Bubble nucleation is ubiquitous in gas evolving reactions that are instrumental for a variety of electrochemical systems. Fundamental understanding of the nucleation process, which is critical to system optimization, remains limited as prior works generally focused on the thermodynamics and have not considered the coupling between surface geometries and different forms of transport in the electrolytes. Here, we establish a comprehensive transport-based model framework to identify the underlying mechanism for bubble nucleation on gas evolving electrodes. We account for the complex effects on the electrical field, ion migration, ion diffusion, and gas diffusion arising from surface heterogeneities and gas pockets initiated from surface crevices. As a result, we show that neglecting these effects leads to significant underprediction of the energy needed for nucleation. Our model provides a non-monotonic relationship between the surface cavity size and the overpotential required for nucleation, which is physically more consistent than the monotonic relationship suggested by a traditional thermodynamics-based model. We also identify the significance of the gas diffuse layer thickness, a parameter controlled by external flow fields and overall electrode geometries, which has been largely overlooked in previous models. Our model framework offers guidelines for practical electrochemical systems whereby, without changing the surface chemistry, nucleation on electrodes can be tuned by engineering the cavity size and the gas diffuse layer thickness.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.langmuir.0c02690 | DOI Listing |
Int J Biol Macromol
December 2024
Hubei Key Laboratory of Advanced Textile Materials & Application, Hubei International Scientific and Technological Cooperation Base of Intelligent Textile Materials & Application, Key Laboratory of Textile Fiber & Product, Ministry of Education, Wuhan Textile University, Wuhan 430200, China; School of Materials Science & Engineering, Hubei University of Automotive Technology, Shiyan 442002, China. Electronic address:
Langmuir
December 2024
School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an 710049, P. R. China.
This study explores the bubble nucleation process and heat transfer characteristics on nanostructured solid surfaces with mixed-wettable pillars using molecular dynamics simulations. Five different surfaces were designed by varying the wettability of the central pillars while keeping the lateral pillars hydrophilic. The nucleation behavior of argon bubbles was observed to differ significantly across these surfaces due to the combined effects of nanostructuring and mixed wettability.
View Article and Find Full Text PDFJ Chem Phys
December 2024
Baikov Institute of Metallurgy and Materials Science, Russian Academy of Sciences, 49 Leninsky Pr., 119334 Moscow, Russian Federation.
Copper and its alloys with transition metals (as good conductors of electricity and heat) are extensively used in electrical industry, electronics, and cooling systems and can be the subject of surface degradation by oxidation. In certain circumstances, surface degradation of copper occurs catastrophically. Predicting catastrophic oxidation kinetics and developing protective technology require understanding the mass transfer mechanisms in the solid/liquid/gas composite scale formed on the copper surface during catastrophic degradation.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Institute of Fluid Dynamics, Helmholtz-Zentrum Dresden-Rossendorf, 01328 Dresden, Germany; Institute of Process Engineering, Technische Universität Dresden, 01069 Dresden, Germany. Electronic address:
Hypothesis: The surface wettability influences the oversaturation-driven growth of gas bubbles on the surface via the contact angle. Larger contact angles on hydrophobic surfaces compared to hydrophilic ones lead to faster growth of bubbles nucleating at microcavities of identical size.
Experiments: Cylindric micro-cavities were etched in silicon wafers as nucleation sites.
Chem Sci
December 2024
Siyuan Laboratory, Guangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy Materials, College of Physics & Optoelectronic Engineering, Department of Physics, Jinan University Guangzhou 510632 China
Due to the minimal electrochemical oxidation-reduction potential, the potassium (K) metal anode has emerged as a focal in K-ion batteries. However, the reactivity of the K metal anode leads to significant side reactions, particularly gas evolution. Mitigating gas generation from K metal anodes has been a persistent challenge in the field.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!