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电化学(中英文)

• 研究论文 •    

碳纳米管穿插钴基卟啉金属有机框架催化ORR

何佩佩 a,1, 师锦华 a,1, 李笑语 a, 刘明杰 a, 方舟 b, 和晶 a,李中坚 a,彭新生 b, 和庆钢 a,*   

  1. a. 浙江大学化学工程与生物工程学院,杭州 310058;b. 浙江大学材料科学与工程学院,杭州 310058
  • 出版日期:2024-10-16 发布日期:2024-10-16
  • 通讯作者: 和庆钢 E-mail:qghe@zju.edu.cn
  • 作者简介:何佩佩 , 师锦华 , 李笑语 , 刘明杰 , 方舟 , 和晶 ,李中坚 ,彭新生 , 和庆钢

A CNT Intercalated Co Porphyrin-based Metal Organic Framework Catalyst for Oxygen Reduction Reaction

Peipei He a,1, Jinhua Shi a,1, Xiaoyu Li a, Mingjie Liu a, Zhou Fang b, Jing He a, Zhongjian Li a, Xinsheng Peng b, Qinggang He a,*   

  1. Peipei He, Jinhua Shi, Xiaoyu Li, Mingjie Liu, Jing He , Prof. Zhongjian Li, Prof. Qinggang He College of Chemical and Biological Engineering Zhejiang University 866 Yuhangtang Road, Hangzhou 310058, P.R. China b Prof. Zhou Fang, Prof. Xinsheng Peng School of materials science and engineering Zhejiang University 866 Yuhangtang Road, Hangzhou 310058, P.R. China
  • Published:2024-10-16 Online:2024-10-16
  • Contact: Qinggang He E-mail:qghe@zju.edu.cn
  • About author:Peipei He, Jinhua Shi, Xiaoyu Li , Mingjie Liu , Zhou Fang , Jing He , Zhongjian Li , Xinsheng Peng , Qinggang He

摘要: 金属有机框架(MOF)材料作为典型的半导体材料,由于其本征的较差电子导电性,严重限制了其在燃料电池电催化领域的直接应用。为此,本文提出了一种解决策略,即在MOF晶体生长过程中加入碳纳米管(CNTs),最终合成了一种具有独特的CNT穿插在MOF晶体结构中的Co金属卟啉基的催化剂TCPPCo-MOF-CNT。物理表征表明,CNTs的插入不仅增强了催化剂整体的导电性,同时也保留了MOF本身的晶体结构和金属卟啉的原始特性。并且,由于CNTs的插入,在催化剂内部形成了大量促进传质的介孔结构,并产生了可以极大提升反应过程中传质效率的分级多孔结构。XPS揭示了插入的CNT中的碳原子改变了催化活性中心Co上的电子云密度,优化了催化中心的电子结构。因此,在中性条件下,TCPPCo-MOF-CNT催化剂的半波电位达到0.77 V(vs. RHE),明显优于未插入CNT的单纯MOF材料制备的催化剂。最后,将TCPPCo-MOF-CNT作为阴极催化剂和Nafion-117组装成PEM微生物燃料电池(MFCs),MFCs显示其最大功率密度可达到约500 mW m-2。因此,TCPPCo-MOF-CNT可作为一种有效的中性环境下ORR催化剂,同时此策略也为其他半导体材料提升电催化活性提供了一种方法。

关键词: 金属有机框架, 碳纳米管穿插, 电催化, 氧还原反应, 微生物燃料电池

Abstract: The poor electronic conductivity of metal−organic framework (MOF) materials hinders their direct application in the field of electrocatalysis in fuel cells. Herein, we proposed a strategy of embedding carbon nanotubes (CNTs) during the growth process of MOF crystals, synthesizing a metalloporphyrin-based MOF catalyst TCPPCo-MOF-CNT with a unique CNT-intercalated MOF structure. Physical characterization revealed that the CNTs enhance the overall conductivity while retaining the original characteristics of the MOF and metalloporphyrin. Simultaneously, the insertion of CNTs, generating adequate mesopores and creating a hierarchical porous structure that enhances mass transfer efficiency. XPS confirmed that the C atom in CNT changed the electron cloud density on the catalytic active center Co, optimizing the electronic structure. Consequently, the E1/2 of the TCPPCo-MOF-CNT catalyst under neutral conditions reaches 0.77 V (vs. RHE), outperforming the catalyst without CNTs. When TCPPCo-MOF-CNT was employed as the cathode catalyst in assembling Microbial Fuel Cells (MFCs) with Nafion-117 as the PEM, the maximum power density of MFCs reached approximately 500 mW m-2.

Key words: Metal organic framework, CNT intercalated, electrocatalysis, ORR, Microbial Fuel Cells