The efficient removal of gas bubbles in (photo)electrochemical gas evolution reactions is an important but underexplored issue. Conventionally, researchers have attempted to impart bubble-repellent properties (so-called superaerophobicity) to electrodes by controlling their microstructures. However, conventional approaches have limitations, as they are material specific, difficult to scale up, possibly detrimental to the electrodes' catalytic activity and stability, and incompatible with photoelectrochemical applications. To address these issues, we report a simple strategy for the realization of superaerophobic (photo)electrodes via the deposition of hydrogels on a desired electrode surface. For a proof-of-concept demonstration, we deposited a transparent hydrogel assembled from M13 virus onto (photo)electrodes for a hydrogen evolution reaction. The hydrogel overlayer facilitated the elimination of hydrogen bubbles and substantially improved the (photo)electrodes' performances by maintaining high catalytic activity and minimizing the concentration overpotential. This study can contribute to the practical application of various types of (photo)electrochemical gas evolution reactions.
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http://dx.doi.org/10.1126/sciadv.aaz3944 | DOI Listing |
J Phys Chem C Nanomater Interfaces
January 2025
Department of Chemistry and Biochemistry, San Francisco State University, 1600 Holloway Ave., San Francisco, California 94132, United States.
Water electrolysis is a green method of storing electrical energy in the chemical bonds of high-energy hydrogen gas (H). However, the anodic oxygen evolution reaction (OER) requires a significant kinetic overpotential, limiting the electrolysis rate. Recently, plasmonic gold nanoparticles (Au NPs) have been introduced to improve charge transfer at the interface between the OER electrocatalysts and the electrolyte under light illumination.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Universität Tübingen, Institute of Physical and Theoretical Chemistry, Auf der Morgenstelle 15, 72076 Tübingen, Germany.
The versatile optoelectronic properties of the material class of III-V semiconductors enable the highest performance in photovoltaic and photoelectrochemical solar cells. While a high level of control and understanding with respect to different surface reconstructions of these compounds in gas-phase ambient has been reached, the situation in an electrochemical environment still poses challenges. Here, we therefore have undertaken a computational study of the InP(100) surface in the presence of hydrogen and chlorine, mimicking the contact with a hydrochloric acid-containing electrolyte, aiming at an understanding of ion adsorption and dominant surface reconstructions with respect to applied potential and electrolyte concentration.
View Article and Find Full Text PDFDalton Trans
January 2025
Shanxi Key Laboratory of Gas Energy Efficient and Clean Utilization, College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan, Shanxi 030024, China.
BiVO is considered as one of the important candidate materials for photoelectrochemical water splitting technology. However, the low efficiency of charge separation and poor kinetics of water oxidation limit its performance in PEC water splitting. In this work, a BiVO/MIL-53(FeNiCo) photoanode was constructed by a facile hydrothermal deposition method, exhibiting excellent water oxidation ability under AM 1.
View Article and Find Full Text PDFLoading with non-metal cocatalysts to regulate interfacial charge transfer and separation has become a prominent focus in current research. In this study, g-CN/CNT composites loaded with non-metallic cocatalysts were prepared through pyrolysis using urea and CNTs. Various characterization techniques, including transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS), photoelectrochemical (PEC) analysis, fluorescence lifetime spectroscopy (TRPL), electron paramagnetic resonance spectroscopy (ESR), and photoluminescence (PL) spectroscopy, were employed to analyze the sample's microstructure, phase composition, elemental chemical states, and photoelectronic properties.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Civil and Environmental Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-Gu, Seoul 04763, Republic of Korea.
In this research, S-scheme heterojunction photocatalysts are prepared through the hybridization of nitrogen-rich g-CN with TiO (coded as TCN-(): as the weight ratio of TiO:g-CN). The photocatalytic potential of TCN-() is evaluated against benzene (1-5 ppm) across varying humidity levels using a dynamic flow packed-bed photocatalytic reactor. Among the prepared composites, TCN-(10) exhibits the highest synergy between g-CN and TiO at "" ratio of 10%, showing superior best benzene degradation performance (e.
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