Dec 3, 2024
3:30pm - 3:45pm
Hynes, Level 1, Room 107
Kristina Ashurbekova1,Mato Knez1,2
CIC nanoGUNE1,IKERBASQUE, Basque Foundation for Science2
Kristina Ashurbekova1,Mato Knez1,2
CIC nanoGUNE1,IKERBASQUE, Basque Foundation for Science2
The development of inorganic, organic and perovskite solar cells (SCs), has witnessed considerable progress over the past decade. Perovskite SCs, while highly efficient, encounter stability and toxicity concerns. Inorganic SCs outperform their organic counterparts in efficiency and durability but lack mechanical flexibility, motivating exploration of alternative technologies. In contrast, organic SCs offer the desired flexibility, but face the mentioned lower efficiency challenges. Despite the inherent limitations of each SC type, they have their own merits, promising a grand step forward if synergy is achieved. Combining the adaptability of organic SCs with the efficiency of inorganic ones may yield a hybrid versatile alternative. Herein, we are introducing new hybrid solar cell materials by applying vapor phase infiltration (VPI) to polymers.<br/>We present a completely new hybrid materials set obtained after growing Sb<sub>2</sub>S<sub>3</sub> and Sb<sub>2</sub>Se<sub>3</sub> by VPI inside the bulk and atop of diverse polymers including Poly(3-hexylthiophene-2,5-diyl) (P3HT), poly(triaryl amine) (PTAA), Poly[N,N’-bis(4-butylphenyl)-N,N’-bisphenylbenzidine] (PolyTPD) and Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS). PTAA, PolyTPD and PEDOT:PSS are excellent hole-transporting semiconducting materials, while P3HT is an efficient light absorber in the visible range. Metal chalcogenide light absorbent materials, such as Sb<sub>2</sub>S<sub>3</sub> and Sb<sub>2</sub>Se<sub>3</sub>, have huge potential in photovoltaics owing to the suitable bandgap of 1.7 and 1.3 eV, and high light absorption coefficient above 10<sup>4</sup> and 10<sup>5</sup> cm<sup>−1</sup>, respectively. For the VPI growth of Sb<sub>2</sub>S<sub>3</sub> and Sb<sub>2</sub>Se<sub>3</sub>, SbCl<sub>3</sub>/H<sub>2</sub>S and SbCl<sub>3</sub>/(Me<sub>3</sub>Si)<sub>2</sub>Se precursors were used, respectively. The hybridization process was monitored <i>in-situ</i> with a Quartz Crystal Microbalance (QCM). The monitoring allowed studying the saturation behavior of the VPI process and quantitatively controlling the loading of the inorganic precursors into the polymer. Scanning electron microscopy (SEM) showed infiltration in form of Sb<sub>2</sub>S<sub>3</sub> and Sb<sub>2</sub>Se<sub>3</sub> crystal growth throughout the whole polymer depth. TEM was used to examine the structure of the crystalline phase of the Sb<sub>2</sub>S<sub>3</sub> and Sb<sub>2</sub>Se<sub>3</sub> grown in the bulk and on top of the polymer.<br/>With the fabricated polymer-inorganic hybrid materials as base, planar p-i-n SCs devices with following structures were fabricated: ITO glass/polymer-Sb<sub>2</sub>S<sub>3</sub>//Sb<sub>2</sub>Se<sub>3</sub> /ETL/Ag and ITO glass/polymer-Sb<sub>2</sub>S<sub>3</sub>//Sb<sub>2</sub>Se<sub>3</sub>/perovskite/ETL/Ag. C60/BCP was used as an electron transport layer (ETL). With those devices, a complete photovoltaic characterization of the new set of hybrid materials was done in 16 ITO pins SCs, including the current density–voltage (J–V) characteristic under illumination, power conversion efficiencies (PCEs) and the external quantum efficiency (EQE). The results are very encouraging and offer new solutions for the design of future flexible and highly efficient SCs.