Colloidal Synthesis of P‐Type Zn3As2 Nanocrystals

Author:

Kim Seongchan1ORCID,Lee Kyumin2,Gwak Namyoung1,Shin Seungki1,Seo Jaeyoung1,Noh Sung Hoon2,Kim Doyeon2,Lee Yunseo1,Kong Hyein1,Yeo Dongjoon1,Kim Tae Ann3,Lee Seung‐Yong1ORCID,Jang Jaeyoung2ORCID,Oh Nuri1ORCID

Affiliation:

1. Division of Materials Science and Engineering Hanyang University 222, Wangsimni‐ro, Seongdong‐gu Seoul 04763 Republic of Korea

2. Department of Energy Engineering Hanyang University 222, Wangsimni‐ro, Seongdong‐gu Seoul 04763 Republic of Korea

3. Convergence Research Center for Solutions to Electromagnetic Interference in Future‐Mobility Korea Institute of Science and Technology Seoul 02792 Republic of Korea

Abstract

AbstractZinc pnictides, particularly Zn3As2, hold significant promise for optoelectronic applications owing to their intrinsic p‐type behavior and appropriate bandgaps. However, despite the outstanding properties of colloidal Zn3As2 nanocrystals, research in this area is lacking because of the absence of suitable precursors, occurrence of surface oxidation, and intricacy of the crystal structures. In this study, a novel and facile solution‐based synthetic approach is presented for obtaining highly crystalline p‐type Zn3As2 nanocrystals with accurate stoichiometry. By carefully controlling the feed ratio and reaction temperature, colloidal Zn3As2 nanocrystals are successfully obtained. Moreover, the mechanism underlying the conversion of As precursors in the initial phases of Zn3As2 synthesis is elucidated. Furthermore, these nanocrystals are employed as active layers in field‐effect transistors that exhibit inherent p‐type characteristics with native surface ligands. To enhance the charge transport properties, a dual passivation strategy is introduced via phase‐transfer ligand exchange, leading to enhanced hole mobilities as high as 0.089 cm2 V−1 s−1. This study not only contributes to the advancement of nanocrystal synthesis, but also opens up new possibilities for previously underexplored p‐type nanocrystal research.

Funder

National Research Foundation of Korea

Publisher

Wiley

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