ZY-4Cl, a modified version of BTP-4Cl-12, belongs to the Y6 non-fullerene acceptors family with a fused thienothienopyrrolo-thienothienoindole (TTP-TTI) core and 5,6-dichloro-1H-indene-1,3(2H)-dione peripheral end groups.
The replacement of the cyano groups with carbonyl groups significantly increases the LUMO energy level of ZY-4Cl due to the reduced electron-withdrawing effect of the carbonyl groups, giving higher open voltage (VOC) however sacrificing its light absorption capability in the NIR region. The modification of the structure also reduces the miscibility between the polymer donor, i.e. P3HT and ZY-4Cl, which improves the phase separation morphology of the P3HT:ZY-4Cl-based active layer for efficient charge transport with reduced charge recombination.
ZY-4Cl can also be added as the third component in organic solar cells not only to improve the device performing efficiency but also to enhance the stability of the device. PM6:Y6-based OPV with ZY-4Cl as the additive exhibited good air stability, maintaining 94% of its initial PCE for over 1390 h (25 °C, 40% humidity).
PCE of 9.46% has been achieved for P3HT based polymer organic solar cells when ZY-4Cl was used as the non-fullerene acceptor. Further device performance improvement to PCE over 10% was observed when a volatilizable solid additive SA4 (2-(thiophen-2-ylmethylene)-1H-indene-1,3(2H)-dione) was introduced in the active layer.
Device structure: ITO/PEDOT:PSS/P3HT:ZY-4Cl/PFN-Br/Al
|Thickness (nm)||VOC (V)||JSC (mA cm-2)||FF (%)||PCE (%)|
|Form||Dark blue to black powder/crystals|
|Molecular weight||1533.87 g/mol|
|HOMO / LUMO||HOMO = -5.64 eV, LUMO = -3.67 eV |
|Classification / Family||NFAs, n-type non-fullerene electron acceptors, organic semiconducting materials, low band-gap small molecule, small molecular acceptor, organic photovoltaics, organic photodetectors (OPDs), polymer solar cells, NF-PSCs|
MSDS DocumentationZY-4Cl MSDS Sheet
Literature and Reviews
- Molecular design of a non-fullerene acceptor enables a P3HT-based organic solar cell with 9.46% efficiency, Energy Environ. Sci., 13, 2864--2869 (2020); DOI: 10.1039/d0ee01763a.
- Thermally stable poly(3-hexylthiophene): Nonfullerene solar cells with efficiency breaking 10%, M. Gao et al., Aggreg., e190 (2022); DOI: 10.1002/agt2.190.
- Achieving over 10% Efficiency in Poly(3-hexylthiophene)-Based Organic Solar Cells via Solid Additives, C. Yang et al., ChemSusChem 14 (17), 3607-3613 (2021); DOI: 10.1002/cssc.202100627.
- Low-cost and efficient organic solar cells based on polythiophene-and poly(thiophene vinylene)-related donors, C. Yang et al., Aggreg., e111 (2021); DOI: 10.1002/agt2.111.
- Ternary strategy enabling high-efficiency rigid and flexible organic solar cells with reduced non-radiative voltage loss, X. Duan et al., Energy Environ. Sci.,15, 1563-1572 (2022); DOI: 10.1039/D1EE03989J.
- Realizing Stable High-Performance and Low-Energy-Loss Ternary Photovoltaics through Judicious Selection of the Third Component, B. Jiang et al., RRL Solar, 5 (9), 2100450 (2021); DOI: 10.1002/solr.202100450.
To the best of our knowledge the information provided here is accurate. However, Ossila assume no liability for the accuracy of this page. The values provided are typical at the time of manufacture and may vary over time and from batch to batch. All products are for laboratory and research and development use only, and may not be used for any other purpose including health care, pharmaceuticals, cosmetics, food or commercial applications.