Direct Solar-to-Electrochemical Energy Storage in a Functionalized Covalent Organic Framework

Angew Chem Int Ed Engl. 2018 Sep 24;57(39):12716-12720. doi: 10.1002/anie.201806596. Epub 2018 Sep 3.

Abstract

A covalent organic framework integrating naphthalenediimide and triphenylamine units (NT-COF) is presented. Two-dimensional porous nanosheets are packed with a high specific surface area of 1276 m2 g-1 . Photo/electrochemical measurements reveal the ultrahigh efficient intramolecular charge transfer from the TPA to the NDI and the highly reversible electrochemical reaction in NT-COF. There is a synergetic effect in NT-COF between the reversible electrochemical reaction and intramolecular charge transfer with enhanced solar energy efficiency and an accelerated electrochemical reaction. This synergetic mechanism provides the key basis for direct solar-to-electrochemical energy conversion/storage. With the NT-COF as the cathode materials, a solar Li-ion battery is realized with decreased charge voltage (by 0.5 V), increased discharge voltage (by 0.5 V), and extra 38.7 % battery efficiency.

Keywords: bifunctional groups; covalent organic frameworks; intramolecular charge transfer; reversible electrochemical reaction; solar energy storage.