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Improved electronic coupling in hybrid organic–inorganic nanocomposites employing thiol-functionalized P3HT and bismuth sulfide nanocrystals

机译:采用巯基官能化p3HT和硫化铋纳米晶的改性电子耦合在有机 - 无机纳米复合材料中的应用

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摘要

In this study, we employ a thiol-functionalized polymer (P3HT-SH) as a leverage to tailor the nanomorphology and electronic coupling in polymer–nanocrystal composites for hybrid solar cells. The presence of the thiol functional group allows for a highly crystalline semiconducting polymer film at low thiol content and allows for improved nanomorphologies in hybrid organic–inorganic systems when employing non-toxic bismuth sulfide nanocrystals. The exciton dissociation efficiency and carrier dynamics at this hybrid heterojunction are investigated through photoluminescence quenching and transient absorption spectroscopy measurements, revealing a larger degree of polaron formation when P3HT-SH is employed, suggesting an increased electronic interaction between the metal chalcogenide nanocrystals and the thiol-functionalized P3HT. The fabricated photovoltaic devices show 15% higher power conversion efficiencies as a result of the improved nanomorphology and better charge transfer mechanism together with the higher open circuit voltages arising from the deeper energy levels of P3HT-SH.
机译:在这项研究中,我们采用硫醇官能化的聚合物(P3HT-SH)作为杠杆,以调整用于混合太阳能电池的聚合物-纳米晶体复合材料的纳米形态和电子耦合。硫醇官能团的存在允许在低硫醇含量下形成高度结晶的半导体聚合物薄膜,并在使用无毒硫化铋纳米晶体时允许杂化有机-无机体系中的纳米形态得到改善。通过光致发光猝灭和瞬态吸收光谱测量研究了该杂化异质结处的激子离解效率和载流子动力学,发现当使用P3HT-SH时极化子形成的程度更大,表明金属硫族化物纳米晶体和硫醇基之间的电子相互作用增加。功能化的P3HT。由于改进的纳米形态和更好的电荷转移机制,以及由于P3HT-SH的能级越深而产生的开路电压越高,所制造的光伏器件显示出高15%的功率转换效率。

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