4.8 Article

Efficient Defect Healing of Transition Metal Dichalcogenides by Metallophthalocyanine

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 10, 期 34, 页码 29145-29152

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b09378

关键词

two-dimensional materials; transition metal dichalcogenides; molybdenum diselenide; phthalocyanine; defects

资金

  1. Ministry of Science and Technology of Taiwan [MOST-104-2112-M-009-007-MY3, MOST 106-2622-M-009-006-CC3]

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Two-dimensional (2D) transition metal dichalcogenides (TMDCs) have attracted great attention as alternatives to graphene with semiconducting band gaps. Mono- or few-layer TMDCs can be prepared by various methods, but regardless of the fabrication methods [such as mechanical exfoliation and chemical vapor deposition (CVD)], TMDCs contain many structural defects, which significantly affect their physical properties and limit their performance in applications. Metallophthalocyanines (MPcs) are organic semiconductors, and as dopants, they are capable of modulating the optical and electrical properties of other semiconducting materials. Here, we report that besides the ability to modulate the optoelectronic properties of 2D TMDCs, MPc molecules can be used to heal defects and improve the physicochemical properties of TMDCs. Doping of planar MPc molecules to TMDCs is achieved by a simple solution dip-coating method and results in a significant improvement in the optical properties and thermal responses of CVD-grown TMDCs, even comparable to those of mechanically exfoliated counterparts. Study of carrier dynamics shows that the adsorption of MPc on the TMDC surface leads to the complete suppression of the mid-gap defect-induced absorption in TMDCs. Furthermore, MPc molecules with a large lateral size are found to effectively reduce the point defects in mechanically exfoliated TMDCs introduced during the preparation process. Our results not only clarify the optoelectronic modulation mechanism of chemical doping but also offer a simple method to control the nanosized defects in 2D TMDCs.

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