Amorphization Process Research Articles

Effect of Cu addition on the properties of Pd-based metallic glasses by experimentation and molecular dynamics simulations

The effect of trace Cu element additions on the properties of Pd-based amorphous alloys was investigated by a combination of experimental and molecular dynamics (MD) simulations. Thin ribbons of Pd40Ni40P20 and containing different proportions of Cu (1 %, 3 %, and 5 %) were prepared, analyzed by X-ray diffraction (XRD) to determine the phase structure, tested for their thermal properties by differential scanning calorimetry (DSC), and nanoindentation to test their mechanical properties. Meanwhile, the amorphization process and compression behavior of these alloys were simulated by MD simulation, and the microstructures of the alloys were resolved by using the radial distribution function (RDF) and the coordination number distribution function (PDF), and the glass transition temperatures (Tg) were deduced from the energy variations. The Voronoi polyhedral analyses showed that the addition of trace amounts of Cu altered the content of the specific clusters, which affected the macroscopic mechanical properties. Both nanoindentation experimental and simulation results confirmed that the addition of trace Cu reduces the Tg and improved the mechanical properties of the Pd40Ni40P20 alloy while maintaining the amorphous structure.

A systematic IR and VUV spectroscopic investigation of ion, electron, and thermally processed ethanolamine ice

ABSTRACT The recent detection of ethanolamine (EtA, HOCH$_2$CH$_2$NH$_2$), a key component of phospholipids, i.e. the building blocks of cell membranes, in the interstellar medium is in line with an exogenous origin of life-relevant molecules. However, the stability and survivability of EtA molecules under inter/circumstellar and Solar System conditions have yet to be demonstrated. Starting from the assumption that EtA mainly forms on interstellar ice grains, we have systematically exposed EtA, pure and mixed with amorphous water (H$_2$O) ice, to electron, ion, and thermal processing, representing ‘energetic’ mechanisms that are known to induce physicochemical changes within the ice material under controlled laboratory conditions. Using infrared (IR) spectroscopy, we have found that heating of pure EtA ice causes a phase change from amorphous to crystalline at 180 K, and further temperature increase of the ice results in sublimation-induced losses until full desorption occurs at about 225 K. IR and vacuum ultraviolet (VUV) spectra of EtA-containing ices deposited and irradiated at 20 K with 1 keV electrons as well as IR spectra of H$_2$O:EtA mixed ice obtained after 1 MeV He$^+$ ion irradiation have been collected at different doses. The main radiolysis products, including H$_2$O, CO, CO$_2$, NH$_3$, and CH$_3$OH, have been identified and their formation pathways are discussed. The measured column density of EtA is demonstrated to undergo exponential decay upon electron and ion bombardment. The half-life doses for electron and He$^+$ ion irradiation of pure EtA and H$_2$O:EtA mixed ice are derived to range between $10.8\!-\!26.3$ eV/16u. Extrapolating these results to space conditions, we conclude that EtA mixed in H$_2$O ice is more stable than in pure form and it should survive throughout the star and planet formation process.

Favored Amorphous LixSi Process with Restrained Volume Change Enabling Long Cycling Quasi-Solid-State SiOx anode.

Silicon-based anodes are becoming promising materials due to their high specific capacity. However, the intrinsically large volume change brought about by the alloying reaction results in the crushing of the active particles and destruction of the electrode structure, which severely limits its practical application. Various structured and modified silica-based anodes exhibit improved cycling stability and the demonstrated ability to mitigate their volume changes through interfacial and binder strategies. However, the issue of large volume changes in silicon-based anodes remains. Herein, we report a gel polymer electrolyte (GPE) prepared through an in situ thermal polymerization process that is suitable for SiOx anode materials and achieving long-term cycling stability. GPE-based cells essentially mitigate the volume change of SiOx anodes by guiding the unique lithiation/delithiation mechanism that tends to favor the formation and delithiation of amorphous-LixSi (a-LixSi) with smaller volume change, thereby mitigating electrode damage and cracking, and achieving the significant improvement in cycling performance. The prepared GPE-SiOx cells retained 693.80 mAh g-1 reversible capacity after 450 cycles at 500 mA g-1. In addition, the prelithiation process was incorporated to mitigate capacity fluctuations and improve the Initial Coulombic Efficiency (ICE), and a reversible capacity of 641.90 mAh g-1 was retained after 480 cycles.

Thermal Transformation of Kaolinite Clays: Analyzing Dehydroxylation and Amorphization for Improved Pozzolanic Performance

This study explores the impact of heat treatment parameters on the dehydroxylation and amorphization processes of kaolinite-based materials, in particular natural kaolin clays. It develops a quantitative method for estimating the amorphous phase in heat-treated kaolinite, using differential thermal analysis/thermogravimetry (DTA/TGA), mass spectrometry, X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). Kaolin clays, subjected to controlled heat treatments between 600°C and 800°C, undergo significant structural transformations. The study identifies the degree of dehydroxylation (DTG) as a crucial measure of kaolinite performance after heat treatment, calculated as a function of sample weight loss. The transition from a crystalline to an amorphous phase strongly influences pozzolanic activity, characterized by its ability to react with portlandite (Ca(OH)₂) in water-rich environments.The materials used, including clay from the Benslimane region of Morocco, were finely ground and subjected to various thermal treatments. Thermal analyses revealed characteristic patterns of mass loss and phase transformation. XRD and FTIR analyses provided detailed information on structural changes, confirming the amorphization of kaolinite after dehydro.

SHG behavior of the solid isomorphic compounds Ni- and Cu-5,10,15,20- tetraphenylporphyrinate. An experimental and theoretical study

We prepared and investigated the SHG behavior in the solid state of the two isomorphic Nickel and Copper 5,10,15,20-tetraphenylporphyrinate, that crystallize in the same acentric I4¯2d space group. The compounds were synthesized and characterized, and the Second Harmonic Generation (SHG) response of powdered samples was measured employing a 1.907 μm pulsed laser radiation. During laser irradiation, for both compounds, a gradual increase of the intensity of the SH signal was observed until, after a few minutes, it reached a plateau of about fifty times (for the Ni-TPP) or ten times (for the Cu-TPP) the initial value. We attempted to understand the origin of this phenomenon both through experimental analysis and theoretical calculations. Absorption and vibrational spectroscopies, in solution and solid state, combined with powder X-ray diffraction, both before and after irradiation, do not evidence any chemical degradation, phase transition or amorphization process. Theoretical calculations on little fragments of the Ni/Cu-TPP structure simulate appropriately the structural features of the complexes and their initial experimental SHG response. Magnetic balance measurement in the solid state before and after irradiation, in conjunction with DFT/B3LYP optimization of excited spin states and TDDFT calculations, highlight a change in the electronic and/or spin state due to the irradiation of the complexes.

In Situ Amorphization of Electrocatalysts

AbstractElectrocatalysis represents an efficient and eco‐friendly approach to energy conversion, enabling the sustainable synthesis of valuable chemicals and fuels. The deliberate engineering of electrocatalysts is crucial to improving the efficacy and scalability of electrocatalysis. Notably, the occurrence of in situ amorphization within electrocatalysts has been observed during various electrochemical processes, influencing the energy conversion efficiency and catalytic mechanism understanding. Of note, the dynamic transformation of catalysts into amorphous structures is complex, often leading to various amorphous configurations. Therefore, revealing this amorphization process and understanding the function of amorphous species are pivotal for elucidating the structure‐activity relationship of electrocatalysts, which will direct the creation of highly efficient catalysts. This review examines the mechanisms behind amorphous structure formation, summarizes characterization methods for detecting amorphous species, and discusses strategies for controlling (pre)catalyst properties and electrochemical conditions that influence amorphization. It also emphasizes the importance of spontaneously formed amorphous species in electrochemical oxidation and reduction reactions. Finally, it addresses challenges in the in situ amorphization of electrocatalysts. aiming to guide the synthesis of electrocatalysts for efficient, selective, and stable electrochemical reactions, and to inspire future advancements in the field.

P‐29: A bias TFT with high photosensitive current for optical sensors

A photosensitive TFT sensor called bias TFT fabricated using simple amorphous silicon process in this paper. The photosensitive current of bias TFT is linearly related to the brightness of the top light source and inversely proportional to the size of the bias region. The photosensitivity current can be up to 10E‐8 amperes under 100 nits illumination. Among four shapes of bias TFTs, L‐type TFTs have the highest photo current.

Study of the entropy and enthalpy of gamma irradiated TiC nanoparticles

The thermal characteristics of nanocrystalline titanium carbide (TiC) particles were systematically compared before and after gamma irradiation through the application of Differential Scanning Calorimetry (DSC) spectroscopy. Utilizing experimental findings, the Gibbs energy of titanium carbide nanoparticles was ascertained within the temperature range spanning from 300 to 1270 K. The investigation of potential phase transitions in nanoparticles and the amorphization processes induced by gamma radiation was investigated employing the Differential Thermal Analysis (DTA) methodology. The enthalpy and entropy of the system comprising nanocrystalline 3C-SiC particles were computed both before and after exposure to gamma irradiation, with theoretical calculations corroborated through comparison with experimental outcomes. The values derived from experimental results for all thermophysical parameters were compared both before and after exposure to gamma radiation.

Rational Design of Amorphous Nanomaterials for Enhanced Electrochemical CO2 and Nitrate Reduction

Amorphous materials are distinguished by their exceptional attributes, notably their expansive surface area and the profusion of active sites they present. Consequently, the amorphization process stands as an efficacious strategy to augment the catalytic efficacy of electrocatalysts. This is achieved through the meticulous construction of the surface architecture and the precise modulation of the electronic configuration of these materials. Therefore, this review aims to offer a thorough examination of the latest progress in the application of amorphous materials for the enhancement of electrocatalytic processes, with a particular emphasis on the nitrate (NO3‐) reduction reaction (NITRR) and the carbon dioxide reduction reaction (CO2RR). Initially, we delve into the structural benefits inherent to amorphous materials, outlining the diverse synthesis techniques and characterization methodologies utilized in their development. Following this, we illustrate the utilization of various amorphous materials in NITRR and CO2RR, accentuating how the amorphous framework influences electrocatalytic activities. Concludingly, we encapsulate the merits and the obstacles encountered in the application of amorphous electrocatalysts for NITRR and CO2RR, whilst also forecasting the future direction for the creation of innovative amorphous electrocatalysts.

Shear localization-induced amorphization in nanocrystals during high strain rate deformation

Shear localization is the predominant form of failure of metals at high strain rates where amorphization often occurs. However, the mechanism and role of amorphization in shear localization are not yet clearly understood. In this work, a series of shear deformations of nanocrystals with different grain sizes at high strain rates are investigated using molecular dynamics simulations. The results show that amorphization is not the result of thermal melting, but a new plastic deformation mechanism in the process of shear localization, which serves as a complement to dislocation and grain boundary to support plastic deformation at a high strain rate. The critical shear strain at which shear localization and amorphization occur is greater for small-grained specimens than for large-grained specimens. This can be attributed to the fact that small-grained specimens have more defects and slip systems that can be activated, which cause amorphization to occur later. The strain rate has a significant influence on shear localization and amorphization. The processes of shear localization and amorphization become more complicated at extremely high strain rates than at relatively low strain rates.

Ab initio study of the vibrational spectra of amorphous boron nitride

Boron Nitride (BN) is an interesting polymorphic insulator that is commonly found in four different crystalline structures, each one with different electrical and mechanical properties which makes it an attractive material for technological and industrial applications. Seeking to improve its features, several experimental and simulational works have studied the amorphous phase (a-BN) focusing on electronic and structural properties, pressure-induced phase transformations, and a hydrogenated form of a-BN. By means of ab initio Molecular Dynamics and our well-proven amorphization process known as the undermelt-quench approach, herein three amorphous supercells were computationally generated, two with 216 atoms (densities of 2.04 and 2.80 g cm−3) and a third one with 254 atoms (density of 3.48 g cm−3). The topology, the vibrational density of states and some thermodynamic properties of the three samples are reported and compared with existing experiments and with other computational results.

The α-crystallin Chaperones Undergo a Quasi-ordered Co-aggregation Process in Response to Saturating Client Interaction

Small heat shock proteins (sHSPs) are ATP-independent chaperones vital to cellular proteostasis, preventing protein aggregation events linked to various human diseases including cataract. The α-crystallins, αA-crystallin (αAc) and αB-crystallin (αBc), represent archetypal sHSPs that exhibit complex polydispersed oligomeric assemblies and rapid subunit exchange dynamics. Yet, our understanding of how this plasticity contributes to chaperone function remains poorly understood. Using biochemical and biophysical analyses combined with single-particle electron microscopy (EM), we examined structural changes in αAc, αBc and native heteromeric lens α-crystallins (αLc) in their apo-states and at varying degree of chaperone saturation leading to co-aggregation, using lysozyme and insulin as model clients. Quantitative single-particle analysis unveiled a continuous spectrum of oligomeric states formed during the co-aggregation process, marked by significant client-triggered expansion and quasi-ordered elongation of the sHSP oligomeric scaffold, whereby the native cage-like sHSP assembly displays a directional growth to accommodate saturating conditions of client sequestration. These structural modifications culminated in an apparent amorphous collapse of chaperone-client complexes, resulting in the creation of co-aggregates capable of scattering visible light. Intriguingly, these co-aggregates maintain internal morphological features of highly elongated sHSP oligomers with striking resemblance to polymeric α-crystallin species isolated from aged lens tissue. This mechanism appears consistent across αAc, αBc and αLc, albeit with varying degrees of susceptibility to client-induced co-aggregation. Importantly, our findings suggest that client-induced co-aggregation follows a distinctive mechanistic and quasi-ordered trajectory, distinct from a purely amorphous process. These insights reshape our understanding of the physiological and pathophysiological co-aggregation processes of α-crystallins, carrying potential implications for a pathway toward cataract formation.

Graphene and MOF Assembly: Enhanced Fabrication and Functional Derivative via MOF Amorphization.

The integration of graphene and metal-organic frameworks (MOFs) has numerous implications across various domains, but fabricating such assemblies is often complicated and time-consuming. Herein, a one-step preparation of graphene-MOF assembly is presented by directly impregnating vertical graphene (VG) arrays into the zeolitic imidazolate framework (ZIF) precursors under ambient conditions. This approach can effectively assemble multiple ZIFs, including ZIF-7, ZIF-8, and ZIF-67, resulting in their uniform dispersion on the VG with adjustable sizes and shapes. Hydrogen defects on the VG surface are critical in inducing such high-efficiency ZIF assembly, acting as the reactive sites to interact with the ZIF precursors and facilitate their crystallisation. The versatility of VG-ZIF-67 assembly is further demonstratedby exploring the process of MOF amorphization. Surprisingly, this process leads to an amorphous thin-film coating formed on VG (named VG-IL-amZIF-67), which preserves the short-range molecular bonds of crystalline ZIF-67 while sacrificing the long-range order. Such a unique film-on-graphene architecture maintains the essential characteristics and functionalities of ZIF-67 within a disordered arrangement, making it well-suited for electrocatalysis. In electrochemical oxygen reduction, VG-IL-amZIF-67 exhibits exceptional activity, selectivity, and stability to produce H2O2 in acid media.

Amorphous Oxyhalide Matters for Achieving Lithium Superionic Conduction.

The recently surged halide-based solid electrolytes (SEs) are great candidates for high-performance all-solid-state batteries (ASSBs), due to their decent ionic conductivity, wide electrochemical stability window, and good compatibility with high-voltage oxide cathodes. In contrast to the crystalline phases in halide SEs, amorphous components are rarely understood but play an important role in Li-ion conduction. Here, we reveal that the presence of amorphous component is common in halide-based SEs that are prepared via mechanochemical method. The fast Li-ion migration is found to be associated with the local chemistry of the amorphous proportion. Taking Zr-based halide SEs as an example, the amorphization process can be regulated by incorporating O, resulting in the formation of corner-sharing Zr-O/Cl polyhedrons. This structural configuration has been confirmed through X-ray absorption spectroscopy, pair distribution function analyses, and Reverse Monte Carlo modeling. The unique structure significantly reduces the energy barriers for Li-ion transport. As a result, an enhanced ionic conductivity of (1.35 ± 0.07) × 10-3 S cm-1 at 25 °C can be achieved for amorphous Li3ZrCl4O1.5. In addition to the improved ionic conductivity, amorphization of Zr-based halide SEs via incorporation of O leads to good mechanical deformability and promising electrochemical performance. These findings provide deep insights into the rational design of desirable halide SEs for high-performance ASSBs.

Changes in the structure of the amorphous phase under heat treatment and deformation

The influence of heat treatment and deformation on the change in the structure of amorphous alloys Co67Fe7Si12B9Nb5, Al87Ni8Y5, Al88Ni6Y6, Al87Ni8Gd5, Al87Ni8La5, Zr50Cu15Ti16Ni19 obtained by melt quen-ching has been studied. It has been established that both heat treatment and deformation lead to the for-mation of a heterogeneous structure, while structure inhomogeneities can be due to formation the regions both with different concentrations of components (during heat treatment) or/and with different density (free volume concentration). At the early stages of crystallization, the phase composition of the emerging struc-ture depends on the type of impact on the amorphous structure and processing parameters (temperature, type and degree of deformation). The sizes of nanocrystals and the fraction of the nanocrystalline component depend on the prehistory of the sample.

Mechanochemically-induced glass formation from two-dimensional hybrid organic-inorganic perovskites.

Hybrid organic-inorganic perovskites (HOIPs) occupy a prominent position in the field of materials chemistry due to their attractive optoelectronic properties. While extensive work has been done on the crystalline materials over the past decades, the newly reported glasses formed from HOIPs open up a new avenue for perovskite research with their unique structures and functionalities. Melt-quenching is the predominant route to glass formation; however, the absence of a stable liquid state prior to thermal decomposition precludes this method for most HOIPs. In this work, we describe the first mechanochemically-induced crystal-glass transformation of HOIPs as a rapid, green and efficient approach for producing glasses. The amorphous phase was formed from the crystalline phase within 10 minutes of ball-milling, and exhibited glass transition behaviour as evidenced by thermal analysis techniques. Time-resolved in situ ball-milling with synchrotron powder diffraction was employed to study the microstructural evolution of amorphisation, which showed that the crystallite size reaches a comminution limit before the amorphisation process is complete, indicating that energy may be further accumulated as crystal defects. Total scattering experiments revealed the limited short-range order of amorphous HOIPs, and their optical properties were studied by ultraviolet-visible (UV-vis) spectroscopy and photoluminescence (PL) spectroscopy.

Direct Observation of Solid-Phase Crystallization of an Amorphous Complex Oxide in the Transmission Electron Microscope

Many complex metal oxides possess intricate structure-function relations, resulting in a wide range of tunable functional properties. The introduction of disorder through amorphization provides additional opportunities for tuning the properties, particularly in the area of electrochemical energy storage and conversion [1]. Consequently, amorphous and partly crystalline complex oxides have garnered growing interest in recent years, with two primary goals: to harness their unique functional properties or to employ them as a chemically-flexible, far-from-equilibrium, thin-film processing platform that offers novel synthesis opportunities [2] due to the minimal energy input required to initiate crystallization and other structural relaxation processes.Relevant to both these aims, the processing-structure-function relationship for amorphous complex oxides is examined by in situ solid-phase crystallization (SPC) in the (scanning) transmission electron microscope ((S)TEM), focusing on perovskite-like (ABO3) mixed ion-electron conducting (MIEC) amorphous complex oxides which make promising low-temperature solid-oxide cell (SOC) electrodes [3] due to the widely observed disorder-mediated oxygen surface-exchange [4]. Key aspects of MIEC amorphous complex oxide processing, such as the evolution of structure and chemistry with temperature and the corresponding effect on conductivity are detailed in the amorphous La0.8Sr0.2MnO3-δ (LSM) system. Further, approaches to direct amorphous complex oxide processing towards desirable synthesis products based on these insights are discussed.Here, we elucidate down to the atomic scale the development of structural characteristics such as porosity, crystallized fraction, crystallite tension, size, curvature, and surface termination, with the aim to establish approaches to tune surface functionality in partly crystalline MIECs by heating or electron beam irradiation [5]. In situ electrical measurements are used to correlate these changes with electrical behavior, revealing that the onset of crystallization is correlated with an increase in electronic conductivity by small polaron hopping, attributed to oxygen-metal-oxygen bond alignment. Further, in the absence of epitaxial constraints, an immiscibility-driven self-organization of amorphous heterointerfacial structures manifests by spinodal decomposition, that is likely to be broadly relevant in low-temperature processing of amorphous complex oxides [6]. Thus, processing from an amorphous complex oxide precursor could be a method to establish uniformly-dispersed nanoscale heterointerfaces of tunable characteristic length scale throughout a thin film volume, while also enabling direct tuning of the porous mesostructure by electron beam irradiation. Overall, case studies of amorphous complex oxide crystallization are limited to relatively few chemical systems and processing conditions. Thus, extending this body of work to explore a broader processing space, and extracting fundamental insights to establish process-structure-function relationships are prerequisites to realizing the full potential of partly crystallineMIEC systems, and provides guidance for processing amorphous complex oxides generally. Acknowledgments The authors acknowledge the UC Irvine School of Engineering new faculty setup funds, the National Science Foundation CAREER award (DMR-2042638) and the UC Irvine Materials Research Institute (IMRI). References S. Yan ... H. Xia, Small (2019)D. Prakash, ... F. Cavallo, Small (2022).J. Zhang ... Y. Chen, Advanced Functional Materials (2022)T. Chen ... N. Perry, ACS Applied Materials & Interfaces (2019)J. Wardini ... W. Bowman (submitted)J. MacManus-Driscoll, Advanced Functional Materials (2010)

Вплив аргонвмісного середовища відпалу на перебіг структурно-фазових перетворень в тонкоплівкових композиціях Ni/Ti

This study is focused on the effect of isothermal annealing in an argon atmosphere (200 Pa) in the temperature range of 200–600 °C on the evolution of diffusion-induced structural phase transformations in Ni/Ti layered thin films with different modulation period but similar total thickness of 60 nm. Changes in the structure and phase composition of nanoscale films have been examined using X-ray diffraction technique, and the chemical composition has been analyzed using secondary ion mass spectrometry. Annealing at 300 °C induces the development of diffusion interaction between the Ni and Ti layers, leading to the formation of intermetallic NixTiy phases of various stoichiometry at higher annealing temperatures. It is shown that an increased number of layers promotes a significant activation of diffusion processes between the components of the system, resulting in a change in its phase composition at lower annealing temperatures. Meanwhile, for all investigated samples, annealing at elevated temperatures (>500 °C) causes the agglomeration of Ti on the free surface with the probable formation of a protective oxide layer. It was established that the decisive influence on thermally induced phase formation is exerted by two competing factors: the use of an argon-containing annealing atmosphere contributes to the intensification of mass transfer processes between the materials of metal nanolayers compared to similar heat treatment in a vacuum, while the decrease of the modulation period of the thin-film system promotes the amorphization processes at the interface between metal layers with a corresponding inhibition of structural ordering processes. Keywords: nanoscale films, NiTi, diffusion, argon, isothermal annealing.

Evolution of structures and internal stress of ZrC-SiC composite under He ion irradiation and post-annealing

Composite ceramics show great potential for utilization in nuclear systems. However, the component phases therein may exhibit large variations in structural response to the ion irradiation including degree of lattice expansion, ability to maintain the crystallinity, types and density of as-formed defects, etc. Such discrepancy may result in the evolution of internal stress and consequently more complicated interactions with respect to the irradiation behavior, which remains less understood. In this study, a ZrC–30 vol% SiC composite is chosen to study the irradiation and helium retention behavior under 540 keV He ion irradiation with a fluence of 1 × 1017/cm2 and subsequent annealing at 1000 °C and 1500 °C. Irradiation-induced volume dilation of ZrC lattice and especially from an amorphization process of SiC leads to a maximum compressive stress of ∼66 GPa at a certain irradiation depth, at which horizontal cracks are generated but only in ZrC grains. During high-temperature annealing, migration of defects, diffusion and coalesce of helium species, growth of He bubbles, recovery of crystal lattices and formation of dislocations are found to be closely correlated to the irradiation-induced gradient of helium retention concentration, lattice damage and internal stress along the irradiation depth along with the recrystallization process of amorphous SiC. The as-observed irradiation behavior and structural evolution during annealing are discussed by theoretical consideration of internal stress in the composite using the COMSOL Multiphysics package.

Enhanced Electrocatalytic Activity of Amorphized LaCoO3 for Oxygen Evolution Reaction.

Amorphous inorganic perovskites have attracted significant attention as efficient electrocatalysts due to their unique structural flexibility and good catalytic activity. In particular, the disordered structure and a surface rich in defects such as oxygen vacancies can contribute to the superior electrocatalytic activity of amorphous oxides compared to their crystalline counterpart. In this work, we report the synthesis of LaCoO3, followed by an amorphization process through urea reduction with tailored modifications. The as-synthesized catalysts were thoroughly tested for their performance in oxygen evolution reaction (OER), Remarkably, the amorphous LaCoO3 synthesized at 450 °C (referred to as LCO-4) exhibits excellent OER catalytic activity. At an overpotential of 310 mV, it achieved a current density of 10 mA/cm-2, exceedingly fast to 1 A/cm-2 at an overpotential of only 460 mV. Moreover, LCO-4 exhibited several advantageous features compared to pristine LaCoO3 and LaCoO3 amorphized at other two temperatures (350 °C, LCO-3, and 550 °C, LCO-5). The amorphized LCO-4 catalyst showed a higher electrochemically active surface area, a key factor in boosting catalytic performance. Additionally, LCO-4 demonstrated the lowest Tafel slope of 70 mVdec-1, further highlighting its exceptional OER activity. Furthermore, the long-term stability of LCO-4 is notably superior than pristine LaCoO3 (LCO-P) and the other amorphized samples (LCO-3 and LCO-5). The enhanced catalytic activity of LCO-4 can be attributed to its unique disordered structure, small crystallite size, and higher concentration of oxygen vacancies in the final catalyst.