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Design and development of unconventional catalytic conversion processes using electrons, photons, and microorganisms

Problem statement

Our long-term commitment to sustainability and a circular carbon economy involves unconventional catalytic conversion processes. We study various processes assisted by electrons, photons, or microorganisms to produce biofuels, chemicals, electricity, or treated water. For example, bio-electro-chemical systems, including microbial fuel cells (MFCs), electrolysis cells (MECs), and photo-assisted cells (PA-MECs), are promising technologies to simultaneously produce renewable energy and clean wastewater using active microorganisms as biocatalysts.

Our work aims to synthesize multi-functional catalysts and reactors to enhance electrical conductivity, photo-efficiency, microbiological affinity, porosity, hydrophilicity, and surface area for carbonaceous electrodes. We work with materials such as graphene oxide, metallic nanoparticles, nitride and carbide basic materials, and MXenes.

We consider new platform technologies to produce renewable biofuel and chemicals and treat wastewater using the nanotechnology and reaction engineering approach as an innovative combination to increase the productivity of these processes.

Goals

  • Develop and scale up electro-photo-bio-catalyst and -reactors
  • Propose novel processes to clean wastewater and produce electricity, chemicals, and bio-hydrogen
  • Model and simulate fuel cell performance
  • Use innovative catalysts (anode and cathode material) and reactor designs to improve fuel cell performance
EPB2023

Related People

Related Publications

Ru-Oᵥ Site-Mediated Product Selectivity Switch for Overall Photocatalytic CO₂ Reduction

by Feng, Hu, Luo, Castaño, Ren, Rueping, Zhang
Adv. Mater. Year: 2025 DOI: https://doi.org/10.1002/adma.202411813

Abstract

The photocatalytic reduction of carbon dioxide (CO2) to methane (CH4) represents a sustainable route for directly converting greenhouse gases into chemicals but poses a significant challenge in achieving high selectivity due to thermodynamic and kinetic limitations during the reaction process. This work establishes Ru-OV active sites on the surface of TiO2 by anchoring coordination unsaturated Ru single-atoms, which stabilize crucial reaction intermediates and facilitate local mass transfer to achieve dual optimization of the thermodynamics and kinetics of the overall photocatalytic CO2reduction. Combining operando spectroscopy with density functional theory (DFT) calculations indicates that oxygen vacancies (OV) inhibits the desorption of *CO, whereas Ru facilitates proton extraction. This configuration not only lowers the overall activation energy barrier but has also been engineered to serve as a selectivity switch, changing the reaction route to produce CH4 instead of CO. Consequently, the Ru-OV/TiO2exhibits a 195.4-fold improvement in the CH4 yield compared to TiO2, accompanied by an increase in selectivity to 81%.

Keywords

EPB HCE