Abstract
Abstract
Self-intercalation is an efficient strategy for tailoring the property of layer structured materials like transition metal dichalcogenides (TMDCs), while the associated kinetics and mechanism remain scarcely explored. In this study, we investigate the atomic-scale dynamics and mechanism of vanadium (V) self-intercalation in multi-layer 1T-VSe2 using in situ high resolution scanning transmission electron microscopy. The results reveal that the self-intercalation of V induces structural transformation of pristine VSe2 into three V-enrich intercalated compounds, i.e. V5Se8, V3Se4 and VSe. The self-intercalated V follows an ordered arrangement of
2
×
2
,
2
×
1
, and
1
×
1
within the interlayer octahedral sites, corresponding to an intercalation concentration of 25%, 50% and 100% in V5Se8, V3Se4 and VSe, respectively. The V intercalants induced lattice distortions to the host 1T-VSe2 such as the dimerization of neighboring lattice V is observed experimentally, which are further supported by density functional theory (DFT) calculations. Finally, a superstructure model generalizing the possible structures of self-intercalated compounds in layered TMDCs is proposed and then validated by the DFT determined formation energy landscape. This study provides comprehensive insights on the kinetics and mechanism of the self-intercalation in layered TMDC materials, contributing to the precise control for the structure and stoichiometry of self-intercalated TMDC compounds.
Funder
the Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering
the National Natural Science Foundation of China
Jihua Laboratory
the Basic and Applied Basic Research Major Program of Guangdong Province
Shanghai Rising-Star Program
the Science and Technology Commission of Shanghai Municipality
the Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning, and the Fundamental Research Funds for the Central Universities
Cited by
2 articles.
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