Alkali Cations Enhance CO2 Conversion in Amine Electrolytes

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current electrochemical techniques for converting chemisorbed CO2 into value-added products, such as carbon monoxide, face inefficiencies and low conversion rates, particularly at higher operating current densities, due to limitations in electron transfer and solubility of CO2 in amine capture solutions.

Innovation Solution

The introduction of alkali cations, such as K+, Rb+, and Cs+, into the amine-CO2 electrolyte disrupts the electrochemical double layer, reducing the distance between chemisorbed CO2 and the electrode, thereby enhancing electron transfer and achieving higher Faradaic efficiency in the conversion of CO2 to CO.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional electrochemical techniques are used for converting chemisorbed CO2, then the process can proceed, but the conversion rate and Faradaic efficiency are low, particularly at higher operating current densities

Engineering Contradiction:
ImproveCO2 conversion rateVSAvoidFaradaic efficiency
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent changes the chemical composition parameter of the electrolyte by introducing alkali metal cations (K+, Rb+, Cs+) into the amine-CO2 electrolyte system. This parameter change modifies the electrochemical double layer structure and enhances electron transfer kinetics, resulting in improved Faradaic efficiency and conversion rates without compromising reliability at higher current densities

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

Alkali metal cations serve as intermediary species that mediate between the electrode and chemisorbed CO2. These cations disrupt the electrochemical double layer and facilitate electron transfer to the carbamate species, acting as a bridge that enhances the overall conversion efficiency while maintaining system stability

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If the distance between chemisorbed CO2 and the electrode is reduced to enhance electron transfer, then conversion efficiency improves, but the structural configuration of the electrolyte must be changed

Engineering Contradiction:
Improveelectron transfer efficiencyVSAvoidelectrolyte composition complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

By modifying the electrolyte composition parameter to include alkali metal cations, the patent achieves a more compact electrochemical double layer structure. This parameter change reduces the effective distance between chemisorbed CO2 and the electrode surface, enhancing electron transfer efficiency while adding only a simple ionic component to the electrolyte

Inventive Principle:
Principle #35Parameter changes

3Reliability

If alkali cations are added to disrupt the electrochemical double layer, then electron transfer to amine-CO2 adduct is enhanced, but the electrolyte composition becomes more complex

Engineering Contradiction:
Improveelectron transfer rateVSAvoidelectrolyte composition
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

Alkali metal cations function as intermediary species that selectively interact with the electrochemical double layer at the electrode interface. These cations mediate the electron transfer process by disrupting the double layer structure and facilitating charge transfer to the amine-CO2 adduct, improving reliability while adding a simple ionic component

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The alkali metal cations exhibit local quality effects by concentrating at the electrode interface where they are most needed for electron transfer enhancement. This localized action disrupts the electrochemical double layer specifically at the reaction interface without requiring uniform composition changes throughout the entire electrolyte volume

Inventive Principle:
Principle #3Local quality

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This approach results in a Faradaic efficiency of up to 72% CO2 conversion to CO at 50 mA/cm2, with improved recyclability of the amine electrolyte and reduced energy costs, simplifying the process flow and lowering the carbon footprint.

Implementation Method 1

The reduction of distance can be achieved by disrupting the electrochemical double layer (EDL) via the presence of alkali cations competing with the ammonium ions from the amine-based electrolyte

Methodology Applied
Scientific EffectElectrochemical double layer disruption:

Implementation Method 2

enhance electron transfer to the amine-CO2 adduct

Methodology Applied
Scientific EffectElectron transfer:

Implementation Method 3

contacting the amine-CO2 electrolyte solution with a working electrode under applied current density for electrolysing the amine-CO2 adduct to form a product mixture comprising carbon monoxide (CO) and an amine

Methodology Applied
Scientific EffectElectrolysis: Electrolysis

Implementation Method 4

the presence of alkali cations competing with the ammonium ions from the amine-based electrolyte

Methodology Applied
Scientific EffectIon competition:

Data Source

PatentUS20230416929A1Enhanced conversion of chemisorbed co2 in aminebased electrochemical systems
Publication Date: 2023.12.28 THE GOVERNING COUNCIL OF THE UNIV OF TORONTO
  • US20230416929A1 patent drawing
  • US20230416929A1 patent drawing
  • US20230416929A1 patent drawing

AI summary

An electrochemical process, and related method and system to upgrade captured CO2 into value-added products. CO2 capture technologies based on chemisorption present the potential to lower net emissions of CO2 into the atmosphere. The use of alkali cations to tailor the electrochemical double layer allows achieving the valorization of chemisorbed CO2 in an aqueous amine-based electrolyte, by placing the CO2 of the amine-CO2 adduct sufficiently close to the site of an heterogeneous reaction at the working electrode. It is revealed, using electrochemical studies and in-situ surface-enhanced Raman spectroscopy, that a smaller double layer distance can correlate with improved activity for CO2 to CO from amine solutions.