2D Nanocrystals Research Articles

Near infrared optically responsive Ag-Cu bimetallic 2D nanocrystals with controllable spatial structures

The optical properties of cost-effective Ag-Cu bimetallic nanocrystals, with synergistically enhanced catalytic and biological activities, are limited within ultraviolet–visible region due to lack of morphology control. In order to overcome this constraint, two-dimensional (2D) Ag-Cu bimetallic heterostructures were designed and synthesized by a seed-mediated colloidal growth method. The conformal Cu domain was epitaxially deposited on Ag nanoplates with different spatial configuration under retention of their 2D shape. Both of the 2D Ag-Cu core@shell and Janus structures display tunable localized surface plasmon resonance from visible to near infrared regions. The results of catalytic reduction of 4-nitrophenol show that the 2D Ag-Cu core@shell structure has better synergistic catalytic performance than Janus structure and Ag plates. In addition to surface-related synergistically enhanced bactericidal performance, their antibacterial effect can also be significantly enhanced by near infrared light irradiation. These results indicate that 2D Ag-Cu heterostructures can benefit from both synergistically improved surface activity and great optical responsive characteristics.

Programmable Birefringent Patterns from Modulating the Localized Orientation of Cellulose Nanocrystals.

Birefringence has been attracting broad attention due to its strong potential for applications in biomedicine and optics, such as biomedical diagnosis, colorimetric sensing, retardant, and polarization encoding. However, engineering architectures with precisely controllable birefringence remains a challenge due to the lack of effective modulation of the localized orientation. Here, by taking advantage of the inherently one-dimensional (1D) anisotropic structure of cellulose nanocrystals (CNCs), we demonstrate an approach to tune the alignment of CNCs with a well-controllable orientation at localized preciseness, which is in contrast to the previously reported unidirectional/radical orientation of CNC-based birefringent structures. The localized modulation of CNC orientation is facilitated by directing the 1D nanocrystals to align along the template periphery and the migrated three-phase contact line during the evaporation. The resultant CNC films exhibit birefringent extinction patterns under polarized light, in which versatile pattern designs can be obtained by employing templates with different shapes and template arrays with varied layouts. Due to the locally modulated orientation of CNCs, the films indicate "kaleidoscope-like" dynamically transformable designs of the birefringent patterns depending on the polarized angle, which has barely been observed previously. Furthermore, an N-nary encoding system for abundant information storage is demonstrated based on the sunlight-transparent CNC films, but with visible extinction patterns under polarized light, which is promising for encryptions, anticounterfeiting, and imaging, enriching the attractive research area of bio-based photonics.

High-Performance Deep Red Colloidal Quantum Well Light-Emitting Diodes Enabled by the Understanding of Charge Dynamics.

Colloidal quantum wells (CQWs) have emerged as a promising family of two-dimensional (2D) optoelectronic materials with outstanding properties, including ultranarrow luminescence emission, nearly unity quantum yield, and large extinction coefficient. However, the performance of CQWs-based light-emitting diodes (CQW-LEDs) is far from satisfactory, particularly for deep red emissions (≥660 nm). Herein, high efficiency, ultra-low-efficiency roll-off, high luminance, and extremely saturated deep red CQW-LEDs are reported. A key feature for the high performance is the understanding of charge dynamics achieved by introducing an efficient electron transport layer, ZnMgO, which enables balanced charge injection, reduced nonradiative channels, and smooth films. The CQW-LEDs based on (CdSe/CdS)@(CdS/CdZnS) ((core/crown)@(colloidal atomic layer deposition shell/hot injection shell)) show an external quantum efficiency of 9.89%, which is a record value for 2D nanocrystal LEDs with deep red emissions. The device also exhibits an ultra-low-efficiency roll-off and a high luminance of 3853 cd m-2. Additionally, an exceptional color purity with the CIE coordinates of (0.719, 0.278) is obtained, indicating that the color gamut covers 102% of the International Telecommunication Union Recommendation BT 2020 (Rec. 2020) standard in the CIE 1931 color space, which is the best for CQW-LEDs. Furthermore, an active-matrix CQW-LED pixel circuit is demonstrated. The findings imply that the understanding of charge dynamics not only enables high-performance CQW-LEDs and can be further applied to other kinds of nanocrystal LEDs but also is beneficial to the development of CQW-LEDs-based display technology and related integrated optoelectronics.

Structural Dynamics and Tunability for Colloidal Tin Halide Perovskite Nanostructures.

Lead halide perovskite nanocrystals are highly attractive for next-generation optoelectronics because they are easy to synthesize and offer great compositional and morphological tunability. However, the replacement of lead by tin for sustainability reasons is hampered by the unstable nature of Sn2+ oxidation state and by an insufficient understanding of the chemical processes involved in the synthesis. Here, an optimized synthetic route is demonstrated to obtain stable, tunable, and monodisperse CsSnI3 nanocrystals, exhibiting well-defined excitonic peaks. Similar to lead halide perovskites, these nanocrystals are prepared by combining a precursor mixture of SnI2 , oleylamine, and oleic acid, with a Cs-oleate precursor. Among the products, nanocrystals with 10nm lateral size in the γ-orthorhombic phase prove to be the most stable. To achieve such stability, an excess of precursor SnI2 as well as substoichiometric Sn:ligand ratios are key. Structural, compositional, and optical investigations complemented by first-principle density functional theory calculations confirm that nanocrystal nucleation and growth follow the formation of (R-NH3 + )2 SnI4 nanosheets, with R = C18 H35 . Under specific synthetic conditions, stable mixtures of 3D nanocrystals CsSnI3 and 2D nanosheets (Ruddlesden-Popper (R-NH3 + )2 Csn -1 Snn I3 n +1 with n> 1) are obtained. These results set a path to exploiting the high potential of Sn halide perovskite nanocrystals for opto-electronic applications.

Self-Assembly in water of C60 fullerene into isotropic nanoparticles or nanoplatelets mediated by a cationic amphiphilic polymer

HypothesisTo disperse high concentration of C60 fullerene in water, we propose to use an emulsification-evaporation process in the presence of an amphiphilic polymer whose chemical structure has been chosen for inducing specific interaction with fullerene The viscosity enhancement provided by self-assembly of the amphiphilic polymers in water should result in high stability of the suspensions. The organic solvent has also to been chosen so as to maximize the initial fullerene concentration. ExperimentsThe concentrations of polymer and fullerene, the solvent type and the volume fraction of the organic phase have been varied. Their influence on the concentration of the fullerene dispersions and on the size and shape of the resulting nanoparticles have been investigated by UV–Visible spectroscopy, light scattering and cryo-transmission electron microscopy experiments. FindingsThe resulting nanoparticles consist of aggregates of C60 fullerene stabilized by the cationic polymer with morphologies/sizes tunable through fullerene and polymer concentration. At high fullerene concentration, nanoplatelets are obtained that consist in thin 2D nanocrystals. Their suspensions are very stable with time due to the viscosity of the dispersing aqueous medium. The concentration of fullerene nanoparticles dispersed in water is as high as 8 g/L which corresponds to an upper limit that has never been reached so far.

Tuning Crystal Plane Orientation in Multijunction and Hexagonal Single Crystalline CsPbBr3 Perovskite Disc Nanocrystals

Two-dimensional-shaped CsPbBr3 platelet nanocrystals are widely studied for their bright high energy emission and self-assembly. These nanostructures are in orthorhombic phase, have a square shape, and have the vertical axis [001] perpendicular to the basal plane. Moreover, these are mostly single-crystalline structures with a continuous lattice and appear like slices of cube nanocrystals. In contrast, herein, multijunction and hexagonal single crystalline 2D discs of CsPbBr3 are reported to have all their vertical axes [100]. These are obtained by using the perovskite derivative of tetragonal Cs3MnBr5 as the parent material and subsequent B-site Pb(II) introduction in the presence of phenacyl bromide at different reaction temperatures. At low temperature, multijunction discs having random orientations of two horizontal axes [010] and [001] from one to another segment are observed. Orientations of planes remained random as both coherent and incoherent twin planes were observed at their boundaries. However, the number of junctions/segments was reduced at higher temperature, and finally hexagonal single crystalline discs remained as the ultimate product. Analysis suggested that the crystal nature of parent Cs3MnBr5 and temperature-dependent variation in the rate of Pb(II) insertions determined the nature of discs having randomly oriented or static planes in the entire nanostructure. Not only in 2D discs but also, 3D nanocrystals having similar segments with different orientations are formed upon Pb(II) exchange with Mn(II) alloyed cubic CsBr. Hexagonal single crystalline and segmented multijunction CsPbBr3 discs remain unique among 2D perovskites nanostructures, and their formation mechanism indeed introduced new fundamentals of the crystallization process of these emerging energy materials.

Nucleation Kinetics and Structure Evolution of Quasi-Two-Dimensional ZnO at the Air-Water Interface: An In Situ Time-Resolved Grazing Incidence X-ray Scattering Study.

The design and synthesis of high-quality two-dimensional (2D) materials with desired morphology are essential for property control. One critical challenge that impedes the understanding and control of 2D crystal nucleation and growth is the inability of direct observation of the nanocrystal evolution process with high enough time resolution. Here, we demonstrated an in situ X-ray scattering approach that directly reveals 2D wurtzite ZnO nanosheet growth at the air-water interface. The time-resolved grazing incidence X-ray diffraction (GID) and grazing incidence X-ray off-specular scattering (GIXOS) results uncovered a lateral to vertical growth kinetics switch phenomenon in the ZnO nanosheet growth. This switch represents the 2D to three-dimensional (3D) crystal structure evolution, which governs the size and thickness of nanosheets, respectively. This phenomenon can guide 2D nanocrystal synthesis with rationally controlled size and thickness. Our work opens a new pathway toward the understanding of 2D nanomaterial growth kinetics based on time-resolved liquid surface grazing incidence X-ray techniques.

2D FeP Nanoframe Superlattices via Space-Confined Topochemical Transformation.

Self-assembled nanocrystal superlattices represent an emergent class of designer materials with potentially programmable functionalities. The ability to construct hierarchically structured nanocrystal superlattices with tailored geometry and porosity is critical for extending their applications. Here, 2D superlattices comprising monolayer FeP nanoframes are synthesized through a space-confined topochemical transformation approach induced by the Kirkendall effect, using carbon-coated Fe3 O4 nanocube superlattices as a precursor. The particle shape and the close-packed nature of Fe3 O4 nanocubes as well as the interconnected carbon layer network contribute to the topochemical transformation process. The resulting 2D FeP nanoframe superlattices possess several unique and advantageous structural features that are unavailable in conventional 3D nanocrystal superlattices, which make them particularly attractive for catalytic applications. As a proof of concept, such 2D FeP nanoframe superlattices are harnessed as highly efficient and durable electrocatalysts for the hydrogen evolution reaction, the performance of which is superior to that of most FeP-based catalysts reported previously. This topochemical transformation approach is scalable and general, representing a new route of designing hierarchical superlattices with highly open features that cannot be accessible by traditional self-assembly methods.

2D-Oriented Attachment of 1D Colloidal Semiconductor Nanocrystals via an Etchant.

The oriented attachment (OA) of 0D semiconductor nanocrystals into 1D and 2D nanostructures with unique properties is useful for the fabrication of quantum confined nanomaterials that are otherwise difficult to produce by direct synthesis. Given that the OA of 1D nanocrystals such as nanorods generally produces linear chains, rod-couple structures, or clustered columns, linking them in a facet-specific manner to produce 2D structures is challenging. Here, we report that 1D Cu2-xS nanorods undergo etching on exposure to hexylphosphonic acid under mild heating, which results in an increased curvature and a reduction in surface ligands at those sites. This causes the nanorods to fuse via their basal tip facets into chains and then cojoin through diametrically opposed side facets, resulting in atomically coupled, 2D raftlike structures. The stepwise OA of 1D nanocrystals into 2D nanostructures illustrated here expands the range of nanoarchitectures that can be produced via solution-processed methods.

Two-dimensional copper based colloidal nanocrystals: synthesis and applications.

Two-dimensional (2D) semiconductor nanocrystals display unconventional physical and opto-electronic properties due to their ultrathin and unique electronic structures. Since the success of Cd-based photoemissive nanocrystals, the development of sustainable and low-cost nanocrystals with enhanced electronic and physical properties has become a central research theme. In this context, copper-based semiconductor 2D nanocrystals, the cost-effective and eco-friendly alternative, exhibit unique plasmonic resonance, transport properties, and high ionic conductivity beneficial for sensing, energy storage, conversion, and catalytic applications. This review summarizes recent progress in the colloidal synthesis, growth mechanisms, properties, and applications of 2D copper-based nanostructures with tunable compositions, dimensions, and crystal phases. We highlight the growth mechanisms concerning their shape evolution in two dimensions. We analyse the effectiveness of cation exchange as a tool to synthesize multinary nanocrystals. Based on the preparation of Cu-based chalcogenide and non-chalcogenide compositions, we discuss synthesis control achieved via colloidal approaches to allow dimension tunability, phase engineering, and plasmonic and thermoelectric property optimization. Furthermore, their potential in various applications of catalysis, energy storage, and sensing is reviewed. Finally, we address the current challenges associated with 2D Cu-based nanocrystal development and provide an outlook pertaining to unexplored research areas.

Nanocrystal-based 3D-printed tablets: Semi-solid extrusion using melting solidification printing process (MESO-PP) for oral administration of poorly soluble drugs

This is the first report on the inclusion of nanocrystals (NCs) within 3D-printed oral solid dosage forms –3D-printed tablets or printlets– produced by the Melting Solidification Printing Process (MESO-PP) 3D printing technique. This method allowed the incorporation of albendazole (ABZ) nanocrystals in a concentration of up to 50% w/w, something not achieved in conventional tablets. An ink of PEG 1500/propylenegycol was used as a carrier and no physicochemical interactions or crystallinity modifications were observed due to the inclusion of ABZ-NCs into the ink, as demonstrated by TGA, DSC, XRD and FT-IR. In particular, the relative crystallinity of the ink loaded with NCs was 97.8% similar to the physical mixture of the components. Moreover, the presence of NCs was observed in the surface and matrix of the printlets by SEM. In addition, the printlet NCs demonstrated to be more effective than NCs included in hard gelatin capsules in improving drug dissolution in HCl 0.1 N. The particle size, crystallinity and chemical stability of the nanocrystals was maintained before and after 180 days of storage. Thus, these findings exhibit relevant pharmaceutical potential for developing stable, fast-release, oral, solid dosage forms of poorly soluble drugs combining 3D printing and nanocrystals. Additionally, this technique could be applied for printing objects using different types of nanocrystals embedded in low melting temperature polymers.

Ripening of two-dimensional colloidal CdSe nanocrystals into zero-dimensional nanodots

SummaryUnderstanding the ripening of two-dimensional (2D) colloidal nanocrystals (NCs) is important for the controllable synthesis of NCs with desired morphology and properties. In this study, we systematically investigate the ripening behavior of the 2D CdSe NCs in the presence of a short-chain acetate ligand and a long-chain oleate ligand. We find that a low acetate/oleate ratio, a low Cd/Se ratio, and a low monomer concentration help in the ripening of the 2D NCs to form 0D NCs. Moreover, a porous nanosheet intermediate is observed when there is a high Cd/Se ratio, whereas in the case of a low Cd/Se ratio, the ripening starts from the edge of the nanosheets, resulting in a saw-like nanosheet intermediate. These findings provide necessary insights into the growth and ripening of 2D CdSe NCs that allow for the controlled synthesis of 0D and 2D CdSe NCs.

Defect detection in atomic-resolution images via unsupervised learning with translational invariance

Crystallographic defects can now be routinely imaged at atomic resolution with aberration-corrected scanning transmission electron microscopy (STEM) at high speed, with the potential for vast volumes of data to be acquired in relatively short times or through autonomous experiments that can continue over very long periods. Automatic detection and classification of defects in the STEM images are needed in order to handle the data in an efficient way. However, like many other tasks related to object detection and identification in artificial intelligence, it is challenging to detect and identify defects from STEM images. Furthermore, it is difficult to deal with crystal structures that have many atoms and low symmetries. Previous methods used for defect detection and classification were based on supervised learning, which requires human-labeled data. In this work, we develop an approach for defect detection with unsupervised machine learning based on a one-class support vector machine (OCSVM). We introduce two schemes of image segmentation and data preprocessing, both of which involve taking the Patterson function of each segment as inputs. We demonstrate that this method can be applied to various defects, such as point and line defects in 2D materials and twin boundaries in 3D nanocrystals.

High Harmonic Generation from Laser-Induced Plasmas of Ni-Doped CsPbBr3 Nanocrystals: Implications for Extreme Ultraviolet Light Sources

The development of versatile two-dimensional (2D) nanocrystals (NCs), with superior nonlinear optical (NLO) properties, is essential for various applications in photonics and optical communications. In this work, we demonstrate efficient high-order harmonic generation (HHG) from the laser-induced plasmas (LIPs) of CsPbBr3 and Ni-doped CsPbBr3 NCs. The present study has been directed at unraveling the role of dopants in the emission of intense harmonics from the LIP of purposefully engineered CsPbBr3 colloidal NCs. The trend observed in the harmonic yield enhancement is found to be similar to the increase in their third-order NLO properties [nonlinear refractive index (n2), nonlinear optical susceptibility (χ(3))] of the same NCs studied at a wavelength of 800 nm. Ni-doped CsPbBr3 NCs containing plasma spreading allowed optimization of the delay between nanosecond (ns) heating pulse and driving pulse (single-color pump) for an enhancement in the conversion efficiency of harmonics. We believe that the emission of harmonics from the LIPs of these pristine, Ni-doped CsPbBr3 colloidal 2D NCs reported here provides the means to address the increase in the efficiency of extreme ultraviolet radiation, useful in attosecond spectroscopic studies.

Fabrication of Three-Dimensional Porous Materials with NiO Nanowalls for Electrocatalytic Oxygen Evolution

Nanosheets are two-dimensional (2D) nanocrystals that exhibit superior electrochemical performance. However, nanosheets are typically stacked horizontally toward the current collector, leading to poor utilization of individual nanosheets. Although most studies have fabricated three-dimensional (3D) structures using nanosheets, the wall thickness was a few hundred nanometers, suggesting that hundreds of nanosheets were restacked along the wall. In this study, we demonstrated the fabrication of a 3D structure constructed by NiO nanowalls with a thickness of 2–3 nm (3D-NiO). The specific surface area of 3D-NiO was found to be 42 m2 g–1, which is 2.6 times larger than that of NiO nanoparticles. The specific capacity of 3D-NiO was 2.5 times higher than that of NiO nanoparticles and could be attributed to the large specific surface area because of the nature of the thin nanowalls. The O2-evolution reaction (OER) activity of 3D-NiO at 1.65 V vs RHE was sixfold greater than that of NiO nanoparticles. The enhanced OER activity of 3D-NiO could be attributed to both the large specific surface area and the fabrication of diffusion paths within the 3D structure. The OER activity of 3D-NiO after 500 cycles was four times higher than that of NiO nanoparticles. Our results show that the 3D structure fabricated with thin nanowalls is a promising porous material for capacitor electrodes and electrocatalysts for applications in electrolysis and fuel cells.

Morphology control of copper hydroxide based nanostructures in liquid phase synthesis

Synthesis and study of copper hydroxide based nanostructures is of continued interest for researchers as these materials act as templates for formation of CuO and because of their individual applications for energy storage and sensing. However, the synthesis mechanisms and the intrinsic properties of these nanostructures are rarely investigated. In this work, we show the template-free bottom-up synthesis and shape control of copper hydroxide based nanostructures grown in liquid phase, from 1D nanowires to 2D layered nanoplatelets and 3D nanocrystals. Precise control over the pH of the solution and the reaction temperature lead to intended tuning of the morphology and chemical composition of the nanostructures. Among the copper hydroxy salts, the botallackite polymorph is known as an intermediate compound which is difficult to stabilise in mother solution. We show here a way to achieve the stable botallackite in form of nanoplatelets. The obtained copper hydroxide based nanostructures are analysed using X-ray Diffraction, X-ray Photoelectron Spectroscopy and absorbance spectra. We contemplate upon the rationale behind this change in shape and material. Having an improved understanding of the formation mechanism of the various nanostructures will enable researchers to have better control over synthesis with designed architecture of nanostructures for targeted applications.

Sb-Doped Metal Halide Nanocrystals: A 0D versus 3D Comparison.

We synthesize colloidal nanocrystals (NCs) of Rb3InCl6, composed of isolated metal halide octahedra (“0D”), and of Cs2NaInCl6 and Cs2KInCl6 double perovskites, where all octahedra share corners and are interconnected (“3D”), with the aim to elucidate and compare their optical features once doped with Sb3+ ions. Our optical and computational analyses evidence that the photoluminescence quantum yield (PLQY) of all these systems is consistently lower than that of the corresponding bulk materials due to the presence of deep surface traps from under-coordinated halide ions. Also, Sb-doped “0D” Rb3InCl6 NCs exhibit a higher PLQY than Sb-doped “3D” Cs2NaInCl6 and Cs2KInCl6 NCs, most likely because excitons responsible for the PL emission migrate to the surface faster in 3D NCs than in 0D NCs. We also observe that all these systems feature a large Stokes shift (varying from system to system), a feature that should be of interest for applications in photon management and scintillation technologies. Scintillation properties are evaluated via radioluminescence experiments, and re-absorption-free waveguiding performance in large-area plastic scintillators is assessed using Monte Carlo ray-tracing simulations.

Programmable two-dimensional nanocrystals assembled from POSS-containing peptoids as efficient artificial light-harvesting systems.

Inspired by the formation of hierarchically structured natural biominerals (e.g., bone and tooth), various sequence-defined polymers have been synthesized and exploited for design and synthesis of functional hybrid materials. Here, we synthesized a series of organic-inorganic hybrid peptoids by using polyhedral oligomeric silsesquioxane (POSS) nanoclusters as side chains at a variety of backbone locations. We further demonstrated the use of these hybrid peptoids as sequence-defined building blocks to assemble a new class of programmable two-dimensional (2D) nanocrystals. They are highly stable and exhibit an enhanced mechanical property and electron scattering due to the incorporated POSS nanoclusters. By varying peptoid side-chain chemistry, we further demonstrated the precise displacement of a large variety of function groups within these 2D nanocrystals and developed a highly efficient aqueous light-harvesting system for live cell imaging. Because these 2D nanocrystals are biocompatible and highly programmable, we expect that they offer unique opportunities for applications.

Modular Construction of Prussian Blue Analog and TiO2 Dual-Compartment Janus Nanoreactor for Efficient Photocatalytic Water Splitting.

Janus structures that include different functional compartments have attracted significant attention due to their specific properties in a diverse range of applications. However, it remains challenge to develop an effective strategy for achieving strong interfacial interaction. Herein, a Janus nanoreactor consisting of TiO2 2D nanocrystals integrated with Prussian blue analog (PBA) single crystals is proposed and synthesized by mimicking the planting process. In situ etching of PBA particles induces nucleation and growth of TiO2 nanoflakes onto the concave surface of PBA particles, and thus enhances the interlayer interaction. The anisotropic PBA–TiO2 Janus nanoreactor demonstrates enhanced photocatalytic activities for both water reduction and oxidation reactions compared with TiO2 and PBA alone. As far as it is known, this is the first PBA‐based composite that serves as a bifunctional photocatalyst for solar water splitting. The interfacial structure between two materials is vital for charge separation and transfer based on the spectroscopic studies. These results shed light on the elaborate construction of Janus nanoreactor, highlighting the important role of interfacial design at the microscale level.

Rapid hydrothermal synthesis of highly crystalline transition metal (Mn & Fe) doped CuSe nanostructures: Applications in wastewater treatment and room temperature gas sensing

In this paper, we report on the rapid hydrothermal synthesis of CuSe 2D nanocrystals. The nanostructures were synthesized for very short reaction durations of 3 h. The influence of two different transition metal inclusions (Mn & Fe) on the growth and properties of CuSe nanocrystals was investigated. Transition metal dopants were found to have a prominent influence on the morphological, magnetic, optical and photocatalytic behavior of the material. Structural properties show that the nanostructures have a single phase with the hexagonal structure. The inclusion of the transition metal dopants (Mn and Fe) had no influence on the phase of the nanostructures although growth along certain crystal directions was restricted. Morphologies like flakes and hexagonal discs were obtained, all in the nanoscale dimensions. Doping resulted in the development of catalytically active edge sites which are more prominent in the case of Fe doping. Magnetic studies reveal conversion of diamagnetic CuSe into paramagnetic material upon doping with Fe and Mn. The gas sensing property of the synthesized nanostructures was tested against NO2 gas. The hexagonal nano-discs showed the highest sensitivity reaching 25% at 40 ppm NO2 concentration. The nanostructures were utilized for the photodegradation of methylene blue (MB) dye under UV-Visible light illumination. Addition of the transition metal dopants resulted in the enhancement of photocatalytic activity of the material, improving the degradation percentage from 59.4% to 64.5%.