Conjugated Radical Polymers

Room-Temperature Quantum Coherence

Stable conjugated polyradicals directly copolymerized from diradical monomers exhibit balanced ambipolar transport and room-temperature quantum coherence, offering processable macromolecular materials for spintronic and quantum information devices.

Liu, Hao · Li, Wenhao · Yi, Yang · Zhang, Zihong · Zhao, Yan · Yang, Kun · Zeng, Zebing

Angewandte Chemie - International Edition 2025

Specifications

Hole Mobility
{'zh': '0.41', 'en': '0.41'} cm2 V-1 s-1
Electron Mobility
{'zh': '0.38', 'en': '0.38'} cm2 V-1 s-1
Longitudinal Quantum Coherence Time (T1)
{'zh': '1.88', 'en': '1.88'} μs
Maximum Diradical Character
{'zh': '0.88', 'en': '0.88'}

Advantages

Facile Synthesis

Direct copolymerization of diradical monomers with DPP units affords stable conjugated polyradicals without complex post-functionalization.

Room-Temperature Quantum Coherence

Thin films exhibit attractive room-temperature quantum coherence times (T1 = 1.88 μs, T2 = 218 ns), promising for quantum information processing.

Balanced Ambipolar Transport

Well-balanced hole/electron mobilities (0.41/0.38 cm² V⁻¹ s⁻¹) enable high-performance ambipolar field-effect transistors.

NIR Absorption Beyond 1000 nm

Intense near-infrared absorptions beyond 1000 nm extend their potential to NIR optoelectronics and bioimaging.

Applications