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具有明确原子排列的合理设计的异金属金属二硫纶配位纳米片。

Rationally Engineered Heterometallic Metalladithiolene Coordination Nanosheets with Defined Atomic Arrangements.

作者信息

Ito Miyu, Fukui Naoya, Takada Kenji, Yu Ziheng, Maeda Hiroaki, Mizuno Katsuya, Nishihara Hiroshi

机构信息

Graduate School of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba, 278-8510, Japan.

Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba, 278-8510, Japan.

出版信息

Small. 2025 Sep;21(38):e2503227. doi: 10.1002/smll.202503227. Epub 2025 May 5.

DOI:10.1002/smll.202503227
PMID:40321071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12462590/
Abstract

Coordination nanosheets are 2D polymers formed by coordination bonds between metal ions and planar organic molecules. They offer high molecular design freedom and unique electronic and chemical properties, making them suitable for various usage. In the two-phase interfacial reaction of metal ions with benzenehexathiol (BHT), highly conductive coordination nanosheets are generated. For nickel ions, porous NiDT (=NiBHT) and nonporous NiBHT (=NiBHT) structures are obtained. However, a rational selective synthesis method for these structures is not well-developed. In this study, selective synthesis of NiDT and NiBHT colloidal solutions is achieved by adjusting the BHT to metal ion ratio in a single phase. These colloidal solutions serve as hydrogen evolution catalysts by coating them on an electrode and NiDT is the better catalyst than NiBHT. CuBHT and ZnBHT colloidal solutions are also successfully prepared. Furthermore, nonporous NiCuBHT and a new material, NiZnBHT are synthesized by filling the NiDT pores with another metal and BHT. These approaches lead to the production of coordination nanosheet inks and the synthesis of heterometallic coordination nanosheets with controlled molecular structures. The introduction of the second metal significantly changes the electrical conductivity. Furthermore, a method is discovered to convert NiBHT to NiCuBHT using a transmetallation reaction.

摘要

配位纳米片是由金属离子与平面有机分子之间的配位键形成的二维聚合物。它们具有高度的分子设计自由度以及独特的电子和化学性质,使其适用于各种用途。在金属离子与苯六硫醇(BHT)的两相界面反应中,会生成高导电性的配位纳米片。对于镍离子,可获得多孔的NiDT(=NiBHT)和无孔的NiBHT(=NiBHT)结构。然而,针对这些结构的合理选择性合成方法尚未得到充分发展。在本研究中,通过在单相中调节BHT与金属离子的比例,实现了NiDT和NiBHT胶体溶液的选择性合成。将这些胶体溶液涂覆在电极上可作为析氢催化剂,并且NiDT是比NiBHT更好的催化剂。还成功制备了CuBHT和ZnBHT胶体溶液。此外,通过用另一种金属和BHT填充NiDT的孔隙,合成了无孔的NiCuBHT和一种新材料NiZnBHT。这些方法导致了配位纳米片油墨的产生以及具有可控分子结构的异金属配位纳米片的合成。第二种金属的引入显著改变了电导率。此外,还发现了一种使用金属转移反应将NiBHT转化为NiCuBHT的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/1b226005e89d/SMLL-21-2503227-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/831294546ce1/SMLL-21-2503227-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/59e85b427494/SMLL-21-2503227-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/c4c9fba51f73/SMLL-21-2503227-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/1b226005e89d/SMLL-21-2503227-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/831294546ce1/SMLL-21-2503227-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/59e85b427494/SMLL-21-2503227-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/c4c9fba51f73/SMLL-21-2503227-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b113/12462590/1b226005e89d/SMLL-21-2503227-g004.jpg

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