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Impact of Conjugated Polymer Characteristics on the Enrichment of Single-Chirality Single-Walled Carbon Nanotubes AITranslate

Security and Disruptive Technologies Research Center, National Research Council Canada;Security and Disruptive Technologies Research Center, National Research Council Canada;Security and Disruptive Technologies Research Center, National Research Council Canada;Security and Disruptive Technologies Research Center, National Research Council Canada;Security and Disruptive Technologies Research Center, National Research Council Canada;Security and Disruptive Technologies Research Center, National Research Council Canada; The University of Sydney; The University of Sydney;Security and Disruptive Technologies Research Center, National Research Council Canada;Advanced Electronics and Photonics Research Center, National Research Council Canada;Security and Disruptive Technologies Research Center, National Research Council Canada;Security and Disruptive Technologies Research Center, National Research Council Canada
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Publisher: ACS
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Abstract AITranslate

Polymer characteristics influence the chiral selectivity and yield in the enrichment of (7,6) from Signis SG76 in toluene by various fluorene homopolymers and copolymers. Fluorene homopolymers such as poly(9,9-di-n-dodecylfluorene) (PFDD) and copolymers with anthracene such as poly[(9,9-dihexylfluorenyl-2,7-diyl)-co-(9,10-anthracene)] (PFH-A) result in high (7,6) selectivities of up to 67 and 72%, respectively. The selectivity is calculated by optical absorption using a known extinction coefficient and also evaluated by Raman scattering and photoluminescence excitation. In contrast, poly[(9,9-dioctyl-2,7-divinylenefluorenylene)-alt-co-(9,10-anthracene)] (PFO=A), with a double-bond spacer, results in (9,5) dominant extractions with the purity of (9,5) up to 80% after ultracentrifugation, which is believed to be the first report on the successful enrichment of (9,5) by conjugated polymers. The chiral selectivity is also greatly impacted by the length of alkyl side chain of fluorene homopolymers: hexyl group has low selectivity, while octyl, dodecyl, and tetradecyl (PFTD) groups show high selectivity toward (7,6), and the octadecyl group is prone to include bigger tubes. Interestingly, a chiral selection transition from (7,6) to (8,6) occurred using PFTD after a few enrichment cycles. The chiral purity of (8,6) was greatly improved from 50 to 86% after slow filtration. Polymer molecular weight (MW, here PFDD) also plays a role in the selectivity and yield. Low MW leads to a low yield, and high MW leads to a low selectivity, with the optimal range (Mn) being ca. 20–35 kDa when the polydisperse index is ca. 2–3. Molecular dynamics simulation confirms that different lengths of side chain of polyfluorene have different wrapping stabilities toward specific chirality, where PFTD shows greater stability toward (8,6) than (7,6).

KeyWords AITranslate

singlewalled carbon nanotube singlechirality enrichment fluorene polymers selectivity and yield polymer backbone Show More
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DOI:https://doi.org/10.1021/acsapm.2c01022

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Citation Information:

Polymer characteristics influence the chiral selectivity and yield in the enrichment of (7,6) from Signis SG76 in toluene by various fluorene homopolymers and copolymers. Fluorene homopolymers such as poly(9,9-di-n-dodecylfluorene) (PFDD) and copolymers with anthracene such as poly[(9,9-dihexylfluorenyl-2,7-diyl)-co-(9,10-anthracene)] (PFH-A) result in high (7,6) selectivities of up to 67 and 72%, respectively. The selectivity is calculated by optical absorption using a known extinction coefficient and also evaluated by Raman scattering and photoluminescence excitation. In contrast, poly[(9,9-dioctyl-2,7-divinylenefluorenylene)-alt-co-(9,10-anthracene)] (PFO=A), with a double-bond spacer, results in (9,5) dominant extractions with the purity of (9,5) up to 80% after ultracentrifugation, which is believed to be the first report on the successful enrichment of (9,5) by conjugated polymers. The chiral selectivity is also greatly impacted by the length of alkyl side chain of fluorene homopolymers: hexyl group has low selectivity, while octyl, dodecyl, and tetradecyl (PFTD) groups show high selectivity toward (7,6), and the octadecyl group is prone to include bigger tubes. Interestingly, a chiral selection transition from (7,6) to (8,6) occurred using PFTD after a few enrichment cycles. The chiral purity of (8,6) was greatly improved from 50 to 86% after slow filtration. Polymer molecular weight (MW, here PFDD) also plays a role in the selectivity and yield. Low MW leads to a low yield, and high MW leads to a low selectivity, with the optimal range (Mn) being ca. 20–35 kDa when the polydisperse index is ca. 2–3. Molecular dynamics simulation confirms that different lengths of side chain of polyfluorene have different wrapping stabilities toward specific chirality, where PFTD shows greater stability toward (8,6) than (7,6).

quote

GB/T 7714-2015 [1] Jianying Ouyang, Homin Shin, Paul Finnie, et al. ACS Applied Polymer Materials, 2022(4). DOI:10.1021/acsapm.2c01022.
MLA [1] Jianying Ouyang, et al., ACS Applied Polymer Materials, no. 4, 2022, https://doi.org/10.1021/acsapm.2c01022.
APA [1] Jianying Ouyang, Homin Shin, Paul Finnie, Jianfu Ding, Chang Guo, Zhao Li, Yuan Chen, Li Wei, Alison J. Wu, Simona Moisa, François Lapointe, & Patrick R. L. Malenfant. (2022). ACS Applied Polymer Materials(4). https://doi.org/10.1021/acsapm.2c01022
IEEE [1] Jianying Ouyang, Homin Shin, Paul Finnie, Jianfu Ding, Chang Guo, Zhao Li, Yuan Chen, Li Wei, Alison J. Wu, Simona Moisa, François Lapointe, and Patrick R. L. Malenfant, ACS Applied Polymer Materials, no. 4, 2022, doi: 10.1021/acsapm.2c01022. keywords: {singlewalled carbon nanotube;singlechirality enrichment;fluorene polymers;selectivity and yield;polymer backbone;Show More}