Deciphering helix assembly in the heliconical nematic phase via tender resonant X-ray scattering

被引:20
作者
Cao, Yu [1 ,2 ]
Feng, Jun [2 ]
Nallapaneni, Asritha [2 ,3 ]
Arakawa, Yuki [4 ]
Zhao, Keqing [5 ]
Zhang, Huijun [1 ]
Mehl, Georg H. [1 ,6 ]
Zhu, Chenhui [2 ]
Liu, Feng [1 ]
机构
[1] Xi An Jiao Tong Univ, Shaanxi Int Res Ctr Soft Matter, Sch Mat Sci & Engn, State Key Lab Mech Behav Mat, Xian 710049, Peoples R China
[2] Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
[3] Univ Akron, Dept Polymer Engn, Akron, OH 44325 USA
[4] Toyohashi Univ Technol, Dept Appl Chem & Life Sci, Grad Sch Engn, Toyohashi, Aichi 4418580, Japan
[5] Sichuan Normal Univ, Coll Chem, Chengdu 610016, Peoples R China
[6] Univ Hull, Dept Chem, Kingston Upon Hull HU6 7RX, N Humberside, England
基金
中国国家自然科学基金;
关键词
LIQUID-CRYSTAL DIMERS; ORIENTATIONAL ORDER; NANOSCALE-PITCH; CHIRALITY; ANGLE;
D O I
10.1039/d1tc02027g
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Being a link between a uniaxial nematic and a chiral nematic, the twist bend nematic (N-TB) has been an intriguing topic for research over the last decade as a key to understanding chirality generation. Accurate description and understanding of resonance effects in helical structures provide crucial knowledge on the phase behavior beyond positional ordering. We examined the manifestation of resonance effects in N(TB)via tender resonant X-ray scattering (TReXS) at the sulfur K-edge. For the first time we demonstrate quantitatively that the energy dependence of the scattering peak in the N-TB phase follows the energy dependence of the complex refractive indices measured by X-ray absorption. Taking advantage of molecular energy calculation, we decipher the distinct helical pitch variation trend for symmetric/asymmetric dimers from the perspective of hybridization and reveal the strong effect of substituting oxygen for sulfur atoms on the helical pitch and the thermal helix extension.
引用
收藏
页码:10020 / 10028
页数:9
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