Synergizing Electron and Heat Flows in Photocatalyst for Direct Conversion of Captured CO₂

We report a ternary hybrid photocatalyst architecture with tailored interfaces that boost the utilization of solar energy for photochemical CO₂ reduction by synergizing electron and heat flows in the photocatalyst. The photocatalyst comprises cobalt phthalocyanine (CoPc) molecules assembled on multiwalled carbon nanotubes (CNTs) that are decorated with nearly monodispersed cadmium sulfide quantum dots (CdS QDs). The CdS QDs absorb visible light and generate electron-hole pairs. The CNTs rapidly transfer the photogenerated electrons from CdS to CoPc. The CoPc molecules then selectively reduce CO₂ to CO. The interfacial dynamics and catalytic behavior are clearly revealed by time-resolved and in situ vibrational spectroscopies. In addition to serving as electron highways, the black body property of the CNT component can create local photothermal heating to activate amine-captured CO₂, namely carbamates, for direct photochemical conversion without additional energy input.

Choi, C.; Zhao, F.; Hart, J.. L; Gao, Y.; Menges, F.; Rooney, C. L.; Harmon, N. J.; Shang, B.; Xu, Z.; Suo, S.; Sam, Q.; Cha, J. J.; Lian, T.; Wang, H. Synergizing Electron and Heat Flows in Photocatalyst for Direct Conversion of Captured CO₂ Angew. Chem. Int. Ed. 2023, 62, e202302152. https://onlinelibrary.wiley.com/doi/10.1002/anie.202302152