ترغب بنشر مسار تعليمي؟ اضغط هنا

Order-disorder transition and alignment dynamics of a block copolymer under high magnetic fields by in situ x-ray scattering

75   0   0.0 ( 0 )
 نشر من قبل Chinedum Osuji
 تاريخ النشر 2012
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

We present results of temperature resolved scattering studies of a liquid crystalline block copolymer undergoing an order-disorder transition (ODT) in the presence of magnetic fields and time-resolved measurements during isothermal field annealing at sub-ODT temperatures. In each case, field interactions produced strongly textured mesophases with the cylindrical microdomains aligned parallel to the field. We find there is no measurable field-induced shift in the ODT temperature ($T_{ODT}$) which suggests that selective melting does not play a role in mesophase alignment during isothermal experiments. Our data indicate instead that sub-ODT alignment occurs by slow, large scale grain rotation whereas alignment during cooling from the disordered melt is rapid and driven by the nucleation of weakly ordered but preferentially aligned material. We identify an optimum sub-cooling that maximizes alignment during isothermal field annealing. This is corroborated by a simple model incorporating the competing effects of an exponentially decreasing mobility and divergent, increasing magnetic anisotropy on cooling below $T_{ODT}$. The absence of measurable field-effects on $T_{ODT}$ is consistent with rough estimates derived from the relative magnitudes of the free energy due to field interaction and the enthalpy of the isotropic-LC transition.

قيم البحث

اقرأ أيضاً

Rare earth (R) half-Heusler compounds, RBiPt, exhibit a wide spectrum of novel ground states. Recently, GdBiPt has been proposed as a potential antiferromagnetic topological insulator (AFTI). We have employed x-ray resonant magnetic scattering to elu cidate the microscopic details of the magnetic structure in GdBiPt below T_N = 8.5 K. Experiments at the Gd L_2 absorption edge show that the Gd moments order in an antiferromagnetic stacking along the cubic diagonal [1 1 1] direction satisfying the requirement for an AFTI, where both time-reversal symmetry and lattice translational symmetry are broken, but their product is conserved.
We elucidate the roles of the isotropic-nematic (I-N) and nematic-smectic A (N-SmA) transitions in magnetic field directed self-assembly of a liquid crystalline block copolymer (BCP), using textit{in situ} x-ray scattering. Cooling into the nematic f rom the disordered melt yields poorly ordered and weakly aligned BCP microdomains. Continued cooling into the SmA however results in an abrupt increase in BCP orientational order with microdomain alignment tightly coupled to the translational order parameter of the smectic layers. These results underscore the significance of the N-SmA transition in generating highly aligned states under magnetic fields in these hierarchically ordered materials.
Using dissipative particle dynamics (DPD) simulation method, we study the phase separation dynamics in block copolymer (BCP) melt in $d=3$, subjected to external stimuli such as light. An initial homogeneous BCP melt is rapidly quenched to a temperat ure $T < T_c$, where $T_c$ is the critical temperature. We then let the system go through alternate light on and off cycles. An on-cycle breaks the stimuli-sensitive bonds connecting both the blocks A and B in BCP melt, and during the off-cycle, broken bonds reconnect. By simulating the effect of light, we isolate scenarios where phase separation begins with the light off (set 1); the cooperative interactions within the system allow it to undergo microphase separation. When the phase separation starts with the light on (set 2), the system undergoes macrophase separation due to the bond breaking. Here, we report the role of alternate cycles on domain morphology by varying bond-breaking probability for both the sets 1 and 2, respectively. We observe that the scaling functions depend upon the conditions mentioned above that change the time scale of the evolving morphologies in various cycles. However, in all the cases, the average domain size respects the power-law growth: $R(t)sim t^{phi}$ at late times, here $phi$ is the dynamic growth exponent. After a short-lived diffusive growth ($phi sim 1/3$) at early times, $phi$ illustrates a crossover from the viscous hydrodynamic ($phi sim 1$) to the inertial hydrodynamic ($phi sim 2/3$) regimes at late times.
122 - Franco Ferrari 2016
An extensive study of single block copolymer knots containing two kinds of monomers $A$ and $B$ is presented. The knots are in a solution and their monomers are subjected to short range interactions that can be attractive or repulsive. In view of pos sible applications in medicine and the construction of intelligent materials, it is shown that several features of copolymer knots can be tuned by changing the monomer configuration. A very fast and abrupt swelling with increasing temperature is obtained in certain multiblock copolymers, while the size and the swelling behavior at high temperatures may be controlled in diblock copolymers. Interesting new effects appear in the thermal diagrams of copolymer knots when their length is increased.
Resonant x-ray scattering (RXS) experiment has been performed for the (3 0 1.5) superlattice reflection in the antiferroquadrupolar and antiferromagnetic phase of DyB2C2. Azimuthal-angle dependence of the resonance enhanced intensities for both dipol ar (E1) and quadrupolar (E2) resonant processes has been measured precisely with polarization analysis. Every scattering channel exhibits distinctive azimuthal dependence, differently from the symmetric reflection at (0 0 0.5) which was studied previously. We have analyzed the results using a theory developed by Lovesey et al., which directly connects atomic tensors with the cross-section of RXS. The fitting results indicate that the azimuthal dependences can be explained well by the atomic tensors up to rank 2. Rank 3 and rank 4 tensors are reflected in the data very little. In addition, The coupling scheme among the 4f quadrupolar moment, 5d ortitals, and the lattice has been determined from the interference among the Thomson scattering from the lattice distortion and the resonant scatterings of E1 and E2 processes. It has also been established from the RXS of the (3 0 1.5) reflection that the canting of the 4f quadrupolar moments exists up to T_Q. We also discuss a possible wavefunction of the ground state from the point-charge model calculation.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا