Ferrocene Organometallic Complexes for Multi-Electron Flow Batteries

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Solution Overview

Problem

Current Redox Flow Batteries (RFBs) face limitations due to low energy density, poor solubility, high cost, and instability of charge carriers, particularly in Vanadium-based systems, which restrict their ability to store multiple electrons effectively.

Innovation Solution

The development of Fc-substituted organometallic complexes, specifically those with Group 13 metals like Al, which enable multi-electron transfer events, enhancing energy density and stability, and are used as analytes in Non-Aqueous Redox Flow Batteries (NRFBs) to overcome these limitations.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If Vanadium-based charge carriers are used in RFBs, then the battery can store electrical energy, but the energy density remains low due to limited solubility and single electron transfer per charge carrier

Engineering Contradiction:
Improveenergy densityVSAvoidlimit to single electron transfer
Core Design Contradiction:
Quantity of substanceVSObject-generated harmful factors

Solution Approach 1:

The patent changes the fundamental parameters of the charge carrier by using Fc-substituted organometallic complexes instead of traditional Vanadium-based species. These complexes enable multi-electron transfer (n ≥ 2) per charge carrier, directly increasing the quantity of substance parameter (energy density) while eliminating the harmful limitation of single electron transfer.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention employs composite organometallic complexes containing ferrocene substituents combined with Group 13 metals (Al, Ga, In). This composite structure integrates the redox activity of ferrocene with the stability and multi-electron transfer capability of the metal center, achieving both high energy density and structural stability.

Inventive Principle:
Principle #40Composite materials

2Quantity of substance

If new RFB analytes with greater energy densities are developed by switching to nonaqueous media, then the solvent window increases and battery cell voltages increase, but the solubility and stability of charge carriers may be compromised

Engineering Contradiction:
Improveenergy densityVSAvoidcharge carrier stability
Core Design Contradiction:
Quantity of substanceVSStability of the object's composition

Solution Approach 1:

The patent uses composite organometallic complexes where the ferrocene-substituted organic ligands provide stability in nonaqueous media while the Group 13 metal center enables multi-electron transfer. This composite structure maintains both high energy density and charge carrier stability in nonaqueous solvents.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The invention introduces ferrocene substituents at specific positions on the organic ligands, creating local redox-active sites that enhance energy density without compromising the overall stability of the complex in nonaqueous media. The local ferrocene groups provide electron transfer capability while the rest of the complex structure maintains stability.

Inventive Principle:
Principle #3Local quality

3Quantity of substance

If charge carriers that store multiple electrons are used, then the energy density increases, but poor solubility and high cost of certain metal ions become limiting factors

Engineering Contradiction:
Improveenergy densityVSAvoidsynthesis complexity and cost
Core Design Contradiction:
Quantity of substanceVSEase of manufacture

Solution Approach 1:

The patent changes the metal center parameter to Group 13 metals (Al, Ga, In) which are more abundant and less costly than traditional multi-electron transfer metals. These metals can still facilitate multi-electron transfer when combined with ferrocene-substituted ligands, achieving high energy density with improved ease of manufacture and lower cost.

Inventive Principle:
Principle #35Parameter changes

4Reliability

If symmetric configuration RFBs are used with the same charge carrier at both electrodes, then the battery can operate with reversible redox couples, but species crossover leads to irreversible capacity loss and fade

Engineering Contradiction:
Improvereversible redox operationVSAvoidcapacity fade due to species crossover
Core Design Contradiction:
ReliabilityVSLoss of substance

Solution Approach 1:

The patent creates local differences between the two half-cells by using different Fc-substituted organometallic complexes with distinct redox potentials and chemical properties at each electrode. This local differentiation allows symmetric configuration operation while preventing harmful species crossover, as the different complexes have different solubilities and electrochemical behaviors that reduce cross-contamination effects.

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

These complexes allow for higher energy storage capacity, improved solubility, and extended cycle stability, maintaining 70% state of charge and 97% Coulombic efficiency for over 100 cycles, with potential for wider temperature operation and compatibility with renewable energy sources.

Implementation Method 1

Fc-substituted organometallic complexes of the present disclosure can be used as multi-electron charge carriers, to enhance, for example, the energy density of RFBs including non-aqueous RFBs (NRFBs)

Methodology Applied
Scientific EffectRedox reactions: Redox Reactions

Data Source

PatentUS12258358B1Ferrocene-substituted organometallic complexes
Publication Date: 2025.03.25 RGT UNIV OF CALIFORNIA
  • US12258358B1 patent drawing
  • US12258358B1 patent drawing
  • US12258358B1 patent drawing

AI summary

Ferrocene (Fc)-substituted organometallic complexes are described. In one example, an Fc-substituted organometallic complex has a structure represented by formula IV:where M is a Group 13 metal, R1 is H or a substituted phenyl, and R2 is 4-ferrocenylphenyl. Non-aqueous redox flow batteries and electrical energy storage systems comprising the Fe-substituted organometallic complexes and methods of storing energy using the Fe-substituted organometallic complexes are provided.