TY - JOUR
T1 - Anode-pressurized water electrolysis with modulated anion exchange membrane architecture
AU - Zhang, Weizhe
AU - Wang, Tao
AU - Zhuo, Yuhang
AU - Li, Shuang
AU - Shi, Jixin
AU - Wei, Haibing
AU - Lin, Weiran
AU - Shi, Yixiang
AU - Wan, Xinhua
AU - Cai, Ningsheng
AU - Wang, Bo
N1 - Publisher Copyright:
© The Author(s) 2026.
PY - 2026/12
Y1 - 2026/12
N2 - Anion exchange membrane water electrolyzers present a promising approach to cost-effective green H2 generation, whereas integration of alkaline media and dry-cathode conditions intrinsically forbids adequate H2O/OH- conduction for efficient operation at high current densities. Herein, we develop a quinuclidinium-functionalized membrane possessing a modulated nano-porous architecture, and exploit its synergy with regulated configuration featuring an anode-to-cathode pressure gradient. By facilitating H2O permeation across interconnected hydrophilic nano-channels, a performance of 11.2 A·cm−2 at 2 V and 90 °C is realized using a NiFe anode, while sufficient membrane robustness and durability enable 2000 h operation at 1 A·cm−2 with suppressed decay of <1 μV·h−1. The narrowed (1-2 nm) gas avenues coordinate with applied pressure gradient to mitigate H2 crossover, improving adaptability to various static-dynamic scenarios. An encouraging levelized cost of H2 of 1.8 $·kg−1 unveils the promise for up-scaled deployment, and this proposed membrane-condition collaboration advances to innovate next-generation energy technologies.
AB - Anion exchange membrane water electrolyzers present a promising approach to cost-effective green H2 generation, whereas integration of alkaline media and dry-cathode conditions intrinsically forbids adequate H2O/OH- conduction for efficient operation at high current densities. Herein, we develop a quinuclidinium-functionalized membrane possessing a modulated nano-porous architecture, and exploit its synergy with regulated configuration featuring an anode-to-cathode pressure gradient. By facilitating H2O permeation across interconnected hydrophilic nano-channels, a performance of 11.2 A·cm−2 at 2 V and 90 °C is realized using a NiFe anode, while sufficient membrane robustness and durability enable 2000 h operation at 1 A·cm−2 with suppressed decay of <1 μV·h−1. The narrowed (1-2 nm) gas avenues coordinate with applied pressure gradient to mitigate H2 crossover, improving adaptability to various static-dynamic scenarios. An encouraging levelized cost of H2 of 1.8 $·kg−1 unveils the promise for up-scaled deployment, and this proposed membrane-condition collaboration advances to innovate next-generation energy technologies.
UR - https://www.scopus.com/pages/publications/105044985251
U2 - 10.1038/s41467-026-72950-3
DO - 10.1038/s41467-026-72950-3
M3 - Article
C2 - 42135292
AN - SCOPUS:105044985251
SN - 2041-1723
VL - 17
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 6433
ER -