TY - JOUR
T1 - Laser-Induced Cooperative Transition in Molecular Electronic Crystal
AU - Hu, Yong
AU - Adhikari, Dasharath
AU - Tan, Andrew
AU - Dong, Xi
AU - Zhu, Taishan
AU - Wang, Xiaoyu
AU - Huang, Yulong
AU - Mitchell, Travis
AU - Yao, Ziheng
AU - Dasenbrock-Gammon, Nathan
AU - Snider, Elliot
AU - Dias, Ranga P.
AU - Huang, Chuankun
AU - Kim, Richard
AU - Neuhart, Ian
AU - Ali, Ahmed H.
AU - Zhang, Jiawei
AU - Bechtel, Hans A.
AU - Martin, Michael C.
AU - Corder, Stephanie N.Gilbert
AU - Hu, Feng
AU - Li, Zheng
AU - Armstrong, Jason N.
AU - Wang, Jigang
AU - Liu, Mengkun
AU - Benedict, Jason
AU - Zurek, Eva
AU - Sambandamurthy, Ganapathy
AU - Grossman, Jeffrey C.
AU - Zhang, Pengpeng
AU - Ren, Shenqiang
N1 - Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2021/10/1
Y1 - 2021/10/1
N2 - The competing and non-equilibrium phase transitions, involving dynamic tunability of cooperative electronic and magnetic states in strongly correlated materials, show great promise in quantum sensing and information technology. To date, the stabilization of transient states is still in the preliminary stage, particularly with respect to molecular electronic solids. Here, a dynamic and cooperative phase in potassium-7,7,8,8-tetracyanoquinodimethane (K-TCNQ) with the control of pulsed electromagnetic excitation is demonstrated. Simultaneous dynamic and coherent lattice perturbation with 8 ns pulsed laser (532 nm, 15 MW cm−2, 10 Hz) in such a molecular electronic crystal initiates a stable long-lived (over 400 days) conducting paramagnetic state (≈42 Ωcm), showing the charge–spin bistability over a broad temperature range from 2 to 360 K. Comprehensive noise spectroscopy, in situ high-pressure measurements, electron spin resonance (ESR), theoretical model, and scanning tunneling microscopy/spectroscopy (STM/STS) studies provide further evidence that such a transition is cooperative, requiring a dedicated charge–spin–lattice decoupling to activate and subsequently stabilize nonequilibrium phase. The cooperativity triggered by ultrahigh-strain-rate (above 106 s−1) pulsed excitation offers a collective control toward the generation and stabilization of strongly correlated electronic and magnetic orders in molecular electronic solids and offers unique electro-magnetic phases with technological promises.
AB - The competing and non-equilibrium phase transitions, involving dynamic tunability of cooperative electronic and magnetic states in strongly correlated materials, show great promise in quantum sensing and information technology. To date, the stabilization of transient states is still in the preliminary stage, particularly with respect to molecular electronic solids. Here, a dynamic and cooperative phase in potassium-7,7,8,8-tetracyanoquinodimethane (K-TCNQ) with the control of pulsed electromagnetic excitation is demonstrated. Simultaneous dynamic and coherent lattice perturbation with 8 ns pulsed laser (532 nm, 15 MW cm−2, 10 Hz) in such a molecular electronic crystal initiates a stable long-lived (over 400 days) conducting paramagnetic state (≈42 Ωcm), showing the charge–spin bistability over a broad temperature range from 2 to 360 K. Comprehensive noise spectroscopy, in situ high-pressure measurements, electron spin resonance (ESR), theoretical model, and scanning tunneling microscopy/spectroscopy (STM/STS) studies provide further evidence that such a transition is cooperative, requiring a dedicated charge–spin–lattice decoupling to activate and subsequently stabilize nonequilibrium phase. The cooperativity triggered by ultrahigh-strain-rate (above 106 s−1) pulsed excitation offers a collective control toward the generation and stabilization of strongly correlated electronic and magnetic orders in molecular electronic solids and offers unique electro-magnetic phases with technological promises.
KW - bistability
KW - dimerization
KW - electronic crystals
KW - hidden phases
KW - photoexcitation
UR - https://www.scopus.com/pages/publications/85112452365
U2 - 10.1002/adma.202103000
DO - 10.1002/adma.202103000
M3 - Article
C2 - 34397123
AN - SCOPUS:85112452365
SN - 0935-9648
VL - 33
JO - Advanced Materials
JF - Advanced Materials
IS - 39
M1 - 2103000
ER -