Low-temperature Phase Transition Research Articles

Phonon Properties and Lattice Dynamics of Two- and Tri-Layered Lead Iodide Perovskites Comprising Butylammonium and Methylammonium Cations—Temperature-Dependent Raman Studies

Hybrid lead iodide perovskites are promising photovoltaic and light-emitting materials. Extant literature data on the key optoelectronic and luminescent properties of hybrid perovskites indicate that these properties are affected by electron–phonon coupling, the dynamics of the organic cations, and the degree of lattice distortion. We report temperature-dependent Raman studies of BA2MAPb2I7 and BA2MA2Pb3I10 (BA = butylammonium; MA = methylammonium), which undergo two structural phase transitions. Raman data obtained in broad temperature (360–80 K) and wavenumber (1800–10 cm−1) ranges show that ordering of BA+ cations triggers the higher temperature phase transition, whereas freezing of MA+ dynamics occurs below 200 K, leading to the onset of the low-temperature phase transition. This ordering is associated with significant deformation of the inorganic sublattice, as evidenced by changes observed in the lattice mode region. Our results show, therefore, that Raman spectroscopy is a very valuable tool for monitoring the separate dynamics of different organic cations in perovskites, comprising “perovskitizer” and interlayer cations.

Experimental assessment of the heat shielding performance by the integration of phase change material and liquid cooling plate

This research focuses on innovative stealth equipment by integrating a liquid cooling plate and phase change material (PCM), and the temperature rise on the cold surface and PCM melting rate is reported to illustrate the PCM thermal behavior in lifting the heat shielding performance. Results show that the integrated PCM system is effective in delaying the temperature rise within a certain time. A slower temperature rise on the cold surface is found at the first 1200 s, and a significant acceleration in the temperature rise is given within 1200 s ∼ 2000 s as the heat flood breaks through the PCM layer. The PCM melting rate increases rapidly and then rises slowly, and the complete melting time is shortened as increasing heat power. The heat shielding performance is significantly reduced with increasing the liquid flow rate, and the influence of the coolant temperature on the temperature rise becomes more and more prominent as the completion of the PCM melting process. A slower temperature rise is observed at the lower PCM phase transition temperature, and a further increase in the PCM covering layer has little influence on the temperature rise at the initial stage.

Phase transition-driven encapsulation of biomolecules using liquid metal with on-demand release for biomedical applications

Robust encapsulation and controllable release of biomolecules have wide biomedical applications ranging from biosensing, drug delivery to information storage. However, conventional biomolecule encapsulation strategies have limitations in complicated operations, optical instability, and difficulty in decapsulation. Here, we report a simple, robust, and solvent-free biomolecule encapsulation strategy based on gallium liquid metal featuring low-temperature phase transition, self-healing, high hermetic sealing, and intrinsic resistance to optical damage. We sandwiched the biomolecules with the solid gallium films followed by low-temperature welding of the films for direct sealing. The gallium can not only protect DNA and enzymes from various physical and chemical damages but also allow the on-demand release of biomolecules by applying vibration to break the liquid gallium. We demonstrated that a DNA-coded image file can be recovered with up to 99.9% sequence retention after an accelerated aging test. We also showed the practical applications of the controllable release of bioreagents in a one-pot RPA-CRISPR/Cas12a reaction for SARS-COV-2 screening with a low detection limit of 10 copies within 40 min. This work may facilitate the development of robust and stimuli-responsive biomolecule capsules by using low-melting metals for biotechnology.

Phase transformation inhibition and improved thermo-mechanical properties of rare earth niobates for thermal barrier coatings

Rare earth niobate Re3NbO7 (Re=Rare earth element) possesses ultra-low thermal conductivity for application as thermal barrier coatings (TBCs). However, Re3NbO7 with large rare earth ion radius (Re =La, Nd, Sm) exhibits both low temperature phase transition and poor facture toughness which is detrimental to the durability of the coatings. In this work, an effective method was proposed to solve those problems by doping. Considering the low-temperature phase transition at about 340K, La3NbO7 is selected as representative material. In order to suppress phase transition, Y3+ with relatively smaller ionic radius is used as a doped ion, and (La1-xYx)3NbO7 (x=0.0,0.1,0.3,0.5) were prepared and investigated. It is shown that, low temperature phase transition of La3NbO7 is effectively suppressed due to Y3+ doped. Facture toughness is increased significantly from 0.5 to 2.3 MPa.m1/2 with the increase of doping concentration. Furthermore, the Vickers hardness is also improved by doping. Considering the phase stability and ultra-low thermal conductivity, (La1-xYx)3NbO7 solid solution (x=0.5) maybe promising candidates for high temperature thermal insulation materials such as TBCs, thermoelectric materials, etc.

Synthesis and characterization of absorption-enhanced alumina solid particle materials for direct irradiation solar-thermal conversion

Based on solar-thermal application more than 1000 °C, a novel combination of sol-gel synthesis and stepwise calcination to prepare metal-ion doped alumina composite particles as heat transfer media were proposed, enhancing solar energy absorption and lowering preparation temperature. Investigations focused on the elemental distribution, phase composition, oxidation states, optical properties and thermal stability of the composites, which were doped with Cr, Co, Cu, Fe, and Mn metal ions in a 100:5 M ratio. The first-principles calculations elucidate the mechanism behind the impact of transition metal ions on alumina’s optical properties. Results show that introducing a small quantity of metal atoms results in new impurity energy levels and electron states around EF = 0. Specifically, the band gap energy of Cu- and Mn–Al2O3 decreases from 6.017 eV to 4.464 eV and 2.170 eV, respectively. Correspondingly, the absorptivity of these composite particles increases from around 20 %–76.6 %. And Tauc analysis indicates a decrease in the optical band gap of the particle materials from 5.37 eV to a range of 2.88–4.90 eV. Additionally, doping with Mn, Fe, and Cu accelerates the in-situ formation of α-Al2O3 crystals, with a phase transition temperature below 1000 °C and a crystallinity exceeding 93 %. Thermal stability tests show that the particles are highly stable, exhibiting a mere 0.49 % mass change between 30 °C and 1200 °C. The stepwise inert annealing strategy and metal-iron doping positively influence the optical performance of alumina, synthesizing long-term high-temperature stable alumina ceramic particles with absorptance enhancement and a low α-Al2O3 phase transition temperature. These attributes make a favorable choice for solar-thermal applications in direct irradiation.

Preparation of CMC-poly(N-isopropylacrylamide) semi-interpenetrating hydrogel with temperature-sensitivity for water retention

The CMC-PNIPAM hydrogel with semi-interpenetrating structure and temperature-sensitivity was prepared by in-situ polymerization of N-isopropylacrylamide (NIPAM) in sodium carboxymethylcellulose (CMC) solution at room temperature. The mass ratio of CMC to NIPAM was a key factor influencing the network structure and property of CMC-PNIPAM hydrogel. The low critical phase transition temperature (LCST) of CMC-PNIPAM hydrogels increased from 34.4 °C to 35.8 °C with the mass ratio of CMC to NIPAM rising from 0 to 1.2. The maximum compressive stress of CMC-PNIPAM hydrogel reached to 26.7 kPa and the relaxation elasticity was 52 % at strain of 60 %. The viscoelasticity of CMC-PNIPAM hydrogel was consistent with the generalized Maxwell model. The maximum swelling ratio in deionized water was 170.25 g·g−1 (dried hydrogel) with swelling rate of 2.57 g·g−1·min−1 at 25 °C. CMC-PNIPAM hydrogel hardly absorbed water above LCST, but the swollen hydrogel could release water at the rate of 0.36 g·g−1·min−1 once exceeding LCST. The test of water retention showed that soil mixed with 2 wt% dried CMC-PNIPAM hydrogel could retain 13.08 wt% water after 30 days at 25 °C that was 4.4 times than that of controlled soil without CMC-PNIPAM hydrogel. The semi-interpenetrating CMC-PNIPAM hydrogel showed a potential to conserve water responding to temperature.

Two‐Photon Direct Laser Writing of pNIPAM Actuators in Microchannels for Dynamic Microfluidics

Microfluidic tools enable to investigate and manipulate various chemical and biological processes at small scales. As a result, it finds widespread applications in lab‐on‐chip devices, drug delivery systems, or miniaturized cell cultures. However, microfluidic devices are still limited in their flexibility and are often designed to fulfill a single functionality. Moreover, technologies to introduce dynamic functionalities with high precision and at high resolution after the development of a continuous phase microfluidic chip remain scarce. Herein, two‐photon polymerization direct laser writing is introduced as a suitable approach to equip continuous phase microfluidic chips with structurally defined thermoresponsive poly(N‐isopropyl‐acrylamide) (pNIPAM) microactuators. Harnessing the lower critical phase transition temperature of pNIPAM, and upon controlling specific design parameters, the efficient catch and release of polystyrene beads of different sizes using a pNIPAM micropillar brush array is demonstrated. Moreover, a biocompatible pNIPAM microgripper array is designed to subsequently capture and release differently sized (single) cell populations. Overall, the method offers great flexibility and a high degree of freedom toward the fabrication of dynamic microfluidic devices with great adaptability to experimental conditions in real time.

Facile and dynamic infrared modulation of durable VO2/CuI films for smart window applications

Vanadium dioxide (VO2) has been widely investigated as a smart window material due to its excellent thermochromic properties. However, with the increasing abundance of studies on VO2-based structures, its low solar modulation capability, environmental durability and high phase transition temperature have limited its commercial applications. Finding a simple way to solve the above problems simultaneously remains challenging. Here, we propose a bilayer structure combining VO2 and a transparent conductive material, copper iodide (CuI), for functional integration of thermochromic smart windows. The CuI layer is used as an anti-reflective layer and a protective layer to ensure high solar modulation capability (ΔTsol=15.41 %) and good expected service life (ESL=27 years), while realizing the dynamic modulation of infrared spectra at room temperature by Joule heating. This facile structure with overall performance offers a new possibility for the commercialization of VO2-based smart windows and room temperature dynamic modulation of infrared devices.

Low-temperature and high-pressure phase transitions of ionic liquid 1-decyl-3-methylimidazolium bromide

The phase behavior of an ionic liquid (IL) was investigated at low temperature (LT) and high pressure (HP). The utilized IL was 1-decyl-3-methylimidazolium bromide ([C10mim][Br]), whose cation possesses a long alkyl side-chain. The LT- and HP-crystal polymorphs of [C10mim][Br] were observed conducting small- and wide-angle X-ray scattering (SWAXS) experiments. Upon cooling, a liquid crystal was formed, which subsequently transformed into crystalline species with the modulated layered structure possessing the double Bragg reflection. In addition to the layered structure, the hybrid layered structure coexisted upon heating. At HP, 00ℓ Bragg reflections representing the layered structure were not observed in SWAXS patterns. The HP-crystal phase of [C10mim][Br] was characterized by double Bragg reflection in the low scattering wavevector region. The non-layered HP-crystal caused the large bulk modulus.

Structural transition, orientational order, and anomalous specific heat in a two-dimensional dimer crystal of core-softened particles.

Systems featuring hard-core-soft-shell repulsive pair potentials can form ordered phases, where particles organize themselves in aggregates with nontrivial geometries. The dimer crystal formed by one such potential, namely, the hard-core plus generalized exponential model of order 4, has been recently investigated, revealing a low-temperature structural phase transition, with the onset of nematic ordering of the dimers. In the present work, we aim to characterize this phase transition via a mean-field theory, by which a detailed analysis of the low-temperature properties of the system is carried out under quadrupole approximation. We determine the transition temperature and identify its order parameter, highlighting the link between the structural transition and the nematic ordering of the system. The first-order character of the transition is established and supported by the Landau expansion of the free energy in powers of the order parameter. The theory is subsequently generalized to take into account lattice vibrations and dimer length fluctuations. Finally, we provide an explanation for the anomalous behavior displayed by the specific heat in the vanishing-temperature limit, which is also supported by Monte Carlo simulations.

Structural changes in Rochelle salt on phase transitions revisited in a multi-temperature single-crystal X-ray diffraction study.

Phase transitions in Rochelle salt [sodium potassium L(+)-tartrate tetrahydrate] are revisited in a single-crystal X-ray diffraction multi-temperature study on cooling from 308 to 100 K across the high-temperature paraelectric (PE) ↔ ferroelectric ↔ low-temperature PE phase transition points. The results of structure refinement using three different models (a harmonic with and without disorder, and an anharmonic) were compared. The temperature dependencies of anisotropic displacement parameters (ADPs) and Ueq, which can be calculated directly from ADPs, for the low-temperature PE phase indicate clearly the dynamic nature of disorder of the K1 atoms. The structures of the low-temperature and the high-temperature PE phases are compared for the first time at multiple temperatures for each phase based on diffraction data collected from the same single crystal. The data indicate that the high-temperature and the low-temperature paraelectric phases are probably not two different phases, as was assumed in earlier works, but are structurally the same phase at different temperatures.

An approach for obtaining thermochromic smart windows with excellent performance and low phase transition temperature based on VO2/tungsten-doped VO2/VO2 composite structure

Tungsten-doped vanadium dioxide (W-VO2) has a low phase transition temperature (Tc), but the poor thermochromic properties hinders its application in the field of smart windows. In this work, we proposed and fabricated VO2(x nm)/W-VO2(x nm)/VO2(x nm) composite films with different thickness (x = 10, 12, 15 and 20) on quartz glass substrate by pulsed laser deposition. The bottom VO2 layer was served as buffer layer to improve the crystallinity of W-VO2 layer, while the top VO2 layer was to strengthen the thermochromic properties of the composite films. With the increase of x from 10 to 20, XRD and SEM results suggested that the crystallinity and grain morphology of the obtained composite films can be largely regulated. In particular, when x = 12, the luminous transmittance (Tlum) and solar modulation ability (ΔTsol) are as high as 61.1 % and 8.0 %, respectively, while maintaining a low Tc of 45.9 °C. Through in-situ annealing treatment, the Tlum and ΔTsol of VO2(12 nm)/W-VO2(12 nm)/VO2(12 nm) further significantly enhanced to 79.3 % and 9.1 %, and Tc also reduced slightly to 41.4 °C. SEM characterization suggested that the improved optical properties can be attributed to the Localized Surface Plasmon Resonance (LSPR) effect of the spherically structured W-VO2 nanoparticles. The results in this study confirmed that the thermochromic properties of W-VO2 could be optimized by controlling its grain morphology, which provided a new strategy for the application of W-VO2 films in the field of smart windows.

Regulating Crystallinity Mismatch Between Donor and Acceptor to Improve Exciton/Charge Transport in Efficient Organic Solar Cells.

Achieving a more balanced charge transport by morphological control is crucial in reducing bimolecular and trap-assisted recombination and enhancing the critical parameters for efficient organic solar cells (OSCs). Hence, a facile strategy is proposed to reduce the crystallinity difference between donor and acceptor by incorporating a novel multifunctional liquid crystal small molecule (LCSM) BDTPF4-C6 into the binary blend. BDTPF4-C6 is the first LCSM based on a tetrafluorobenzene unit and features a low liquid crystal phase transition temperature and strong self-assembly ability, conducive to regulating the active layer morphology. When BDTPF4-C6 is introduced as a guest molecule into the PM6 : Y6 binary, it exhibits better compatibility with the donor PM6 and primarily resides within the PM6 phase because of the similarity-intermiscibility principle. Moreover, systematic studies revealed that BDTPF4-C6 could be used as a seeding agent for PM6 to enhance its crystallinity, thereby forming a more balanced and favourable charge transport with suppressed charge recombination. Intriguingly, dual Förster resonance energy transfer was observed between the guest molecule and the host donor and acceptor, resulting in an improved current density. This study demonstrates a facile approach to balance the charge mobilities and offers new insights into boosting the efficiency of single-junction OSCs beyond 20 %.

Regulating Crystallinity Mismatch Between Donor and Acceptor to Improve Exciton/Charge Transport in Efficient Organic Solar Cells

AbstractAchieving a more balanced charge transport by morphological control is crucial in reducing bimolecular and trap‐assisted recombination and enhancing the critical parameters for efficient organic solar cells (OSCs). Hence, a facile strategy is proposed to reduce the crystallinity difference between donor and acceptor by incorporating a novel multifunctional liquid crystal small molecule (LCSM) BDTPF4‐C6 into the binary blend. BDTPF4‐C6 is the first LCSM based on a tetrafluorobenzene unit and features a low liquid crystal phase transition temperature and strong self‐assembly ability, conducive to regulating the active layer morphology. When BDTPF4‐C6 is introduced as a guest molecule into the PM6 : Y6 binary, it exhibits better compatibility with the donor PM6 and primarily resides within the PM6 phase because of the similarity‐intermiscibility principle. Moreover, systematic studies revealed that BDTPF4‐C6 could be used as a seeding agent for PM6 to enhance its crystallinity, thereby forming a more balanced and favourable charge transport with suppressed charge recombination. Intriguingly, dual Förster resonance energy transfer was observed between the guest molecule and the host donor and acceptor, resulting in an improved current density. This study demonstrates a facile approach to balance the charge mobilities and offers new insights into boosting the efficiency of single‐junction OSCs beyond 20 %.

Polymorphism and Red Photoluminescence Emission from 5s2 Electron Pairs of Sb(III) in a New One-Dimensional Organic-Inorganic Hybrid Based on Methylhydrazine: MHy2SbI5.

We explore the crystal structure and luminescent properties of a new 1D organic-inorganic hybrid, MHy2SbI5, based on methylhydrazine. The compound reveals the red photoluminescence (PL) originating from the 5s2 electron pairs of Sb(III) as well as complex structural behavior. MHy2SbI5 crystalizes in two polymorphic forms (I and II) with distinct thermal properties and structural characteristics. Polymorph I adopts the acentric P212121 chiral space group confirmed by SHG, and, despite a thermally activated disorder of MHy, does not show any phase transitions, while polymorph II undergoes reversible low-temperature phase transition and high-temperature reconstructive transformation to polymorph I. The crystal structures of both forms consist of 1D perovskite zig-zag chains of corner-sharing SbI6 octahedra. The intriguing phase transition behavior of II is associated with the unstable arrangement of the [SbI5]2-∞ chains in the structure. The energy band gap (Eg) values, estimated based on the UV-Vis absorption spectra, indicate that both polymorphs have band gaps, with Eg values of 2.01 eV for polymorph I and 2.12 eV for polymorph II.

CUTE: A Cryogenic Underground TEst facility at SNOLAB

Low-temperature cryogenics open the door for a range of interesting technologies based on features like superconductivity and superfluidity, low-temperature phase transitions or the low heat capacity of non-metals in the milli-Kelvin range. Devices based on these technologies are often sensitive to small energy depositions as can be caused by environmental radiation. The Cryogenic Underground TEst facility (CUTE) at SNOLAB is a platform for testing and operating cryogenic devices in an environment with low levels of background. The large experimental chamber (O(10) L) reaches a base temperature of ∼ 12 mK; it can hold a payload of up to ∼ 20 kg and provides a radiogenic background event rate as low as a few events/kg/keV/day in the energy range below about 100 keV, as well as a negligible muon rate (O1)/month). CUTE was designed and built in the context of the Super Cryogenic Dark Matter Search experiment (SuperCDMS) that uses cryogenic detectors to search for interactions of dark matter particles with ordinary matter. The facility has been used to test SuperCDMS detectors since its commissioning in 2019. In 2021, it was handed over to SNOLAB to become a SNOLAB user facility after the completion of the testing of detectors for SuperCDMS. The facility will be available for projects that benefit from these special conditions, based on proposals assessed for their scientific and technological merits. This article describes the main design features and operating parameters of CUTE.

Phase transitions, baro- and piezocaloric effects in single crystal and ceramics of ferroelectric NH4HSeO4

A study of heat capacity, thermal dilatation and sensitivity to hydrostatic and uniaxial pressure was carried out on single-crystal and ceramic samples of NH4HSeO4. The main parameters of low-temperature successive phase transitions B2 (T1) ↔ incommensurate IC (T2) ↔ ferroelectric P1 (T3) ↔ non-ferroelectric did not depend on the type of samples. The behavior of the volumetric strain and the results of direct measurements of T3(p) contributed to the resolution of the longstanding problem associated with the ambiguity of the sign of the corresponding volumetric baric coefficient. The role of thermal expansion anisotropy in the formation of the piezocaloric effect (PCE) near the ferroelectric phase transition at T3 has been studied. Due to the strong difference in the linear baric coefficients, the main contribution to the barocaloric effect (BCE) comes from the inverse intensive and extensive PCE associated with the a-axis. Compared to a single crystal, ceramics demonstrate lower BCE values, which, however, exist in a wider temperature range, which leads to close values of integral caloric parameters. The strong decrease in both BCE and PCE at low-temperature transformations in NH4HSeO4 compared to the ferroelectrics NH4HSO4 and NH4NH4SO4 is associated with a small change in entropy during three low-temperature phase transitions, ΣΔSi = 2.52 J/mol∙K, which is a consequence of a high degree of structural ordering in selenate as a result of a high-temperature transformation at T0 between the superionic and B2 phases, accompanied by a giant change in entropy, ΔS0≈Rln21.

Organic ferroelastic enantiomers with high Tc and large dielectric switching ratio triggered by order-disorder and displacive phase transition

Molecular-based ferroelastics with dielectric switching properties are highly desirable for their applications on microelectronic dielectric switches, sensors, data storage, and so on. However, the current reports mostly focus on organic-inorganic hybrids containing toxic heavy metal atoms, and the relatively low phase transition temperature limits their application. In this paper, low-toxic organic salt ferroelastic enantiomers (R/S)-4-fluoro-1-azabicyclo[3.2.1]octonium chloride [(R/S)-F-321] were designed and synthesized under the introducing chirality strategy. They undergo a 432F422-type ferroelastic phase transition with a high Curie temperature (Tc) of 470 K, simultaneously exhibiting excellent dielectric switching characteristics. In addition to the ordered-disordered movement of cations, the significant displacement of anions is also responsible for such high Tc and large dielectric switching ratios, which is very rare in molecular-based switching materials. This work enriches the development of molecular ferroelastic switching materials and gives inspiration for the exploration of environmentally friendly high Tc organic salt ferroelastics with prominent switching performances.

Revisiting a (001)-oriented layered lead chloride templated by 1,2,4-triazolium: structural phase transitions, lattice dynamics and broadband photoluminescence.

This study revisits a (001)-oriented layered lead chloride templated by 1,2,4-triazolium, Tz2PbCl4, which recently has been an object of intense research but still suffers from gaps in characterization. Indeed, the divergent reports on the crystal structures of Tz2PbCl4 at various temperatures, devoid of independent verification of chiral phases through second harmonic generation (SHG), have led to an unresolved debate regarding the existence of a low-temperature phase transition (PT) and the noncentrosymmetric nature of the low-temperature phase. Now, by combining differential scanning calorimetry, single-crystal X-ray diffraction, dielectric, as well as linear and nonlinear optical spectroscopies on Tz2PbCl4, we reveal a sequence of reversible PTs at T1 = 361 K (phase I-II), T2 = 339 K (phase II-III), and T3 = 280 K (phase III-IV). No SHG activity could be registered for any of the four crystal phases, as checked by wide-temperature range SHG screening, supporting their centrosymmetry. The dipole relaxation processes indicate a decrease in activation energy with increasing temperature, from 0.60, 0.38, to 0.24 eV observed for phase IV (space group P21/c), phase III (Pnma), and phase II (Cmcm), respectively. This change is interpreted as a result of the diminishing strength of H-bonds as the system transforms from phase IV to III and subsequently to II. The weaker H-bonds facilitate the reorientation of Tz+ cations in the presence of an external electric field. The photoluminescence spectra of Tz2PbCl4 reveal an intriguing interplay of narrow and broadband emission, linked respectively to free excitons and excitons trapped on defects. Notably, as the temperature decreases from 300 K to 16 K, both the emission bands exhibit distinctive blue and red shifts, indicative of increased in-plane octahedral distortion. This dynamic behaviour transforms the photoluminescence of Tz2PbCl4 from greenish-blue at 300 K to yellowish-green at 13 K, enriching our understanding of 2D lead halide perovskites and highlighting the optoelectronic potential of Tz2PbCl4.

Stabilization Effect of Potato Starch on Characteristic Flavor Compounds in Onion Sauce

AbstractThe food industry is experiencing a substantial demand for transitioning to natural flavors. Nonetheless, the challenge lies in the inherent instability of most flavor molecules when removed from their original sources. Three representative flavor compounds, including dipropyl disulfide (DD), allyl mercaptan (AM), and dimethyl trisulfide (DT), are selected to form composites with potato starch (PS) to protect them from decomposition or transformation. Then, their physicochemical properties and microstructures are investigated using combined methods. PS can combine with these sulfides mainly through its amylose, and thioethers are more likely to interact with PS than mercaptan. All the composites have lower phase transition temperature and higher enthalpy values than PS, and PS‐AM exhibits the largest stability followed by PS‐DD and PS‐DT. The sulfides interact with PS by entering into the helical cavity of its amylose mainly through hydrophobic interaction and increase the long‐range ordered degree and short‐range ordered degree of the composites. DD, AM, and DT can form V‐type inclusion composites with PS, which reserves more DD and AM to delay flavor degradation and enhances the flavor stability of onion sauce. This study can provide valuable reference for the preservation of characteristic flavors of allium food products during thermal processing and storage.