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Sub-second ultrafast yet programmable wet-chemical synthesis
Wet-chemical synthesis via heating bulk solution is powerful to obtain nanomaterials. However, it still suffers from limited reaction rate, controllability, and massive consumption of energy/reactants, particularly for the synthesis on specific substrates. Herein, we present an innovative wet-interf...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439120/ https://www.ncbi.nlm.nih.gov/pubmed/37596259 http://dx.doi.org/10.1038/s41467-023-40737-5 |
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author | Zhang, Lin Peng, Li Lu, Yuanchao Ming, Xin Sun, Yuxin Xu, Xiaoyi Xia, Yuxing Pang, Kai Fang, Wenzhang Huang, Ning Xu, Zhen Ying, Yibin Liu, Yingjun Fu, Yingchun Gao, Chao |
author_facet | Zhang, Lin Peng, Li Lu, Yuanchao Ming, Xin Sun, Yuxin Xu, Xiaoyi Xia, Yuxing Pang, Kai Fang, Wenzhang Huang, Ning Xu, Zhen Ying, Yibin Liu, Yingjun Fu, Yingchun Gao, Chao |
author_sort | Zhang, Lin |
collection | PubMed |
description | Wet-chemical synthesis via heating bulk solution is powerful to obtain nanomaterials. However, it still suffers from limited reaction rate, controllability, and massive consumption of energy/reactants, particularly for the synthesis on specific substrates. Herein, we present an innovative wet-interfacial Joule heating (WIJH) approach to synthesize various nanomaterials in a sub-second ultrafast, programmable, and energy/reactant-saving manner. In the WIJH, Joule heat generated by the graphene film (GF) is confined at the substrate-solution interface. Accompanied by instantaneous evaporation of the solvent, the temperature is steeply improved and the precursors are concentrated, thereby synergistically accelerating and controlling the nucleation and growth of nanomaterials on the substrate. WIJH leads to a record high crystallization rate of HKUST-1 (~1.97 μm s(−1)), an ultralow energy cost (9.55 × 10(−6) kWh cm(−2)) and low precursor concentrations, which are up to 5 orders of magnitude faster, −6 and −2 orders of magnitude lower than traditional methods, respectively. Moreover, WIJH could handily customize the products’ amount, size, and morphology via programming the electrified procedures. The as-prepared HKUST-1/GF enables the Joule-heating-controllable and low-energy-required capture and liberation towards CO(2). This study opens up a new methodology towards the superefficient synthesis of nanomaterials and solvent-involved Joule heating. |
format | Online Article Text |
id | pubmed-10439120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104391202023-08-20 Sub-second ultrafast yet programmable wet-chemical synthesis Zhang, Lin Peng, Li Lu, Yuanchao Ming, Xin Sun, Yuxin Xu, Xiaoyi Xia, Yuxing Pang, Kai Fang, Wenzhang Huang, Ning Xu, Zhen Ying, Yibin Liu, Yingjun Fu, Yingchun Gao, Chao Nat Commun Article Wet-chemical synthesis via heating bulk solution is powerful to obtain nanomaterials. However, it still suffers from limited reaction rate, controllability, and massive consumption of energy/reactants, particularly for the synthesis on specific substrates. Herein, we present an innovative wet-interfacial Joule heating (WIJH) approach to synthesize various nanomaterials in a sub-second ultrafast, programmable, and energy/reactant-saving manner. In the WIJH, Joule heat generated by the graphene film (GF) is confined at the substrate-solution interface. Accompanied by instantaneous evaporation of the solvent, the temperature is steeply improved and the precursors are concentrated, thereby synergistically accelerating and controlling the nucleation and growth of nanomaterials on the substrate. WIJH leads to a record high crystallization rate of HKUST-1 (~1.97 μm s(−1)), an ultralow energy cost (9.55 × 10(−6) kWh cm(−2)) and low precursor concentrations, which are up to 5 orders of magnitude faster, −6 and −2 orders of magnitude lower than traditional methods, respectively. Moreover, WIJH could handily customize the products’ amount, size, and morphology via programming the electrified procedures. The as-prepared HKUST-1/GF enables the Joule-heating-controllable and low-energy-required capture and liberation towards CO(2). This study opens up a new methodology towards the superefficient synthesis of nanomaterials and solvent-involved Joule heating. Nature Publishing Group UK 2023-08-18 /pmc/articles/PMC10439120/ /pubmed/37596259 http://dx.doi.org/10.1038/s41467-023-40737-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhang, Lin Peng, Li Lu, Yuanchao Ming, Xin Sun, Yuxin Xu, Xiaoyi Xia, Yuxing Pang, Kai Fang, Wenzhang Huang, Ning Xu, Zhen Ying, Yibin Liu, Yingjun Fu, Yingchun Gao, Chao Sub-second ultrafast yet programmable wet-chemical synthesis |
title | Sub-second ultrafast yet programmable wet-chemical synthesis |
title_full | Sub-second ultrafast yet programmable wet-chemical synthesis |
title_fullStr | Sub-second ultrafast yet programmable wet-chemical synthesis |
title_full_unstemmed | Sub-second ultrafast yet programmable wet-chemical synthesis |
title_short | Sub-second ultrafast yet programmable wet-chemical synthesis |
title_sort | sub-second ultrafast yet programmable wet-chemical synthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10439120/ https://www.ncbi.nlm.nih.gov/pubmed/37596259 http://dx.doi.org/10.1038/s41467-023-40737-5 |
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