Single-atom cobalt-incorporating carbon nitride for photocatalytic solar hydrogen conversion: An X-ray spectromicroscopy study

The use of carbon nitride-based materials and light to drive catalytic water splitting has enormous potential for the production of hydrogen. Revealing the processes of molecular conjugation, nucleation, and crystallization in crystalline carbon nitride is expected to enhance the photocatalytic activity through the creation of isotype heterojunctions and active sites. In this work, the addition of cobalt salts in ionothermal synthesis was found to promote the phase transition of heptazine-based crystalline carbon nitride (CCN) to triazine-based poly (triazine imide) (PTI), resulting in the formation of a single-atom cobalt-doped coordinated isotype CCN/PTI heterojunction. The new hybrid orbital modulates the atomic/electronic structure and the band gap of the CCN/PTI heterojunction, and synergistically increases the absorption of visible light, accelerating the separation and transfer of photoexcited electrons and holes. Synchrotron-based X-ray spectroscopy and microscopy are used to identify the origin of the improved performance of the single-atom cobalt-doped CCN/PTI heterojunction in the photocatalytic hydrogen evolution reaction. This work demonstrates that synchrotron X-ray spectroscopy is a promising tool for designing materials aimed at enhancing photocatalytic activity in solar energy conversion applications.

Automated summary

The use of carbon nitride-based materials and light for catalytic water splitting has great potential for hydrogen production. This study explores the processes of molecular conjugation, nucleation, and crystallization in crystalline carbon nitride to enhance photocatalytic activity. The addition of cobalt salts in ionothermal synthesis promotes the phase transition of carbon nitride, resulting in a cobalt-doped heterojunction. Synchrotron-based X-ray spectroscopy and microscopy confirm the improved performance of the cobalt-doped heterojunction in the photocatalytic hydrogen evolution reaction. This study highlights the potential of synchrotron X-ray spectroscopy for designing materials to enhance photocatalytic activity in solar energy conversion.