Clean Energy Research Center, University of Yamanashi, 4 Takeda, Kofu 400-8510, Japan.
Hydrogen Fuel Cell Nanomaterials Center, University of Yamanashi, 6-43 Miyamae, Kofu 400-0021, Japan.
ACS Appl Mater Interfaces. 2023 Mar 15;15(10):13219-13227. doi: 10.1021/acsami.3c01392. Epub 2023 Feb 28.
Polymer electrolyte membranes (PEMs) for fuel cells are chemically degraded by the attack of ·OH radicals generated from the decomposition of HO, which is predominantly produced at the Pt/C hydrogen anode. The incorporation of conventional radical scavengers into the PEM suffers from a decrease in the output performance. We, for the first time, demonstrate that the addition of hygroscopic silica nanoparticles (NPs) to the Pt/C anode catalyst layer provides a remarkably prolonged (ca. 4 times) lifetime of a Nafion membrane in an accelerated stress test and open circuit voltage (OCV) holding at 90 °C, accompanied by improved output () performances at low relative humidity. It has been found that the use of silica NPs decreases HO formation rate from the OCV to a practical H oxidation potential in a half-cell using 0.1 M HClO at 90 °C and provides reduced ohmic resistance (increase in water content) and effective utilization of Pt cathode catalyst in a single cell, by which the improvement of the durability of the PEM and increased output performance are explained rationally.
用于燃料电池的聚合物电解质膜 (PEM) 会受到来自 HO 分解产生的·OH 自由基的化学攻击,HO 主要在 Pt/C 氢阳极产生。将传统的自由基清除剂掺入 PEM 会导致输出性能下降。我们首次证明,将吸湿性二氧化硅纳米颗粒 (NPs) 添加到 Pt/C 阳极催化剂层中,可显著延长 Nafion 膜在加速应力测试和 90°C 开路电压 (OCV) 保持下的使用寿命(约 4 倍),同时在低相对湿度下提高输出 () 性能。已经发现,在使用 0.1 M HClO 在 90°C 的半电池中从 OCV 到实际 H 氧化电势的情况下,使用二氧化硅 NPs 可降低 HO 的形成速率,并在单电池中提供降低的欧姆电阻(增加含水量)和对 Pt 阴极催化剂的有效利用,由此可以合理地解释 PEM 耐久性的提高和输出性能的提高。