4.8 Article

Atomically Resolved Quantum-Confined Electronic Structures at Organic-Inorganic Interfaces of Two-Dimensional Ruddlesden- Popper Halide Perovskites

期刊

NANO LETTERS
卷 21, 期 19, 页码 8066-8072

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.1c02409

关键词

two-dimensional perovskites; scanning tunneling microscopy; quantum-well electronic structure; organic-inorganic interface

资金

  1. Ministry of Science and Technology (MOST), Taiwan [108-2923-M-002-002-MY2, MOST 109-2628-M-002-005-MY3]
  2. National Taiwan University [NTU-109L7848]
  3. Center of Atomic Initiative for New Materials (AI-Mat), National Taiwan University, from the Featured Areas Research Center Program by the Ministry of Education in Taiwan [108L9008]

向作者/读者索取更多资源

This study demonstrates the direct visualization of atomically resolved quantum-confined electronic structures at organic-inorganic interfaces of 2D RPPs using STM and STS techniques. The presence of quantum-well-like type-I heterojunction band alignment and edge states due to organic cation vacancies are observed at these interfaces. Real-space visualization of atomic-scale structural phase transition behavior and changes in local electronic band structures are obtained simultaneously.
This work demonstrates the direct visualization of atomically resolved quantum-confined electronic structures at organic-inorganic heterointerfaces of two-dimensional (2D) organic-inorganic hybrid Ruddlesden-Popper perovskites (RPPs); this is accomplished with scanning tunneling microscopy (STM) and scanning tunneling spectroscopy (STS) by using solvent engineering to prepare perpendicularly oriented 2D RPPs. Atomically resolved band mapping images across the organic-inorganic interfaces of 2D RPPs yield typical quantum-well-like type-I heterojunction band alignment with band gaps depending on the thicknesses or n values of the inorganic perovskite slabs. The presence of edge states within the band gap due to organic cation vacancies is also observed. In addition, real-space visualization of atomic-scale structural phase transition behavior and changes in local electronic band structures are obtained simultaneously. Our results provide an unequivocal observation and explanation of the quantum-confined electronic structures formed at organic-inorganic interfaces of 2D RPPs.

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