arXiv subjects

Chenhui Zhu

Publications and source records attributed to Chenhui Zhu.

30 records · Page 2Linked to original sources

arXiv2022

Traps and transport resistance: the next frontier for stable state-of-the-art non-fullerene acceptor solar cells

Stability is one of the most important challenges facing organic solar cells (OSC) on their path to commercialization. In the high-performance material system PM6:Y6 studied here, investigate degradation mechanisms of inverted photovoltaic devices. We have identified two distinct degradation pathways: one requires presence of both illumination and oxygen and features a short-circuit current reduction, the other one is induced thermally and marked by severe losses of open-circuit voltage and fill factor. We focus our investigation on the thermally accelerated degradation. Our findings show that bulk material properties and interfaces remain remarkably stable, however, aging-induced defect state formation in the active layer remains the primary cause of thermal degradation. The increased trap density leads to higher non-radiative recombination, which limits open-circuit voltage and lowers charge carrier mobility in the photoactive layer. Furthermore, we find the trap-induced transport resistance to be the major reason for the drop in fill factor. Our results suggest that device lifetimes could be significantly increased by marginally suppressing trap formation, leading to a bright future for OSC.

cond-mat.mtrl-sci↗

arXiv2021

Antiferroelectric Smectic Ordering as a Prelude to the Ferroelectric Nematic:Introducing the Smectic $Z_A$ Phase

We have structurally characterized the liquid crystal phase that appears as an intermediate state when a dielectric nematic, having polar disorder of its molecular dipoles, transitions to the almost perfectly polar-ordered ferroelectric nematic. This intermediate phase, which fills a 100-year-old void in the taxonomy of smectics and which we term the "smectic $Z_A$", is antiferroelectric, with the nematic director and polarization oriented parallel to smectic layer planes, and the polarization alternating in sign from layer to layer. The period of this polarization wave ($\sim$180 A) is mesoscopic, corresponding to $\sim$40 molecules side-by-side, indicating that this lamellar structure is collectively stabilized. A Landau free energy, originally formulated to model incommensurate antiferroelectricity in crystals, describes the key features of the nematic-Sm$Z_A$-ferroelectric nematic phase sequence.

cond-mat.soft↗

arXiv2020

The interplay between spatial and heliconical bond order in twist-bend nematic materials

The nanostructure of two novel sulfur containing dimer materials has been investigated experimentally by hard and by resonant tender X-ray scattering techniques. On cooling the dimers through the nematic to twist-bend nematic (N-NTB) phase transition, the correlation length associated with short-range positional order drops, while the heliconical orientational order becomes more correlated. The heliconical pitch shows a stronger temperature dependence near the N-NTB transition than observed in previously studied dimers, such as the CBnCB series of compounds. We explain both this strong variation and the dependence of the heliconical pitch on the length of the spacer connecting the monomer units by taking into account a temperature dependent molecular bend and intermolecular overlap. and. The heliconical structure is observed even in the upper 3-4°C range of the smectic phase that forms just below the NTB state. The coexistence of smectic layering and the heliconical order indicates a SmCTB -type phase where the rigid units of the dimers are tilted with respect to the layer normal in order to accommodate the bent conformation of the dimers, but the tilt direction rotates along the heliconical axis. This is potentially similar to the SmCTB phase reported by Abberley et al (Nat. Commun. 2018, 9, 228) below a SmA phase.

cond-mat.soft↗

arXiv2020

Identification of New Assembly Mode in the Heliconical Nematic Phase via Tender Resonant X-ray Scattering

Helical structures are exciting and are utilized in numerous applications ranging from biotechnology to displays to medicine. Accurate description and understanding of resonance effects in helical structures provides crucial knowledge on molecular packing beyond positional ordering. We exam-ined the manifestation of resonance effects in a nematic phase with heliconical structure, the so called twist bend nematic (NTB) via tender resonant X-ray scattering (TReXS) at the sulfur K-edge. We demonstrate for the first time quantitatively that the energy dependence of the scattering peak in the NTB phase follows the energy dependence of the complex refractive indices measured by X-ray absorption. This allows us to identify a new self-assembly mode for specific sets of liquid crystal dimers in the NTB phase. We anticipate that new avenues in the exploration of complex orientational structures both in static as well as in dynamic modes induced by external stimuli will be pursued.

cond-mat.soft↗

arXiv2019

Multi-level Chirality in Liquid Crystals Formed by Achiral Molecules

In many biological materials with a hierarchical structure there is an intriguing and unique mechanism responsible for the 'propagation' of order from the molecular to the nano- or micro-scale level. Here we present a much simpler molecular system built of achiral mesogenic dimeric molecules that shows a similar complexity with four levels of structural chirality (i) layer chirality, (ii) helicity of a basic 4-layer repeating unit, (iii) a helix with a pitch of several layers and (iv) mesoscopic helical filaments. As seen in many biological systems, there is a coupling between chirality at different levels. The structures were identified by a combination of hard and soft x-ray diffraction measurements, optical studies and theoretical modelling.

cond-mat.soft↗

arXiv2018

Distinct differences in the nanoscale behaviors of the twist-bend liquid crystal phase of a flexible linear trimer and homologous dimer

We synthesized the liquid crystal dimer and trimer members of a series of flexible linear oligomers and characterized their microscopic and nanoscopic properties using resonant soft x-ray scattering and a number of other experimental techniques. On the microscopic scale, the twist-bend phases of the dimer and trimer appear essentially identical. However, while the liquid crystal dimer exhibits a temperature-dependent variation of its twist-bend helical pitch varying from 100 - 170 Å on heating, the trimer exhibits an essentially temperature-independent pitch of 66 Å, significantly shorter than those reported for other twist-bend forming materials in the literature. We attribute this to a specific combination of intrinsic conformational bend of the trimer molecules and a sterically favorable intercalation of the trimers over a commensurate fraction (two-thirds) of the molecular length. We develop a geometric model of the twist-bend phase for these materials with the molecules arranging into helical chain structures, and we fully determine their respective geometric parameters.

cond-mat.soft↗

arXiv2017

Heliconical smectic phases formed by achiral molecules

A series of asymmetric dimers with an odd number of atoms in the spacer were found to form different types of twisted structures despite being achiral. The formation of a variety of helical structures is accompanied by a gradual freezing of molecular rotation. The tight pitch heliconical nematic (NTB) phase and heliconical tilted smectic C (SmCTB) phase are formed. In the lowest temperature smectic phase, HexI, the twist is expressed through the formation of hierarchical structure: nano-scale helices and mesoscopic helical filaments. The short pitch helical structure in smectic phases is confirmed by resonant x-ray measurements.

cond-mat.soft↗

arXiv2017

Structure of nanoscale-pitch helical phases: blue phase and twist-bend nematic phase resolved by resonant soft X-ray scattering

Periodic structures of phases with orientational order of molecules, but homogenous electron density distribution: a short pitch cholesteric, blue phase and twist-bend nematic phase, were probed by a resonant soft x-ray scattering (RSoXS) at the carbon K-edge. The theoretical model shows that in case of a simple heliconical nematic structure two resonant signals corresponding to the full and half pitch band should be present, while only the full pitch band is observed in experiment. This suggests that the twist-bend nematic phase has complex structure with a double-helix, built of two interlocked, shifted helices. We confirm that the helical pitch in the twist-bend nematic phase is in a 10 nm range, for both, the chiral and achiral materials. We also show that the symmetry of a blue phase can unambiguously be determined through a resonant enhancement of x-ray diffraction signals, by including polarization effects, which are found to be an important indicator in phase structure determination.

cond-mat.soft↗

arXiv2017

Double-Helical Tiled Chain Structure of the Twist-Bend Liquid Crystal phase in CB7CB

The twist-bend nematic liquid crystal phase is a three-dimensional fluid in which achiral bent molecules spontaneously form an orientationally ordered macroscopically chiral heliconical winding of molecular scale pitch, in absence of positional ordering. Here we characterize the structure of the ground state of the twist-bend phase of the bent dimer CB7CB and its mixtures with 5CB over a wide range of concentrations and temperatures, showing that the contour length along the molecular direction for a single turn of the helix is approximately equal to 2πRmol, where Rmol is the radius of bend curvature of a single all-trans CB7CB molecule. This relation emerges from a model which simply relates the macroscopic characteristics of the helical structure, which is mostly biaxial twist and has little bend, to the bent molecular shape. This connection comes about through the presence in the fluid of self-assembled oligomer-like correlations of interlocking molecules, arising from the nanosegregation of rigid and flexible molecular subcomponents, forming a brickwork tiling of pairs of molecular strands into a duplex double-helical chain.

cond-mat.soft↗

arXiv2016

Interaction of Molecular Oxygen with Hexagonally Reconstructed Au (001) Surface

Kinetics of molecular oxygen / Au (001) surface interaction has been studied at high temperature and near atmospheric pressures of O2 gas with in situ x-ray scattering measurements. We find that the hexagonal reconstruction (hex) of Au (001) surface lifts to (1x1) in the presence of O2 gas, indicating that the (1x1) is more favored when some oxygen atoms present on the surface. The measured lifting rate constant vs. temperature is found to be highest at intermediate temperature exhibiting a 'volcano'-type behavior. At low temperature, the hex-to-(1x1) activation barrier (Eact = 1.3(3) eV) limits the lifting. At high temperature, oxygen adsorption energy (Eads = 1.6(2) eV) limits the lifting. The (1x1)-to-hex activation barrier (Ehex = 0.41(14) eV) is also obtained from hex recovery kinetics. The pressure-temperature (PT) surface phase diagram obtained in this study shows three regions: hex at low P and T, (1x1) at high P and T, and coexistence of the hex and (1x1) at the intermediate P and T.

cond-mat.mtrl-sci↗

arXiv2016

Spontaneous Liquid Crystal and Ferromagnetic Ordering of Colloidal Magnetic Nanoplates

Ferrofluids are familiar as colloidal suspensions of ferromagnetic nanoparticles in aqueous or organic solvents. The dispersed particles are randomly oriented but their moments become aligned if a magnetic field is applied, producing a variety of exotic and useful magneto-mechanical effects. A longstanding interest and challenge has been to make such suspensions macroscopically ferromagnetic, that is having uniform magnetic alignment in absence of a field. Here we report a fluid suspension of magnetic nanoplates which spontaneously aligns into an equilibrium nematic liquid crystal phase that is also macroscopically ferromagnetic. Its zero-field magnetization produces distinctive magnetic self-interaction effects, including liquid crystal textures of fluid block domains arranged in closed flux loops, and makes this phase highly sensitive, with it dramatically changing shape even in the Earth's magnetic field.

cond-mat.soft↗

arXiv2016

Resonant carbon K-edge soft x-ray scattering from lattice-free heliconical molecular ordering: soft dilative elasticity of the twist-bend liquid crystal phase

Resonant x-ray scattering shows that the bulk structure of the twist-bend liquid crystal phase, recently discovered in bent molecular dimers, has spatial periodicity without electron density modulation, indicating a lattice-free heliconical nematic precession of orientation that has helical glide symmetry. In situ study of the bulk helix texture for the dimer CB7CB shows an elastically-confined temperature-dependent minimum helix pitch, but a remarkable elastic softness of pitch in response to dilative stresses. Scattering from the helix is not detectable in the higher temperature nematic phase.

cond-mat.soft↗