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One-Step Preparation of ZnO Electron Transport Layers Functionalized with Benzoic Acid Derivatives One-Step Preparation of ZnO Electron Transport Layers Functionalized with Benzoic Acid Derivatives AITranslate

Monash University; Monash University; Monash University;Australian Synchrotron;CSIRO Manufacturing, Ian Wark Laboratories; Monash University; Flinders University; Flinders University; Flinders University; Monash University; Monash University; Monash University; Monash University
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Publisher: ACS
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Abstract AITranslate

ZnO is a common electron transport layer in organic solar cells that typically requires treatment with an additional layer to passivate surface traps to optimize the device performance. Here, we present a “one-step” approach to modifying ZnO electron transport layers (ETLs) used in organic solar cells. This approach involves adding benzoic acid (BZA) derivatives directly to the ZnO precursor solution, which are then present at the surface of the resulting ZnO film. We demonstrate this approach for three different BZA derivatives, namely, benzoic acid, 4-chlorobenzoic acid, and 4-hydrazinobenzoic acid. For all molecules, improved device performance and stability is demonstrated in solar cells using an active layer blend of PTQ10 (donor) and ITIC-Br (nonfullerene acceptor) compared to such cells prepared using untreated ZnO. Furthermore, similar or improved device performance and stability is demonstrated compared to conventional PEIE treatment of ZnO. The presence of the BZA derivatives at the surface after processing is established using X-ray photoelectron spectroscopy and near-edge X-ray absorption fine-structure spectroscopy. From atomic force microscopy analysis and X-ray diffraction studies, the addition of BZA derivatives appears to restrict ZnO grain growth; however, this does not negatively impact the device performance. ZnO layers treated with BZA derivatives also exhibit a higher water contact angle and lower work function compared to untreated ZnO. Improved device performance is attributed to reduced surface recombination at the ETL/active layer interface, while improved device stability is attributed to the increased hydrophobicity of the ETL. This approach enables simplification of device manufacture while still allowing for optimization of the surface properties of metal oxide ETLs.

KeyWords AITranslate

electron transport layers zinc oxide organic solar cells surface modification interfaces
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Basic Information:

DOI:https://doi.org/10.1021/acsaelm.3c01517

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Citation Information:

ZnO is a common electron transport layer in organic solar cells that typically requires treatment with an additional layer to passivate surface traps to optimize the device performance. Here, we present a “one-step” approach to modifying ZnO electron transport layers (ETLs) used in organic solar cells. This approach involves adding benzoic acid (BZA) derivatives directly to the ZnO precursor solution, which are then present at the surface of the resulting ZnO film. We demonstrate this approach for three different BZA derivatives, namely, benzoic acid, 4-chlorobenzoic acid, and 4-hydrazinobenzoic acid. For all molecules, improved device performance and stability is demonstrated in solar cells using an active layer blend of PTQ10 (donor) and ITIC-Br (nonfullerene acceptor) compared to such cells prepared using untreated ZnO. Furthermore, similar or improved device performance and stability is demonstrated compared to conventional PEIE treatment of ZnO. The presence of the BZA derivatives at the surface after processing is established using X-ray photoelectron spectroscopy and near-edge X-ray absorption fine-structure spectroscopy. From atomic force microscopy analysis and X-ray diffraction studies, the addition of BZA derivatives appears to restrict ZnO grain growth; however, this does not negatively impact the device performance. ZnO layers treated with BZA derivatives also exhibit a higher water contact angle and lower work function compared to untreated ZnO. Improved device performance is attributed to reduced surface recombination at the ETL/active layer interface, while improved device stability is attributed to the increased hydrophobicity of the ETL. This approach enables simplification of device manufacture while still allowing for optimization of the surface properties of metal oxide ETLs.

quote

GB/T 7714-2015 [1] Hao Liu, Chao Wang, Wen Liang Tan, et al. ACS Applied Electronic Materials, 2024(6). DOI:10.1021/acsaelm.3c01517.
MLA [1] Hao Liu, et al., ACS Applied Electronic Materials, no. 6, 2024, https://doi.org/10.1021/acsaelm.3c01517.
APA [1] Hao Liu, Chao Wang, Wen Liang Tan, Lars Thomsen, Anthony S. R. Chesman, Yvonne Hora, Martyn Jevric, Jonas M. Bjuggren, Mats R. Andersson, Yahui Tang, Linjing Tang, Doan Vu, & Christopher R. McNeill. (2024). ACS Applied Electronic Materials(6). https://doi.org/10.1021/acsaelm.3c01517
IEEE [1] Hao Liu, Chao Wang, Wen Liang Tan, Lars Thomsen, Anthony S. R. Chesman, Yvonne Hora, Martyn Jevric, Jonas M. Bjuggren, Mats R. Andersson, Yahui Tang, Linjing Tang, Doan Vu, and Christopher R. McNeill, ACS Applied Electronic Materials, no. 6, 2024, doi: 10.1021/acsaelm.3c01517. keywords: {electron transport layers zinc oxide organic solar cells surface modification interfaces}