过电位
塔菲尔方程
密度泛函理论
共轭体系
共价键
共价有机骨架
材料科学
结晶度
带隙
化学
纳米技术
化学工程
电化学
电极
计算化学
有机化学
光电子学
聚合物
复合材料
物理化学
工程类
作者
Chunhua Yang,Z. R. Yang,Hong Dong,Ning Sun,Lu Yang,Fengming Zhang,Guiling Zhang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-08-26
卷期号:4 (9): 2251-2258
被引量:145
标识
DOI:10.1021/acsenergylett.9b01691
摘要
It is a great challenge to obtain oriented design and synthesis of new two-dimensional covalent organic frameworks (2D-COFs) with proper CN stoichiometry, N position, and band structures as specific electrocatalysts. Driven by density functional theory (DFT) calculations, we designed and synthesized a new phenazine-linked 2D-COF (COF-C4N) by solvothermal reaction of triphenylenehexamine (TPHA) and hexaketocyclohexane (HKH). Structural analysis confirmed that COF-C4N possesses an ordered crystalline structure with a highly conjugated basal plane and better stability. COF-C4N exhibited OER performance with a low overpotential of 349 mV at 10 mA cm–2 and a Tafel slope of 64 mV dec–1. A combination of theoretical and experimental studies revealed that better OER performance is attributed to better crystallinity and stability, an appropriate band gap, and an N position that promotes the formation of C active sites around N atoms. The strategy of theory-driven design and targeting synthesis of 2D-COFs for OER may provide a new way to further develop metal-free materials for clean energy application.
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