TY - JOUR
T1 - Open framework–based Brønsted acid–Lewis base interfaces boost proton transfer in the fuel cells
AU - Ma, Qianli
AU - Yang, Jiarui
AU - Li, Jie
AU - Zhao, Zihan
AU - Yue, Feiyu
AU - Yang, Jianwei
AU - Zhao, Shuang
AU - Sheng, Wenhan
AU - Wang, Tang
AU - Zhao, Shangnan
AU - Zhou, Junwen
AU - Xu, Wenli
AU - Lu, Yanli
AU - Wu, Ke
AU - Han, Xianghao
AU - Jia, Xilin
AU - Yang, Wenxiu
AU - Wang, Qianyou
AU - Li, Yujing
AU - Zhao, Zipeng
AU - Han, Yu
AU - Sun, Shucheng
AU - Zhang, Teng
AU - Feng, Xiao
AU - Wang, Bo
N1 - Publisher Copyright:
© 2026 American Association for the Advancement of Science. All rights reserved.
PY - 2026/9/10
Y1 - 2026/9/10
N2 - Limited proton conductivity within the catalyst layer induces severe ohmic polarizations and constrains power output at high hydrogen-to-electricity efficiencies in proton exchange membrane fuel cells. We demonstrate that proton transfer can be boosted by constructing brønsted acid–Lewis base interfaces through integrating organic open frameworks with Nafion. these confined interfaces mediate low-barrier relay pathways, disrupt hydrogen bonding to expedite water network reorganization, facilitate consecutive proton transfer, and enrich protons locally. Compared with Nafion, the complexes exhibit an order-of-magnitude increase in proton self-diffusion coefficient, a 6.5-fold rise in proton conductivity, and a 55% reduction in activation energy. When integrated with commercial platinum on carbon, they deliver a fourfold increase in rated power output relative to the baseline, outperforming representative state-of-the-art membrane electrode assemblies with advanced catalysts under similar conditions.
AB - Limited proton conductivity within the catalyst layer induces severe ohmic polarizations and constrains power output at high hydrogen-to-electricity efficiencies in proton exchange membrane fuel cells. We demonstrate that proton transfer can be boosted by constructing brønsted acid–Lewis base interfaces through integrating organic open frameworks with Nafion. these confined interfaces mediate low-barrier relay pathways, disrupt hydrogen bonding to expedite water network reorganization, facilitate consecutive proton transfer, and enrich protons locally. Compared with Nafion, the complexes exhibit an order-of-magnitude increase in proton self-diffusion coefficient, a 6.5-fold rise in proton conductivity, and a 55% reduction in activation energy. When integrated with commercial platinum on carbon, they deliver a fourfold increase in rated power output relative to the baseline, outperforming representative state-of-the-art membrane electrode assemblies with advanced catalysts under similar conditions.
UR - https://www.scopus.com/pages/publications/105050207284
U2 - 10.1126/science.adp3564
DO - 10.1126/science.adp3564
M3 - Article
C2 - 42721239
AN - SCOPUS:105050207284
SN - 0036-8075
VL - 393
JO - Science
JF - Science
IS - 6816
M1 - eadp3564
ER -