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Ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis

Two-dimensional conjugated metal–organic frameworks (2D c-MOFs) have recently emerged for potential applications in (opto-)electronics, chemiresistive sensing, and energy storage and conversion, due to their excellent electrical conductivity, abundant active sites, and intrinsic porous structures. H...

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Detalles Bibliográficos
Autores principales: Wang, Zhiyong, Wang, Gang, Qi, Haoyuan, Wang, Mao, Wang, Mingchao, Park, SangWook, Wang, Huaping, Yu, Minghao, Kaiser, Ute, Fery, Andreas, Zhou, Shengqiang, Dong, Renhao, Feng, Xinliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159486/
https://www.ncbi.nlm.nih.gov/pubmed/34094144
http://dx.doi.org/10.1039/d0sc01408g
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author Wang, Zhiyong
Wang, Gang
Qi, Haoyuan
Wang, Mao
Wang, Mingchao
Park, SangWook
Wang, Huaping
Yu, Minghao
Kaiser, Ute
Fery, Andreas
Zhou, Shengqiang
Dong, Renhao
Feng, Xinliang
author_facet Wang, Zhiyong
Wang, Gang
Qi, Haoyuan
Wang, Mao
Wang, Mingchao
Park, SangWook
Wang, Huaping
Yu, Minghao
Kaiser, Ute
Fery, Andreas
Zhou, Shengqiang
Dong, Renhao
Feng, Xinliang
author_sort Wang, Zhiyong
collection PubMed
description Two-dimensional conjugated metal–organic frameworks (2D c-MOFs) have recently emerged for potential applications in (opto-)electronics, chemiresistive sensing, and energy storage and conversion, due to their excellent electrical conductivity, abundant active sites, and intrinsic porous structures. However, developing ultrathin 2D c-MOF nanosheets (NSs) for facile solution processing and integration into devices remains a great challenge, mostly due to unscalable synthesis, low yield, limited lateral size and low crystallinity. Here, we report a surfactant-assisted solution synthesis toward ultrathin 2D c-MOF NSs, including HHB-Cu (HHB = hexahydroxybenzene), HHB-Ni and HHTP-Cu (HHTP = 2,3,6,7,10,11-hexahydroxytriphenylene). For the first time, we achieve single-crystalline HHB-Cu(Ni) NSs featured with a thickness of 4–5 nm (∼8–10 layers) and a lateral size of 0.25–0.65 μm(2), as well as single-crystalline HHTP-Cu NSs with a thickness of ∼5.1 ± 2.6 nm (∼10 layers) and a lateral size of 0.002–0.02 μm(2). Benefiting from the ultrathin feature, the synthetic NSs allow fast ion diffusion and high utilization of active sites. As a proof of concept, when serving as a cathode material for Li-ion storage, HHB-Cu NSs deliver a remarkable rate capability (charge within 3 min) and long-term cycling stability (90% capacity retention after 1000 cycles), superior to the corresponding bulk materials and other reported MOF cathodes.
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spelling pubmed-81594862021-06-04 Ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis Wang, Zhiyong Wang, Gang Qi, Haoyuan Wang, Mao Wang, Mingchao Park, SangWook Wang, Huaping Yu, Minghao Kaiser, Ute Fery, Andreas Zhou, Shengqiang Dong, Renhao Feng, Xinliang Chem Sci Chemistry Two-dimensional conjugated metal–organic frameworks (2D c-MOFs) have recently emerged for potential applications in (opto-)electronics, chemiresistive sensing, and energy storage and conversion, due to their excellent electrical conductivity, abundant active sites, and intrinsic porous structures. However, developing ultrathin 2D c-MOF nanosheets (NSs) for facile solution processing and integration into devices remains a great challenge, mostly due to unscalable synthesis, low yield, limited lateral size and low crystallinity. Here, we report a surfactant-assisted solution synthesis toward ultrathin 2D c-MOF NSs, including HHB-Cu (HHB = hexahydroxybenzene), HHB-Ni and HHTP-Cu (HHTP = 2,3,6,7,10,11-hexahydroxytriphenylene). For the first time, we achieve single-crystalline HHB-Cu(Ni) NSs featured with a thickness of 4–5 nm (∼8–10 layers) and a lateral size of 0.25–0.65 μm(2), as well as single-crystalline HHTP-Cu NSs with a thickness of ∼5.1 ± 2.6 nm (∼10 layers) and a lateral size of 0.002–0.02 μm(2). Benefiting from the ultrathin feature, the synthetic NSs allow fast ion diffusion and high utilization of active sites. As a proof of concept, when serving as a cathode material for Li-ion storage, HHB-Cu NSs deliver a remarkable rate capability (charge within 3 min) and long-term cycling stability (90% capacity retention after 1000 cycles), superior to the corresponding bulk materials and other reported MOF cathodes. The Royal Society of Chemistry 2020-04-21 /pmc/articles/PMC8159486/ /pubmed/34094144 http://dx.doi.org/10.1039/d0sc01408g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wang, Zhiyong
Wang, Gang
Qi, Haoyuan
Wang, Mao
Wang, Mingchao
Park, SangWook
Wang, Huaping
Yu, Minghao
Kaiser, Ute
Fery, Andreas
Zhou, Shengqiang
Dong, Renhao
Feng, Xinliang
Ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
title Ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
title_full Ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
title_fullStr Ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
title_full_unstemmed Ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
title_short Ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
title_sort ultrathin two-dimensional conjugated metal–organic framework single-crystalline nanosheets enabled by surfactant-assisted synthesis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159486/
https://www.ncbi.nlm.nih.gov/pubmed/34094144
http://dx.doi.org/10.1039/d0sc01408g
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