4.8 Article

Chemically Driven Interfacial Coupling in Charge-Transfer Mediated Functional Superstructures

期刊

NANO LETTERS
卷 16, 期 4, 页码 2851-2859

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.6b00712

关键词

Nanoferroics; organic crystallization; materials design; and multifuctionality

资金

  1. Army Research Office - Young Investigator Program [W911NF-15-1-0610]
  2. U.S. Department of Energy-Basic Energy Sciences Award [DE-SC0014902]
  3. Department of Energy (DOE), Office of Science, Basic Energy Science (BES) [DE-SC0010307]
  4. U.S. Department of Energy (DOE) [DE-SC0010307, DE-SC0014902] Funding Source: U.S. Department of Energy (DOE)

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据