Doping two-dimensional (2D) semiconductors beyond their degenerate levels provides the opportunity to investigate extreme carrier density-driven superconductivity and phase transition in 2D systems. Chemical functionalization and the ionic gating have achieved the high doping density, but their effective ranges have been limited to ∼1 nm, which restricts the use of highly doped 2D semiconductors. Here, we report on electron diffusion from the 2D electride [CaN]·e to MoTe over a distance of 100 nm from the contact interface, generating an electron doping density higher than 1.6 × 10 cm and a lattice symmetry change of MoTe as a consequence of the extreme doping. The long-range lattice symmetry change, suggesting a length scale surpassing the depletion width of conventional metal-semiconductor junctions, was a consequence of the low work function (2.6 eV) with highly mobile anionic electron layers of [CaN]·e. The combination of 2D electrides and layered materials yields a novel material design in terms of doping and lattice engineering.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.nanolett.6b05199DOI Listing

Publication Analysis

Top Keywords

long-range lattice
8
lattice engineering
8
doping density
8
lattice symmetry
8
symmetry change
8
doping
5
engineering mote
4
mote electride
4
electride doping
4
doping two-dimensional
4

Similar Publications

Spin Glass Transition of Magnetic Ionic Liquids Induced by Self-Assembly.

Langmuir

January 2025

School of Materials Science and Engineering, Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin 300350, China.

Spin glass (SG), in which the spins are glassy, has attracted broad attention for theoretical study and prospective application. SG states are generally related to disordered or frustrated spin systems, which are usually observed in inorganic magnets. Herein, supramolecular magnetic ionic liquid (TMTBDI[FeCl]) self-assemblies are prepared by solution self-assembly via hydrophobic and π-π stacking interactions.

View Article and Find Full Text PDF

Magnetoplumbites are one of the most broadly studied families of hexagonal ferrites, typically with high magnetic ordering temperatures, making them excellent candidates for permanent magnets. However, magnetic frustration is rarely observed in magnetoplumbites. Herein, the discovery, synthesis, and characterization of the first Mn-based magnetoplumbite, as well as the first magnetoplumbite involving pnictogens (Sb), ASbMnO (A = K or Rb) are reported.

View Article and Find Full Text PDF

Frustrated Magnetism and Spin Anisotropy in a Buckled Square Net YbTaO.

Inorg Chem

January 2025

School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.

The interplay between quantum effects from magnetic frustration, low-dimensionality, spin-orbit coupling, and crystal electric field in rare-earth materials leads to nontrivial ground states with unusual magnetic excitations. Here, we investigate YbTaO, which hosts a buckled square net of Yb ions with = 1/2 moments. The observed Curie-Weiss temperature is about -1 K, implying an antiferromagnetic coupling between the Yb moments.

View Article and Find Full Text PDF

Resonant Quantum Magnetodielectric Effect in Multiferroic Metal-Organic Framework [CHNH]Co(HCOO).

Small

December 2024

Department of Applied Physics and Center of Quantum Materials and Devices, Chongqing University, Chongqing, 401331, China.

The observation of both resonant quantum tunneling of magnetization (RQTM) and resonant quantum magnetodielectric (RQMD) effect in the perovskite multiferroic metal-organic framework [CHNH]Co(HCOO).is reported. An intrinsic magnetic phase separation emerges at low temperatures due to the hydrogen-bond-modified long-range super-exchange interaction, leading to the coexistence of canted antiferromagnetic order and single-ion (Co) magnets.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!