Chemically Driven Interfacial Coupling in Charge-Transfer Mediated Functional Superstructures

• Main Authors: Xu, Beibei (Author), Li, Huashan (Contributor), Li, Haoqi (Author), Wilson, Andrew J. (Author), Zhang, Lin (Author), Chen, Ke (Author), Willets, Katherine A. (Author), Ren, Fei (Author), Grossman, Jeffrey C. (Contributor), Ren, Shenqiang (Author)
• Other Authors: Massachusetts Institute of Technology. Department of Materials Science and Engineering (Contributor), Massachusetts Institute of Technology. Research Laboratory of Electronics (Contributor)
• Format: Article
• Language: English
• Published: American Chemical Society (ACS), 2017-10-10T19:45:54Z.
• Subjects: Article
• Online Access: Get fulltext

 Organic charge-transfer superstructures are enabling new interfacial electronics, such as organic thermoelectrics, spin-charge converters, and solar cells. These carbon-based materials could also play an important role in spin-based electronics due to their exceptionally long spin lifetime. However, to explore these potentials a coherent design strategy to control interfacial charge-transfer interaction is indispensable. Here we report that the control of organic crystallization and interfacial electron coupling are keys to dictate external stimuli responsive behaviors in organic charge-transfer superstructures. The integrated experimental and computational study reveals the importance of chemically driven interfacial coupling in organic charge-transfer superstructures. Such degree of engineering opens up a new route to develop a new generation of functional charge-transfer materials, enabling important advance in all organic interfacial electronics.