Molybdenum‐Pocket Driven Low‐Platinum Oxygen Reduction Catalysts for 100‐Watt‐Scale Fuel Cell Stacks

Y Yue Cheng (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering) H Haoran Sun (State Key Laboratory of Rare Earth Resource Utilization) Y Yang Shen (Beijing National Laboratory for Condensed Matter Physics, Institute of Physics) C Changhong Zhan (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering) Z Zhongliang Huang (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering) W Wei‐Hsiang Huang (National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan) C Chih‐Wen Pao (National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan) D Dong Su (Beijing National Laboratory for Condensed Matter Physics, Institute of Physics) W Wei Liu X Xiaoqing Huang (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering) N Nanjun Chen (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering)

Abstract

ABSTRACT Developing highly efficient and low‐platinum (Pt) proton exchange membrane fuel cell (PEMFC) stacks is imperative for their commercialization. However, ultralow‐loading Pt catalysts (<0.10 mg cm −2 ) are inherently less active and unstable due to high oxygen resistance, particularly under practical stack operating conditions. Here, we present a molybdenum oxide‐pocket‐driven Pt 2 Co (MoO 3 ‐Pt 2 Co) alloy to tackle the aforementioned challenge, where MoO 3 with abundant oxygen vacancies can act as the pivotal “oxygen storage pocket” to boost the oxygen reduction reaction (ORR) activity and minimize the leaching of Co. Consequently, the MoO 3 ‐Pt 2 Co/C‐based membrane electrode assembly (MEA) enables exceptional peak power densities of 3.20 W cm −2 and 1.73 W cm −2 in H 2 ‐O 2 and H 2 ‐air, respectively, with a low Pt loading of 0.10 mg cm −2 , outperforming cutting‐edge MEAs. Meanwhile, the MoO 3 ‐Pt 2 Co/C‐based MEA can retain a record‐breaking mass activity of 1.68 A mg −1 after 30k‐cycle accelerated stress tests and can be operated stably at 0.65 V beyond 550 h. Most importantly, we develop a MoO 3 ‐Pt 2 Co/C‐based fuel cell stack that delivers an excellent rated power of 123 W in H 2 ‐air, which can project Pt utilization of 0.0975 g Pt kW −1 for a 100‐kW hydrogen fuel cell vehicle, exceeding the US Department of energy (DOE) ultimate target of 0.10 g Pt kW −1 .

Article Details

Volume / Issue Vol. 38, Issue 36
Published June 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (11)

Y

Yue Cheng

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering

H

Haoran Sun

State Key Laboratory of Rare Earth Resource Utilization

Y

Yang Shen

Beijing National Laboratory for Condensed Matter Physics, Institute of Physics

C

Changhong Zhan

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering

Z

Zhongliang Huang

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering

W

Wei‐Hsiang Huang

National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan

C

Chih‐Wen Pao

National Synchrotron Radiation Research Center (NSRRC) Hsinchu 300092 Taiwan

D

Dong Su

Beijing National Laboratory for Condensed Matter Physics, Institute of Physics

W

Wei Liu

X

Xiaoqing Huang

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering

N

Nanjun Chen

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering