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氰基桥联的铜镍配位聚合物纳米片及其热转化为混合铜镍氧化物

Cyano-Bridged Cu-Ni Coordination Polymer Nanoflakes and Their Thermal Conversion to Mixed Cu-Ni Oxides.

作者信息

Azhar Alowasheeir, Young Christine, Kaneti Yusuf Valentino, Yamauchi Yusuke, Badjah Ahmad Yacine, Naushad Mu, Habila Mohamed, Wabaidur Saikh, Alothman Zeid A, Kim Jeonghun

机构信息

Key Laboratory of Eco-Chemical Engineering, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.

International Research Center for Materials Nanoarchitechtonics (WPI-MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.

出版信息

Nanomaterials (Basel). 2018 Nov 23;8(12):968. doi: 10.3390/nano8120968.

DOI:10.3390/nano8120968
PMID:30477166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6315628/
Abstract

Herein, we demonstrate the bottom-up synthesis of 2D cyano-bridged Cu-Ni coordination polymer (CP) nanoflakes through a controlled crystallization process and their conversion to Cu-Ni mixed oxides via a thermal treatment in air. The chelating effect of citrate anions effectively prevents the rapid coordination reaction between Cu and K₂[Ni(CN)₄], resulting in the deceleration of the crystallization process of CPs. Specifically, with addition of trisodium citrate dehydrate, the number of nuclei formed at the early stage of the reaction is decreased. Less nuclei undergo a crystal growth by interacting with [Ni(CN)₄], leading to the formation of larger Cu-Ni CP nanoflakes. Following heat treatment in air, the -CN- groups present within the CP nanoflakes are removed and nanoporous Cu-Ni mixed oxide nanoflakes are generated. When tested as an electrode material for supercapacitors using a three-electrode system, the optimum Cu-Ni mixed oxide sample shows a maximum specific capacitance of 158 F g at a current density of 1 A g. It is expected that the proposed method will be useful for the preparation of other types of 2D and 3D CPs as precursors for the creation of various nanoporous metal oxides.

摘要

在此,我们展示了通过可控结晶过程自下而上合成二维氰基桥联铜镍配位聚合物(CP)纳米片,并通过在空气中进行热处理将其转化为铜镍混合氧化物。柠檬酸根阴离子的螯合作用有效地阻止了铜与K₂[Ni(CN)₄]之间的快速配位反应,从而导致配位聚合物结晶过程的减速。具体而言,加入柠檬酸三钠二水合物后,反应初期形成的核的数量减少。较少的核通过与[Ni(CN)₄]相互作用而经历晶体生长,从而导致形成更大的铜镍配位聚合物纳米片。在空气中进行热处理后,配位聚合物纳米片中存在的 -CN- 基团被去除,并生成了纳米多孔铜镍混合氧化物纳米片。当使用三电极系统作为超级电容器的电极材料进行测试时,最佳的铜镍混合氧化物样品在电流密度为1 A g时显示出最大比电容为158 F g。预计所提出的方法将有助于制备其他类型的二维和三维配位聚合物,作为制备各种纳米多孔金属氧化物的前体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/069c5487bc95/nanomaterials-08-00968-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/85e26348e203/nanomaterials-08-00968-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/e96c8cb7aac1/nanomaterials-08-00968-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/6fdf6bf26d81/nanomaterials-08-00968-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/4fc82175ffab/nanomaterials-08-00968-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/cb748c414071/nanomaterials-08-00968-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/069c5487bc95/nanomaterials-08-00968-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/85e26348e203/nanomaterials-08-00968-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/e96c8cb7aac1/nanomaterials-08-00968-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/6fdf6bf26d81/nanomaterials-08-00968-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/4fc82175ffab/nanomaterials-08-00968-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/cb748c414071/nanomaterials-08-00968-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40c/6315628/069c5487bc95/nanomaterials-08-00968-g006.jpg

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