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一种加速电化学析氢的多孔质子中继金属有机骨架材料。

A porous proton-relaying metal-organic framework material that accelerates electrochemical hydrogen evolution.

作者信息

Hod Idan, Deria Pravas, Bury Wojciech, Mondloch Joseph E, Kung Chung-Wei, So Monica, Sampson Matthew D, Peters Aaron W, Kubiak Cliff P, Farha Omar K, Hupp Joseph T

机构信息

Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, USA.

Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University, Evanston, Illinois 60208, USA.

出版信息

Nat Commun. 2015 Sep 14;6:8304. doi: 10.1038/ncomms9304.

Abstract

The availability of efficient hydrogen evolution reaction (HER) catalysts is of high importance for solar fuel technologies aimed at reducing future carbon emissions. Even though Pt electrodes are excellent HER electrocatalysts, commercialization of large-scale hydrogen production technology requires finding an equally efficient, low-cost, earth-abundant alternative. Here, high porosity, metal-organic framework (MOF) films have been used as scaffolds for the deposition of a Ni-S electrocatalyst. Compared with an MOF-free Ni-S, the resulting hybrid materials exhibit significantly enhanced performance for HER from aqueous acid, decreasing the kinetic overpotential by more than 200 mV at a benchmark current density of 10 mA cm(-2). Although the initial aim was to improve electrocatalytic activity by greatly boosting the active area of the Ni-S catalyst, the performance enhancements instead were found to arise primarily from the ability of the proton-conductive MOF to favourably modify the immediate chemical environment of the sulfide-based catalyst.

摘要

高效析氢反应(HER)催化剂的可用性对于旨在减少未来碳排放的太阳能燃料技术至关重要。尽管铂电极是出色的HER电催化剂,但大规模制氢技术的商业化需要找到一种同样高效、低成本且储量丰富的替代物。在此,高孔隙率金属有机框架(MOF)薄膜已被用作沉积Ni-S电催化剂的支架。与无MOF的Ni-S相比,所得的杂化材料在酸性水溶液中析氢性能显著增强,在10 mA cm(-2)的基准电流密度下,动力学过电位降低了200多毫伏。尽管最初的目标是通过大幅增加Ni-S催化剂的活性面积来提高电催化活性,但结果发现性能增强主要源于质子传导性MOF能够有利地改变硫化物基催化剂的直接化学环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04fb/4647847/5023e90c674a/ncomms9304-f1.jpg

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