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用于提高燃料电池氧化稳定性和氧还原反应的聚[2,2'-(4,4'-联吡啶)-5,5'-联苯并咪唑]功能化炭黑

Poly[2,2'-(4,4'-bipyridine)-5,5'-bibenzimidazole] functionalization of carbon black for improving the oxidation stability and oxygen reduction reaction of fuel cells.

作者信息

Berber Mohamed R, Mustafa Mohamad Y

机构信息

Chemistry Department, College of Science, Jouf University Sakaka 2014 Saudi Arabia

Chemistry Department, Faculty of Science, Tanta University Tanta 31527 Egypt

出版信息

RSC Adv. 2020 Aug 20;10(51):30776-30784. doi: 10.1039/d0ra04289g. eCollection 2020 Aug 17.

Abstract

The rapid oxidation of carbon black (CB) is a major drawback for its use as a catalyst support in polymer electrolyte fuel cells. Here, we synthesize poly[2,2'-(4,4'-bipyridine)-5,5'-bibenzimidazole] (BiPyPBI) as a conducting polymer and use it to functionalize the surface of CB and homogenously anchor platinum metal nanoparticles (Pt-NPs) on a CB surface. The as-prepared materials were confirmed by different spectroscopic techniques, including nuclear magnetic resonance spectroscopy, energy-dispersive X-ray, thermal gravimetric analysis, and scanning-transmittance microscopy. The as-fabricated polymer-based CB catalyst showed an electrochemical surface area (ECSA) of 63.1 cm mg , giving a catalyst utilization efficiency of 74.3%. Notably, the BiPyPBI-based CB catalyst exhibited remarkable catalytic activity towards oxygen reduction reactions. The onset potential and the diffusion-limiting current density reached 0.66 V and 5.35 mA cm, respectively. Furthermore, oxidation stability testing showed a loss of only 16% of Pt-ECSA for BiPyPBI-based CB compared to a 36% loss of Pt-ECSA for commercial Pt/CB after 5000 potential cycles. These improvements were related to the synergetic effect between the nitrogen-rich BiPyPBI polymer, which promoted the catalytic activity through the structural nitrogen atoms, and demolished the degradation of CB the wrapping process.

摘要

炭黑(CB)的快速氧化是其在聚合物电解质燃料电池中用作催化剂载体的一个主要缺点。在此,我们合成了聚[2,2'-(4,4'-联吡啶)-5,5'-联苯并咪唑](BiPyPBI)作为导电聚合物,并将其用于功能化CB表面,使铂金属纳米颗粒(Pt-NPs)均匀地锚定在CB表面。通过不同的光谱技术对所制备的材料进行了确认,包括核磁共振光谱、能量色散X射线、热重分析和扫描透射显微镜。所制备的基于聚合物的CB催化剂的电化学表面积(ECSA)为63.1 cm² mg⁻¹,催化剂利用效率为74.3%。值得注意的是,基于BiPyPBI的CB催化剂对氧还原反应表现出显著的催化活性。起始电位和扩散极限电流密度分别达到0.66 V和5.35 mA cm⁻²。此外,氧化稳定性测试表明,经过5000次电位循环后,基于BiPyPBI的CB的Pt-ECSA仅损失16%,而商业Pt/CB的Pt-ECSA损失36%。这些改进与富氮BiPyPBI聚合物之间的协同效应有关,该聚合物通过结构氮原子促进催化活性,并在包裹过程中抑制了CB的降解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc93/9056374/7891b3151e2a/d0ra04289g-f1.jpg

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