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Construction of 1T@2H MoS(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries
Natural molybdenite, an inexpensive and naturally abundant material, can be directly used as an anode material for lithium-ion batteries. However, how to release the intrinsic capacity of natural molybdenite to achieve high rate performance and high capacity is still a challenge. Herein, we introduc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042300/ https://www.ncbi.nlm.nih.gov/pubmed/35497512 http://dx.doi.org/10.1039/d1ra05565h |
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author | Peng, ChengLong Shi, Mingming Li, Fei Wang, Yang Liu, Xueqin Liu, HuaSheng Li, Zhen |
author_facet | Peng, ChengLong Shi, Mingming Li, Fei Wang, Yang Liu, Xueqin Liu, HuaSheng Li, Zhen |
author_sort | Peng, ChengLong |
collection | PubMed |
description | Natural molybdenite, an inexpensive and naturally abundant material, can be directly used as an anode material for lithium-ion batteries. However, how to release the intrinsic capacity of natural molybdenite to achieve high rate performance and high capacity is still a challenge. Herein, we introduce an innovative, effective, and one-step approach to preparing a type of heterostructure material containing 1T@2H MoS(2) crafted from insertion and expansion of natural molybdenite. The metallic 1T phase formed in situ can significantly improve the electronic conductivity of MoS(2). At the same time, 1T@2H MoS(2) heterostructures can provide an internal electric field (E-field) to accelerate the migration rate of electrons and ions, promote the charge transfer behaviour, and ensure the reaction reversibility and lithium storage kinetics. Such worm-like 1T@2H MoS(2) heterostructures also have a large specific surface area and a large number of defects, which will help shorten the lithium-ion transmission distance and provide more ion transmission channels. As a result, it exhibits a discharge capacity of 788 mA h g(−1) remarkably at 100 mA g(−1) after 485 cycles and stable cycling performance. It also shows excellent magnification performance of 727 mA h g(−1) at 1 A g(−1), compared to molybdenite concentrate. Briefly, this work's heterostructure architectures open up a new avenue for applying natural molybdenite in lithium-ion batteries, which has the potential to achieve large-scale commercial applications. |
format | Online Article Text |
id | pubmed-9042300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90423002022-04-28 Construction of 1T@2H MoS(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries Peng, ChengLong Shi, Mingming Li, Fei Wang, Yang Liu, Xueqin Liu, HuaSheng Li, Zhen RSC Adv Chemistry Natural molybdenite, an inexpensive and naturally abundant material, can be directly used as an anode material for lithium-ion batteries. However, how to release the intrinsic capacity of natural molybdenite to achieve high rate performance and high capacity is still a challenge. Herein, we introduce an innovative, effective, and one-step approach to preparing a type of heterostructure material containing 1T@2H MoS(2) crafted from insertion and expansion of natural molybdenite. The metallic 1T phase formed in situ can significantly improve the electronic conductivity of MoS(2). At the same time, 1T@2H MoS(2) heterostructures can provide an internal electric field (E-field) to accelerate the migration rate of electrons and ions, promote the charge transfer behaviour, and ensure the reaction reversibility and lithium storage kinetics. Such worm-like 1T@2H MoS(2) heterostructures also have a large specific surface area and a large number of defects, which will help shorten the lithium-ion transmission distance and provide more ion transmission channels. As a result, it exhibits a discharge capacity of 788 mA h g(−1) remarkably at 100 mA g(−1) after 485 cycles and stable cycling performance. It also shows excellent magnification performance of 727 mA h g(−1) at 1 A g(−1), compared to molybdenite concentrate. Briefly, this work's heterostructure architectures open up a new avenue for applying natural molybdenite in lithium-ion batteries, which has the potential to achieve large-scale commercial applications. The Royal Society of Chemistry 2021-10-13 /pmc/articles/PMC9042300/ /pubmed/35497512 http://dx.doi.org/10.1039/d1ra05565h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Peng, ChengLong Shi, Mingming Li, Fei Wang, Yang Liu, Xueqin Liu, HuaSheng Li, Zhen Construction of 1T@2H MoS(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries |
title | Construction of 1T@2H MoS(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries |
title_full | Construction of 1T@2H MoS(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries |
title_fullStr | Construction of 1T@2H MoS(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries |
title_full_unstemmed | Construction of 1T@2H MoS(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries |
title_short | Construction of 1T@2H MoS(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries |
title_sort | construction of 1t@2h mos(2) heterostructures in situ from natural molybdenite with enhanced electrochemical performance for lithium-ion batteries |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042300/ https://www.ncbi.nlm.nih.gov/pubmed/35497512 http://dx.doi.org/10.1039/d1ra05565h |
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