Insights Into The Dynamics Of Liquid Metal Nanoparticles During CO2 Reduction Reaction Using In-Situ Electrochemical Liquid Phase TEM
Krishna Kumar a, Coline Boulanger a, Seyedmohamadjavad Chabok a, Anna Loiudice a, Raffaella Buonsanti a
a Laboratory of Nanochemistry for Energy (LNCE), Institute of Chemical Sciences and Engineering (ISIC), Ecole Polytechnique Fédérale de Lausanne, Sion, CH-1950, Switzerland
Materials for Sustainable Development Conference (MATSUS)
Proceedings of MATSUS Fall 2024 Conference (MATSUSFall24)
#PECCO2 - Advances in (Photo)Electrochemical CO2 Conversion to Chemicals and Fuels
Lausanne, Switzerland, 2024 November 12th - 15th
Organizers: Deepak PANT, Adriano Sacco and juqin zeng
Poster, Krishna Kumar, 375
Publication date: 28th August 2024

Gallium (Ga)-based liquid metals (LM) have recently emerged as a promising class of advanced material due to their unique physicochemical properties, including high electrical and thermal conductivities, combined with water-like fluidity [1]. Nanoparticles of Ga and its alloys exhibit a liquid metallic core surrounded by a native oxide skin [2]. These materials have gained significant attention as electrocatalysts, particularly for their dynamic surfaces and inherent resistance to coke formation, attributed to the reconfigurable nature of the oxide layer [3-4]. However, the relationship between the structural evolution of LM-based catalysts and their catalytic activity remains unexplored. Understanding the dynamic interactions that drive reactions is crucial for further development as LM-based reconfigurable catalysts.
In this work, we utilize in-situ electrochemical liquid-phase TEM to study the dynamic evolution of liquid metal nanoparticles under near-operating CO2 reduction conditions. We will demonstrate how Ga-based nanoparticles evolve as a function of size and applied potential, providing insights into the structural changes under CO2 reduction conditions.

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