Realization of a Photoelectrochemical Cascade for the Generation of Methanol: A Liquid Solar Fuel

Biochemical networks use reaction cascades to selectively reduce CO<sub>2</sub> using energy from sunlight, but can similar selectivity be achieved by applying a cascade approach to an engineered system? Here, we report the design and implementation of a two-step photoelectrochemical (PEC) cascade to a liquid solar fuel: reduction of CO<sub>2</sub> to CO and subsequent reduction of CO to methanol. The potentials required to perform the reductions were generated using custom-made III-V-based three-terminal tandem (3TT) solar cells. Cobalt phthalocyanine immobilized on multiwalled carbon nanotubes (CoPc/MWCNT) catalyzed both reactions. Multiphysics simulations of electrolyte flow and nonilluminated electrochemical measurements were used to narrow the operating parameters for the CoPc/MWCNT 3TT photocathodes. The champion integrated photocathode produced methanol with 3.8 ± 0.4% Faradaic efficiency (FE), with tested photocathodes having 0.7-3.8% methanol FE. Products were quantified by nuclear magnetic resonance spectroscopy and gas chromatography. The current output of the tested photocathodes was highly stable, and methanol production continued over multiple experiments. The low methanol yield is attributed to insufficient CO flux to, and CO<sub>2</sub> depletion at, the methanol-producing subcell when both contacts are active, which is supported by the observation that a control photoelectrode slightly outperformed the methanol production of the 3TT device. Methanol production ceased when the 3TT subcell driving CO reduction was deactivated, supporting the assignment of a cascade mechanism. The major factors resulting in low methanol FE by the CoPc/MWCNT 3TT photocathodes are insufficient CO<sub>2</sub> depletion at the methanol-producing contact and uncertainty in operating potential selection using the 3TT design. Although the CoPc/MWCNT 3TT photocathode is not yet highly selective, this work develops the basic science principles underlying the PEC cascade, demonstrates the co-design of a 3TT-based photoelectrode to produce carbon-based fuels, and finally discusses routes for improving product yields with this concept, including CO<sub>2</sub> supply optimization and alternative photoelectrode and catalyst materials.

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Publication Details

Journal
Energy & Fuels
Published
2024-12-23
DOI
https://doi.org/10.1021/acs.energyfuels.4c04779
Citations
3
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
Field-Weighted Citation Impact
0.31

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article

Realization of a Photoelectrochemical Cascade for the Generation of Methanol: A Liquid Solar Fuel

Clifford P. Kubiak, Emily L. Warren, Darci Collins, Myles A. Steiner et al.
3 citations
Energy & Fuels
CO2 Reduction Techniques and Catalysts
0.31
article

Realization of a Photoelectrochemical Cascade for the Generation of Methanol: A Liquid Solar Fuel

Clifford P. Kubiak, Emily L. Warren, Darci Collins, Myles A. Steiner, Adele C. Tamboli, Mickey J. Wilson, Thomas Chan, Grace A. Rome, Joel W. Ager, Ann L. Greenaway, Alex J. King, Rajiv Ramanujam Prabhakar, Calton J. Kong, Michelle Young, Sarah A. Collins
article en
3 citations

Abstract

Biochemical networks use reaction cascades to selectively reduce CO<sub>2</sub> using energy from sunlight, but can similar selectivity be achieved by applying a cascade approach to an engineered system? Here, we report the design and implementation of a two-step photoelectrochemical (PEC) cascade to a liquid solar fuel: reduction of CO<sub>2</sub> to CO and subsequent reduction of CO to methanol. The potentials required to perform the reductions were generated using custom-made III-V-based three-terminal tandem (3TT) solar cells. Cobalt phthalocyanine immobilized on multiwalled carbon nanotubes (CoPc/MWCNT) catalyzed both reactions. Multiphysics simulations of electrolyte flow and nonilluminated electrochemical measurements were used to narrow the operating parameters for the CoPc/MWCNT 3TT photocathodes. The champion integrated photocathode produced methanol with 3.8 ± 0.4% Faradaic efficiency (FE), with tested photocathodes having 0.7-3.8% methanol FE. Products were quantified by nuclear magnetic resonance spectroscopy and gas chromatography. The current output of the tested photocathodes was highly stable, and methanol production continued over multiple experiments. The low methanol yield is attributed to insufficient CO flux to, and CO<sub>2</sub> depletion at, the methanol-producing subcell when both contacts are active, which is supported by the observation that a control photoelectrode slightly outperformed the methanol production of the 3TT device. Methanol production ceased when the 3TT subcell driving CO reduction was deactivated, supporting the assignment of a cascade mechanism. The major factors resulting in low methanol FE by the CoPc/MWCNT 3TT photocathodes are insufficient CO<sub>2</sub> depletion at the methanol-producing contact and uncertainty in operating potential selection using the 3TT design. Although the CoPc/MWCNT 3TT photocathode is not yet highly selective, this work develops the basic science principles underlying the PEC cascade, demonstrates the co-design of a 3TT-based photoelectrode to produce carbon-based fuels, and finally discusses routes for improving product yields with this concept, including CO<sub>2</sub> supply optimization and alternative photoelectrode and catalyst materials.

Energy & FuelsVol. 39(8)
National Laboratory of the Rockies (US), Lawrence Berkeley National Laboratory (US), Colorado School of Mines (US), University of California System (US), University of California San Diego (US), Institute of Materials Science (VN), Division of Materials Science and Engineering (AU), NOAA Chemical Sciences Laboratory (US), Computational Physics (United States) (US), Advanced Energy Systems (United States) (US), University of California, Berkeley (US)
National Science Foundation, U.S. Department of Energy, Office of Science, Oak Ridge Institute for Science and Education, Basic Energy Sciences, Workforce Development for Teachers and Scientists
Affordable and clean energy
Openalex Percentile: Top 51%
CO2 Reduction Techniques and Catalysts
0.31
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