Ternary Organic Photovoltaics at a Turning Point: Mechanistic Perspectives on Their Constraints

Ternary organic photovoltaics (OPVs) are considered as the next step beyond binary systems, aiming to achieve synergistic improvements in absorption, energetic alignment, and charge transport. However, despite their conceptual appeal, most ternary blends do not outperform binary counterparts, particularly under indoor illumination where photon flux and carrier dynamics impose strict limitations. To comprehensively understand this discrepancy, multiple ternary systems were systematically examined to ensure that the observed behaviors are representative rather than case specific. In this study, we systematically investigate this discrepancy by comparing representative donor-donor-acceptor (D-D-A) and donor-acceptor-acceptor (D-A-A) systems under both AM 1.5G and TL84 lighting. In all cases, the broadened absorption fails to yield effective photocurrent; instead, redundant excitations, reduced driving forces for charge separation, and disrupted percolation networks collectively diminish device performance. Recombination and transient analyses reveal that the third component often introduces energetic disorder and trap-assisted recombination instead of facilitating beneficial cascade pathways. Although the film morphology remains smooth, interfacial instability under low-light conditions further intensifies performance losses. The inclusion of several systems allows the identification of consistent mechanistic trends across different ternary architectures, reinforcing the generality of the conclusions. This work establishes a mechanistic framework linking molecular miscibility, energetic alignment, and percolation continuity to device-level behavior, clarifying why ternary strategies rarely deliver consistent efficiency improvements. Ultimately, indoor OPV performance is determined not by spectral breadth but by maintaining balanced charge transport and stable energetic landscapes, which represents an essential paradigm for advancing ternary OPVs from concept to practical application.

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Publication Details

Journal
Nanomaterials
Published
2025-11-11
DOI
https://doi.org/10.3390/nano15221702
Primary Topic
Organic Electronics and Photovoltaics
Type
article
Field-Weighted Citation Impact
0.00

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article

Ternary Organic Photovoltaics at a Turning Point: Mechanistic Perspectives on Their Constraints

Yu‐Ching Huang, Hui-Chun Wu, Chia-Feng Li, Hou‐Chin Cha et al.
Nanomaterials
Organic Electronics and Photovoltaics
article

Ternary Organic Photovoltaics at a Turning Point: Mechanistic Perspectives on Their Constraints

Yu‐Ching Huang, Hui-Chun Wu, Chia-Feng Li, Hou‐Chin Cha, Kang‐Wei Chang, Yihan Wang, Shin-Puu Jeng
article en

Abstract

Ternary organic photovoltaics (OPVs) are considered as the next step beyond binary systems, aiming to achieve synergistic improvements in absorption, energetic alignment, and charge transport. However, despite their conceptual appeal, most ternary blends do not outperform binary counterparts, particularly under indoor illumination where photon flux and carrier dynamics impose strict limitations. To comprehensively understand this discrepancy, multiple ternary systems were systematically examined to ensure that the observed behaviors are representative rather than case specific. In this study, we systematically investigate this discrepancy by comparing representative donor-donor-acceptor (D-D-A) and donor-acceptor-acceptor (D-A-A) systems under both AM 1.5G and TL84 lighting. In all cases, the broadened absorption fails to yield effective photocurrent; instead, redundant excitations, reduced driving forces for charge separation, and disrupted percolation networks collectively diminish device performance. Recombination and transient analyses reveal that the third component often introduces energetic disorder and trap-assisted recombination instead of facilitating beneficial cascade pathways. Although the film morphology remains smooth, interfacial instability under low-light conditions further intensifies performance losses. The inclusion of several systems allows the identification of consistent mechanistic trends across different ternary architectures, reinforcing the generality of the conclusions. This work establishes a mechanistic framework linking molecular miscibility, energetic alignment, and percolation continuity to device-level behavior, clarifying why ternary strategies rarely deliver consistent efficiency improvements. Ultimately, indoor OPV performance is determined not by spectral breadth but by maintaining balanced charge transport and stable energetic landscapes, which represents an essential paradigm for advancing ternary OPVs from concept to practical application.

NanomaterialsVol. 15(22)
Ming Chi University of Technology (TW), National Taiwan University (TW), Chang Gung University (TW)
National Science and Technology Council
Openalex Percentile: Top 67%
Organic Electronics and Photovoltaics
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