Molecule level precise construction of donor-acceptor polymeric carbon nitride for photocatalytic hydrogen evolution
Fanglei Yao1, Liming Dai1, Chenchen Fang1
1Key Laboratory for Soft Chemistry and Functional Materials, Ministry of Education, Nanjing University of Science and Technology, Nanjing 210094, China.
Abstract:
Constructing donor-acceptor structures in polymeric carbon nitride (CN) provides an attractive pathway for facilitating charge carrier separation in photocatalytic reactions. However, achieving the implantation of donor or acceptor moieties at molecule level precision remains challenging. Here we develop a three-dimensional (3D) porous thiophene implanted carbon nitride (TCN) with donor-acceptor structure via a supramolecular assembly strategy. The specific-designed triazine derivatives with similar hydrogen bonding sites allow for the uniform introduction of thiophene groups at molecule level precision during the supramolecular assemble stage. The electron-donating thiophene groups in TCN can continuously tune electronic band structure, expand visible light absorption range, and promote charge carriers' separation. The optimized properties enable TCN-3 an outstanding H2 evolution rate of 5620 μmol h-1 g-1, greatly exceeding bulk CN (95 μmol h-1 g-1). Briefly, our work may offer opportunities to prepare highly active photocatalysts with molecule level precise donor-acceptor structure.
More Related Videos
13:56Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations
Published on: October 12, 2019
12:19Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
Published on: November 29, 2018
Related Concept Videos
Catalysis
Aldehydes and Ketones with HCN: Cyanohydrin Formation Mechanism
Aldehydes and Ketones with HCN: Cyanohydrin Formation Overview
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
