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源自金属有机框架的中空Ni/NiO/C复合材料作为析氢反应的高效电催化剂。

Hollow Ni/NiO/C composite derived from metal-organic frameworks as a high-efficiency electrocatalyst for the hydrogen evolution reaction.

作者信息

Do Ha Huu, Tekalgne Mahider Asmare, Le Quyet Van, Cho Jin Hyuk, Ahn Sang Hyun, Kim Soo Young

机构信息

School of Chemical Engineering and Materials Science, Chung-Ang University, 84 Heukseok-Ro, Dongjak-Gu, Seoul, 06974, Republic of Korea.

Department of Materials Science and Engineering, Institute of Green Manufacturing Technology, Korea University, 145 Anam-Ro, Seongbuk-Gu, Seoul, 02841, Republic of Korea.

出版信息

Nano Converg. 2023 Feb 2;10(1):6. doi: 10.1186/s40580-023-00354-w.

Abstract

Metal-organic frameworks (MOFs) constitute a class of crystalline porous materials employed in storage and energy conversion applications. MOFs possess characteristics that render them ideal in the preparation of electrocatalysts, and exhibit excellent performance for the hydrogen evolution reaction (HER). Herein, H-Ni/NiO/C catalysts were synthesized from a Ni-based MOF hollow structure via a two-step process involving carbonization and oxidation. Interestingly, the performance of the H-Ni/NiO/C catalyst was superior to those of H-Ni/C, H-NiO/C, and NH-Ni/NiO/C catalysts for the HER. Notably, H-Ni/NiO/C exhibited the best electrocatalytic activity for the HER, with a low overpotential of 87 mV for 10 mA cm and a Tafel slope of 91.7 mV dec. The high performance is ascribed to the synergistic effect of the metal/metal oxide and hollow architecture, which is favorable for breaking the H-OH bond, forming hydrogen atoms, and enabling charge transport. These results indicate that the employed approach is promising for fabricating cost-effective catalysts for hydrogen production in alkaline media.

摘要

金属有机框架材料(MOFs)是一类用于存储和能量转换应用的晶体多孔材料。MOFs具有的特性使其在制备电催化剂方面非常理想,并且在析氢反应(HER)中表现出优异的性能。在此,通过碳化和氧化两步法从镍基金属有机框架空心结构合成了H-Ni/NiO/C催化剂。有趣的是,对于析氢反应,H-Ni/NiO/C催化剂的性能优于H-Ni/C、H-NiO/C和NH-Ni/NiO/C催化剂。值得注意的是,H-Ni/NiO/C对析氢反应表现出最佳的电催化活性,在10 mA cm时过电位低至87 mV,塔菲尔斜率为91.7 mV dec。高性能归因于金属/金属氧化物与空心结构的协同效应,这有利于打破H-OH键、形成氢原子并实现电荷传输。这些结果表明,所采用的方法对于在碱性介质中制备具有成本效益的制氢催化剂具有广阔前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86e0/9895561/bc8696979f35/40580_2023_354_Fig1_HTML.jpg

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