TY - JOUR
T1 - Local alkalinity enables high-performance pure water anion exchange membrane electrolysis
AU - Guo, Jiaxin
AU - Wang, Ruguang
AU - Yang, Yuting
AU - Zhang, Qinhao
AU - Cao, Fahe
AU - Zhao, Jiong
AU - Pan, Caofeng
AU - Ling, Tao
N1 - Publisher Copyright:
© The Author(s) 2026.
PY - 2026/12
Y1 - 2026/12
N2 - Anion exchange membrane water electrolyser is a highly promising electrolyser technology, but its performance in pure water is severely limited by the unsatisfactory OH− conductivity of the membrane. To overcome this critical challenge, we develop a local alkalinity engineering strategy that employs TiO2 nanoparticles in catalyst layers. These nanoparticles enrich OH− in the electric double layer at both electrodes, creating self-sustaining alkaline microenvironments (pH ~ 14), as confirmed by a scanning electrochemical microscopy technique integrating pH microelectrodes. As a result, the engineered electrolyser achieves a high current density of 3.0 A cm−2 at 2.08 V, approaching that of the precious-metal-based proton exchange membrane water electrolyser under identical conditions. In addition, the local alkalinity alleviates the degradation of non-noble metal catalysts and membrane, thus enabling the electrolyser to realise long-term stability of ~ 1400 h at 1.0 A cm−2. We also demonstrate that this local alkalinity strategy can be readily extended to different types of membranes and scaled up, providing a universal tactic to boost the performance of anion exchange membrane water electrolysers.
AB - Anion exchange membrane water electrolyser is a highly promising electrolyser technology, but its performance in pure water is severely limited by the unsatisfactory OH− conductivity of the membrane. To overcome this critical challenge, we develop a local alkalinity engineering strategy that employs TiO2 nanoparticles in catalyst layers. These nanoparticles enrich OH− in the electric double layer at both electrodes, creating self-sustaining alkaline microenvironments (pH ~ 14), as confirmed by a scanning electrochemical microscopy technique integrating pH microelectrodes. As a result, the engineered electrolyser achieves a high current density of 3.0 A cm−2 at 2.08 V, approaching that of the precious-metal-based proton exchange membrane water electrolyser under identical conditions. In addition, the local alkalinity alleviates the degradation of non-noble metal catalysts and membrane, thus enabling the electrolyser to realise long-term stability of ~ 1400 h at 1.0 A cm−2. We also demonstrate that this local alkalinity strategy can be readily extended to different types of membranes and scaled up, providing a universal tactic to boost the performance of anion exchange membrane water electrolysers.
UR - https://www.scopus.com/pages/publications/105033342873
U2 - 10.1038/s41467-026-69053-4
DO - 10.1038/s41467-026-69053-4
M3 - 文章
C2 - 41634033
AN - SCOPUS:105033342873
SN - 2041-1723
VL - 17
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 2335
ER -