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

Author:

Choi Chungseok12,Zhao Fengyi3,Hart James L4,Gao Yuanzuo12,Menges Fabian1,Rooney Conor L.12,Harmon Nia J.12,Shang Bo12,Xu Zihao3,Suo Sa3,Sam Quynh4,Cha Judy J.4,Lian Tianquan3,Wang Hailiang12ORCID

Affiliation:

1. Department of Chemistry Yale University New Haven CT 06511 USA

2. Energy Sciences Institute Yale University West Haven CT 06516 USA

3. Department of Chemistry Emory University Atlanta GA 30322 USA

4. Department of Materials Science and Engineering Cornell University Ithaca NY 14853 USA

Abstract

AbstractWe 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.

Funder

U.S. Department of Energy

Publisher

Wiley

Subject

General Medicine

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