流子寿命的提高(从未加TAPC时的84 μsec提高到加TAPC后的87 μsec)来检测界面质量指标,进一步支持了这一结果。
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11%-Efficiency hybrid organic/silicon-nanowire heterojunction solar cell with an intermediate 1,1-bis[(di-4-tolylamino)phenyl]cyclohexane layer
Hybrid organic-inorganic heterojunction solar cells based on silicon nanowires (SiNWs) are promising candidates for next-generation photovoltaics owing to potentials for low fabrication cost and high efficiency. The SiNW array, fabricated by a simple metal-assisted wet chemical etching method, produces a large surface-area-to-volume ratio, hence allowing efficient light harvesting and charge collection via the formation of a core-sheath p-n junction. However, previously reported power conversion efficiencies (PCEs) are approximately capped at 10%, which is largely depicted by the interface defect densities that limit the open-circuit voltage (Voc) and fill factor (FF). In this work, we introduce a solution-processed, intermediate 1,1-bis[(di-4-tolylamino)phenyl]cyclohexane (TAPC) layer to mitigate the interface recombination loss for hybrid heterojunction solar cells consisted of SiNWs and conjugate polymer poly(3,4-ethylenedioxy-thiophene): poly(styrenesulfonate) (PEDOT:PSS). A record PCE of 11.0% is achieved in contrast to 9.6% from a reference counterpart without TAPC, which represents an enhancement factor of 14.2% ascribed to noticeable improvement in the Voc and FF. The result is further supported by examining indicators for the interface quality via a suppressed dark saturation current and an enhanced minority carrier lifetime which exhibits an increase from 84 μsec without TAPC to 87 μsec with TAPC.
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