Intermolecular naphthylamine cyclization-based synthesis of bandgap-modulated carbon dots for multicolor light-emitting diodes

被引:0
作者
Park, Sehyeon [1 ]
Lee, Su Hwan [2 ]
Kim, Yujin [3 ]
Park, Hyeonjin [1 ]
Kim, Gui-Min [3 ]
Kim, Young-Hoon [2 ]
Kwon, Woosung [1 ,4 ]
机构
[1] Sookmyung Womens Univ, Dept Chem & Biol Engn, 100 Cheongpa Ro 47 Gil, Seoul 04310, South Korea
[2] Hanyang Univ, Dept Energy Engn, 222 Wangsimni Ro, Seoul 04763, South Korea
[3] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, 291 Daehak Ro, Daejeon 34141, South Korea
[4] Sookmyung Womens Univ, Inst Adv Mat & Syst, 100 Cheongpa Ro 47 Gil, Seoul 04310, South Korea
基金
新加坡国家研究基金会;
关键词
Carbon dot; Nitrogen doping; Electronic transition; Dual emission; Light-emitting diode; QUANTUM DOTS; INSIGHTS; NITROGEN;
D O I
10.1016/j.optmat.2024.116313
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Owing to their tunable optical properties, N-doped carbon dots (CDs) have a broad scope of optoelectronic applications. However, the difficulty of precisely controlling nitrogen incorporation limits our understanding of its impact on CD electronic structure and emission behavior. To address this gap, N-doped CDs with tunable bandgaps are herein synthesized via the solvothermal carbonization of 1-naphthylamine in the presence of a controlled amount of nitric acid to obtain single-source emitters with two distinct emission wavelengths. The amount of nitric acid determines the extent of nitrogen incorporation through the intermolecular cyclization of 1-naphthylamine and, hence, the proportions of pyrrolic/pyridinic N-heterocycles (red emission, similar to 600 nm) and polycyclic aromatic hydrocarbons (blue emission, similar to 400 nm). For a practical utility demonstration, the prepared N-doped CDs are used to fabricate high-color-purity multicolor light-emitting diodes. By establishing a correlation between nitrogen incorporation modes and photophysical properties, this study paves the way for the rational design of advanced N-doped CDs for next-generation optoelectronic devices.
引用
收藏
页数:10
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