Issue 18, 2024

Self-assembled monolayers for electrostatic electrocatalysis and enhanced electrode stability in thermogalvanic cells

Abstract

Waste heat is ubiquitous; as such, sustainable and long-lasting devices are required to convert it into more useful forms of energy that can make use of this abundant potential resource. Thermogalvanic cells (or thermocells) can use the thermoelectrochemical properties of redox couples to achieve this; entropy-driven redox reactions allow them to act as liquid thermoelectrics. However, excellent electrocatalysis at the electrode surface is required for optimum conversion efficiency. Serendipitous observation of Nafion-based electrocatalysis prompted the exploration of electrostatically charged self-assembled monolayers (SAMs) inside a thermocell. Both electrostatic electrocatalysis and improved electrode stability were observed; in an aqueous K3[Fe(CN)6]/K4[Fe(CN)6]-based cell, modification with (3-trimethylammonium bromide)thiopropane resulted in higher electrical power, and protection against [Fe(CN)6]3−/4−-induced gold passivation, relative to bare gold. Molecular-based electrostatic electrocatalysis could be an alternative to precious metal-based nanomaterial electrocatalysis, and could be integrated with (nano)carbon-based electrodes to further enhance the ability of thermogalvanic and other electrochemical energy conversion devices, e.g. redox flow batteries.

Graphical abstract: Self-assembled monolayers for electrostatic electrocatalysis and enhanced electrode stability in thermogalvanic cells

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Article information

Article type
Edge Article
Submitted
16 Dec 2023
Accepted
02 Apr 2024
First published
03 Apr 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2024,15, 6958-6964

Self-assembled monolayers for electrostatic electrocatalysis and enhanced electrode stability in thermogalvanic cells

K. Laws, M. A. Buckingham and L. Aldous, Chem. Sci., 2024, 15, 6958 DOI: 10.1039/D3SC06766A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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