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Electronic Structure Modulation in MoO(2)/MoP Heterostructure to Induce Fast Electronic/Ionic Diffusion Kinetics for Lithium Storage

Transition metal oxides (TMOs) are considered as the prospective anode materials in lithium‐ion batteries (LIBs). Nevertheless, the disadvantages, including large volume variation and poor electrical conductivity, obstruct these materials to meet the needs of practical application. Well‐designed mes...

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Autores principales: Shen, Yuanhao, Jiang, Yalong, Yang, Zhongzhuo, Dong, Jun, Yang, Wei, An, Qinyou, Mai, Liqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867142/
https://www.ncbi.nlm.nih.gov/pubmed/35001551
http://dx.doi.org/10.1002/advs.202104504
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author Shen, Yuanhao
Jiang, Yalong
Yang, Zhongzhuo
Dong, Jun
Yang, Wei
An, Qinyou
Mai, Liqiang
author_facet Shen, Yuanhao
Jiang, Yalong
Yang, Zhongzhuo
Dong, Jun
Yang, Wei
An, Qinyou
Mai, Liqiang
author_sort Shen, Yuanhao
collection PubMed
description Transition metal oxides (TMOs) are considered as the prospective anode materials in lithium‐ion batteries (LIBs). Nevertheless, the disadvantages, including large volume variation and poor electrical conductivity, obstruct these materials to meet the needs of practical application. Well‐designed mesoporous nanostructures and electronic structure modulation can enhance the electron/Li‐ions diffusion kinetics. Herein, a unique mesoporous molybdenum dioxide/molybdenum phosphide heterostructure nanobelts (meso‐MoO(2)/MoP‐NBs) composed of uniform nanoparticles is obtained by one‐step phosphorization process. The Mott–Schottky tests and density functional theory calculations demonstrated that meso‐MoO(2)/MoP‐NBs possesses superior electronic conductivity. The detailed lithium storage mechanism (solid solution reaction for MoP and partial conversion for MoO(2)), small change ratio of crystal structure and fast electronic/ionic diffusion behavior of meso‐MoO(2)/MoP‐NBs are systematically investigated by operando X‐ray diffraction, ex situ transmission electron microscopy, and kinetic analysis. Benefiting from the synergistic effects, the meso‐MoO(2)/MoP‐NBs displays a remarkable cycling performance (515 mAh g(−1) after 1000 cycles at 1 A g(−1)) and excellent rate capability (291 mAh g(−1) at 8 A g(−1)). These findings can shed light on the behavior of the electron/ion regulation in heterostructures and provide a potential route to develop high‐performance lithium‐ion storage materials.
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spelling pubmed-88671422022-02-27 Electronic Structure Modulation in MoO(2)/MoP Heterostructure to Induce Fast Electronic/Ionic Diffusion Kinetics for Lithium Storage Shen, Yuanhao Jiang, Yalong Yang, Zhongzhuo Dong, Jun Yang, Wei An, Qinyou Mai, Liqiang Adv Sci (Weinh) Research Articles Transition metal oxides (TMOs) are considered as the prospective anode materials in lithium‐ion batteries (LIBs). Nevertheless, the disadvantages, including large volume variation and poor electrical conductivity, obstruct these materials to meet the needs of practical application. Well‐designed mesoporous nanostructures and electronic structure modulation can enhance the electron/Li‐ions diffusion kinetics. Herein, a unique mesoporous molybdenum dioxide/molybdenum phosphide heterostructure nanobelts (meso‐MoO(2)/MoP‐NBs) composed of uniform nanoparticles is obtained by one‐step phosphorization process. The Mott–Schottky tests and density functional theory calculations demonstrated that meso‐MoO(2)/MoP‐NBs possesses superior electronic conductivity. The detailed lithium storage mechanism (solid solution reaction for MoP and partial conversion for MoO(2)), small change ratio of crystal structure and fast electronic/ionic diffusion behavior of meso‐MoO(2)/MoP‐NBs are systematically investigated by operando X‐ray diffraction, ex situ transmission electron microscopy, and kinetic analysis. Benefiting from the synergistic effects, the meso‐MoO(2)/MoP‐NBs displays a remarkable cycling performance (515 mAh g(−1) after 1000 cycles at 1 A g(−1)) and excellent rate capability (291 mAh g(−1) at 8 A g(−1)). These findings can shed light on the behavior of the electron/ion regulation in heterostructures and provide a potential route to develop high‐performance lithium‐ion storage materials. John Wiley and Sons Inc. 2022-01-09 /pmc/articles/PMC8867142/ /pubmed/35001551 http://dx.doi.org/10.1002/advs.202104504 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Shen, Yuanhao
Jiang, Yalong
Yang, Zhongzhuo
Dong, Jun
Yang, Wei
An, Qinyou
Mai, Liqiang
Electronic Structure Modulation in MoO(2)/MoP Heterostructure to Induce Fast Electronic/Ionic Diffusion Kinetics for Lithium Storage
title Electronic Structure Modulation in MoO(2)/MoP Heterostructure to Induce Fast Electronic/Ionic Diffusion Kinetics for Lithium Storage
title_full Electronic Structure Modulation in MoO(2)/MoP Heterostructure to Induce Fast Electronic/Ionic Diffusion Kinetics for Lithium Storage
title_fullStr Electronic Structure Modulation in MoO(2)/MoP Heterostructure to Induce Fast Electronic/Ionic Diffusion Kinetics for Lithium Storage
title_full_unstemmed Electronic Structure Modulation in MoO(2)/MoP Heterostructure to Induce Fast Electronic/Ionic Diffusion Kinetics for Lithium Storage
title_short Electronic Structure Modulation in MoO(2)/MoP Heterostructure to Induce Fast Electronic/Ionic Diffusion Kinetics for Lithium Storage
title_sort electronic structure modulation in moo(2)/mop heterostructure to induce fast electronic/ionic diffusion kinetics for lithium storage
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8867142/
https://www.ncbi.nlm.nih.gov/pubmed/35001551
http://dx.doi.org/10.1002/advs.202104504
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