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Characterization of Interfacial Structure in Polymer-Fullerene Bulk Heterojunctions via 13C {2H} Rotational Echo Double Resonance NMR

机译:聚合物-富勒烯本体异质结中界面结构的13C {2H}旋转回波双共振NMR表征

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摘要

Weintroduce a new application of solid state NMR measurements towards characterizing the donor- acceptor interfaces within bulk heterojunction (BHJ) films. Rotational echo double resonance (REDOR) is used to measure dipolar couplings between 13C nuclei on the acceptor phenyl-C61-butyric acid methyl ester (PCBM) fullerene cage, which is ≈18% isotopically enriched with 13C, and beta hydrogens on the donor poly(3-hexyl thiophene) (P3HT) main chain, which are >95% isotopically enriched with 2H. The 13C — 2H dipolar couplings are used for constraining possible models of molecular packing in the amorphous mixed phase of a P3HT/PCBM BHJ. The films studied are highly mixed (>80%) and have a maximum length scale of composition nonuniformity of ≈6 nm in the mixed phase, as demonstrated by 1H spin diffusion NMR and supported by TEM. The REDOR results show that despite the lack of phase separation at length scales greater than ≈6 nm, neat P3HT and PCBM clusters exist on ≈3 nm size scales, and, for the average PCBM molecule, the number of nearest neighbors P3HTs is two.
机译:我们引入了固态NMR测量的新应用,以表征本体异质结(BHJ)薄膜中的供体-受体界面。旋转回波双共振(REDOR)用于测量受体苯基-C61-丁酸甲酯(PCBM)富勒烯笼上 13 C核之间的偶极耦合,同位素富集了≈18%的< sup> 13 C,以及供体聚(3-己基噻吩)(P3HT)主链上的β氢,这些同位素> 95%地富含 2 H。 13 C — 2 H双极偶合用于约束P3HT / PCBM BHJ非晶混合相中分子堆积的可能模型。所研究的薄膜是高度混合的(> 80%),并且在混合相中的组成不均匀性的最大长度尺度为≈6nm,如 1 H自旋扩散NMR所证明并得到TEM的支持。 REDOR结果表明,尽管在大于约6 nm的长度尺度上没有相分离,但是纯净的P3HT和PCBM簇以≈3 nm的尺度存在,并且对于平均PCBM分子而言,最邻近的P3HT数为2。

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