Delai Wang , Guoyu Lin , Hai-Qun Xu , Zihao Zhai , Chang Mei , Xiang Chen , Guangshun Wu , Zheng Cao , Zhen Jin , Shilong Xu , Di Wang , Lei Wang , Weiwei Dong , Xiaoran Niu , Yi Ding
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引用次数: 0
Abstract
Proton exchange membrane fuel cells (PEMFCs) are promising for mobile and renewable energy storage due to their high efficiency and zero-carbon emissions. However, the slow kinetics of the oxygen reduction reaction (ORR) at the cathode remains a significant challenge. In this work, we successfully synthesized an L10-PtZn intermetallic compound (IMC) with a core–shell structure using a thiourea molecule-assisted strategy based on strong metal–support interactions with Pt–S bonding. The as-prepared PtZn-IMC catalyst exhibited significantly enhanced oxygen reduction reaction (ORR) performance, achieving a mass activity (MA) of 1.50 A mgPt−1, approximately six-fold higher than that achieved by commercial Pt/C nanoparticles. Moreover, the catalyst demonstrated remarkable stability, retaining 93% of MA in rotating disk electrode (RDE) tests and showing only a 7.9% peak power density loss in membrane electrode assembly (MEA) measurements. Density functional theory (DFT) calculations reveal that the ordered PtZn structure lowered the Pt d-band center, improving the ORR kinetics and structural stability. This work demonstrates the potential of core–shell structure PtZn-IMC as an efficient and stable catalyst for PEMFC applications.
质子交换膜燃料电池(pemfc)由于其高效率和零碳排放,在移动和可再生能源存储方面前景广阔。然而,阴极氧还原反应(ORR)的缓慢动力学仍然是一个重大的挑战。在这项工作中,我们利用硫脲分子辅助策略,基于与Pt-S键的强金属支持相互作用,成功合成了具有核壳结构的L10-PtZn金属间化合物(IMC)。制备的PtZn-IMC催化剂表现出显著增强的氧还原反应(ORR)性能,达到1.50 a mgPt−1的质量活性(MA),比商用Pt/C纳米颗粒高约6倍。此外,该催化剂表现出了显著的稳定性,在旋转圆盘电极(RDE)测试中保留了93%的MA,在膜电极组装(MEA)测试中仅显示出7.9%的峰值功率密度损失。密度泛函理论(DFT)计算表明,有序的PtZn结构降低了Pt d带中心,提高了ORR动力学和结构稳定性。这项工作证明了核壳结构PtZn-IMC作为一种高效稳定的PEMFC催化剂的潜力。
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A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis.
Editor-in-chief: Bert Weckhuysen
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