Jia Xinrui, Zhang Juan, Gong Jian Ru
CAS Center of Excellence for Nanoscience, CAS Key Laboratory for Nanosystem & Hierarchical Fabrication, National Center for Nanoscience and Technology, 11 Beiyitiao Zhongguancun, Beijing 100190, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
ACS Appl Mater Interfaces. 2024 Sep 25;16(38):50826-50833. doi: 10.1021/acsami.4c11066. Epub 2024 Sep 11.
The reduced nicotinamide adenine dinucleotide (NADH) is a vital biomolecule involved in many biocatalytic processes, and the high cost makes it significant to regenerate NADH in vitro. The photoelectrochemical approach is a promising and environmentally friendly method for sustainable NADH regeneration. However, the free Rh-based mediator ([Cp*Rh (bpy)HO]) in the electrolyte suffers from low efficiency due to the sluggish charge transfer controlled by the diffusion process. Herein, we report an efficient and facile covalent bonding of the Rh-based mediator with the Si-based photocathode for NADH regeneration. The bipyridine-containing covalent organic framework (BpyCOF) layer ensures the even distribution of mediators throughout the surface of the photoelectrode. The graphene interlayer provides a pathway for charge transport and prevents silicon from corrosion. Furthermore, during the synthesis of BpyCOF, it functions as a substrate to promote the growth of the oriented BpyCOF film. The imitated contact between the components of the photocathode favors the charge transfer to the surface to participate in a chemical reaction, thus improving the catalytic performance and the NADH regeneration efficiency, which is four times higher than the reported photocathode modified by the Rh-based mediator. This study offers a new strategy for the construction of photoelectrochemical solar energy conversion devices.