TY - JOUR
T1 - Thiophene Sulfone Single Crystal as a Reversible Thermoelastic Linear Actuator with an Extended Stroke and Second-Harmonic Generation Switching
AU - Wang, Zhihua
AU - Shi, Rongchao
AU - Tahir, Ibrahim
AU - Karothu, Durga Prasad
AU - Cheng, Puxin
AU - Han, Wenqing
AU - Li, Liang
AU - Zheng, Yongshen
AU - Naumov, Panče
AU - Xu, Jialiang
AU - Bu, Xian He
N1 - Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society.
PY - 2025/3/5
Y1 - 2025/3/5
N2 - Dynamic organic crystals are becoming recognized as some of the fastest materials for converting light or heat to mechanical work. The degree of deformation and the response time of any actuating material are often exclusive of each other; however, both factors influence the material’s overall performance limits. Unlike polymers, whose disordered structures are not conducive to rapid energy transfer, cooperative phase transitions in dynamic molecular crystals that are amenable to rapid and concerted martensitic-like structure switching could help circumvent that limitation. Here, we report that single crystals of a dibenzothiophene sulfone derivative exhibit extraordinarily large, rapid, and reversible elongation when they undergo a thermally induced phase transition. The value for the linear stroke of ∼15% along the long crystal axis with retention of macroscopic integrity of this material is remarkable and capitalizes on an anisotropic lattice switching with relative changes of 14.8% and −9.5% along its crystallographic a and c axes, respectively, resulting in a visible macroscopic elongation of the crystal. The transitioning crystals deliver forces ranging from 0.19 to 15 μN and a work density of ∼7 × 10-3 J m-3. The phase transformation is accompanied by a change in symmetry between centrosymmetric and noncentrosymmetric space groups and a significant change in both the fluorescence and the second-order nonlinear optical (NLO) response. The combination of these properties makes this material a favorable choice for low-power, precise, and small-scale NLO actuation applications.
AB - Dynamic organic crystals are becoming recognized as some of the fastest materials for converting light or heat to mechanical work. The degree of deformation and the response time of any actuating material are often exclusive of each other; however, both factors influence the material’s overall performance limits. Unlike polymers, whose disordered structures are not conducive to rapid energy transfer, cooperative phase transitions in dynamic molecular crystals that are amenable to rapid and concerted martensitic-like structure switching could help circumvent that limitation. Here, we report that single crystals of a dibenzothiophene sulfone derivative exhibit extraordinarily large, rapid, and reversible elongation when they undergo a thermally induced phase transition. The value for the linear stroke of ∼15% along the long crystal axis with retention of macroscopic integrity of this material is remarkable and capitalizes on an anisotropic lattice switching with relative changes of 14.8% and −9.5% along its crystallographic a and c axes, respectively, resulting in a visible macroscopic elongation of the crystal. The transitioning crystals deliver forces ranging from 0.19 to 15 μN and a work density of ∼7 × 10-3 J m-3. The phase transformation is accompanied by a change in symmetry between centrosymmetric and noncentrosymmetric space groups and a significant change in both the fluorescence and the second-order nonlinear optical (NLO) response. The combination of these properties makes this material a favorable choice for low-power, precise, and small-scale NLO actuation applications.
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U2 - 10.1021/jacs.4c17448
DO - 10.1021/jacs.4c17448
M3 - Article
C2 - 39989406
AN - SCOPUS:85218909569
SN - 0002-7863
VL - 147
SP - 7749
EP - 7756
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 9
ER -