Liquid Phase Exfoliation of Few‐Layer Non‐Van der Waals Chromium Sulfide

Author:

Su Wenjie1,Kuklin Artem2,Jin Ling hua1,Engelgardt Dana34,Zhang Han5,Ågren Hans2ORCID,Zhang Ye1

Affiliation:

1. School of Chemistry and Chemical Engineering University of South China Hengyang 421001 China

2. Department of Physics and Astronomy Uppsala University Box 516 Uppsala SE‐751 20 Sweden

3. Department of Chemistry College of Natural Sciences Kyungpook National University 80 Daehakro, Bukgu Daegu 41556 South Korea

4. International Research Center of Spectroscopy and Quantum Chemistry – IRC SQC Siberian Federal University 79 Svobodny pr. Krasnoyarsk 660041 Russia

5. Collaborative Innovation Center for Optoelectronic Science & Technology International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education Institute of Microscale Optoelectronics Shenzhen University Shenzhen 518060 China

Abstract

AbstractExfoliation of 2D non‐Van der Waals (non‐vdW) semiconductor nanoplates (NPs) from inorganic analogs presents many challenges ahead for further exploring of their advanced applications on account of the strong bonding energies. In this study, the exfoliation of ultrathin 2D non‐vdW chromium sulfide (2D Cr2S3) by means of a combined facile liquid‐phase exfoliation (LPE) method is successfully demonstrated. The morphology and structure of the 2D Cr2S3 material are systematically examined. Magnetic studies show an obvious temperature‐dependent uncompensated antiferromagnetic behavior of 2D Cr2S3. The material is further loaded on TiO2 nanorod arrays to form an S‐scheme heterojunction. Experimental measurements and density functional theory (DFT) calculations confirm that the formed TiO2@Cr2S3 S‐scheme heterojunction facilitates the separation and transmission of photo‐induced electron/hole pairs, resulting in a significantly enhanced photocatalytic activity in the visible region.

Funder

University of South China

Russian Science Foundation

Vetenskapsrådet

Publisher

Wiley

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