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一种具有三方相 MoS2 结构的新型氮化钼催化剂,用于加氢应用。

A new molybdenum nitride catalyst with rhombohedral MoS2 structure for hydrogenation applications.

机构信息

∥Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.

‡Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan, Shanxi 030001, China.

出版信息

J Am Chem Soc. 2015 Apr 15;137(14):4815-22. doi: 10.1021/jacs.5b01446. Epub 2015 Apr 1.

Abstract

Nitrogen-rich transition-metal nitrides hold great promise to be the next-generation catalysts for clean and renewable energy applications. However, incorporation of nitrogen into the crystalline lattices of transition metals is thermodynamically unfavorable at atmospheric pressure; most of the known transition metal nitrides are nitrogen-deficient with molar ratios of N:metal less than a unity. In this work, we have formulated a high-pressure route for the synthesis of a nitrogen-rich molybdenum nitride through a solid-state ion-exchange reaction. The newly discovered nitride, 3R-MoN2, adopts a rhombohedral R3m structure, isotypic with MoS2. This new nitride exhibits catalytic activities that are three times more active than the traditional catalyst MoS2 for the hydrodesulfurization of dibenzothiophene and more than twice as high in the selectivity to hydrogenation. The nitride is also catalytically active in sour methanation of syngas with >80% CO and H2 conversion at 723 K. Our formulated route for the synthesis of 3R-MoN2 is at a moderate pressure of 3.5 GPa and, thus, is feasible for industrial-scale catalyst production.

摘要

富氮过渡金属氮化物有望成为下一代清洁能源应用的催化剂。然而,在常压下,氮掺入过渡金属的晶体点阵在热力学上是不利的;大多数已知的过渡金属氮化物都存在氮缺陷,N:金属的摩尔比小于 1。在这项工作中,我们通过固态离子交换反应制定了一种在高压下合成富氮氮化钼的方法。新发现的氮化钼 3R-MoN2 采用三方 R3m 结构,与 MoS2 同晶型。这种新型氮化物在二苯并噻吩加氢脱硫反应中的催化活性比传统催化剂 MoS2 高 3 倍,加氢选择性高 2 倍以上。该氮化物在合成气的酸性甲烷化反应中也具有催化活性,在 723 K 时 CO 和 H2 的转化率超过 80%。我们制定的 3R-MoN2 合成路线的压力适中,为 3.5 GPa,因此适用于工业规模的催化剂生产。

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