共轭体系
聚合物
接受者
材料科学
高分子化学
化学物理
化学
物理
凝聚态物理
复合材料
作者
Kundu Thapa,Madison Mooney,Guorong Ma,Zhiqiang Cao,Gage T. Mason,Naresh Eedugurala,Surabhi Jha,Derek L. Patton,Jason David Azoulay,Simon Rondeau‐Gagné,Xiaodan Gu
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-04-29
卷期号:58 (9): 4780-4789
被引量:8
标识
DOI:10.1021/acs.macromol.4c02778
摘要
The significant differences in scattering cross sections between deuterium and protium are unique to neutron scattering techniques and have been a long-standing area of interest within the neutron scattering community. Researchers have explored selective deuteration to manipulate scattering contrast in soft matter systems, leading to the widespread use of deuterium labeling in materials development. As deuteration changes the atomic mass, it alters physical properties such as molecular volume, polarizability, and polarity, which in turn may affect noncovalent interactions and crystal ordering. Despite previous studies, there remains a limited understanding of how deuteration impacts donor-acceptor (DA) conjugated polymers. To address this, we synthesized deuterated DPP polymers and systematically investigated the effects of side-chain deuteration on their thermal stability, crystal packing, morphology, and optoelectronic properties. We found that deuteration increased the melting and crystallization temperatures of DPP polymers, although it did not significantly alter their morphology, molecular packing, or charge mobility. These properties were assessed by using atomic force microscopy (AFM), X-ray scattering, and thin-film transistor device measurements, respectively, for DPP polymers. Our work shows that deuterium labeling could be a powerful method for controlling scattering length density, enabling neutrons to study the structure and dynamics of conjugated polymers without impacting their electronic performance.
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