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Atomic Scale Control and Visualization of Topological Quantum Phase Transition in π‐Conjugated Polymers Driven by Their Length

Quantum phase transitions (QPTs) driven by quantum fluctuations are transitions between distinct quantum phases of matter. At present, they are poorly understood and not readily controlled. Here, scanning tunneling microscopy (STM) and noncontact atomic force microscopy (nc‐AFM) are used to explore...

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Bibliographic Details
Published in:Advanced materials (Weinheim) 2021-11, Vol.33 (44), p.e2104495-n/a
Main Authors: González‐Herrero, Héctor, Mendieta‐Moreno, Jesús I., Edalatmanesh, Shayan, Santos, José, Martín, Nazario, Écija, David, Torre, Bruno, Jelinek, Pavel
Format: Article
Language:English
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Summary:Quantum phase transitions (QPTs) driven by quantum fluctuations are transitions between distinct quantum phases of matter. At present, they are poorly understood and not readily controlled. Here, scanning tunneling microscopy (STM) and noncontact atomic force microscopy (nc‐AFM) are used to explore atomic scale control over quantum phase transitions between two different topological quantum states of a well‐defined π‐conjugated polymer. The phase transition is driven by a pseudo Jahn–Teller effect that is activated above a certain polymer chain length. In addition, theoretical calculations indicate the presence of long‐lasting coherent fluctuations between the polymer's two quantum phases near the phase transition, at finite temperature. This work thus presents a new way of exploring atomic‐scale control over QPTs and indicates that emerging quantum criticality in the vicinity of a QPT can give rise to new states of organic matter. Length control of π‐conjugated pentacene polymers leads to the observation of a topological quantum phase transition. The transition is marked by the emergence of a zero‐energy in‐gap edge state. A pseudo Jahn–Teller effect is identified as the driving mechanism by theoretical calculations. Furthermore, atomic manipulation with scanning tunneling microscopy allows for engineering polymers.
ISSN:0935-9648
1521-4095
DOI:10.1002/adma.202104495