光催化
激子
共轭体系
材料科学
异质结
共价键
化学物理
接受者
制氢
光子
电子转移
催化作用
纳米技术
光化学
氢
碳纤维
化学
光电子学
聚合物
物理
复合数
有机化学
复合材料
量子力学
凝聚态物理
作者
Enquan Jin,Zhi‐An Lan,Qiuhong Jiang,Keyu Geng,Guosheng Li,Xinchen Wang,Donglin Jiang
出处
期刊:Chem
[Elsevier]
日期:2019-05-02
卷期号:5 (6): 1632-1647
被引量:459
标识
DOI:10.1016/j.chempr.2019.04.015
摘要
Photo-to-chemical energy conversion requires a systematic and complex molecular design to manage consecutive photochemical processes, including energy harvesting, exciton migration, electron transfer, charge separation, and charge transport. However, such an integrated design remains a substantial challenge. Here, we report a seamless system in managing these photochemical events on the basis of two-dimensional sp2 carbon-conjugated covalent organic frameworks. The frameworks are designed to be fully π conjugated for harvesting a wide range of visible to near-infrared light and to constitute built-in donor-acceptor heterojunction interfaces for splitting excitons. The frameworks create dense yet ordered columnar π arrays that offer pathways to facilitate exciton migration and charge transport. Loading reaction centers in pores or on surface shortens the electron-transfer distance and promotes the accumulation of electrons at the reaction centers. These three molecular mechanisms are seamlessly integrated in the frameworks and render the system able to efficiently produce hydrogen that is driven by low-energy photons.
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