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氮掺杂碳纳米管壳包裹的镍铁金属核通过结构协同作用提高甲醇氧化反应中的催化稳定性。

N-Doped Carbon Nanotube Shell Encapsulating the NiFe Metal Core for Enhanced Catalytic Stability in Methanol Oxidation Reaction by the Structural Cooperation Mechanism.

机构信息

College of Chemistry & Chemical Engineering, Chongqing University, Chongqing400044, P. R. China.

出版信息

Langmuir. 2022 Dec 13;38(49):15198-15208. doi: 10.1021/acs.langmuir.2c02289. Epub 2022 Dec 2.

DOI:10.1021/acs.langmuir.2c02289
PMID:36459487
Abstract

Exploitation of high-efficiency catalysts toward methanol oxidation is a pivotal step to promote the commercialization of direct methanol fuel cells. Herein, a strategy is demonstrated to prepare nitrogen-doped carbon nanotubes with NiFe metal particles (NiFe@N-CNT) as the carrier material of Pt nanoparticles. Combining SEM and TEM, NiFe metal particles are fully encapsulated in N-CNTs, and they form the metal core and carbon nanotube shell structure based on the structural cooperation mechanism. Surprisingly, the as-prepared Pt/NiFe@N-CNT catalyst shows superior catalytic activity (1023 mA mg) compared to commercial Pt/C (392 mA mg), Pt/Ni@N-CNT (331 mA mg), and Pt/Fe@N-CNT (592 mA mg). After 1000 cycles, Pt/NiFe@N-CNT maintains the optimal catalytic activity (588 mA mg), and its mass activity loss is 42.5%, which is better than those of commercial Pt/C (64.0%), Pt/Ni@N-CNT (67.7%), and Pt/Fe@N-CNT (59.6%) catalysts, indicating that the Pt/NiFe@N-CNT catalyst achieves excellent catalytic activity and stability, which stems chiefly from the homodispersed Pt nanoparticles and the generation of the metal core-carbon nanotube shell based on the structural cooperation mechanism. This study reports the facile construction of a metal core-carbon nanotube shell structure, which intrinsically ameliorates structural collapse of carrier material, thereby improving the catalytic stability of the Pt-based catalyst and broadening the view for design of other desire catalysts in methanol oxidation.

摘要

开发高效催化剂用于甲醇氧化是推动直接甲醇燃料电池商业化的关键步骤。本文展示了一种策略,即用氮掺杂碳纳米管作为担载 Pt 纳米粒子的载体材料来制备 NiFe 金属粒子(NiFe@N-CNT)。通过 SEM 和 TEM 结合观察,NiFe 金属粒子完全被包裹在 N-CNTs 中,它们基于结构协同机制形成了金属核和碳纳米管壳结构。令人惊讶的是,所制备的 Pt/NiFe@N-CNT 催化剂表现出比商业 Pt/C(392 mA mg)、Pt/Ni@N-CNT(331 mA mg)和 Pt/Fe@N-CNT(592 mA mg)更高的催化活性(1023 mA mg)。经过 1000 次循环后,Pt/NiFe@N-CNT 保持了最佳的催化活性(588 mA mg),其质量活性损失为 42.5%,优于商业 Pt/C(64.0%)、Pt/Ni@N-CNT(67.7%)和 Pt/Fe@N-CNT(59.6%)催化剂,表明 Pt/NiFe@N-CNT 催化剂具有优异的催化活性和稳定性,这主要归因于均匀分散的 Pt 纳米粒子和基于结构协同机制生成的金属核-碳纳米管壳。本研究报告了一种简便构建金属核-碳纳米管壳结构的方法,这种结构从本质上改善了载体材料的结构塌陷,从而提高了 Pt 基催化剂的催化稳定性,并为甲醇氧化中其他理想催化剂的设计拓宽了视野。

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