Thin Films of PNDI(2HD)2T and PCPDTBT Polymers Deposited Using the Spin Coater Technique for Use in Solar Cells
Source abstract
Abstract
Conductive polymers play a crucial role in the advancement of modern technologies, particularly in the field of organic photovoltaics (OPVs). Due to advantages such as flexibility, low specific weight, ease of processing, and low production costs, polymeric materials present an attractive alternative to traditional photovoltaic materials. This study investigates the properties of a polymer blend composed of PCPDTBT (donor) and PNDI(2HD)2T (acceptor), used as the active layer in bulk heterojunction (BHJ) solar cells. The motivation behind this research was the search for a novel n-type polymer material with potentially better properties than the commonly used P(NDI2OD-T2). Comprehensive characterization of thin films made from the individual polymers and their blend was conducted using Fourier Transform Infrared Spectroscopy (FTIR), Atomic Force Microscopy (AFM), Scanning Electron Microscopy (SEM), Ultraviolet-Visible Spectroscopy (UV-Vis), four-point probe conductivity measurements, and photovoltaic testing. The prepared films were continuous, uniform, and exhibited low surface roughness (Ra < 2.5 nm). Spectroscopic analysis showed that the blend absorbs light in a broad range of the spectrum, with slight bathochromic shifts compared to individual polymers. Electrical measurements indicated that the blend’s conductivity (9.1 µS/cm) was lower than that of pure PCPDTBT but higher than that of PNDI(2HD)2T, with an optical band gap of 1.34 eV. Photovoltaic devices fabricated using the blend demonstrated an average power conversion efficiency (PCE) of 6.45%, with a short-circuit current of 14.37 mA/cm2 and an open-circuit voltage of 0.89 V. These results confirm the feasibility of using PCPDTBT:PNDI(2HD)2T blends as active layers in BHJ solar cells and provide a promising direction for further optimization in terms of polymer ratio and processing conditions.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Optoelectronics, Faculty of Electrical Engineering, Silesian University of Technology, Krzywoustego 2, 44-100 Gliwice, Poland
Department of Engineering and Biomedical Materials, Faculty of Mechanical Engineering, Silesian University of Technology, Konarskiego 18a, 44-100 Gliwice, Poland
Scientific and Didactic Laboratory of Nanotechnology and Material Technologies, Faculty of Mechanical Engineering, Silesian University of Technology, Towarowa 7, 44-100 Gliwice, Poland
References (29)
Show source-provided references
1. Czerwiński, W., Kaczmarek, H., Kędziera, D., Kowalonek, J., Nowaczyk, J., and Olewnik, E. (2012). Przewodzące i Fotoczułe Materiały Polimerowe, Faculty of Chemistry at Nicolaus Copernicus University (UMK).
2. Review on Conducting Polymers and Their Applications
3. Lelek-Borkowska, U. (2021). Podstawy Chemii Polimerów, Akademia Górniczo-Hutnicza im. St. Staszica w Krakowie.
4. Polimery Przewodzące i ich Zastosowanie
5. Conductive Polymers: Opportunities and Challenges in Biomedical Applications10.1021/acs.chemrev.6b00275 ↗
6. Oskay, W., and Barrett, R. (2016). Make: The Annotated Build-It-Yourself Science Laboratory, O’Reilly.
7. Exploring polymer/nanoparticle hybrid solar cells in tandem architecture10.1039/c3ra43842b ↗
8. Polymer-based solar cells10.1016/S1369-7021(07)70276-6 ↗
9. Understanding of Imine Substitution in Wide-Bandgap Polymer Donor-Induced Efficiency Enhancement in All-Polymer Solar Cells10.1021/acs.chemmater.9b03570 ↗
10. Achieving efficient polymer solar cells based on benzodithiophene-thiazolecontaining wide band gap polymer donors by changing the linkage patterns of two thiazoles10.1039/D0NJ02483J ↗
11. Bithieno[3,4-c]pyrrole-4,6-dione-Mediated Crystallinity in Large Bandgap Polymer Donors Directs Charge Transportation and Recombination in Efficient Nonfullerene Polymer Solar Cells10.1021/acsenergylett.9b02842 ↗
12. Rationally Designed Donor-Acceptor Random Copolymers with Optimized Complementary Light Absorption for Highly Efficient All-Polymer Solar Cells
13. PTB7-Th /Non-fullerene acceptors for organic solar cells
14. Organic solar cells based on conjugated polymers: History and recent advances10.1007/s11814-014-0154-8 ↗
15. Photoconductivity of a low-bandgap conjugated polymer10.1002/adfm.200600199 ↗
16. Highly Crystalline Films of PCPDTBT with Branched Side Chains by Solvent Vapor Crystallization: Influence on Opto-Electronic Properties
17. Synthesis of Poly(4,4-dialkyl-cyclopenta[2,1-b:3,4-b′]dithiophene-alt-2,1,3-benzothiadiazole) (PCPDTBT) in a Direct Arylation Scheme10.1021/mz300093w ↗
18. Guided crystallization of P3HT in ternary blend solar cell based on P3HT:PCPDTBT:PCBM10.1039/C4EE02004A ↗
19. Side Chain Optimization of Naphthalenediimide-Bithiophene-Based Polymers to Enhance the Electron Mobility and the Performance in All-Polymer Solar Cells10.1002/adfm.201504191 ↗
20. Controlling Molecural Orientation of Naphthalenediimide-Based Polymer Acceptors for High Performance All-Polymers Solar Cells
21. High-Performance Flexible Organic Solar Cells with Enhanced Stability via Novel Interface Engineering
22. Polymer solar cells10.1038/nphoton.2012.11 ↗
23. An electron acceptor challenging fullerenes for efficient polymer solar cells10.1002/adma.201404317 ↗
24. Non-fullerene acceptors for organic solar cells10.1038/natrevmats.2018.3 ↗
25. Vertical Phase Separation for Highly Efficient Organic Solar Cells Incorporating Conjugated-Polyelectrolytes10.1002/admi.201801396 ↗
26. FTIR Study of the Impact of PC[60]BM on the Photodegradation of the Low Band Gap Polymer PCPDTBT under O2 Environment10.1021/acs.chemmater.5b00268 ↗
27. Optoelectronic Properties of PCPDTBT for Photovoltaics: Morphology Control and Molecular Doping10.1007/978-3-319-28338-8_5 ↗
28. Ossila (2025, May 12). PNDI(2HD)2T|Copolymer of Naphthalene & Bithiophene. Available online: https://www.ossila.com/products/pndi2hd2t.
29. P(NDI2OD-T2) Revisited—Aggregation Control as Key for High Performance n-Type Applications10.1016/j.synthmet.2019.04.017 ↗