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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

机译:聚[2,2' - (4,4'-bibyridine)-5,5'-二苯并咪唑]炭黑的官能化,用于提高燃料电池的氧化稳定性和氧还原反应

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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 ~(2) mg _(Pt) ~(?1) , 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 ~(?2) , 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 via the wrapping process.
机译:炭黑(CB)的快速氧化是其用作聚合物电解质燃料电池中的催化剂载体的主要缺点。在此,我们将聚[2,2'-(4,4'-bibyridine)-5,5,5,5'-苄硫代咪唑](BiPyPbi)合成为导电聚合物,并使用它使Cb的表面和均匀的锚定铂金属纳米颗粒( pt-nps)在Cb表面上。通过不同的光谱技术证实了AS制备的材料,包括核磁共振光谱,能量分散X射线,热重分析和扫描透射率显微镜。制造的基于聚合物的CB催化剂显示电化学表面积(ECSA)为63.1cm〜(2)mg _(Pt)〜(α1),催化剂利用效率为74.3%。值得注意的是,基于BiPBI的CB催化剂表现出显着的催化活性朝向氧还原反应。发作电位和扩散限流电流密度分别达到0.66V和5.35mA cm〜(Δ2)。此外,氧化稳定性测试表明,在5000个潜在循环之后的商业Pt / Cb的Pt-Ecsa的36%损失,仅为BiPBI的CB的损失仅为Pt-ECSA的损失。这些改进与富含氮的培养基聚合物之间的协同作用有关,其通过结构氮原子促进催化活性,并通过包装过程拆除CB的降解。

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