Tuning Electron Cloud Density in MOF Nanosheets for Enhanced Proton Conduction in PEMFCs
Dongxu Shen, Yarong Liu, Chongchong Chen, Zhirong Yang, Hao Li, Shang-Hao Xiao, Wenjia Wu, Jingtao Wang
Abstract
Abstract Precise construction of proton transfer pathways and modulation of proton carrier microenvironments are crucial for achieving high proton conduction in proton exchange membranes (PEMs). Despite extensive efforts to tailor these microenvironments, the underlying regulation of electron cloud density around proton carriers, intrinsically linked to proton conduction, remains largely overlooked. Herein, MIL‐53‐SO 3 H‐X (X = –F, –Br, –H, –CH 3 ) nanosheets are synthesized via solvothermal coordination of Cr 3+ ions with functionalized terephthalic acid (BDC‐X) ligands, followed by post‐synthetic sulfonation at unsaturated Cr 3+ sites to anchor –SO 3 H groups. Density functional theory (DFT) calculations and experimental results reveal that electron‐withdrawing –F groups enhance the electron cloud density around –SO 3 H sites, shortening transfer distance, aligning water molecules, and lowering the proton transfer barrier. Conversely, electron‐donating –CH 3 groups deplete the electron cloud density in the –SO 3 H region, disrupting proton transport pathways. The MIL‐53‐SO 3 H‐F nanosheet achieves an intrinsic proton conductivity of 298.3 mS cm −1 at 80 °C and 98% RH, a 4.5‐fold increase over MIL‐53‐SO 3 H‐CH 3 nanosheets (65.5 mS cm −1 ), as measured by the comb electrode. The corresponding lamellar membrane delivers a high peak power density of 734.8 mW cm −2 and remains stable for over 100 h in H 2 /O 2 PEM fuel cells (PEMFCs).