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退火钴-苯并三氮唑/CNTs 催化剂对氧还原反应的电化学性能。

Electrochemical performance of annealed cobalt-benzotriazole/CNTs catalysts towards the oxygen reduction reaction.

机构信息

CEA-Saclay, DSM/IRAMIS/SPCSI/LCSI, 91191 Gif-sur-Yvette Cedex, France.

出版信息

Phys Chem Chem Phys. 2011 Dec 28;13(48):21600-7. doi: 10.1039/c1cp23199e. Epub 2011 Nov 9.

Abstract

One of the major limitations yet to the global implementation of polymer electrolyte membrane fuel cells (PEMFCs) is the cathode catalyst. The development of efficient platinum-free catalysts is the key issue to solve the problem of slow kinetics of the oxygen reduction reaction (ORR) and high cost. We report a promising catalyst for ORR prepared through the annealing treatment under inert conditions of the cobalt-benzotriazole (Co-BTA) complex supported on carbon nanotubes (CNTs). The N-rich benzotriazole precursor was chosen based on its ability to complex Co(II) ions and generate under annealing highly reactive radicals able to tune the physicochemical properties of CNTs. X-Ray photoelectron spectroscopy (XPS) was used to follow the surface structure changes and highlight the active electrocatalytic sites towards the ORR. To achieve further evaluation of the catalysts in acidic medium, voltamperometry, rotating disk electrode (RDE), rotating ring-disk electrode (RRDE) and half-cell measurements were performed. The resulting catalysts (Co/N/CNTs) all show catalytic activity towards the ORR, the most active one resulting from annealing at 700 °C. The overall electron transfer number for the catalyzed ORR was determined to be ∼3.7 with no change upon the catalyst loading, suggesting that the ORR was dominated by a 4e(-) transfer process. The results indicate a promising alternative cathode catalyst for ORR in fuel cells, although its performance is still lower (overpotential around 110 mV evaluated by RDE and RRDE) than the reference Pt/C catalyst.

摘要

聚合物电解质膜燃料电池(PEMFCs)在全球范围内应用的主要限制之一是阴极催化剂。开发高效的无铂催化剂是解决氧气还原反应(ORR)动力学缓慢和成本高的关键问题。我们报告了一种通过在惰性条件下退火处理负载在碳纳米管(CNTs)上的钴苯并三唑(Co-BTA)配合物制备的 ORR 有希望的催化剂。选择富氮苯并三唑前体是基于其络合 Co(II) 离子的能力,并在退火下生成高反应性自由基,能够调整 CNTs 的物理化学性质。X 射线光电子能谱(XPS)用于跟踪表面结构变化,并突出对 ORR 具有活性电催化作用的位点。为了在酸性介质中进一步评估催化剂,进行了伏安法、旋转圆盘电极(RDE)、旋转环盘电极(RRDE)和半电池测量。所得催化剂(Co/N/CNTs)均对 ORR 表现出催化活性,在 700°C 退火时最具活性。催化 ORR 的总电子转移数约为 3.7,催化剂负载量不变,表明 ORR 主要由 4e(-)转移过程主导。结果表明,对于燃料电池中的 ORR,这是一种很有前途的阴极催化剂替代方案,尽管其性能仍然低于参考 Pt/C 催化剂(通过 RDE 和 RRDE 评估的过电势约为 110 mV)。

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