109
Views
0
CrossRef citations to date
0
Altmetric
Research Article

Flowable capacitive cathode for efficiency carbon dioxide reduction in photoelectrochemical cell

, , , , , , & show all
Pages 7294-7302 | Received 08 Feb 2023, Accepted 28 Mar 2023, Published online: 19 Jun 2023
 

ABSTRACT

Photoelectrochemical (PEC) Cell reduction carbon dioxide (CO2) is a promising avenue for converting CO2 into valuable products. In this work, a flowable electrode with a rotating impeller collector was proposed to enhance the efficiency of the carbon dioxide reduction reaction (CO2RR) in a photoelectrochemical system. Titanium carbide (Ti3C2), with its capacitive properties, serves as a catalyst and is fluidized in the cathode chamber. The frequent contact between the Ti3C2 catalysts and the rotating impeller collector extends the catalytic reaction throughout the catholyte and enhances the efficiency of CO2RR. The feasibility of the design was verified through suspension characterization, CO2 diffusion concentration measurement, capacitance characterization, and experimental factor analysis. The PEC with a flow electrode exhibits CO and CH4 production rates of 1.64 μmol g−1h −1and 9.62 μmol g−1h−1, respectively, which are 3.5 and 7.2 times higher than those of the fixed cathode. The Faradaic efficiency for CH4 reaches 92.4%. Moreover, the collision probability of the flow electrode is 17.7%, which is significantly higher than that of the conventional bubbling fluidized electrode. In addition, the capacitive properties of Ti3C2 particles favor the continuous CO2RR under open circuit conditions, which was verified by an EDS test of Na+. Finally, the operational mechanism of the PEC system is described.

Highlights

  • A novel rotating impeller collector was proposed to support the PEC system.

  • Ti3C2, which has great capacitive properties, was introduced as a fluidized cathode.

  • The PEC system displayed excellent suspension properties for Ti3C2 particles.

  • Yields of CO and CH4 that were 3.5 and 7.2 times higher than those of a fixed cathode were obtained.

Acknowledgements

We acknowledgments the Science and Technology Department Project of Henan Province (222102320109).

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

The work was supported by the Science and Technology Department Project of Henan Province [222102320109].

Notes on contributors

Jun Zhang

Jun Zhang is an associate professor at Zhengzhou University of Light Industry, mainly engaged in research on fuel cells.

Ankang Fang

Ankang Fang is a master's student at Zhengzhou University of Light Industry, involved in research on photocatalytic carbon dioxide reduction.

Jili Zheng

Jili Zheng is a lecturer at Zhengzhou University of Light Industry, specializing in research on fuel cells.

Penglin Yang

Penglin Yang is a master's student at Zhengzhou University of Light Industry, focusing on research on photoelectric catalysis for the degradation of pollutants.

Shuai Lv

Shuai Lv is a master's student at Zhengzhou University of Light Industry, engaged in research on photocatalytic carbon dioxide reduction.

Chuanxiao Cheng

Chuanxiao Cheng is an associate professor at Zhengzhou University of Light Industry, conducting research on hydrate energy storage.

Peiyuan Xu

Peiyuan Xu is a professor at Zhengzhou University of Light Industry, primarily involved in research on chemical process and equipment.

Shuang Cao

Shuang Cao is a lecturer at Zhengzhou University of Light Industry, specializing in research on energy system optimization and design.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.