Li Min, Liu Feng, Pei Supeng, Zhou Zongshang, Niu Kai, Wu Jianbo, Zhang Yongming
School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules, Center of Hydrogen Science, and Shanghai Key Lab of Electrical Insulation & Thermal Aging, Shanghai Jiao Tong University, Shanghai 200240, China.
School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 201418, China.
Nanomaterials (Basel). 2023 Jan 21;13(3):444. doi: 10.3390/nano13030444.
Platinum-based catalysts are widely used for efficient catalysis of the acidic oxygen reduction reaction (ORR). However, the agglomeration and leaching of metallic Pt nanoparticles limit the catalytic activity and durability of the catalysts and restrict their large-scale commercialization. Therefore, this study aimed to achieve a uniform distribution and strong anchoring of Pt nanoparticles on a carbon support and improve the ORR activity and durability of proton-exchange membrane fuel cells. Herein, we report on the facile one-pot synthesis of a novel ORR catalyst using metal-nitrogen-carbon (M-N-C) bonding, which is formed in situ during the ion exchange and pyrolysis processes. An ion-exchange resin was used as the carbon source containing R-N(CH) groups, which coordinate with PtCl to form nanosized Pt clusters confined within the macroporous framework. After pyrolysis, strong M-N-C bonds were formed, thereby preventing the leaching and aggregation of Pt nanoparticles. The as-synthesized Pt supported on the N-doped hierarchically porous carbon catalyst (Pt/NHPC-800) showed high specific activity (0.3 mA cm) and mass activity (0.165 A mg), which are approximately 2.7 and 1.5 times higher than those of commercial Pt/C, respectively. The electrochemical surface area of Pt/NHPC-800 remained unchanged (~1% loss) after an accelerated durability test of 10,000 cycles. The mass activity loss after ADT of Pt/NHPC-800 was 18%, which is considerably lower than that of commercial Pt/C (43%). Thus, a novel ORR catalyst with highly accessible and homogeneously dispersed Pt-N-C sites, high activity, and durability was successfully prepared via one-pot synthesis. This facile and scalable synthesis strategy for high-efficiency catalysts guides the further synthesis of commercially available ORR catalysts.
铂基催化剂被广泛用于高效催化酸性氧还原反应(ORR)。然而,金属铂纳米颗粒的团聚和浸出限制了催化剂的催化活性和耐久性,并阻碍了它们的大规模商业化。因此,本研究旨在实现铂纳米颗粒在碳载体上的均匀分布和牢固锚定,并提高质子交换膜燃料电池的ORR活性和耐久性。在此,我们报道了一种使用金属-氮-碳(M-N-C)键合的新型ORR催化剂的简便一锅合成方法,该键合在离子交换和热解过程中原位形成。一种离子交换树脂被用作含有R-N(CH)基团的碳源,这些基团与PtCl配位形成限制在大孔框架内的纳米级铂簇。热解后,形成了强M-N-C键,从而防止了铂纳米颗粒的浸出和聚集。负载在氮掺杂分级多孔碳催化剂(Pt/NHPC-800)上的合成铂表现出高比活性(0.3 mA cm)和质量活性(0.165 A mg),分别比商业Pt/C高约2.7倍和1.