Fuel Cell Catalyst Layer Pore Structure for Water Management

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Solution Overview

Problem

Fuel cell electrode catalyst layers face challenges in balancing water retention and drainage, leading to issues of flooding or dry-out, particularly due to the hydrophobic nature of carbon-based supports, which affect power output and humidity dependence.

Innovation Solution

A porous electrode catalyst layer using a particulate inorganic oxide support with a specific pore size distribution, measured by mercury intrusion porosimetry, featuring a first peak in 0.005 to 0.1 μm and a second peak in 0.1 to 1 μm, with a peak intensity ratio of 0.2 to 10, to enhance water retention and drainage efficiency.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If carbon-based support is used in the catalyst layer, then water drainage is improved, but the catalyst layer becomes prone to dry-out

Engineering Contradiction:
Improvewater drainageVSAvoidmoisture retention
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The invention changes the material parameter of the catalyst support from carbon-based (hydrophobic) to inorganic oxide-based (hydrophilic). This parameter change fundamentally alters the water interaction characteristics, improving moisture retention while maintaining adequate drainage through optimized pore structure. The hydrophilic surface of inorganic oxide supports reduces water contact angle, preventing excessive water drainage and dry-out conditions.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention uses inorganic oxide materials (such as metal oxides) as composite support structures instead of pure carbon. These composite inorganic oxide-based catalyst layers combine the hydrophilic properties of oxide surfaces with controlled pore architecture, achieving a balance between water retention and drainage that pure carbon supports cannot provide.

Inventive Principle:
Principle #40Composite materials

2Reliability

If inorganic oxide support is used in the catalyst layer, then moisture retention is improved, but water accumulation and flooding occur

Engineering Contradiction:
Improvemoisture retentionVSAvoidwater drainage
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The invention employs porous inorganic oxide support materials with specifically controlled pore size distributions. The porous structure provides capillary channels that facilitate water drainage while the hydrophilic oxide surface maintains moisture retention. The pore size distribution (with peaks at 0.005-0.1 μm and 0.1-1 μm) creates a hierarchical drainage system that prevents flooding by efficiently removing excess water through capillary action.

Inventive Principle:
Principle #31Porous materials

Solution Approach 2:

The invention modifies the pore structure parameters of the inorganic oxide support, specifically controlling the pore size distribution with dual peaks. This parameter optimization allows the material to exhibit both high moisture retention (due to hydrophilic surface) and effective water drainage (through controlled pore channels), resolving the contradiction between these two opposing requirements.

Inventive Principle:
Principle #35Parameter changes

3Ease of operation

If carbon-based support is used, then water drainage is enhanced, but power output and humidity dependence deteriorate

Engineering Contradiction:
Improvewater drainageVSAvoidpower output
Core Design Contradiction:
Ease of operationVSPower

Solution Approach 1:

The invention changes the fundamental material parameter from carbon-based to inorganic oxide-based support, which alters the hydrophobicity/hydrophilicity balance. This parameter change improves power output by maintaining optimal moisture content in the catalyst layer, which is critical for efficient electrochemical reactions. The inorganic oxide support reduces humidity dependence by providing stable moisture retention across varying environmental conditions.

Inventive Principle:
Principle #35Parameter changes

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 configuration improves power output and reduces humidity dependence, ensuring efficient water drainage and reaction gas diffusion, thereby enhancing the performance of fuel cells under varying humidity conditions.

Implementation Method 1

the porous structure having a pore size distribution, measured by mercury intrusion porosimetry, showing a first peak in a range of from 0.005 to 0.1 μm and a second peak in a range of from greater than 0.1 μm to 1 μm

Methodology Applied
Scientific EffectCapillary action: Capillary Action

Implementation Method 2

an electroconductive oxide support that has recently been proposed as a new support has a hydrophilic surface and is therefore less prone to develop the dry-out problem

Methodology Applied
Scientific EffectAdsorption: Adsorption

Data Source

PatentUS10629935B2Fuel cell electrode catalyst layer, production method therefor, membrane electrode assembly, and solid polymer fuel cell
Publication Date: 2020.04.21 MITSUI MINING & SMELTING CO LTD
  • US10629935B2 patent drawing
  • US10629935B2 patent drawing
  • US10629935B2 patent drawing

AI summary

In this fuel cell electrode catalyst layer, a catalyst is supported on a carrier comprising inorganic oxide particles. The fuel cell electrode catalyst layer is provided with a porous structure. When a mercury penetration method is used to measure the pore size distribution of the porous structure, a peak is observed in the range spanning from 0.005 μm to 0.1 μm inclusive, and a peak is also observed in the range spanning from over 0.1 μm to not more than 1 μm. When P1 represents the peak intensity in the range spanning from 0.005 μm to 0.1 μm inclusive, and P2 represents the peak intensity in the range spanning from over 0.1 μm to not more than 1 μm, the value of P2/P1 is 0.2-10 inclusive. It is preferable that the inorganic oxide be tin oxide.