(521ac) Molecular Catalyst-Functionalized Silicon Photocathode for Aqueous Photoelectrocatalytic CO2 Reduction to Methanol | AIChE

(521ac) Molecular Catalyst-Functionalized Silicon Photocathode for Aqueous Photoelectrocatalytic CO2 Reduction to Methanol

Authors 

Wang, H., Yale University
Recent research has shown that immobilizing cobalt phthalocyanine (CoPc) molecules onto carbon nitride results in high-performance conversion of CO2 into CO.1 Building on this, we developed a molecular catalyst-based photocathode that is active for aqueous CO2 reduction to CO and methanol. The photoelectrode is composed of CoPc molecules anchored on graphene oxide which is integrated via a (3-aminopropyl)triethoxysilane linker to p-type silicon protected by a thin film of titanium dioxide. The photocathode reduces CO2 to CO with high selectivity at potentials as mild as 0 V versus the reversible hydrogen electrode (vs RHE). Methanol production is observed at an onset potential of −0.36 V vs RHE, and reaches a peak turnover frequency of 0.18 s-1. To date, this is the only molecular catalyst-based photoelectrode that is active for the six-electron reduction of CO2 to methanol.2

This work puts forth a strategy for interfacing molecular catalysts to p-type semiconductors and demonstrates state-of-the-art performance for photoelectrochemical CO­2 reduction to CO and methanol.

References

(1) Shang, B.; Zhao, F.; Choi, C.; Jia, X.; Pauly, M.; Wu, Y.; Tao, Z.; Zhong, Y.; Harmon, N.; Maggard, P. A.; Lian, T.; Hazari, N.; Wang, H., Monolayer Molecular Functionalization Enabled by Acid–Base Interaction for High-Performance Photochemical CO2 Reduction. ACS Energy Letters 2022, 7 (7), 2265-2272.

(2) Shang, B.; Rooney, C. L.; Gallagher, D. J.; Wang, B. T.; Krayev, A.; Shema, H.; Leitner, O.; Harmon, N. J.; Xiao, L.; Sheehan, C., Aqueous Photoelectrochemical CO2 Reduction to CO and Methanol over a Silicon Photocathode Functionalized with a Cobalt Phthalocyanine Molecular Catalyst. Angewandte Chemie 2023, 135 (4), e202215213.

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