Wafer‐Scale Atomic Assembly for 2D Multinary Transition Metal Dichalcogenides for Visible and NIR Photodetection

Author:

Jeon Hye Yoon12,Song Da Som1,Shin RoSa1,Kwon Yeong Min1,Jo Hyeong‐ku1,Lee Do Hyung1,Lee Eunji1,Jang Moonjeong3,So Hee‐Soo1,Kang Saewon1,Yim Soonmin1,Myung Sung1,Lee Sun Sook1,Yoon Dae Ho2,Kim Chang Gyoun1,Lim Jongsun1,Song Wooseok14ORCID

Affiliation:

1. Thin Film Materials Research Center Korea Research Institute of Chemical Technology Daejeon 34114 Republic of Korea

2. School of Advanced Materials Science and Engineering Sungkyunkwan University Suwon 16419 Republic of Korea

3. National Nano Fab Center (NNFC) Daejeon 34141 Republic of Korea

4. School of Electronic and Electrical Engineering Sungkyunkwan University Suwon 16149 South Korea

Abstract

AbstractThe tunable properties of 2D transition‐metal dichalcogenide (TMDs) materials are extensively investigated for high‐performance and wavelength‐tunable optoelectronic applications. However, the precise modification of large‐scale systems for practical optoelectronic applications remains a challenge. In this study, a wafer‐scale atomic assembly process to produce 2D multinary (binary, ternary, and quaternary) TMDs for broadband photodetection is demonstrated. The large‐area growth of homogeneous MoS2, Ni0.06Mo0.26S0.68, and Ni0.1Mo0.9S1.79Se0.21 is carried out using a succinct coating of the single‐source precursor and subsequent thermal decomposition combined with thermal evaporation of the chalcogen powder. The optoelectrical properties of the multinary TMDs are dependent on the combination of heteroatoms. The maximum photoresponsivity of the MoS2‐, Ni0.06Mo0.26S0.68‐, and Ni0.1Mo0.9S1.79Se0.21‐based photodetectors is 3.51 × 10−4, 1.48, and 0.9 A W−1 for 532 nm and 0.063, 0.42, and 1.4 A W−1 for 1064 nm, respectively. The devices exhibited excellent photoelectrical properties, which is highly beneficial for visible and near‐infrared (NIR) photodetection.

Funder

National Research Foundation of Korea

Publisher

Wiley

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