Solution Processing Research Articles

Tuning the bandgap without compromising efficiency: ambient solution processing of Ge-alloyed (Ag,Cu)2Zn(Sn,Ge)(S,Se)4 kesterite thin-film solar cells

The photovoltaic sector currently experiences a growing demand for deeply-integrated technologies in agriculture, buildings, vehicles, among others. Kesterite compounds provide a versatile solution through their tunable bandgap via isovalent alloying. However, this should be done while preserving material opto-electronic quality and device performance, which is an unresolved challenge. Indeed, tuning the bandgap of kesterites must ensure low crystalline disorder to counteract the associated open-circuit voltage (Voc) losses when used in solar cells. To achieve this goal, this work introduces a simple molecular ink recipe realized in ambient air to process single-phase high-quality Ag,Gealloyed kesterite absorbers. By varying the Ge content from 0 to 100%, the absorber bandgap covers the range from 1.15 to 1.5 eV, in which the Urbach energy remains close to 20 meV and promisingly low Voc deficits are observed. In particular, the champion efficiency of 12.1% obtained with 40% Ge breaks the record for Ge-alloyed kesterites with a 1.2 eV bandgap by remarkably reaching 62% of the Shockley-Queisser limit for Voc. This study demonstrates a promising strategy to solve the issue of large band tailing and low opto-electronic quality in widebandgap kesterites while establishing a foundation for solution-processed kesterite solar cells with tunable bandgap and promising performance.

A Survey Paper on Plastic Solar Cell Technology

The demand of energy is increasing day by day so non-conventional source of energy has to be used. Sun is the nonconventional source of energy. Conventional solar panels convert solar energy into electrical energy. A plastic solar cell is the type of photovoltaic that makes use of organic electronics dealing with conductive organic polymers or small molecules for light absorption and charge transport to produce electricity from sunlight by the photovoltaic effect. Polymers Provide the Advantage of Solution Processing at Room Temperature, which is Less Expensive and Enables One to Use Plastics. Therefore, If Silicon Is Replaced with Polymer Nanowires, The Solar Cell Would Be Much Lighter and Ultimately Less Costly. These Solar Cells are Thin, Several Microns in Diameter, and Scavenge All the Rays from the Sun's Radiation. Plastic Solar Cell Technology is Based on Conjugated Polymers and Molecules. Polymer Solar Cells have Generated Considerable Interest Since it Provides Environmentally Friendly, Flexible, Lightweight, Low Cost, Possibility of High-Efficiency Solar Cells in the Last Couple of Decades. Plastic Solar Cells are More Efficient and Viable in Usage. This dissertation focuses on the development and optimization of plastic solar cell technology, in particular this potential towards flexible, lightweight, and cost-effective alternative sources to traditional silicon-based solar cells. The focus of the present research work is to find optimum organic materials for higher efficiency and stability in plastic solar cells, varying from conjugated polymers to small organic molecules. Some of the main goals are improving the charge transport mechanisms and optimizing the architecture of devices through state-of-the-art techniques of fabrication, like roll-to-roll printing and layer-by-layer deposition. The other key aspect is that the project assesses the environmental aspects and lifecycle of plastic solar cells to ensure an environmentally friendly production process. Huge preliminary results were achieved at high power conversion efficiencies and durability has been greatly improved, targeting very wide spread application from portable electronics up to building-integrated photovoltaics. Therefore, the discovery of plastic solar cells might be a major step for applicable solutions in renewable energy and towards overcoming the world's increasing energy challenges.

Electron-Deficient Organic Molecules Based on B←N Unit: A N-Type Room-Temperature Chemiresistive Sensors with Moisture Resistance.

Organic molecules with tailorable chemical structures, high stability, and solution processability have great potential in the sensing field. Compared with p-type organic small molecules (OSMs), the electron-dominated n-type analogs show superior conductivity when exposed to reducing gases, which can achieve outstanding sensor signal-to-noise ratios. However, inadequate humidity resistance at room temperature hinders the development of such molecules. Herein, an A-D-π-D-A molecular design strategy is proposed based on electron-deficient B←N units, which results in effective intramolecular charge transport and sensitive responses by extending the π-conjugation bridge. As a result, the ST-2BP with A-D-π-D-A configuration shows a prominent sensitivity of 787 (Ra/Rg) in 20ppm NH3 at room temperature and an almost initial and stable response under different relative humidity conditions, which is the highest among currently reported OSM sensors. Supported by theoretical calculations and in situ FTIR spectra, it is revealed that B←N units, which function as the active centers mediate the specific ammonia adsorption. This study provides a new understanding of the design of high-performance room temperature gas sensing materials by decorating B←N units.

An Instructive CO2 Adsorption Model for DAC: Wave Solutions and Optimal Processes

We present and investigate a simple yet instructive model for the adsorption of CO2 from air in porous media as used in direct air capture (DAC) processes. Mathematical analysis and non-dimensionalization reveal that the sorbent is characterized by the sorption timescale and capacity, while the adsorption process is effectively wavelike. The systematic evaluation shows that the overall adsorption rate and the recommended charging duration depend only on the wave parameter that is found as the ratio of capacity and dimensionless air flow velocity. Specifically, smaller wave parameters yield a larger overall charging rate, while larger wave parameters reduce the work required to move air through the sorbent. Thus, optimal process conditions must compromise between a large overall adsorption rate and low work requirements.

Tetraoctylammonium Bromide Interlayer between NiLiOx and Perovskite for Light-Emitting Diodes.

Physical vapor deposition is a favorable technique for fabricating light-emitting diodes (LEDs) due to its scalability and reproducibility. However, the performances of LEDs fabricated via this method are worse than those prepared via solution processing owing to the generation of high defect densities. In this study, we introduce a layer of tetraoctylammonium bromide (TOABr), an interfacial-modification compound containing four long octyl chains that are symmetrically arranged around an N atom, to reduce nonradiative recombination and trap densities in CsPbBr3. We examined the impacts of adding TOABr on perovskite thin films deposited on hole injection layers made of Li-doped NiOx and poly(3,4-ethylenedioxythiophene)/polystyrenesulfonate. Our investigations reveal that TOABr addition slightly increases crystallinity, dramatically increases photoluminescence, and achieves the preferred orientation in the perovskite films. Additionally, the interfacial layer passivates defects and improves charge balance in the device, thereby enhancing performance. Consequently, perovskite LEDs with a TOABr layer exhibit a lower turn-on voltage of 3 V than their pristine counterparts, achieving a maximum luminance of 11,133 cd m-2 and an external quantum efficiency of 1.24%, whereas the pristine perovskite LEDs achieve an EQE of 0.015%. The approach proposed in this study can be used to fabricate efficient vacuum-thermal-evaporated perovskite LEDs.

Solution-based processing of Ge2Sb2Se4Te optical phase change materials

Phase change materials (PCMs) are important building blocks in solid-state memory and photonic devices. Solution-based processing promises large-area, cost-effective, conformal coating of optical PCMs (O-PCMs) for photonic applications. In this work, a solution processing route was developed for Ge2Sb2Se4Te1 (GSST), a target PCM of interest due to its large optical contrast, broadband transparency, and improved glass-forming capability. An alkahest solvent mixture of ethanedithiol and ethylenediamine was used as a solvent system to fabricate solution-derived GSST thin films and films from these solutions were prepared and characterized using SEM, XRD, and Raman spectroscopy.

Single‐Component White Emissive Organic–Inorganic Hybrid Copper Halide Composite Films for Remote UV‐pumped White Light‐Emitting Diodes with High Color Rendering Index

AbstractLead‐free organic–inorganic metal halides (OIMHs) are highly desirable owing to their remarkable properties including low toxicity, structural diversity, high stability, and solution processability. Nevertheless, the development of their single‐component white emissive films remains a formidable challenge for remote white light‐emitting diodes (WLEDs) application. In this work, (C16H36N)2Cu2I4/polyvinylidene fluoride (PVDF) white emissive composite film is successfully fabricated through an in situ solvent evaporation crystallization process at room temperature. The elemental analysis and bonding between (C16H36N)2Cu2I4 and PVDF are demonstrated by X‐ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) measurements. In addition, this composite film exhibits a broadband white emission with two peaks. Notably, the best photoluminescence quantum yields (PLQYs) of the PVDF based composite film reaches an impressive 96.7%. A (C16H36N)2Cu2I4/PVDF based remote UV‐pumped WLEDs with an impressive color rendering index of 95.5 is realized. Finally, the in situ fabrication method is expanded to fabricate (C16H36N)2Cu2I4/polyacrylonitrile (PAN) composite films, and we further realized their single component remote WLEDs.

Solution Processed Bilayer Metal Halide White Light Emitting Diodes.

Metal halide perovskites and perovskite-related organic metal halide hybrids (OMHHs) have recently emerged as a new class of luminescent materials for light emitting diodes (LEDs), owing to their unique and remarkable properties, including near-unity photoluminescence quantum efficiencies, highly tunable emission colors, and low temperature solution processing. While substantial progress has been made in developing monochromatic LEDs with electroluminescence across blue, green, red, and near-infrared regions, achieving highly efficient and stable white electroluminescence from a single LED remains a challenging and under-explored area. Here, a facile approach to generating white electroluminescence is reported by combining narrow sky-blue emission from metal halide perovskites and broadband orange/red emission from zero-dimensional (0D) OMHHs. For the proof of concept, utilizing TPPcarz+ passivated two-dimensional (2D) CsPbBr3 nanoplatelets (NPLs) as sky blue emitter and 0D TPPcarzSbBr4 as orange/red emitter (TPPcarz+ = triphenyl (9-phenyl-9H-carbazol-3-yl) phosphonium), white LEDs (WLEDs) with a solution processed bilayer structure have been fabricated to exhibit a peak external quantum efficiency (EQE) of 4.8% and luminance of 1507 cd m-2 at the Commission Internationale de L'Eclairage (CIE) coordinate of (0.32, 0.35). This work opens a new pathway for creating highly efficient and stable WLEDs using metal halide perovskites and related materials.

Multi-layered quasi-2D perovskite based triboelectric nanogenerator

Inorganic-organic perovskites are considered as one of the emerging candidates as a tribopositive material in triboelectric nanogenerators (TENG) owing to their unique functionalities. Among them, quasi-two-dimensional (quasi-2D) perovskites are promising materials for TENG due to layered nature, excellent environmental and chemical stability, tunability, and excellent electrical properties. Herein, we investigate the performance of TENG based on multiple series of perovskite layers using simple solution processing technique. The dimensionality of the perovskite layers is attained by changing the stoichiometric ratios of phenylethylammonium iodide (PEAI), lead iodide (PbI2), methylammonium iodide (MAI). The quasi-2D based TENG generates the maximum output electrical performance with a voltage of 306 V, current of 4.71 µA, and maximum power density of 3.48 µW/cm2 at the optimum value of (<n> = 5) due to the higher concentration of C–N and N–H groups. Moreover, the fabricated device shows stable performance for 12,000 cycles. The TENG device is further utilized to charge the various commercially available capacitors, for lightning of light-emitting diodes (LEDs), and to power up low-power electronic devices. These results demonstrate the effect of the dimensionality of perovskites on the output performance of the TENG for use in next-generation energy harnessing.

Molecular Engineering for High-Performance X-ray Scintillators.

X-ray scintillators, materials that convert high-energy radiation into detectable light in the ultraviolet to visible spectrum, are widely used in industrial and medical applications. Organic and organic-inorganic hybrid systems have emerged as promising alternatives for X-ray detection and imaging due to their mechanical flexibility, lightweight, tunable excited states, and solution processability for large-scale fabrication. However, these systems often suffer from weak X-ray absorption and insufficient exciton utilization, which seriously affects their scintillation performance, limiting their potential for broader application and commercialization. This review highlights recent advances in molecular engineering for developing high-performance X-ray scintillators. Itfocuses on molecular design principles, such as the heavy atom effect, donor-acceptor/host-guest strategies, hydrogen/halogen bonding, molecular sensitization, and crystal packing, for enhancing scintillation performance. By leveraging these approaches, researchers have made significant strides in improving X-ray scintillation efficiency and advancing the potential of these materials for commercial applications.

Strain-Induced Tunable Enhancement of Piezoelectricity in a Novel Molecular Multiferroic Material.

Multiferroics are appealing because of application potentials in data storage devices, sensors, transducers, and energy harvesters. Molecular multiferroics emerge as a promising alternative to inorganic multiferroics due to flexibility, light weight, low toxicity, solution processing, structural diversity, and chemical tunability. While researches have predominantly focused on perovskite structures, studies on molecular ionic multiferroics remain relatively limited. It is urgent to creatively build a novel platform for studying and developing the coupling and interaction between the stress, electricity, and magnetism. Knowing this, the work focuses on a novel organic-inorganic hybrid multiferroic N-ethyl-N-(fluoromethyl)-N-methylethylammonium tetrabromoferrate (III) showing coexisting magnetic and electric orderings. It undergoes antiferromagnetic, ferroelectric, and ferroelastic transitions. Notably, under a strain of 2.0%, the piezoelectric response increases tenfold, and the coercive field of ferroelectric polarization is reduced by half. The strain-induced enhancement of piezoelectricity is rarely reported in molecular multiferroics. Density functional theory is employed to predict that the mechanism of the large piezoelectric response under strain engineering is related to the cation rotation and phase switching between the stable phase and an energetically competitive metastable phase. This study creates a new paradigm to develop molecular multiferroics and future microelectronic devices for energy conversion.

Numerical simulation of electrically pumped active vertical‐cavity surface‐emitting lasers diodes based on metal halide perovskite

AbstractMetal halide perovskites (MHP)‐based electrically pumped vertical‐cavity surface‐emitting lasers (EPVCSEL) are promising candidates in optoelectronics due to low‐carbon footprint solution processing method. However, significant challenges impede MHP‐EPVCSEL manufacturing: (1) Distributed Bragg Reflectors (DBRs) composed of typical electron transport layers (ETLs) and hole transport layers (HTLs) are not conductive enough. (2) Due to large mobility difference of typical ETLs and HTLs, carriers‐unbalanced injection leads to severe performance degradation. Herein, we propose a potential strategy to address such challenges using MAPbCl3 and CsSnCl3 as carrier transport layers with mobility 3 orders larger than typical ETLs and HTLs. Via transfer matrix method calculations, we find that the reflectance of DBRs composed of MAPbCl3 (130.5 nm)/CsSnCl3 (108 nm) is larger than 91% with 10 pairs of DBRs. Furthermore, the proposed EPVCSEL device simulation shows that MHP‐EPVCSEL has the potential to achieve room temperature continuous wave lasing with a threshold current density of ∼69 A cm−2 and output optical power ∼10−4 W. This work can provide a deep insight into the practical realization of MHP‐EPVCSEL.

Unravelling the Electrical Field Induced Ion Migration in Flexible OLEDs with PEDOT:PSS Electrodes.

The development of flexible organic light-emitting didoes (FOLEDs) has spurred the research on flexible transparent electrodes (FTEs). Poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS) is one of the most attractive FTEs due to its adjustable conductivity and compatibility with low-cost and large-scale solution processing techniques. Significantly, highly efficient FOLEDs have been achieved with modified PEDOT:PSS FTEs. However, the intrinsic mechanisms that contribute to device degradation of FOLEDs utilizing PEDOT:PSS FTEs have not yet been fully elucidated. In this work, three ionic liquids (ILs) are used to enhance the electrical conductivity and mechanical flexibility of PEDOT:PSS FTEs. Simultaneously, the influence of the electric field induced ion migration from PEDOT:PSS FTEs on the operational stability of FOLEDs is unraveled. We find that the ILs with larger ionic radii and higher steric hindrance are beneficial to suppressing the electrical field induced ion migration and improving the operational stability of FOLEDs. Finally, large-area and high-performance FOLEDs are achieved based on the IL of 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide modified PEDOT:PSS FTEs, which demonstrate a high current efficiency of 98.1 cd/A and a longer lifetime of 66.7 min. This finding may promote the practical application of PEDOT:PSS FTEs in flexible optoelectronics.

Volatile Additive Assists Binary Layer‐by‐Layer Solution Processing Organic Solar Cells to Achieve 19% Efficiency

Comprehensive SummaryLayer‐by‐layer (LbL) solution processing is an efficient method to realize high performance organic solar cells (OSCs). One of the drawbacks of the LbL‐processed active layer is the large difference in the crystallinity of the donor and acceptor, which will lead to imbalance charge transfer and result in unfavorable charge recombination. Herein, we combined a novel volatile additive 3,5‐dichloro‐2,4,6‐ trifluorobenzotrifluoride (DTBF) with the LbL method to realize high‐efficiency OSCs. DTBF interacts with the non‐fullerene acceptor BTP‐4F by non‐covalent bonding, which enhances the crystallinity and compact stacking of BTP‐4F. DTBF doped OSC has balanced and efficient electron transport properties, longer carrier lifetime, higher exciton dissociation and charge collection efficiencies, lower energetic disorder than the control OSC without any additives. Benefiting from the optimization of charge dynamics and micro‐morphology by DTBF, the binary LbL‐processed OSC achieved synergistic improvements in open‐circuit voltage, short‐circuit current density and fill factor. As a result, a champion power conversion efficiency (PCE) of 19% is realized for DTBF‐optimized OSC, which is superior to the control OSC (17.55%). This work demonstrates a promising approach to modulate active layer morphology and fabricate high performance OSCs.

Enhancing Efficiency and Stability of Inverted Perovskite Solar Cells through Solution‐Processed and Structurally Ordered Fullerene

AbstractThe electron transporting layer (ETL) used in high performance inverted perovskite solar cells (PSCs) is typically composed of C60, which requires time‐consuming and costly thermal evaporation deposition, posing a significant challenge for large‐scale production. To address this challenge, herein, we present a novel design of solution‐processible electron transporting material (ETM) by grafting a non‐fullerene acceptor fragment onto C60. The synthesized BTPC60 exhibits an exceptional solution processability and well‐organized molecular stacking pattern, enabling the formation of uniform and structurally ordered film with high electron mobility. When applied as ETL in inverted PSCs, BTPC60 not only exhibits excellent interfacial contact with the perovskite layer, resulting in enhanced electron extraction and transfer efficiency, but also effectively passivates the interfacial defects to suppress non‐radiative recombination. Resultant BTPC60‐based inverted PSCs deliver an impressive power conversion efficiency (PCE) of 25.3 % and retain almost 90 % of the initial values after aging at 85 °C for 1500 hours in N2. More encouragingly, the solution‐processed BTPC60 ETL demonstrates remarkable film thickness tolerance, and enables a high PCE up to 24.8 % with the ETL thickness of 200 nm. Our results highlight BTPC60 as a promising solution‐processed fullerene‐based ETM, opening an avenue for improving the scalability of efficient and stable inverted PSCs.

Inhibiting Cation Segregation to Enable Highly Efficient Perovskite Light‐Emitting Diodes

AbstractPerovskite light‐emitting diodes (PeLEDs) present potential applications for next‐generation displays due to their excellent luminescent properties and solution processing. The formamidinium‐caesium lead bromide (FAxCs1−xPbBr3) mixed cation strategy is one of the primary methods to achieve high‐performance of Cs‐dominate PeLEDs system. However, the inhomogeneous distribution of cations is detrimental to the photoelectronic performance of Cs‐dominated PeLEDs. Here, in mixed FA/Cs perovskite films, it is observed that Cs, Br and trace Pb elements precipitated on the surface of the perovskite films. It is found that the segregation of cations is induced by the uncontrollable crystallization process of Cs/FA cations. By introducing biuret additive, the hydrogen bonding interaction of biuret and FA cation balances crystallization rate, which therefore significantly improves the crystal quality and cations distribution of perovskite films. As a result, green PeLEDs with a high external quantum efficiency of 28.8% are obtained, and represent five times enhancement in half‐life time (T50) of 2.48 h at an initial luminance of 100 cd m−2 relative to the control device. The results help to understand the relationship between cationic distribution and PeLEDs properties, offering significant insights for modulating the performance of PeLEDs.

Boosting the Efficiency of Perovskite/Organic Tandem Solar Cells via Enhanced Near-Infrared Absorption and Minimized Energy Losses.

The compatibility of perovskite and organic photovoltaic materials in solution processing provides a significant advantage in the fabrication of high-efficiency perovskite/organic tandem solar cells. However, additional recombination losses can occur during exciton dissociation in organic materials, leading to energy losses in the near-infrared region of tandem devices. Consequently, a ternary organic rear subcell is designed containing two narrow-bandgap non-fullerene acceptors to enhance the absorption of near-infrared light. Simultaneously, a unique diffusion-controlled growth technique is adopted to optimize the morphology of the ternary active layer, thereby improving exciton dissociation efficiency. This innovation not only broadens the absorption range of near-infrared light but also facilitates the generation and effective dissociation of excitons. Owing to these technological improvements, the power conversion efficiency (PCE) of organic solar cells increased to 19.2%. Furthermore, a wide-bandgap perovskite front subcell is integrated with a narrow-bandgap organic rear subcell to develop a perovskite/organic tandem solar cell. Owing to the reduction in near-infrared energy loss, the PCE of this tandem device significantly improved, reaching 24.5%.

Limitation and Potential of Lignin-Assisted Stabilisation of Oriented Liquid Crystalline Cellulosic Mesophase

This study aimed at progressing in the fundamental understanding of the lignin-assisted microstructural stabilisation observed in solution-processed materials based on the polymer blend of hydroxypropyl cellulose and hardwood organosolv lignin. Mechanical analysis, polarised infrared spectroscopy and wide-angle X-ray scattering of shear cast blend films revealed that the effect of lignin on the flow-oriented cellulosic mesophase is also valid for blends composed of ethyl cellulose as liquid crystalline matrix polymer and lignin derived oligomers from base-catalysed depolymerisation as dispersed “microstructural cementing agent”. The results underline the significant role of the solvent diffusion between the continuous cellulosic and the dispersed lignin phase, which is ascribed to polymer-/oligomer-solvent interactions. An abundance of the solvent within the lignin phase caused the disruption of the microstructural stabilisation effect. The concept of a balanced proton-donor activity was introduced linking the solvent diffusion with the lyotropic liquid crystalline phase formation, the macro- and microstructural blend morphology and aspects regarding the solution processing.

Composition design of fullerene-based hybrid electron transport layer for efficient and stable wide-bandgap perovskite solar cells

Fullerene derivatives [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) has been routinely used as the electron transport layer (ETL) in perovskite solar cells due to its suitable energy levels and good solution processability. However, its electron mobility and conductivity still need to be further enhanced for constructing high performance perovskite solar cells (PSCs). Herein, by doping the PC61BM with a p-type polymer PM6 and n-type molecule ITIC, efficient wide-bandgap perovskite solar cells with improved efficiency and operational/storage stability are obtained. Further spectroscopy and electric measurements indicate PM6 and ITIC can both passivate defects at the perovskite/ETL interface, meanwhile ITIC can elevate the Fermi level of PC61BM to enhance conductivity and PM6 can improve the photo-induced electron mobility of the ETL, facilitating charge extraction and reducing charge recombination. As the results, Cs0.17FA0.83Pb(I0.83Br0.17)3 wide-bandgap PSCs with PM6:PC61BM:ITIC as the ETL demonstrates a superior efficiency of 22.95%, compared to 20.89% of the PC61BM assisted device.

Engineering PLA-MXene nanocomposite with balanced mechanical properties for enhanced shape memory effect

AbstractPoly(lactic acid) (PLA) as shape memory material has gained attention due to its biocompatibility, biodegradability, and ease of processing by 3D printing. PLA’s environmentally friendly nature makes it an attractive candidate for sustainable and recyclable shape memory applications. However, PLA’s slow shape recovery rate and low shape fixation percentage hinder its applicability as shape memory material. In the present study, we report MXene-modified PLA (PLA/Mx) nanocomposite with enhanced shape memory effect. Solution processing methods mediated the loading of the MXene in the PLA matrix. Different samples were prepared by varying the weight% of the MXene in the PLA matrix. The structure and morphology of samples were analyzed by XRD and TEM characterization. Thermogravimetric analysis was performed to measure the thermal stability of the composite. Compared with pure PLA, with MXene loading, the PLA/Mx composites show an increase in thermal. The shape recovery study on PLA/Mx samples used temperature as an external stimulus. The PLA/Mx composite exhibited a significantly improved shape memory effect than the PLA alone. The study exhibits that a shape memory effect can be improved by tuning the MXene additive loading in the PLA matrix. The material shape recovery effect was validated by fabricating the spiral structure. The fast shape recovery time 3s and shape fixation/recovery of &gt; 95% was observed for 1 wt% of PLA/Mx. The PLA/Mx composite is expected to contribute significantly to implementing innovative shape memory applications, particularly in the biomedical field for sutures, controlled drug release, and minimally invasive devices.