Dielectric Research Articles

Effect of hydrogen on the integration process of photosensitive polyimide and its feasibility in advanced packaging

To reduce the resistive-capacitive (RC) delay, low-k materials are employed in advanced packaging systems that cover the redistribution layers (RDL). Owing to its remarkable properties, photosensitive polyimide (PSPI) is one of the most widely used interlayer dielectric (ILD) materials. Industries usually employ the forming gas annealing (FGA) (5 % H2 / 95 % N2 at 350 °C) in processes which help to reduce the dangling bonds at interfaces of Si/SiO2. Considering this, we have studied the effect of FGA onto photopatterned PSPI films and compared it with nitrogen gas annealing. The imidization in films at different ambientes is confirmed by Fourier Transform Infrared Spectroscopy (FTIR). X-ray photoelectron spectroscopy (XPS), and Elemental Dispersive Spectroscopy (EDS) implied to study the compositional change in PSPI after different ambient annealing. Our study reveals that FGA causes more imidization, but it forms impurities in PSPI leading to reduction in its mechanical strength and causes carbon from PSPI to diffuse inside copper interconnects. We hope the proposed research will help to understand the adverse effect of FGA annealing on the PSPI. Interestingly, N2 gas annealing is more feasible for PSPI than that of FGA 350 °C.

Theoretical investigation of the optical and plasmonic properties of the nanocomposite media composed of silver nanoparticles embedded in rubidium

This theoretical study investigates, the optical response of a metal-dielectric nanocomposite of silver and rubidium (Ag/Rb) is theoretically studied via Maxwell-Garnett Model by varying the size, shape and volume ratio of the silver nanoparticles (AgNPs) in the coherently driven four levels rubidium dielectric atomic media. The rubidium being an alkali metal behaves as dielectric under quantum coherence effect. It was found that the optical response of this nanocomposite media strongly depends on the coherent driving fields applied in the atomic ensemble, the volume fraction of the AgNPs as well as their size and the applied frequencies. It was found that the dielectric function decreases with the increase in AgNPs’ size, while increase in Rabi frequency increases the refractive index. Similarly, the dispersion and absorption decrease with decrease in volume fraction of the AgNPs. Our results suggest important applications of this nanocomposite in various fields such as energy harvesting, photovoltaics and quantum plasmonics. The modeling approach developed in this study provides great freedom for tuning optical properties of the metal-dielectric nanocomposites.

Polyetherimide copolymer film with room-temperature self-healing properties and high breakdown field strength

With the waste of resources caused by human activities, it has gradually become an increasingly prominent social problem. The development of self-healing polymers in the field of insulation has attracted widespread attention. Develop polymer matrices with efficient healing efficiency and sound insulation properties to achieve green and sustainable resource conservation. In addition, improving the dielectric properties of intrinsic self-healing matrices has been a hot topic. In this work, we developed a new PEI matrix-modified self-healing polymer substrate that provides a breakdown field strength of 240 kV/mm and self-healing properties at room temperature, this has significantly improved the dielectric properties over other previously reported self-healing polymers. In addition to the abovementioned performance, we found significant differences in thermodynamic behavior in the synthesized end-modified polymers. By dielectric characterization (LCR), the breakdown composite can be left at room temperature for 60 min, and the material can recover 80 % of the initial properties without external intervention(This is demonstrated by the fact that its DC conductivity at 60 min of autonomous healing was significantly changed from that of the freshly electrically pierced DC conductivity and remained around 5.38 × 10−11 S/cm for a longer period of time thereafter). The microscopic morphology of the modified PEI matrix was observed by scanning electron microscopy (SEM) and EDS surface elemental analysis, which further supports the existence of metal coordination structures. These findings can further deepen the thinking of self-healing dielectric composites. The work inspired by this may break the limits and take self-healing composite dielectric materials to a new height.

Solvent-free Acrylate/BCB drop-on-demand (DOD) inkjet dielectric ink for 3D printing

Currently, drop-on-demand (DOD) inkjet-printed dielectric inks used to produce next-generation high-frequency electronic devices fail to meet the requirements of circuit board substrates in terms of thermal, mechanical, and dielectric properties. To address this gap, we synthesized a low-viscosity acrylate monomer featuring an intrinsically low dielectric structure (hexafluorobisphenol A) and multiple cross-linking sites, and a benzocyclobutene monomer with low curing shrinkage and excellent thermomechanical properties. By mixing these monomers with other reactive diluents and verifying them through theoretical calculations and printing, we have developed a range of dielectric inks suitable for inkjet 3D printing. To enhance the overall performance of the cured inks, a sequential UV/thermal curing strategy was employed to form interpenetrating networks (IPNs). The optimal ink formulations met the requirements of circuit board substrates, demonstrating excellent heat resistance (Td5% = 334 °C, Tg = 181 °C), mechanical properties (tensile strength = 85 MPa, elongation at break = 13.5 %), and dielectric properties (Dk = 2.526 and Df = 0.113 at 15 GHz). These formulations meet the performance requirements for circuit board substrates and lead the industry in mechanical and dielectric properties. Furthermore, the feasibility of inkjet printing heterogeneous integrated electronic devices was verified, showing excellent print resolution and continuity of the conductive network. This work provides new insights into the future development of dielectric materials for inkjet 3D printing.

Effect of Surface Morphology on the Response Speed of Moisture Sensors

Relative humidity sensors are used for high-humidity measurement and moisture sensor or dew point sensors are used for low-humidity measurement (<1 ppmv). We fabricated moisture sensors using α-Al2O3 films as porous dielectric materials deposited by anodic spark deposition. In this study, a variety number of small pores has been studied to investigate the response speed of moisture sensors. Three different surface morphologies have been studied using scanning electron microscopy. One sample has the maximum number of small pores, one sample has the medium number of small pores, and the last sample has the minimum number of small pores. Small pores are defined as pore size ranging from 40 nm to 200 nm. We found that the sensor made as porous material with the maximum number of small pores has the fastest response speed, and that from the minimum number of small pores has the slowest response speed either from high humidity to low humidity or from low humidity to high humidity.

Dielectric and photocatalytic characteristics of novel CaCu3Ti4O12 modified Ba0.5Sr0.5TiO3-based heterojunction synthesized by wet-chemistry method

The study presents a comprehensive investigation into the synthesis, characterization, and application of barium strontium titanate-calcium copper titanate (BST-CCTO) heterojunction, offering insights into their potential for high-energy-density capacitors and photocatalytic applications. It discusses the synthesis methods for BST, CCTO nanoparticles and their heterojunction. It delves into the structural analysis of prepared heterojunctions using techniques like X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The photocatalytic performance of heterojunctions, particularly in the degradation of organic dyes and pharmaceutical waste under visible light, is explored. Results demonstrate the superior photocatalytic efficiency of BST-CCTO heterojunction, i.e., B2 (99.5 % for RhB) compared to individual BST (78.4 %), suggesting potential applications in environmental remediation. This study also explores the development and properties of dielectric materials, particularly focusing on polyvinylidene fluoride (PVDF) and its composites with high-dielectric ceramics such as BST and CCTO. Various aspects of dielectric behavior, including polarization mechanisms and frequency dependence, are also discussed. Dielectric studies reveal the enhanced dielectric constant (50.93 at 1 kHz for 3 wt% loading of B3) of PBCT-3 composite as compared to pure PVDF composite (10 at 1 kHz), attributed to factors such as interface engineering, complementary electrical properties, and grain boundary effects. The mechanisms underlying the interaction between fillers and PVDF matrix are elucidated, highlighting the role of interface engineering and polarization enhancement in optimizing dielectric performance.

Enhanced energy storage capability of hydroxylated BiFeO3/PVDF composites designed by compositionally gradient multilayer structures

With the development of the microelectronics industry, there is a huge demand for flexible polymer dielectrics with excellent dielectric energy storage capacity, aimed at increasing dielectric constant and enhancing breakdown strength. In this study, the hydroxylated BiFeO3-loaded polyvinylidene fluoride(PVDF) composite films were prepared by electrostatic spinning techniques and the energy storage properties have been investigated. The results show that the dielectric constant and breakdown strength of the composites are effectively influenced by the hydroxylation modification and spatial structure. More interestingly, the seven-grade hydroxylated composite films exhibit a great enhancement of the excellent energy storage performances (Ue, ∼13.21 J/cm3; η, ∼66.2 %). This study demonstrates the immense potential of these composites as highly efficient dielectric materials suitable for use in energy storage capacitors.

Selective IR wavelengths multichannel filter based on the one-dimensional topological photonic crystals comprising hyperbolic metamaterial

In this research article, we have theoretically introduced a one-dimensional topological photonic crystal (1D TPC) design to provide a better stability due to imperfections and fluctuations in geometry compared to the traditional PC structures. The considered structure is designed by the combination of two different PCs, i.e., PC1 and PC2. PC1 consists of two layers of silicon (Si) and magnesium fluoride (MgF2), while PC2 contains a multilayer stack of MgF2 and hyperbolic metamaterial (HMM). Interestingly, the HMM layer is introduced as a composite of a dielectric material of indium arsenide (InAs), and nanocomposite of Ag nanoparticles inside a hosting medium of Y2O3. The foundations of our theoretical framework are based on Effective Medium Theory (EMT), the Transfer Matrix Method (TMM), and the Maxwell-Garnett model. Our research primarily focuses on utilizing our design as a pass/stop band filter for near-infrared (NIR) applications. Notably, this proposed design exhibits significant stability in the face of imperfections and variations. Our numerical findings highlight the influence of several geometric parameters including the refractive index of hosting medium for Ag nanoparticles, thicknesses, and filling fraction on the characteristics of the resulting filter. Remarkably, the results also reveal the emergence of multiple resonance peaks that maintain high stability against geometric tolerances. We believe our work presents a finite photonic crystal (PC) whose wave localization properties are resilient to random geometric imperfections, making it suitable for NIR filtering applications.

Rapid fabrication of Ba1–xSrxTiO3 ceramics via reactive flash sintering

Ba1–xSrxTiO3 (BST) ceramics are promising dielectric materials. However, their fabrication is usually laborious, requiring long preparation stages and high temperatures, which are not favorable for tuning the grain size and dielectric properties. In this study, (Ba1–xSrx)TiO3 (x = 0.1, 0.3, 0.5) ceramics were produced via reactive flash sintering (RFS) of a mixture of BaCO3, SrCO3 and TiO2 powders at 900 °C and relatively short times (15–90 s). The electric field (E-field) with a strength of 400 V/cm and the current densities of 25–75 mA mm−2 were applied during RFS. Once the Sr2+ content increased, the incubation time for the RFS decreased, suggesting that the addition of Sr2+ facilitated the RFS process. At the RFS time above 15 s, a single-phase Ba0.6Sr0.4TiO3 perovskite structure was formed. When the time and the applied current density increased, both the densities and grain sizes within the ceramics increased. This increased the real part (ε’) of the complex permittivity compared to that of the conventionally sintered (CS) ceramic. Moreover, the enhancement of mass transport by E-field-induced oxygen vacancies was considered the predominant mechanism of RFS in the production of BST ceramics.

Discovery of high-performance dielectric materials with machine-learning-guided search

Discovery of high-performance dielectric materials with machine-learning-guided search

Enhanced low‐field energy storage performance in Nd3+‐doped (Bi0.40K0.2Na0.2Sr0.2)TiO3 high‐entropy ceramics

AbstractThe burgeoning requirement for compact electronic devices has intensified research into lead‐free dielectric ceramics that offer superior recoverable energy storage density and efficiency at low electric fields. In this study, we report the synthesis of Nd3+‐doped (Bi0.4K0.2Na0.2Sr0.2)TiO3 perovskite ceramics via the solid‐state reaction technique. The synthesized ceramics adopted a tetragonal crystal structure. As the concentration of Nd3+ ions increased, both the maximum dielectric constant (εm) and its corresponding temperature (Tm) decrease. The incorporation of Nd3+ ions perturbed the long‐range ferroelectric order, leading to diminished maximum polarization (Pm) and remanent polarization (Pr). The ceramics achieved optimal properties with 12 mol% Nd3+ doping, showcasing a significant recoverable energy storage density of 1.50 J/cm3 at a low electric field of 140 kV/cm, along with an exceptional storage efficiency of 94.6%. This research not only highlights a promising candidate for dielectric materials in low electric field applications but also introduces an innovative approach to enhance energy storage performance.

Flexible poly (ethylene-co-vinyl acetate)/copper oxide nanocomposites: A promising avenue for energy storage applications

The use of metal oxide nanoparticles in polymeric materials to improve optical properties, dielectric constant, mechanical strength, and electrical conductivity has generated significant interest in fabricating flexible optoelectronic and energy storage devices. Herein, copper oxide (CuO) nanoparticle-reinforced poly (ethylene-co-vinyl acetate) (EVA) nanocomposites were prepared using a solvent-free two roll mill mixing method. Fourier transform infrared (FTIR) analysis reveals the distinct absorption peaks of CuO in the EVA matrix. The addition of CuO nanoparticles improved the crystallinity of EVA, as confirmed by X-ray diffraction (XRD). The addition of CuO to EVA led to an increase in the refractive index and a decrease in bandgap energy, as well as a broadening and intensification of UV–visible absorption, indicating strong interactions between CuO nanoparticles and the EVA matrix. Field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM) revealed a homogeneous dispersion of CuO nanoparticles throughout the EVA matrix. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) demonstrated that the incorporation of CuO nanoparticles into EVA significantly enhanced its thermal properties. The electrical characteristics studies showed that the AC conductivity and dielectric constant of EVA increased significantly with increasing temperatures and CuO nanoparticle loading levels. EVA containing 5 wt% CuO exhibited the highest conductivity and the lowest activation energy. CuO nanoparticle reinforcement significantly enhanced the tensile, tear, and impact strength of EVA while reducing elongation at break up to a particular concentration. The nanocomposites containing 5 wt% CuO exhibited the highest tensile, tear resistance, and impact strengths, outperforming virgin EVA by 85 %, 103.6 %, and 83.16 %, respectively. These findings suggest that EVA/CuO nanocomposites are promising candidates for flexible dielectric materials.

Achieving ultra-high energy storage performance in simple systems through minimal element substitution

Dielectric capacitors are essential components of modern advanced electronic devices and power systems based on their ultra-fast charging and discharging speeds and supreme power densities. Nevertheless, how to comprehensively boost their energy storage density and storage efficiency is still an insurmountable challenge. Here, we report a simple micro-chemical polarizability modulation strategy that enables SrTiO3-based dielectric materials to achieve excellent energy storage properties. The energy density and energy efficiency are increased to as high as 76 J∙cm−3 and 72 % from 0.4 J∙cm−3 and 46.7 % of pure STO, respectively, which is the largest value in micro-substitution (less than 3 %). Our results show that the introduction of trace amounts of elements with high ionic polarizabilities (Mn, V) facilitates the increase of chemical disorder and the formation of stable and highly dynamic polar nanoregions (PNRs), which reduces the hysteresis of the polarization switching and improves the polarization at the breakdown field strength, synergistically fostering the energy storage performance. The results of X-ray photoelectron spectroscopy and scanning electron microscopy reveal that the micro-substitution of Mn and V promote the reduction of oxygen vacancies and grain size, improving the breakdown resistance and stability of the capacitor. This present approach is expected to be widely used in the development of high-performance dielectrics.

Structural designs and synthesis of co-polycarbonates with cyclohexyl and fluorene structures: Low-dielectric constant, high solubility, and superior mechanical properties

The rapid developments of high-speed communication and large-scale integrated circuits have accelerated the research for insulating dielectric materials with low dielectric constant, low dielectric loss, and good mechanical properties. In this study, a series of polycarbonate resins containing cyclohexyl and fluorene structures are synthesized by melt transesterification, which is low dielectric, highly thermally resistant, and soluble. The effects of fluorene structure contents on the properties of a co-polycarbonate resin were studied systematically. The results showed that the non-polar fluorene group could reduce the molecular polarization of co-polycarbonate, resulting in low permittivity of co-polycarbonate are 2.41-2.71@1MHz. In addition, the resin has excellent solubility and can be dissolved in NMP, CH2Cl2, THF, and other solvents at room temperature. Furthermore, the co-polycarbonate resins also exhibit superior heat resistance with glass transition temperature (Tg) of 160.6-173.1 °C as well as admirable mechanical properties with a tensile strength of 50.54-70.72 MPa. This makes it a promising candidate for high-speed communications and large-scale integrated circuits.

CSEM Optimization Using the Correspondence Principle

Traditionally, 3D modeling of marine controlled-source electromagnetic (CSEM) data (in the frequency domain) involves high-memory demand, requiring solving a large linear system for each frequency. To address this problem, we propose to solve Maxwell’s equations in a fictitious dielectric medium with time-domain finite-difference methods, with the support of the correspondence principle. As an advantage of this approach, we highlight the possibility of its implementation for execution with GPU accelerators, in addition to multi-frequency data modeling with a single simulation. Furthermore, we explore using the correspondence principle to the inversion of CSEM data by calculating the gradient of the least-squares objective function employing the adjoint-state method to establish the relationship between adjoint fields in a conductive medium and their counterparts in the fictitious dielectric medium, similar to the approach used in forward modeling. We validate this method through 2D inversions of three synthetic CSEM datasets, computed for a simple model consisting of two resistors in a conductive medium, a model adapted from a CSEM modeling and inversion package, and the last one based on a reference model of turbidite reservoirs on the Brazilian continental margin. We also evaluate the differences between the results of inversions using the steepest descent method and our proposed momentum method, comparing them with the limited-memory BFGS (Broyden–Fletcher–Goldfarb–Shanno) algorithm (L-BFGS-B). In all experiments, we use smoothing by model reparameterization as a strategy for regularizing and stabilizing the iterations throughout the inversions. The results indicate that, although it requires more iterations, our modified momentum method produces the best models, which are consistent with results from the L-BFGS-B algorithm and require less storage per iteration.

Roll‐to‐Roll Production of High‐Performance All‐Organic Polymer Nanocomposites for High‐Temperature Capacitive Energy Storage

AbstractDielectric materials with significant performance in high temperatures are highly desired, especially in harsh environments. However, the polymer‐based dielectric films have developed so far, the production scale remains at the state of the lab. Here, an all‐organic strategy is proposed by introducing phenyl‐acid‐based polymer nanodots (PAPD) into Polyetherimide (PEI), achieving high capacitive energy storage properties even at 200 °C and mass production by an industrial continuous roll‐to‐roll process. The abundant hydrogen bonding between PAPD and PEI chains ensures uniform distribution for the enhanced interaction between nanofillers and polymer matrix. Under UV irradiation, the electron‐affinity and band gap of the film are further extended, which impede charge transfer and reduction of conductive loss. A low loading (0.3 wt.%) of PAPD renders the membrane significant improvement in breakdown strength and charge–discharge efficiency. An ultrahigh energy storage density of 5.1 J cm−3 with a charge–discharge efficiency of over 90% and charge–discharge cycle stability up to 2 × 104 cycles at 150 °C is observed. Furthermore, a 1000 m long roll of polymeric film is roll‐to‐roll fabricated on an industrial solution‐casting production line and the low cost makes practical commercial scale application possible. Considering the low loading and low cost of nanofiller, this all‐organic design strategy sheds light on the industrial application of high‐temperature dielectric materials.

Room‐Temperature Lasing of Dual‐Metal Nanoparticle Surface Lattice Resonance with Monolithic InGaAs Multiple Quantum Wells on GaAs Substrates

This study demonstrates the surface lattice resonance (SLR) laser utilizing asymmetric dual‐metallic nanoparticle arrays, incorporating a high‐refractive‐index material, which exhibits a confinement factor of 16%, enhancing the coupling between metal and dielectric materials. Multiple quantum wells (MQWs) are integrated with plasmonic SLR in the proposed structure. Through theoretical design and experimental validation, the MQW plasmonic SLR laser exhibits excellent high Q‐factor and stable operation at room temperature. This demonstration enhances laser performance and achieves low‐threshold operation with a laser threshold as low as ≈2.39 MW cm−2. This study's design of plasmonic SLR lasers further advances the realization of optoelectronic device applications.

3D printed hernia mesh implant: a conformability study

Aim: This study aims to explore the sensing capabilities of polyvinylidene fluoride-hydroxyapatite-chitosan (PVDF-HAP-CS) composite-based hernia mesh implants (of conformal/planar design), followed by in-vitro analysis for better understanding of the bio-stability in the patient’s body. Methods: For analyzing the sensing capabilities, a microstrip patch antenna (MPA)-based implantable sensor [with 17-4 precipitate hardened (PH) stainless steel (SS) (bio-compatible) and Cu alloy (non-biocompatible) materials as conducting plane/patch with PVDF-HAP-CS as dielectric material] has been considered separately in this study. Primarily, in this study, the 3D models of the hernia mesh implant have been designed in the high-frequency structure simulator (HFSS) software, and the sensing behaviour of the same has been recorded. Results: The HFSS results represent that for the 17-4PH SS-based sensor, resonant frequency (fr) decreases from 2.3953 to 2.3800 GHz, whereas the gain increases from 0.54 to 4.02 dB with a SAR value of 1.077 W/kg. The fr for Cu alloy increases up to 30° conformal angle and, after that, starts decreasing, whereas the gain reaches 3.24 dB with a SAR value of 1.238 W/kg. The in-vitro study highlights that both materials (17-4PH SS and Cu alloy) possess a low corrosion rate. Conclusions: The simulation-based comparison of the biosensors with conducting elements 17-4PH SS and Cu alloy for different conformal angles indicates that the 17-4PH SS shows promising results over Cu in terms of higher gain (up to 4.02 dB) and low SAR value (1.077 W/kg) with the fr lying in the industry scientific and medical (ISM) band and therefore may be used for implantable sensor applications and possesses the capability to be used as 3D-printed hernia mesh implant. The in-vitro results with the low corrosion rate ≈ of 5.1 × 10–8 mm/year, 17-4PH SS may be a suitable material for the fabrication of hernia mesh implant.

Combined design of dielectric material and layer structure of vanadium nitride/graphene composites for ultra-broadband microwave absorption

Combined design of dielectric material and layer structure of vanadium nitride/graphene composites for ultra-broadband microwave absorption

Au Nanorings/TiO2 NPs@MXene-Based Metasurfaces with a Magnetic Mirror-Modulated ECL Strategy for Extracellular Vesicle Detection.

A metasurface as an artificial electromagnetic structure can concentrate optical energy into nanometric volumes to strongly enhance the light-matter interaction, which has been becoming a powerful platform for optical sensing, nonlinear effects, and quantum optics. Herein, we developed a novel hybrid plasmonic-dielectric metasurface consisting of Au nanorings (Au NRs) and TiO2 nanoparticles derived from MXene (TiO2 NPs@MXene). The hybrid metasurface simultaneously benefited from the high near-field enhancement effect of plasmonic materials and the low loss of dielectric materials. Furthermore, the optical modulation efficiency of the hybrid metasurface can be regulated by a magnetic mirror configuration. The magnetic mirror acted like a mirror, confining the electrons to a limited region and increasing the density of the surface plasmon. Moreover, the electrochemiluminescence (ECL) of the Cu2BDC metal-organic framework (Cu2BDC-MOF) served as a light source for the Au NRs/TiO2 NPs@MXene metasurface. Due to the exceptional light manipulation capability of the hybrid metasurface and the coordination of the magnetic mirror, the isotropic ECL signal can be dynamically amplified and converted into polarized emission. Finally, a metasurface-regulated ECL (MECL)-based biosensor with a dual-positive membrane protein recognition strategy was developed for the accurate identification of gastric cancer-derived extracellular vesicles. The novel MECL research opened up a new route in the realization of dynamically tunable metasurfaces for optical sensing and novel nanophotonic devices.