Ethynyl‐Linked Donor–Acceptor Covalent Organic Framework for Highly Efficient Photocatalytic H<sub>2</sub>O<sub>2</sub> Production
Bowen Li, Junjin Chen, Kang Wang, Dongdong Qi, Tianyu Wang, Jianzhuang Jiang
Abstract
Abstract Photocatalytic H 2 O 2 synthesis from H 2 O and O 2 is considered to be one of the most promising alternative approaches for manufacturing H 2 O 2 . Developing highly active and selective photocatalysts is of significant in achieving efficient H 2 O 2 photosynthesis. Herein, an ethynyl‐linked donor–acceptor covalent organic framework (COF), named EBBT‐COF, is prepared from the condensation reaction between an electron‐deficient unit 4,4′,4″‐(1,3,5‐benzenetriyltri‐2,1‐ethynediyl)tris‐benzenamine and an electron‐rich unit benzo[1,2‐b:3,4‐b′:5,6‐b″]trithiophene‐2,5,8‐tricarboxaldehyde. Powder X‐ray diffraction and N 2 adsorption isotherm unveil the crystalline porous hcb network of EBBT‐COF with pores size centered at ca . 2.3 nm. Spectroscopic characterizations demonstrate the excellent visible‐light absorption capacity and enhanced photo‐induced charge separation and transport efficiency of EBBT‐COF owing to its donor–acceptor architecture. Density functional theory calculations and electrochemical tests indicate the high activity and selectivity of EBBT‐COF toward 2e − O 2 reduction reaction and 2e − water oxidation reaction with triethynylbenzene and trithiophene moieties to accelerate O 2 ‐to‐H 2 O 2 and H 2 O‐to‐H 2 O 2 conversion, respectively. These merits enable EBBT‐COF to be a promising photocatalyst toward H 2 O 2 generation from H 2 O and O 2 with a H 2 O 2 yield rate of 5 686 µmol g −1 h −1 , an optimal apparent quantum yield of 15.14%, a solar‐to‐chemical conversion efficiency of 1.17% (λ > 400 nm), representing one of the best performance among COF‐based photocatalysts reported thus far.