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环境条件下用于定制电子产品的MoS和WS结构的层选择性合成

Layer-Selective Synthesis of MoS and WS Structures under Ambient Conditions for Customized Electronics.

作者信息

Park Seoungwoong, Lee Aram, Choi Kwang-Hun, Hyeong Seok-Ki, Bae Sukang, Hong Jae-Min, Kim Tae-Wook, Hong Byung Hee, Lee Seoung-Ki

机构信息

Functional Composite Materials Research Center, Institute of Advanced Composite Materials, Korea Institute of Science and Technology (KIST), 92 Chudong-ro, Bongdong-eup, Wanju-gun, Jeonbuk 55324, Republic of Korea.

Department of Chemistry, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea.

出版信息

ACS Nano. 2020 Jul 28;14(7):8485-8494. doi: 10.1021/acsnano.0c02745. Epub 2020 Jun 29.

Abstract

Transition metal dichalcogenides (TMDs) have attracted significant interest as one of the key materials in future electronics such as logic devices, optoelectrical devices, and wearable electronics. However, a complicated synthesis method and multistep processes for device fabrication pose major hurdles for their practical applications. Here, we introduce a direct and rapid method for layer-selective synthesis of MoS and WS structures in wafer-scale using a pulsed laser annealing system (λ = 1.06 μm, pulse duration ∼100 ps) in ambient conditions. The precursor layer of each TMD, which has at least 3 orders of magnitude higher absorption coefficient than those of neighboring layers, rigorously absorbed the incoming energy of the laser pulse and rapidly pyrolyzed in a few nanoseconds, enabling the generation of a MoS or WS layer without damaging the adjacent layers of SiO or polymer substrate. Through experimental and theoretical studies, we establish the underlying principles of selective synthesis and optimize the laser annealing conditions, such as laser wavelength, output power, and scribing speed, under ambient condition. As a result, individual homostructures of patterned MoS and WS layers were directly synthesized on a 4 in. wafer. Moreover, a consecutive synthesis of the second layer on top of the first synthesized layer realized a vertically stacked WS/MoS heterojunction structure, which can be treated as a cornerstone of electronic devices. As a proof of concept, we demonstrated the behavior of a MoS-based field-effect transistor, a skin-attachable motion sensor, and a MoS/WS-based heterojunction diode in this study. The ultrafast and selective synthesis of the TMDs suggests an approach to the large-area/mass production of functional heterostructure-based electronics.

摘要

过渡金属二硫属化物(TMDs)作为未来电子领域(如逻辑器件、光电器件和可穿戴电子产品)的关键材料之一,已引起了广泛关注。然而,复杂的合成方法和器件制造的多步骤工艺对其实际应用构成了重大障碍。在此,我们介绍一种在环境条件下使用脉冲激光退火系统(λ = 1.06μm,脉冲持续时间约100ps)在晶圆级进行MoS和WS结构层选择性合成的直接且快速的方法。每个TMD的前驱体层,其吸收系数比相邻层至少高3个数量级,严格吸收激光脉冲的入射能量,并在几纳秒内迅速热解,从而能够生成MoS或WS层而不损坏SiO或聚合物衬底的相邻层。通过实验和理论研究,我们确立了选择性合成的基本原理,并在环境条件下优化了激光退火条件,如激光波长、输出功率和划片速度。结果,在4英寸晶圆上直接合成了图案化的MoS和WS层的单个同质结构。此外,在第一个合成层之上连续合成第二层,实现了垂直堆叠的WS/MoS异质结结构,这可被视为电子器件的基石。作为概念验证,我们在本研究中展示了基于MoS的场效应晶体管、可附着在皮肤上的运动传感器以及基于MoS/WS的异质结二极管的性能。TMDs的超快和选择性合成提出了一种实现基于功能异质结构的电子产品大面积/大规模生产的方法。

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