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Precise engineering of quantum dot array coupling through their barrier widths

Author

Listed:
  • Ignacio Piquero-Zulaica

    (Centro de Física de Materiales CSIC/UPV-EHU-Materials Physics Center)

  • Jorge Lobo-Checa

    (CSIC-Universidad de Zaragoza
    Universidad de Zaragoza)

  • Ali Sadeghi

    (Shahid Beheshti University)

  • Zakaria M. Abd El-Fattah

    (Al-Azhar University)

  • Chikahiko Mitsui

    (The University of Tokyo)

  • Toshihiro Okamoto

    (The University of Tokyo
    PRESTO, Japan Science and Technology Agency)

  • Rémy Pawlak

    (University of Basel)

  • Tobias Meier

    (University of Basel)

  • Andrés Arnau

    (Centro de Física de Materiales CSIC/UPV-EHU-Materials Physics Center
    Donostia International Physics Center (DIPC)
    Universidad del País Vasco)

  • J. Enrique Ortega

    (Centro de Física de Materiales CSIC/UPV-EHU-Materials Physics Center
    Donostia International Physics Center (DIPC)
    Universidad del País Vasco)

  • Jun Takeya

    (The University of Tokyo)

  • Stefan Goedecker

    (University of Basel)

  • Ernst Meyer

    (University of Basel)

  • Shigeki Kawai

    (PRESTO, Japan Science and Technology Agency
    University of Basel
    National Institute for Materials Science)

Abstract

Quantum dots are known to confine electrons within their structure. Whenever they periodically aggregate into arrays and cooperative interactions arise, novel quantum properties suitable for technological applications show up. Control over the potential barriers existing between neighboring quantum dots is therefore essential to alter their mutual crosstalk. Here we show that precise engineering of the barrier width can be experimentally achieved on surfaces by a single atom substitution in a haloaromatic compound, which in turn tunes the confinement properties through the degree of quantum dot intercoupling. We achieved this by generating self-assembled molecular nanoporous networks that confine the two-dimensional electron gas present at the surface. Indeed, these extended arrays form up on bulk surface and thin silver films alike, maintaining their overall interdot coupling. These findings pave the way to reach full control over two-dimensional electron gases by means of self-assembled molecular networks.

Suggested Citation

  • Ignacio Piquero-Zulaica & Jorge Lobo-Checa & Ali Sadeghi & Zakaria M. Abd El-Fattah & Chikahiko Mitsui & Toshihiro Okamoto & Rémy Pawlak & Tobias Meier & Andrés Arnau & J. Enrique Ortega & Jun Takeya , 2017. "Precise engineering of quantum dot array coupling through their barrier widths," Nature Communications, Nature, vol. 8(1), pages 1-6, December.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00872-2
    DOI: 10.1038/s41467-017-00872-2
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    Cited by:

    1. Zhen-Yu Yi & Xue-Qing Yang & Jun-Jie Duan & Xiong Zhou & Ting Chen & Dong Wang & Li-Jun Wan, 2022. "Evolution of Br⋯Br contacts in enantioselective molecular recognition during chiral 2D crystallization," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    2. Xinnan Peng & Harshitra Mahalingam & Shaoqiang Dong & Pingo Mutombo & Jie Su & Mykola Telychko & Shaotang Song & Pin Lyu & Pei Wen Ng & Jishan Wu & Pavel Jelínek & Chunyan Chi & Aleksandr Rodin & Jion, 2021. "Visualizing designer quantum states in stable macrocycle quantum corrals," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
    3. Liangliang Cai & Tianhao Gao & Andrew T. S. Wee, 2024. "Topology selectivity of a conformationally flexible precursor through selenium doping," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    4. Ruoting Yin & Xiang Zhu & Qiang Fu & Tianyi Hu & Lingyun Wan & Yingying Wu & Yifan Liang & Zhengya Wang & Zhen-Lin Qiu & Yuan-Zhi Tan & Chuanxu Ma & Shijing Tan & Wei Hu & Bin Li & Z. F. Wang & Jinlon, 2024. "Artificial kagome lattices of Shockley surface states patterned by halogen hydrogen-bonded organic frameworks," Nature Communications, Nature, vol. 15(1), pages 1-11, December.

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