Nanotrap Architectures for Mitigating Interfacial Transport Limitations in Cathode Catalyst Layers of Proton Exchange Membrane Fuel Cells

Z Zhiyin Huang (Huangpu Hydrogen Energy Innovation Centre School of Chemistry and Chemical Engineering Guangzhou University Guangzhou Guangdong China) Y Yuqin Peng Z Zhiguo Qu (Key Laboratory of Thermo‐Fluid Engineering and Science of MOE School of Energy and Power Engineering Xi'an Jiaotong University Xi'an Shaanxi China) L Lixin Xing (Huangpu Hydrogen Energy Innovation Centre School of Chemistry and Chemical Engineering Guangzhou University Guangzhou Guangdong China) R Ruyi Zhong (Huangpu Hydrogen Energy Innovation Centre School of Chemistry and Chemical Engineering Guangzhou University Guangzhou Guangdong China) Z Zenan Wu (Huangpu Hydrogen Energy Innovation Centre School of Chemistry and Chemical Engineering Guangzhou University Guangzhou Guangdong China) S Siyu Ye (Department of Cell Biology and Center for Cell Dynamics, School of Medicine, Johns Hopkins University) Y Yutong Mu (School of Human Settlements and Civil Engineering Xi'an Jiaotong University Xi'an Shaanxi China) L Liguang Wang (College of Chemical and Biological Engineering) L Lei Du (State Key Laboratory of Microbial Technology)

Abstract

ABSTRACT Efficient gas transport and abundant triple‐phase boundaries (TPBs) are vital for thick cathode catalyst layers (CCLs) in proton exchange membrane fuel cells (PEMFCs), yet remain challenging to realize. In this work, we introduce a carbon‐based nanotrap architecture functionalized with pyrrolic‐N groups, which reorganizes the Pt–carbon–ionomer interface to enhance local oxygen supply. These nanotraps simultaneously confine Pt nanoparticles and ionomer, forming continuous pathways for oxygen, protons, and electrons, thereby significantly increasing active TPB density. The underlying enhancement mechanism is validated by x‐ray tomography and 3D two‐phase flow simulations. Using a 15.5 µm‐thick CCL, the optimized electrode achieves peak power densities of 1940 mW cm −2 in H 2 /O 2 and 1410 mW cm −2 in H 2 /Air—improvements of ∼30% and ∼80%, respectively. Moreover, it exhibits a good stability, with a voltage decay rate of only 43.8 µV h −1 at 1.5 A cm −2 over 1000 h. This nanotrap concept offers a versatile interfacial design strategy for advanced gas‐diffusion electrodes in energy conversion technologies.

Article Details

Volume / Issue Vol. 38, Issue 40
Published July 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

Z

Zhiyin Huang

Huangpu Hydrogen Energy Innovation Centre School of Chemistry and Chemical Engineering Guangzhou University Guangzhou Guangdong China

Y

Yuqin Peng

Z

Zhiguo Qu

Key Laboratory of Thermo‐Fluid Engineering and Science of MOE School of Energy and Power Engineering Xi'an Jiaotong University Xi'an Shaanxi China

L

Lixin Xing

Huangpu Hydrogen Energy Innovation Centre School of Chemistry and Chemical Engineering Guangzhou University Guangzhou Guangdong China

R

Ruyi Zhong

Huangpu Hydrogen Energy Innovation Centre School of Chemistry and Chemical Engineering Guangzhou University Guangzhou Guangdong China

Z

Zenan Wu

Huangpu Hydrogen Energy Innovation Centre School of Chemistry and Chemical Engineering Guangzhou University Guangzhou Guangdong China

S

Siyu Ye

Department of Cell Biology and Center for Cell Dynamics, School of Medicine, Johns Hopkins University

Y

Yutong Mu

School of Human Settlements and Civil Engineering Xi'an Jiaotong University Xi'an Shaanxi China

L

Liguang Wang

College of Chemical and Biological Engineering

L

Lei Du

State Key Laboratory of Microbial Technology