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  • Jang, Yongchan  (2)
  • 1
    In: Journal of Materials Chemistry A, Royal Society of Chemistry (RSC), Vol. 11, No. 6 ( 2023), p. 3008-3017
    Abstract: Non-fullerene acceptor-based polymer solar cells (NFA-PSCs) can exhibit high morphological stability under thermal stress, often resulting in the fabrication of thermally stable NFA-PSCs. Here, our stability study with systematic steps shows that high morphological stability of active layers does not necessarily guarantee high thermal stability for NFA-PSCs. Furthermore, a degradation pathway is elucidated by using two NFA-PSCs comprising well-known polymer donors and non-fullerene acceptors such as PTB7-Th, PBDB-T-2Cl, and ITIC-4F. Morphologies of the PTB7-Th:ITIC-4F and PBDB-T-2Cl:ITIC-4F blends are highly stable at a high temperature of 110 °C. However, the corresponding NFA-PSCs degrade severely at the same temperature. For example, all the NFA-PSCs show an efficiency reduction of greater than 30% within an hour, particularly owing to the significant decrease in the short-circuit current density ( J SC ) and fill factor (FF). A series of experiments, including time-of-flight secondary ion mass spectrometry measurements, demonstrate that the penetration of metal oxide molecules into the photoactive layer occurs upon heating, resulting in degradation. The diffused molecules can act as charge recombination centers, leading to decreases in J SC and FF. Finally, we provide insights, from a material design perspective, into the prevention of undesirable penetration of metal oxide molecules.
    Type of Medium: Online Resource
    ISSN: 2050-7488 , 2050-7496
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2702232-8
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  • 2
    In: Macromolecular Rapid Communications, Wiley, Vol. 43, No. 19 ( 2022-10)
    Abstract: Organic indoor photovoltaics (IPVs) are attractive energy harvesting devices for low‐power consumption electronic devices and the Internet of Things (IoTs) owing to their properties such as being lightweight, semitransparent, having multicoloring capability, and flexibility. It is important to match the absorption range of photoactive materials with the emission spectra of indoor light sources that have a visible range of 400–700 nm for IPVs to provide sustainable, high‐power density. To this end, benzo[1,2‐b:4,5‐b′]dithiophene‐based homopolymer (PBDTT) is synthesized as a polymer donor, which is a classical material that has a wide bandgap with a deep highest occupied molecular orbitals (HOMO) level, and a series of random copolymers by incorporating thieno[3,4‐c] pyrrole‐4,6,‐dione (TPD) as a weak electron acceptor unit in PBDTT. The composition of the TPD unit is varied to fine tune the absorption range of the polymers; the polymer containing 70% TPD (B30T70) perfectly covers the entire range of indoor lamps such as light‐emitting diodes (LEDs) and fluorescent lamp (FL). Consequently, B30T70 shows a dramatic enhancement of the power conversion efficiency (PCE) from 1‐sun (PCE: 6.0%) to the indoor environment (PCE: 18.3%) when fabricating organic IPVs by blending with PC 71 BM. The simple, easy molecular design guidelines are suggested to develop photoactive materials for efficient organic IPVs.
    Type of Medium: Online Resource
    ISSN: 1022-1336 , 1521-3927
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1475027-2
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