The imperative to address CO emissions has prompted the search for alternative approaches to capture this gas with minimal energy consumption. In this context, leveraging the CO reduction reaction (CORR) as an oxidant in fuel cells has emerged as a sophisticated strategy to convert this gas into usable energy. This study introduces a hybrid microfluidic photo fuel cell (μPFC) designed for the efficient conversion of CO and glycerol into electrical energy. The prototype integrates 3D-printed components with glass sealing, enabling precise control over the reactant flow and the use of light-sensitive catalysts. The anodic glycerol electrooxidation was investigated on Pt/C dispersed on carbon paper (CP), while the CORR was carried out on CuBiO/CP and CuBiO/CuO/CP in the presence of solar light. Half-cell measurements demonstrate the photoactivity of CuBiO/CuO/CP and CuBiO/CP electrodes for the CORR under light exposure at low onset potential in a neutral pH solution, generating a positive theoretical open-circuit voltage of 0.89-0.91 V when coupled to glycerol electrooxidation in an alkaline medium. The use of the mixed medium in the membraneless system equipped with the photosensitive catalysts allowed the building of this galvanic cell. However, the feasibility of using CuBiO/CP is hindered by the disruption of the colaminar channel caused by hydrogen bubbles produced during concurrent water splitting. In contrast, the μPFC equipped with a CuBiO/CuO/CP photocathode demonstrates a stable and reproducible performance, delivering a maximum power density of 0.9 mW cm. The formation of the CuBiO/CuO heterojunction effectively suppresses photocatalytic water splitting, allowing for efficient CO conversion without disruption of the laminar flow channel. This innovative approach highlights the potential of μPFCs as sustainable energy converters for the utilization of CO in aqueous solutions, offering a pathway toward carbon-neutral energy production.
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http://dx.doi.org/10.1021/acsomega.4c05943 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
Key Laboratory for Advanced Ceramics and Machining Technology of Ministry of Education, Institute of New-Energy, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China.
The development of water splitting technology in alkaline medium requires the exploration of electrocatalysts superior to Pt/C to boost the alkaline hydrogen evolution reaction (HER). Ruthenium oxides with strong water dissociation ability are promising candidates; however, the lack of hydrogen combination sites immensely limits their performance. Herein, we reported a unique RuO catalyst with metallic Ru on its surface through a simple cation exchange method.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Applied Chemistry, Chuo University, Tokyo 112-8551, Japan.
We employed machine learning (ML) techniques combined with potential-dependent photoelectrochemical impedance spectroscopy (pot-PEIS) to gain deeper insights into the charge transport mechanisms of hematite (α-FeO) photoanodes. By the Shapley Additive exPlanations (SHAP) analysis from the ML model constructed from a small data set (dozens of samples) of electrical parameters obtained from pot-PEIS and the PEC performance, we identified the dominant factors influencing the electron transport to the back contact in the bulk and hole transfer to a solution at the hematite/electrolyte interface. The results revealed that shallow defect states significantly enhance electron transport, while deep defect states impede it, and also one of the surface states enhances the hole transfer to the electrolyte solution.
View Article and Find Full Text PDFJ Phys Chem Lett
January 2025
Department of Nature and Environment, Faculty of Liberal Arts, The Open University of Japan, Chiba 261-8586, Japan.
In this work, we study the plexciton in the far-ultraviolet region formed between indium nanoclusters and water molecules. The indium clusters are fabricated on graphene under ultrahigh vacuum conditions and show a strong localized surface plasmon polariton (LSP) absorption band at 6-7 eV. Adsorption of water molecules onto the clusters at 115 K induces a band splitting larger than 1 eV, indicating a strong coupling between the LSP and water 4a ← 1b transition.
View Article and Find Full Text PDFPlant J
January 2025
Systems Biotechnology Group, Department Microbial Biotechnology, Helmholtz Centre for Environmental Research - UFZ, Leipzig, 04318, Germany.
Biophotovoltaics offers a promising low-carbon footprint approach to utilize solar energy. It aims to couple natural oxygenic photosynthetic electrons to an external electron sink. This lays the foundation for a potentially high light-to-energy efficiency of the Biophotovoltaic process.
View Article and Find Full Text PDFACS Cent Sci
January 2025
Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, United States.
As a vital process for solar fuel synthesis, water oxidation remains a challenging reaction to perform using durable and cost-effective systems. Despite decades of intense research, our understanding of the detailed processes involved is still limited, particularly under photochemical conditions. Recent research has shown that the overall kinetics of water oxidation by a molecular dyad depends on the coordination between photocharge generation and the subsequent chemical steps.
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