TY - JOUR
T1 - Unraveling two distinct polymorph transition mechanisms in one n-type single crystal for dynamic electronics
AU - Davies, Daniel William
AU - Seo, Bumjoon
AU - Park, Sang Kyu
AU - Shiring, Stephen B.
AU - Chung, Hyunjoong
AU - Kafle, Prapti
AU - Yuan, Dafei
AU - Strzalka, Joseph W.
AU - Weber, Ralph
AU - Zhu, Xiaozhang
AU - Savoie, Brett M.
AU - Diao, Ying
N1 - Y.D., D.D., S.K.P., and H.C. acknowledge the Sloan Foundation for a Sloan Research Fellowship in Chemistry and a 3M Nontenured Faculty Award. D.D. acknowledges support of DuPont Graduate Fellowship and A. T. Widiger Chemical Engineering Fellowship. Y.D. and P.K. acknowledge partial support by the NSF MRSEC: Illinois Materials Research Center under grant number DMR-1720633 and NSF CAREER award under Grant No. 18-47828. X.Z. acknowledges the National Key R&D Program of China (2017YFA0204700). B.S. and B.M.S. acknowledge support by the NSF under Grant No. 2045887-CBET. This work was conducted in part in the Frederick Seitz Materials Research Laboratory Central Facilities. Portions of this research were carried out at the Advanced Photon Source, a U.S. Department of Energy (DOE), Office of Science User Facility, operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. D.D. acknowledges Dr. Joseph G. Manion (CGFigures) for his tutorials on using 3D rending software for scientific illustrations.
PY - 2023/12
Y1 - 2023/12
N2 - Cooperativity is used by living systems to circumvent energetic and entropic barriers to yield highly efficient molecular processes. Cooperative structural transitions involve the concerted displacement of molecules in a crystalline material, as opposed to typical molecule-by-molecule nucleation and growth mechanisms which often break single crystallinity. Cooperative transitions have acquired much attention for low transition barriers, ultrafast kinetics, and structural reversibility. However, cooperative transitions are rare in molecular crystals and their origin is poorly understood. Crystals of 2-dimensional quinoidal terthiophene (2DQTT-o-B), a high-performance n-type organic semiconductor, demonstrate two distinct thermally activated phase transitions following these mechanisms. Here we show reorientation of the alkyl side chains triggers cooperative behavior, tilting the molecules like dominos. Whereas, nucleation and growth transition is coincident with increasing alkyl chain disorder and driven by forming a biradical state. We establish alkyl chain engineering as integral to rationally controlling these polymorphic behaviors for novel electronic applications.
AB - Cooperativity is used by living systems to circumvent energetic and entropic barriers to yield highly efficient molecular processes. Cooperative structural transitions involve the concerted displacement of molecules in a crystalline material, as opposed to typical molecule-by-molecule nucleation and growth mechanisms which often break single crystallinity. Cooperative transitions have acquired much attention for low transition barriers, ultrafast kinetics, and structural reversibility. However, cooperative transitions are rare in molecular crystals and their origin is poorly understood. Crystals of 2-dimensional quinoidal terthiophene (2DQTT-o-B), a high-performance n-type organic semiconductor, demonstrate two distinct thermally activated phase transitions following these mechanisms. Here we show reorientation of the alkyl side chains triggers cooperative behavior, tilting the molecules like dominos. Whereas, nucleation and growth transition is coincident with increasing alkyl chain disorder and driven by forming a biradical state. We establish alkyl chain engineering as integral to rationally controlling these polymorphic behaviors for novel electronic applications.
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U2 - 10.1038/s41467-023-36871-9
DO - 10.1038/s41467-023-36871-9
M3 - Article
C2 - 36944642
AN - SCOPUS:85150671873
SN - 2041-1723
VL - 14
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 1304
ER -