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Crystallization from a Droplet: Single-Crystalline Arrays and Heterojunctions for Organic Electronics

期刊

ACCOUNTS OF CHEMICAL RESEARCH
卷 54, 期 24, 页码 4498-4507

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.accounts.1c00537

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资金

  1. National Key Research and Development Program of China [2019YFE0116700, 2019YFA0705900]
  2. MOST
  3. National Natural Science Foundation of China [51625304, 51873182, 52103231]
  4. Zhejiang Province Science and Technology Plan [2021C04012]
  5. Zhejiang Provincial Department of Science and Technology

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Organic semiconductor (OSC) single crystals are promising for flexible electronic/optoelectronic applications due to their high mobility and intrinsic flexibility, but challenges arise in forming large, uniform, and defect-free single crystals. The droplet-pinned crystallization (DPC) method developed in 2012 offers a time- and cost-effective way to grow high-quality OSC single crystals, accelerating studies on charge-transport mechanisms and addressing the general lagging of electron mobility in OSC materials. The method allows flexibility in OSC materials and solvents, facilitating the formation of single-crystal OSC heterojunctions with promising potentials in circuits, photovoltaics, and photodiodes.
CONSPECTUS: Single crystals of organic semiconductors (OSCs) are believed to have both high mobility and intrinsic flexibility, making them promising candidates for flexible electronic/optoelectronic applications and being consistently pursued by researchers. The van der Waals force in OSC enables low-temperature solution processing of single crystals, but the relatively weak binding energy brings challenges in forming large, uniform, and defect-free single crystals. To promote the study on OSC single crystals, a generalized method that grows high-quality crystals in an easy-to-handle, time/resource-saving, and repeatable manner is apparently necessary. In 2012, Li et al. developed a droplet-pinned crystallization (DPC) method that uses a rather simple strategy to create a steadily receding contact line for the growth of OSC single crystals. Instead of setting up expensive equipment, controlling strict deposition parameters, or waiting for days or weeks for countable crystal seeds, the DPC method offers a time- and cost-effective way to obtain OSC single crystals for further study of the tendency of crystallization, single-crystal mobility, and molecular packing information. The DPC method is primarily a powerful tool for studying the charge-transport mechanisms in OSC single crystals. In pioneering work, high-mobility single crystals of both p-type 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS-PEN) and n-type C60 materials were obtained. Driven by the demands from practical applications, we then focused on the general lagging of electron mobility in OSC materials. The ambipolar property of TIPS-PEN was studied, and a strong correlation between electron mobility and polar species (polar solvent residuals and surface hydroxyl groups) was observed. The latter further guided the harvest of electron mobility in a series of OSC materials. Undoubtfully, the facile DPC method accelerated these studies by providing a time-efficient, reliable, and repeatable testing platform. Additionally, flexibility on OSC materials and solvents, where not only one-component but also binary systems were allowed, is another critical integrity of the DPC method. The m-xylene/carbon tetrachloride binary solvent was proven to be efficient for growing ribbon-like C60 single crystals rather than needle-like crystals from typical one-component solvents. Afterward, a variety of OSC materials (including p-type, n-type, and ambipolar ones) and a series of solvents (including aromatic, aliphatic, and polar ones) were studied. The crystallization of OSC single crystals was primarily found at either the top liquid-air interface or the bottom solid-liquid interface. The interactions between OSC molecules and substrate surfaces were deduced as the qualitative determining factor. By utilizing the top interface crystallization, the two-step sequential deposition of single-crystalline OSC heterojunctions was enabled. Moreover, by selecting appropriate pairs of OSC materials that crystallize at separate interfaces, the facile one-step formation of single-crystalline OSC heterojunctions was achieved. The OSC single crystals and heterojunctions (including horizontal, vertical, and bulk heterojunctions) thereof exhibit promising potentials in circuits, photovoltaics, and photodiodes and would probably provide new insights for the future development of organic electronics.

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