Reduction Step Research Articles

MRI-quality and morphometric MRI analysis to identify focal cortical dysplasia: An exploratory study

BackgroundIn the pre-surgical evaluation of people with focal epilepsy and a normal MRI, Morphometric Analysis Program v2018 (MAP18) aids in detecting visually inconspicuous focal cortical dysplasia (FCD). We investigated the impact of MRI scans with reduced signal-to-noise ratio (SNR) and spatial resolution (SR) on FCD detection by MAP18, aiming to improve the chances of achieving seizure freedom through epilepsy surgery. MethodsThirty MRI scans with the identified lesion using MAP18 radiologically confirmed as FCD by a neuroradiologist, were retrospective analysed. SNR and SR were artificially reduced in ten steps, and their impact on MAP18 outcomes was assessed using multilevel analysis. ResultsThere was a significant effect after reducing SR and SNR for z-score and volume of the FCD cluster, the total number of detected clusters, and volume of these clusters. After SNR reduction, there was also a significant effect for z-score of the total number of detected clusters. FCD became undetectable by MAP18 after six steps of SR reduction (voxel size 2.8 × 2.8 × 2.8 mm³) and after two steps of SNR reduction. ConclusionsThis exploratory study suggests that reduced SR and SNR negatively affect FCD detection with MRI post-processing (MAP18). The MAP18 evaluator should screen MRI quality before post-processing, particularly for scans with significant visual noise or voxel sizes of 2.8 × 2.8 × 2.8 mm³ and upwards, as repeating a low-quality MRI scan is less burdensome than the adverse effects of continued seizures due to failure to detect FCD.

Kesehatan Mental Siswa Pasca Pembelajaran Daring di SMA N 2 Pulau Punjung Kabupaten Dharmasraya

This study was motivated by the fact that some students felt stressed, had feelings of insecurity and discomfort with the changing learning system. They also often feel tired, lethargic in the teaching and learning process, they also often experience anxiety and feelings of stress. Some students also feel less confident, less good at understanding themselves, and less satisfied with their social relationships so that they do not feel happy with the learning system and they also find it difficult to adapt to their environment as a result of post-online learning. This type of research is descriptive qualitative research that describes the mental health of students after online learning at SMAN 2 Pulau Punjung. In collecting data, researchers used observation and interview techniques. Meanwhile, to analyze it, researchers used data reduction, data presentation, and data verification steps. The results of the study showed that the mental health of students after carrying out online learning at SMAN 2 Pulau Punjung, namely students have good mental health. More students have good mental health than bad, students have a healthy mentality characterized by students feeling comfortable and safe while studying, having high self-confidence, being able to understand themselves, getting satisfaction in social relationships (social interactions), having emotional maturity that is appropriate for their age, not having a disturbed personality, and being able to adapt to their environment and being happy with their current situation.

Adsorption and Catalytic Reduction of Nitrogen Oxides (NO, N2O) on Disulfide Cluster Complexes of Cobalt and Iron-A Density Functional Study.

The reactivity of nitrogen oxide, NO, as a ligand in complexes with [Fe2-S2] and [Co2-S2] non-planar rhombic cores is examined by density functional theory (DFT). The cobalt-containing nitrosyl complexes are less stable than the iron complexes because the Co-S bonds in the [Co2-S2] core are weakened upon NO coordination. Various positions of NO were examined, including its binding to sulfur centers. The release of NO molecules can be monitored photochemically. The ability of NO to form a (NO)2 dimer provides a favorable route of electrochemical reduction, as protonation significantly stabilizes the dimeric species over the monomers. The quasilinear dimer ONNO, with trans-orientation of oxygen atoms, gains higher stability under protonation and reduction via proton-electron transfer. The first two reduction steps lead to an N2O intermediate, whose reduction is more energy demanding: in the two latter reaction steps the highest energy barrier for Co2S2(CO)6 is 109 kJ mol-1, and for Fe2S2(CO)6, it is 133 kJ mol-1. Again, the presence of favorable light absorption bands allows for a photochemical route to overcome these energy barriers. All elementary steps are exothermic, and the final products are molecular nitrogen and water.

Electrochemical Study of Zr from Anodic Dissolution using a Consumable Zirconium Nitride Anode

Zirconium nitride (ZrN) has proved to be a promising new catalyst material. Bearing in mind its recyclability at end-of-life, the objective of this work was to demonstrate recovery of Zr in an electrochemical process using a consumable ZrN anode. A mechanically stable ZrN anode was made from synthetic ZrN powder by spark plasma sintering. The anodic dissolution was carried out in an equimolar NaCl-KCl molten salt at 727 °C (1000 K) by potentiostatic polarization. Cyclic voltammetry of the molten salt was performed before and after the anodic dissolution. It was successfully demonstrated that Zr ions were dissolved into the molten salt. The electrochemical characterization of the electroactive species showed a two-step electrochemical process, related to the reduction steps Zr(IV)/Zr(II), and Zr(II)/Zr. Analysis of voltammograms showed diffusion controlled electrochemical reactions and the diffusion coefficients calculated correlated well with values reported in the literature.

Square-Planar Nickel Bis(phosphinopyridyl) Complexes for Long-Lived Photocatalytic Hydrogen Evolution.

Phosphinopyridyl ligands are used to synthesize a class of Ni(II) bis(chelate) complexes, which have been comprehensively characterized in both solid and solution phases. The structures display a square-planar configuration within the primary coordination sphere, with axially positioned labile binding sites. Their electrochemical data reveal two redox couples during the reduction process, suggesting the possibility of accessing two-electron reduction states. Significantly, these complexes serve as robust catalysts for homogeneous photocatalytic H2 evolution. In a system utilizing an organic photosensitizer and a sacrificial electron donor, an optimal turnover number of 27,100 is achieved in an alcohol-containing aqueous solution. A series of photophysical and electrochemical measurements were conducted to elucidate the reaction mechanism of photocatalytic hydrogen generation. Density function theory calculations propose a catalytic pathway involving two successive one-electron reduction steps, followed by two proton discharges. The sustained photocatalytic activity of these complexes stems from their distinct ligand system, which includes phosphine and pyridine donors that aid in stabilizing the low oxidation states of the Ni center.

A 1,4-benzoquinone with counteracting inductive donor and acceptor substituents

Investigation of a published route to produce 3,5-di- tert-butylphenol, starting from commercial 3,5-di- tert-butylbenzoic acid via 3,5-di- tert-butylanlinium hydrogen sulfate, unexpectedly yielded 2,6-dintitro-3,5-di- tert-butylphenol. Attempts to increase the yield of the latter resulted, instead, in the previously unreported 2,6-dinitro-3,5-di- tert-butylcyclohexa-2,5-dien-1,4-dione. Single-crystal X-ray diffraction structures are reported for the anilinium salt, the nitrated phenol, and the quinone. Voltammetry of the quinone shows two chemically reversible reductions in anhydrous solution and the radical anion produced from the first reduction step has been characterized by electron paramagnetic resonance spectroscopy. This compound fits well to the middle range of electron-poor quinones, indicating that the inductive effects of the tert-butyl and nitro groups counteract each other. This conclusion is also supported by the infrared spectroscopic data where the ν(C=O) and ν(C=C) bands are of very similar energy to those of 2,3,5,6-tetrachloro-1,4-benzoquinone.

Application of Interface Reduction Methods to Rotordynamic Casing Models

Abstract As the use of digital twins for the purpose of structural health monitoring increases, so does the demand for high-quality models. In the area of rotating machines, this means that the casing must also be taken into account. These are often geometrically complex assemblies that require the use of finite element models. The models are then reduced in size by established reduction methods like the Craig-Bampton reduction in order to keep the solution time, e.g. for a forced response analysis as low as possible. In case of nonlinear contact forces, e.g. friction in bolted joints, a secondary reduction step has to be applied. Here, three different interface reduction methods are investigated and used for a rotor-casing assembly including frictional damping. The necessary basics and terms are presented. The performance of the methods is evaluated for a linear model on substructure and assembly level and for a nonlinear model on the assembly level. The implementation of the interface reduction within the Harmonic Balance Method is presented and tested for different unbalance excitation cases.

Dynamic Asymmetric Diamination of Allylic Alcohols through Borrowing Hydrogen Catalysis: Diastereo-Divergent Synthesis of Tetrahydrobenzodiazepines.

We present herein a catalytic enantioconvergent diamination of racemic allylic alcohols with the construction of two C-N bonds and 1,3-nonadjacent stereocenters. This iridium/chiral phosphoric acid cooperative catalytic system operates through an atom-economical borrowing hydrogen amination/aza-Michael cascade, and converts readily available phenylenediamines and racemic allylic alcohols to 1,5-tetrahydrobenzodiazepines in high enantioselectivity. An intriguing solvent-dependent switch of diastereoselectivity was also observed. Mechanistic studies suggested a dynamic kinetic resolution process involving racemization through a reversible Michael addition, making the last step of asymmetric imine reduction the enantiodetermining step of this cascade process.

Modification of Co3O4 by Al2O3: Influence on the reducibility

In this study, we used a coprecipitation method followed by calcination at 500 °C to synthesize undoped and Al3+-doped Co3O4 nanoparticles with different aluminum fractions (x = Al/(Co + Al) = 1/60, 1/30, 1/15, 1/75, 1/6 and 1/5). An addition of Al3+ ions led to a decrease in the average crystallite size from 29 to 11 nm, and growth of the specific surface area from 28 to 91 m2/g. TEM images indicated round and platelet shapes of the nanoparticles. According to HAADF-STEM combined with EDS elemental mapping, the platelet shape particles are Al3+-enriched, while the round shape particles are Al3+-depleted. The origin of Al3+ distribution over the oxide volume is conditioned by the state of the hydroxide precursor. It was shown by XRD that the coprecipitation yielded homogeneous hydroxides only for Al fractions x = 0 and x = 1/5. For the intermediate compositions, the precursors represent a mixture of Co6(CO3)2(OH)8*H2O and Co0.8Al0.2(OH)2(CO3)0.1*nH2O. On the TPR-H2 profiles, reduction peaks for three (Co,Al)3O4 oxides differing in the Al3+ concentration (y) can be found. Two of these oxides with y = 0 and y = 0.2 are formed from different hydroxides, and third one with y ∼0.05 is the result of their mutual interaction. In situ XRD allowed us to interpret the TPR peaks correctly and showed that the reduction of all the oxides occurs in two steps. In the first step, Co3+ → Co2+, and (Co1-yAly)3O4 oxides transform to (Co,Al)O. In the second step, Co2+ → Co0, and (Co,Al)O is reduced into metallic cobalt. In undoped Co3O4, Co3+ → Co2+ and Co2+ → Co0 reduction steps occur at T1 = 280 and T2 = 325 °C, respectively. For Al-depleted (Co1-yAly)3O4 (y ∼ 0.05 in the interior of particles), both reduction steps shift toward higher temperatures T1 = 305 and T2 = 405 °C, respectively. The reduction of Al-enriched (Co0.8Al0.2)3O4 is more difficult; first and second reduction steps occur at T1 = 345 and T2 = 610−690 °C. Therefore, Al3+ ions have a little effect on the first step and very significantly influence the second one. Additionally, it was shown by TEM that after the reduction at 700 °C metallic cobalt particles were surrounded by the Al-enriched oxide shell. Apparently, that is why the addition of even a small amount of Al3+ ions prevents a quick sintering of metallic cobalt observed for pure Co3O4.

Organically coordinated Cu(II) activated peroxymonosulfate for enhanced degradation of emerging contaminants

Copper ion Cu(II) is generally considered ineffective in activating peroxymonosulfate (PMS). However, our study demonstrates that organically coordinated Cu(II), namely, org-Cu(II) with contaminants such as amoxicillin (AMO), ofloxacin (OFX), sulfadiazine (SDZ), and tetracycline (TET) can efficiently activate PMS under neutral conditions, leading to faster degradation of these emerging contaminants. In contrast, organic contaminants that do not coordinate with Cu(II) do not facilitate PMS activation. Unlike traditional PMS-induced advanced oxidation processes (AOPs), our study identifies trivalent Cu(III) as the primary oxidant intermediate, with monovalent Cu(I) serving as its precursor. In addition, basic conditions was found to be beneficial for the degradation of target pollutants in org-Cu(II)/PMS systems. Moreover, this promotion effect extends to realistic wastewater, suggesting promising application prospects. The potential mechanism of the rate-limiting reduction step from Cu(II) to Cu(I) was further investigated. The interaction strength between the lowest unoccupied molecular orbital (LUMO) of the copper complex formed with organic compounds and the highest occupied molecular orbital (HOMO) of PMS influences the energy of the bonding orbitals. Coordination with organic ligands alters the LUMO of Cu(II), facilitating electron transfer from the HOMO of PMS to copper. This process activates PMS, ultimately leading to the production of Cu(I) and Cu(III). These findings deepen our understanding of PMS-induced AOPs for degrading emerging contaminants and underscore the importance of further research into PMS activation by Org-Cu(II).

Biomimetic and Concise Total Syntheses of Prenylated and Bicyclo[2.2.2]diazaoctane-Containing Indole Alkaloids Including Taichunamide A, Notoamide N and Versicolamide B.

Total syntheses of the title prenylated indole alkaloids together with seven others are reported. Biogenetic considerations have been employed in devising the reaction sequences leading to these targets with, in the opening stages, electrochemically-derived indole-3-carboxaldehyde 15 being subject to an aldol-type condensation reaction involving diketopiperazine derivative 19. This led, after prototopic shifts, intramolecular Diels-Alder cycloaddition and hydrolysis/deprotection steps, to the racemic forms of the bicyclo[2.2.2]diazaoctane-containing natural product stephacidin A (2) and its C6 epimer 3. Epoxidation of the last compound afforded, following rearrangement of the primary oxidation products, a mixture of (±)-taichunamide A [(±)-4] and (±)-versicolamide B [(±)-7]. Related protocols allowed for the conversion of (±)-stephacidin A [(±)-2] into (±)-notoamide B [(±)-5]. Analogous aldol condensation, nucleophilic reduction, and epoxidation steps led to the formation of (-)-notoamide E and its conversion into notoamide C as well as the indole fragmentation product amoenamide E. A late-stage chlorination reaction applied to (±)-stephacidin A provided access to the spirocyclic oxindole (±)-notoamide N [(±)-6].

Borohydride Compounds Catalyze the Selective 4e- Reduction of CO2 with 9-BBN.

The selective double hydroboration of CO2 into bis(boryl)acetal (BBA) is a challenging yet appealing reduction process since BBA can be used as a versatile C1 and Cn sources for the synthesis of value-added products. In the present study, we demonstrate that simple borohydride compounds are efficient and selective catalysts for the synthesis of BBA when using 9-borabicyclo(3.3.1)nonane (9-BBN) as a reductant. The experimental and theoretical investigations show that while the borohydride species catalyzes the first reduction step of CO2 into formoxyborane (2e- reduction intermediate), the observed 4e- reduction selectivity is mostly due to the ability of 9-BBN to reduce the formoxyborane into BBA without a catalyst. Notably, 0.2 mol % of LiH2BBN catalyzed the hydroboration of CO2 with 9-BBN as a reductant into the corresponding BBA in 77% yield with TON and TOF of 385 and 196 h-1, respectively. The simplicity of borohydride contrasts with the more elaborate catalytic systems used so far for the 4e- reduction of CO2.

SpQuant-SNN: ultra-low precision membrane potential with sparse activations unlock the potential of on-device spiking neural networks applications.

Spiking neural networks (SNNs) have received increasing attention due to their high biological plausibility and energy efficiency. The binary spike-based information propagation enables efficient sparse computation in event-based and static computer vision applications. However, the weight precision and especially the membrane potential precision remain as high-precision values (e.g., 32 bits) in state-of-the-art SNN algorithms. Each neuron in an SNN stores the membrane potential over time and typically updates its value in every time step. Such frequent read/write operations of high-precision membrane potential incur storage and memory access overhead in SNNs, which undermines the SNNs' compatibility with resource-constrained hardware. To resolve this inefficiency, prior works have explored the time step reduction and low-precision representation of membrane potential at a limited scale and reported significant accuracy drops. Furthermore, while recent advances in on-device AI present pruning and quantization optimization with different architectures and datasets, simultaneous pruning with quantization is highly under-explored in SNNs. In this work, we present SpQuant-SNN, a fully-quantized spiking neural network with ultra-low precision weights, membrane potential, and high spatial-channel sparsity, enabling the end-to-end low precision with significantly reduced operations on SNN. First, we propose an integer-only quantization scheme for the membrane potential with a stacked surrogate gradient function, a simple-yet-effective method that enables the smooth learning process of quantized SNN training. Second, we implement spatial-channel pruning with membrane potential prior, toward reducing the layer-wise computational complexity, and floating-point operations (FLOPs) in SNNs. Finally, to further improve the accuracy of low-precision and sparse SNN, we propose a self-adaptive learnable potential threshold for SNN training. Equipped with high biological adaptiveness, minimal computations, and memory utilization, SpQuant-SNN achieves state-of-the-art performance across multiple SNN models for both event-based and static image datasets, including both image classification and object detection tasks. The proposed SpQuant-SNN achieved up to 13× memory reduction and >4.7× FLOPs reduction with < 1.8% accuracy degradation for both classification and object detection tasks, compared to the SOTA baseline.

Tuning the Thermal Stability of Tetra-o-chloroazobenzene Derivatives by Transforming Push-Pull to Push-Push Systems.

Molecular photoswitches provide interesting tools to reversibly control various biological functions with light. Thanks to its small size and easy introduction into the biomolecules, azobenzene derivatives have been widely employed in the field of photopharmacology. All visible-light switchable azobenzenes with controllable thermostability are highly demanded. Based on the reported tetra-o-chloroazobenzenes, we synthesized push-pull systems, by introducing dialkyl amine and nitro groups as strong electron-donating and electron-withdrawing groups on the para-positions, and then transformed to push-push systems by a simple reduction step. The developed push-pull and push-push tetra-o-chloroazobenzene derivatives displayed excellent photoswitching properties, as previously reported. The half-life of the Z-isomers can be tuned from milliseconds for the push-pull system to several hours for the push-push system. The n-π* and π-π* transitions have better resolution in the push-push molecules, and excitation at different wavelengths can tune the E/Z ratio at the photostationary state. For one push-pull molecule, structure and absorption spectra obtained from theoretical calculations are compared with experimental data, along with data on the push-push counterpart.

Revealing the potential-determining steps of reduction of nitrate to ammonia on transition metal porphyrins catalysts

The reduction reaction of nitrate (NO3RR) to ammonia by electrocatalytic methods is a promising method for sustainable ammonia synthesis, yet it remains a great challenge. In this work, we report a class of transition metal coordination porphyrins (TM-PP) as a cost-effective, high activity and selectivity electrocatalysts for NO3RR. By large-scale density functional theory calculations, our investigation into the catalytic mechanism of TM-PP sheds light on the underlying principles of their enhanced activity. It's worth noting that through systematic study of potential-determining steps, we proposed for the first time that the Gibbs free energy change of the 7th step (*NOH→*N) reaction can serve as an effective catalytic descriptor for NO3RR and unveiled its underlying mechanism. We theoretically demonstrate that Mo-PP and Ru-PP stand out among 23 TM-PP and showcasing superior performance supported by systematic analyses of kinetics, thermodynamics, and electrochemical stabilities. Mo-PP boast a significantly reduced additional voltage requirement of merely –0.16 V compared to existing catalysts. Furthermore, both Mo-PP and Ru-PP demonstrate the capacity to suppress the competing HER and effectively prevent the generation of by-products. Overall, our work presents a promising NO3RR catalyst with great potential for practical applications and provides valuable insights into the NO3RR intricate mechanisms.

Implementation of Management Functions at PT Pegadaian (Persero)

This research aims to investigate and analyze the implementation of management functions at PT. Pegadaian (Persero) Lebong Regency. Considering the many functions of management, this research will only discuss four management functions, namely, planning, organizing, supervising, and directing. This research uses descriptive and qualitative research methods. In the data collection process in this research, researchers used observation, interview, and documentation techniques. In analyzing the data, researchers used data analysis techniques with data reduction steps, data presentation, and drawing conclusions. The research results show that employees already have their respective duties and obligations in dividing tasks as well as arranging activities by planning in advance. Apart from planning the division of tasks according to the abilities of each employee, PT. Pegadaian (Persero) Lebong Regency also provides good guidance to employees. By carrying out training activities that all employees must participate in. Then, in terms of supervision of PT Pegadaian (Persero), Lebong Regency also did well. Supervision is very important in a company so that the evaluation process runs smoothly.

Influence of cerium addition and redox state on silicate structure and viscosity

AbstractThe viscosities of Ce‐free and Ce‐bearing (∼1.3 mol%, ∼6.5 wt.% Ce2O3) soda lime silicate (window glass) melts were measured with respect to oxidation state. Experiments were performed isothermally using a concentric‐cylinder viscometer on melts equilibrated with successively reducing CO–CO2 gas mixtures within a gas tight vertical tube furnace at 1 atm. Viscosity measurement and sampling were performed at the end of each melt reduction step. Further, viscosities in the glass transition temperature range were estimated using the shift factor method applied to glass transition temperature values determined using differential scanning calorimetry (DSC) measurements on quenched glasses. The Ce speciation at each stepwise melt reduction was probed using Ce L3‐edge X‐ray absorption near‐edge structure (XANES) spectroscopy, while structural information upon Ce addition and reduction was provided by Raman spectroscopy. The viscosities of these materials remain constant at this level of Ce addition and do not vary significantly with redox state at high temperature. Conversely, viscosity values in the glass transition temperature range increase upon both Ce addition and reduction. Our analysis, based on the glass composition analyses obtained via electron probe microanalyzer (EPMA), viscosity calculations, and observations of silicate structural changes, leads to the conclusion that the observed viscosity increase around the glass transition temperature is explained by the high ionic field strength of Ce ions as well as the polymerization behavior of the silicate matrix occurring during reduction of Ce. Because of its low concentration, resulting from its low solubility, Ce redox changes exert only minimal effects on the viscosity of this melt.

Conversion of CO2(g) to CO(g) via reverse water–gas shift cycle on mixed cerium/praseodymium oxides at 500 °C

Reactions of cerium/praseodymium oxides under hydrogen atmospheres, and subsequently, carbon dioxide, involved in chemical looping reverse water–gas shift cycles (RWGS) at 500 °C were investigated by in-situ high-temperature X-ray powder diffraction, FTIR and thermogravimetry. The RWGS cycle is a critical chemical process for converting carbon dioxide into useful products, such as carbon monoxide, which can be used to synthesize fuels and chemicals. The mixed oxides exploit the redox properties of Ce and Pr, which can switch between oxidation states, making them suitable for oxygen incorporation and release during the RWGS process allowing them to react with H2(g), and subsequently with CO2(g), promoting their interaction and conversion into H2O(g) and CO(g). Pure cerium and praseodymium oxides showed poor CO2(g) conversion efficiency. However, we found that nanometric Ce/Pr mixed oxides exhibit enhanced oxyreduction performance suitable for this application, particularly with a composition of 75 mol% Ce and 25 mol% Pr, significantly improved performance, achieving an average CO(g) yield of 0.6 mmol/(goxide.cycle) and a maximum rate of 0.26 mmol/(goxide.min). Pr enhances oxygen mobility in CeO2, which improves the dissociation of C═O bonds in CO2(g). This is because the remaining oxygen atoms are delivered more quickly to the support sink, thereby cleaning up the vacant sites generated during the reduction step. These findings suggest that Ce/Pr mixed oxides are highly effective for CO2(g) conversion to CO(g) via RWGS cycle, offering a potentially viable option for industrial application.

Partisipasi Masyarakat dalam Pengelolaan Pariwisata Berkelanjutan Desa Wisata Samiran, Kecamatan Kabupaten Boyolali

Samiran Tourism Village has developed since 2009 based on community empowerment, so it is necessary to identify its management aspects to realize sustainable tourism. The research method is a qualitative approach through data collection of literature studies, observation, in-depth and semi-structured interviews. The interview informants were Samiran Tourism Village stakeholders who were determined by purposive sampling method tailored to the research objectives. Data analysis was conducted descriptively qualitatively through three steps of reduction, data presentation, and conclusion drawing. Samiran Tourism Village has achieved sustainable tourism management by involving various stakeholders but still placing the community as the main actor through the management structure and framework, stakeholder involvement, and management of change. The level of participation was identified through 5 stages. The high category level is at the implementation stage of enjoying results, and reporting because the community is fully involved in it, while the moderate level of participation is at the decision-making and evaluation stages, where the community still plays a role but is not independent / cooperates with other stakeholders. The factors that determine the level of participation can be divided into two, internal and external. Internal factors that influence are gender, social position, length of stay, and local hero, while external factors are influenced by policies made by the government, so that it is beyond the authority of the tourist village and cannot be controlled.Keywords: participation, management, sustainability, tourism village

Implementasi Pembelajaran Pendidikan Agama Islam melalui Media Sosial Youtube di Kelas IV SDI Alexandria Kota Tangerang

The use of YouTube Social Media is a new thing in learning Islamic Religious Education at SDI Alexandria Tangerang City. The implementation of YouTube Social Media on the material Aku anak Saleh is expected to be able to make students reflect the attitude of Saleh in their daily activities. This study aims to determine how the implementation of Islamic Religious Education Learning through YouTube Social Media in Class IV SDI Alexandria. This research uses descriptive qualitative methods using data collection techniques in the form of interviews, observations and documentation studies. Data validity checks using triangulation. Data were analyzed through the steps of data collection, data reduction, data presentation and conclusion drawing. Interviews were conducted with an Islamic Religious Education teacher and 5 class IV students. The results of this research are that the implementation of Islamic Religious Education Learning via YouTube Social Media in class IV SDI Alexandria is said to be effective and improves students' ability to understand the material of I'm Saleh's Child in accordance with the research focus.