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通过L1 -Pt M金属间化合物核实现Pt壳层的定制晶格压缩应变以实现高效氧还原

Tailored Lattice Compressive Strain of Pt-Skins by the L1 -Pt M Intermetallic Core for Highly Efficient Oxygen Reduction.

作者信息

Wang Zichen, Chen Suhao, Wu Wei, Chen Runzhe, Zhu Yu, Jiang Haoran, Yu Liyue, Cheng Niancai

机构信息

College of Materials Science and Engineering, Fuzhou University, Fuzhou, 350108, P. R. China.

Key Laboratory of Fuel Cell Technology of Guangdong Province, Guangzhou, 510641, P. R. China.

出版信息

Adv Mater. 2023 Sep;35(36):e2301310. doi: 10.1002/adma.202301310. Epub 2023 Jul 20.

DOI:10.1002/adma.202301310
PMID:37196181
Abstract

The sluggish kinetics of oxygen reduction reaction (ORR) and unsatisfactory durability of Pt-based catalysts are severely hindering the commercialization of proton-exchange-membrane fuel cells (PEMFCs). In this work, the lattice compressive strain of Pt-skins imposed by Pt-based intermetallic cores is tailored for highly effective ORR through the confinement effect of the activated nitrogen-doped porous carbon (a-NPC). The modulated pores of a-NPC not only promote Pt-based intermetallics with ultrasmall size (average size of <4 nm), but also efficiently stabilizes intermetallic nanoparticles and sufficient exposure of active sites during the ORR process. The optimized catalyst (L1 -Pt Co@ML-Pt/NPC ) achieves excellent mass activity (1.72 A mg ) and specific activity (3.49 mA cm ), which are 11- and 15-fold that of commercial Pt/C, respectively. Besides, owing to the confinement effect of a-NPC and protection of Pt-skins, L1 -Pt Co@ML-Pt/NPC retains 98.1% mass activity after 30 000 cycles, and even 95% for 100 000 cycles, while Pt/C retains only 51.2% for 30 000 cycles. Rationalized by density functional theory, compared with other metals (Cr, Mn, Fe, and Zn), L1 -Pt Co closer to the top of "volcano" induces a more suitable compressive strain and electronic structure on Pt-skin, leading to an optimal oxygen adsorption energy and a remarkable ORR performance.

摘要

氧还原反应(ORR)缓慢的动力学以及铂基催化剂不尽人意的耐久性严重阻碍了质子交换膜燃料电池(PEMFC)的商业化。在这项工作中,通过活性氮掺杂多孔碳(a-NPC)的限域效应,对铂基金属间化合物核施加的铂壳晶格压缩应变进行了调整,以实现高效的ORR。a-NPC调制的孔不仅促进了超小尺寸(平均尺寸<4nm)的铂基金属间化合物的形成,而且在ORR过程中有效地稳定了金属间纳米颗粒并充分暴露了活性位点。优化后的催化剂(L1-Pt Co@ML-Pt/NPC)具有出色的质量活性(1.72 A mg)和比活性(3.49 mA cm),分别是商业Pt/C的11倍和15倍。此外,由于a-NPC的限域效应和铂壳的保护,L1-Pt Co@ML-Pt/NPC在30000次循环后保留了98.1%的质量活性,在100000次循环后甚至保留了95%,而Pt/C在30000次循环后仅保留了51.2%。通过密度泛函理论进行合理化分析,与其他金属(Cr、Mn、Fe和Zn)相比,更接近“火山”顶部的L1-Pt Co在铂壳上诱导出更合适的压缩应变和电子结构,从而导致最佳的氧吸附能和卓越的ORR性能。

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