Long Tang, Xingyun Liu, Zeyong Zhu, Junjie Luo, Song Zhao, Wenyi Wang
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引用次数: 0
摘要
以氮气条件下原位热解钴-金属有机框架(MOF)(Co-PTA-MOF)前驱体为基础,在不同热解温度下以高N含量的H-1,2,4-三唑-3-胺有机配体为原料,成功制备了Co/Co-Nx嵌入介孔三维花状碳片(Co/Co-N-MC-800)催化剂。缺陷位点较多的介孔 Co/Co-N-MC-800 催化剂的金属活性中心位于带正电的 0 ~ + 2 处,键间距与共卟啉的 Co-N4 平面结构一致。所获得的 Co/Co-N-MC-800 具有优异的氧还原反应性能,其起始电位(0.92 V vs RHE)和半波电位(0.76 V vs RHE)更接近于 Pt/C,并且具有出色的长期稳定性,89 h 后的电流保持率为 89.1%,在空气呼吸阴极微生物燃料电池(MFC)中的可选功率密度为 1079.3 ± 22.5mW-m-2。催化性能的提高可能归功于特殊的三维纳米结构、嵌入式钴纳米颗粒(形成 Co-Nx)和掺杂 N 的介孔碳片材料的结合。本研究为利用非贵金属和含 N 有机配体制备的 MOF 阴极改性实现 ORR 提供了技术和理论依据。
Metal Organic Framework–Derived Co and Co-Nx Embedded Mesoporous Carbon Sheets as an Efficient Electrocatalyst Toward the Oxygen Reduction Reaction for Air-Breath Cathode Microbial Fuel Cells
The Co/Co-Nx-embedded mesoporous 3D flower-like carbon sheet (Co/Co-N-MC-800) catalyst is successfully prepared from high N content H-1,2,4-Triazol-3-amine organic-ligand at different pyrolysis temperatures based on in situ pyrolysis Co-metal organic frame (MOF) (Co-PTA-MOF) precursor under nitrogen. The metal active center of the mesoporous Co/Co-N-MC-800 catalyst with more defect sites is situated in the positively charged 0 ~ + 2, and the bond spacing is consistent with the Co-N4 plane structure of the co-porphyrin. The obtained Co/Co-N-MC-800 possesses an excellent oxygen reduction reaction performance with a higher onset potential (0.92 V vs RHE) and half-wave potential (0.76 V vs RHE), which is closer to Pt/C and outstanding long-term stability with 89.1% current retention after 89 h and displays an optional power density of 1079.3 ± 22.5mW·m−2 in air-breath cathode microbial fuel cell (MFC). The improved catalytic performance maybe attributes to combination of the special 3D nanostructure, embedded cobalt nanoparticles (forming Co-Nx) and N-doped mesoporous carbon sheet material. The present study provides the technical and theoretical basis for the ORR through the cathode modification of MOF prepared from non-precious metal and N content organic-ligand.
期刊介绍:
Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis.
The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.