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涉及用于催化氨合成的旋转结构转变的Ca CrN H的拓扑化学合成。

Topochemical Synthesis of Ca CrN H Involving a Rotational Structural Transformation for Catalytic Ammonia Synthesis.

作者信息

Cao Yu, Kirsanova Maria A, Ochi Masayuki, Al Maksoud Walid, Zhu Tong, Rai Rohit, Gao Shenghan, Tsumori Tatsuya, Kobayashi Shintaro, Kawaguchi Shogo, Abou-Hamad Edy, Kuroki Kazuhiko, Tassel Cédric, Abakumov Artem M, Kobayashi Yoji, Kageyama Hiroshi

机构信息

Department of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510, Japan.

Center for Energy Science and Technology, Skolkovo Institute of Science and Technology, Nobel str. 3, 121205, Moscow, Russia.

出版信息

Angew Chem Int Ed Engl. 2022 Sep 26;61(39):e202209187. doi: 10.1002/anie.202209187. Epub 2022 Aug 23.

Abstract

Topochemical reactions have led to great progress in the discovery of new metastable compounds with novel chemical and physical properties. With these reactions, the overall crystal structure of the host material is generally maintained. Here we report a topochemical synthesis of a hexagonal nitride hydride, h-Ca CrN H, by heating an orthorhombic nitride, o-Ca CrN , under hydrogen at 673 K, accompanied by a rotational structural transformation. The hydrogen intercalation modifies the Ca-N rock-salt-like atomic packing in o-Ca CrN to a face-sharing octahedral chain in h-Ca CrN H, mimicking a "hinged tessellation" movement. In addition, the h-Ca CrN H exhibited stable ammonia synthesis activity when used as a catalyst.

摘要

拓扑化学反应在发现具有新颖化学和物理性质的新亚稳化合物方面取得了巨大进展。通过这些反应,主体材料的整体晶体结构通常得以保持。在此,我们报告了一种六方氮氢化物h-CaCrNH的拓扑合成方法,即在673K的氢气氛围下加热正交氮化物o-CaCrN,同时伴随着旋转结构转变。氢嵌入将o-CaCrN中类似岩盐的Ca-N原子堆积转变为h-CaCrNH中的共面八面体链,类似于“铰接镶嵌”运动。此外,h-CaCrNH用作催化剂时表现出稳定的氨合成活性。

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