Stoichiometric Ratio Research Articles

Atomically Precise Rhodium‐Gold Carbonyl Nanoclusters: In‐Depth Synthesis and Multivalence Investigation of [Rh16Au6(CO)36]6−, and its Correlation with [Rh10Au(CO)26]3−

AbstractThe synthesis of the previously‐reported atomically‐precise [Rh16Au6(CO)36]6− (1) nanocluster has been optimized by screening different reaction variables like solvent, stoichiometric ratio, counterion and atmosphere. Its multivalence properties have also been studied by means of electrochemical and spectroelectrochemical techniques; the results pointed out a remarkable electron‐sponge behaviour, as under such experimental conditions 1 is capable to release one electron and accept up to four more, while retaining its molecular structure. This scarce structural variation has been confirmed through DFT calculations on those species whose redox processes showed the maximum reversibility, namely [Rh16Au6(CO)36]7− and [Rh16Au6(CO)36]5−. Moreover, we report herein the isolation and characterization of the new [Rh10Au(CO)26]3− (2) nanocluster, which represents one of the major fallouts of the synthetic pathway investigation of 1. Finally, we disclosed the existence of further species that, from preliminary results, appear to be new large atomically‐precise Rh−Au nanoclusters, which will be the subject of future investigations. Cluster 2 has been identified via single‐crystal X‐ray diffraction analysis, and the characterization of both clusters 1 and 2 completed by infrared (IR) spectroscopy and Electrospray Ionization Mass Spectrometry (ESI‐MS).

Experimental Analysis of Long-Term Fuel Trim Performance in a Gasoline Engine Under Various Operating Conditions

This paper analyzes the effect of operating conditions on the enrichment of the fuel-air mixture in a car engine due to a decrease in air mass with increasing altitude above sea level. This study focuses on fuel trim, particularly long-term fuel trim, in optimizing the composition of the fuel-air mixture before it enters the engine's combustion chamber. Experimental studies were conducted on the Bishkek–Osh highway in the Kyrgyz Republic, a road characterized by flat, mountainous, and high-altitude sections with complex terrain. Based on the research objectives, experimental results were obtained, and graphs of long-term fuel trim as a percentage of terrain altitude were constructed and analyzed for flat, mountainous, and high-altitude sections of the Bishkek–Osh highway. The study established that fuel trim indicators can be used to analyze changes in the air-fuel mixture's air excess coefficient (λ = 1, stoichiometric ratio). The reduction in long-term fuel trim was observed in flat, mountainous, and high-altitude sections as air density and pressure decreased with increasing altitude above sea level. The results show that with a reduction in long-term fuel trim to -6.25% to -7.81% at altitudes between 1500 and 3000 meters above sea level, the air excess coefficient (λ) drops to 0.92–0.94. At an altitude of 770 meters (flat terrain), λ was measured at 0.97. The difference in λ (0.03–0.05) indicates that an increase in altitude significantly affects the air-fuel ratio (AFR), impacting mixture formation during vehicle operation in mountainous and high-altitude conditions.

Generating Tooth Organoids Using Defined Bioorthogonally Cross-Linked Hydrogels.

Generating teeth in vitro requires mimicking tooth developmental processes. Biomaterials are essential to support 3D tooth organoid formation, but their properties must be finely tuned to achieve the required biomimicry for tooth development. For the first time, we used bioorthogonally cross-linked hydrogels as defined 3D matrixes for tooth developmental engineering, and we highlighted how their properties play a pivotal role in enabling 3D tooth organoid formation in vitro. We prepared hydrogels by mixing gelatin precursors modified either with tetrazine (Tz) or norbornene (Nb) moieties. We tuned the hydrogel properties (E = 2-7 kPa; G' = 500-1500 Pa) by varying the gelatin concentration (8% vs 12% w/V) and stoichiometric ratio (Tz:Nb = 1 vs 0.5). We encapsulated dental epithelial-mesenchymal cell pellets in a library of hydrogels and identified a hydrogel formulation that enabled successful growth kinetics and morphogenesis of tooth germs, introducing a defined tunable platform for tooth organoid engineering and modeling.

The role of surface substitution in the atomic disorder-to-order phase transition in multi-component core-shell structures.

Intermetallic phases with atomic ordering are highly active and stable in catalysts. However, understanding the atomistic mechanisms of disorder-to-order phase transition, particularly in multi-component systems, remains challenging. Here, we investigate the atom diffusion and phase transition within Pd@Pt-Co cubic nanoparticles during annealing, using in-situ electron microscopy and ex-situ atomic resolution element analysis. We reveal that initial outward diffusing Pd partially substitutes Pt, forming a (Pt, Pd)-Co ternary system in the surface region, enabling the phase transition at a low temperature of 400 °C, followed by shape-preserved inward propagation of the ordered phase. At higher temperatures, excessive interdiffusion across the interface changes the stoichiometric ratio, diminishing the atomic ordering, leading to obvious change in morphology. Calculations indicate that the Pd-substitute in (Pt, Pd)-Co system leads to a significantly lower phase transition temperature compared to that of Pt-Co alloy and thus a lower activation energy for atomic diffusion. These insights into atomistic behavior are crucial for future design of multi-component systems.

Soil microbial carbon use efficiency and the constraints

Abstract Background Microbial contributions to soil organic carbon formation have received increasing attention, and microbial carbon use efficiency is positively correlated with soil organic carbon storage. Mainbody This work reviews the impact on microbial carbon use efficiency from six constraints, including plant community composition and diversity, soil pH, substrate quality, nutrient availability and stoichiometric ratios, soil texture and aggregates, water and thermal constraints, and external nutrient inputs. In general, the response of microbial carbon use efficiency showed large uncertainty to above constraints, including positive-, negative-, or non-correlation. However, some factors are biased, more likely to promote or inhibit carbon use efficiency. For example, external nutrient input (N, P, K, Ca) tended to promote carbon use efficiency, while climate warming showed more negative influence. Conclusion Further, overwhelming works focused on single constraint, we suggest the importance to consider the synergistic influence of multiple environmental variables on microbial carbon use efficiency, special for the regulation mechanism of biological-environmental interactions.

FEATURES OF ELEMENTAL ANALYSIS OF DOLOMITES OF THE LOWER PERMIAN DEPOSITS BY X-RAY FLUORESCENCE SPECTROSCOPY

In this work, using the methods of scanning electron microscopy (SEM), X-ray phase analysis (XRF), X-ray fluorescence spectrometry (XFS) and thermogravimetric analysis (TGA), the physicochemical properties of dolomite rocks selected from one well at different depths of occurrence were studied. The SEM method shows that, depending on the depth of occurrence, dolomite is characterized by both ordinary crystals of rhombohedral morphology, the size of which varies from 50 to 80 microns along the diagonal axis, and unusual shapes, in the form of hexagonal plates up to 1 microns thick and 1 to 10 microns in diameter. It has been found that dolomite plates in places form spherical aggregates ranging in size from 20 to 40 microns. According to the RF analysis data, it was found that in samples of dolomite rock (of ordinary and unusual shape), after calcination at 1000 °C for 5 hours, there is a twofold increase in the molar stoichiometric ratio of Mg and Ca, compared with the initial (non-calcined) state of dolomite. By the XRD method, it was found that during calcination of dolomite samples, a phase transformation (CaMg(CO3)2 → CaO + MgO + 2CO2) is observed, in which lime (CaO) and periclase (MgO) phases are formed. Precision SEM studies have shown that periclase nanocrystals, whose size varies from 100 nm to 300 nm, are evenly distributed on the surface of larger lime fragments. As a result of numerous measurements of the X-ray spectra of the RF, it was found that the overlap of lime fragments with numerous periclase nanocrystals is the cause of a significant overestimation of the magnesium content after calcination of dolomite samples. It is concluded that in order to correctly conduct elemental analysis and obtain adequate information about the weight fraction of rock-forming oxides in dolomite samples, they must first be dissolved in hydrochloric acid. The method of sample preparation proposed by the authors for the correct elemental analysis of dolomite rocks has been tested on numerous samples, which showed convincing convergence of the data obtained by XRF (decomposition into rock-forming oxides) and XRF analysis.

Enhancing the Energy Release Performance of Al/CuO Nanothermites through Hierarchical Structure

ABSTRACT The objective of this study is to enhance the mixing uniformity and contact efficiency between nano-Al and oxidizers through structural control, while suppressing the “pre – ignition fusion” effect of nanothermites. We employed biotemplate approach, utilizing Lycopodium japonicum Thunb. spores (LP) and Papilio maackii wings (PW) as sacrificial templates, to successfully fabricate hierarchically structured Al/PW-CuO and Al/LP-CuO nanothermites. At a stoichiometric ratio of Ф = 1.5, Al/PW-CuO exhibited the highest heat release of 2278.00 J/g, whereas Al/LP-CuO also achieved a substantial heat release of 1969.08 J/g. These outstanding performances are attributed to the unique structures of PW-CuO and LP-CuO, especially the spine-like plate structure of PW-CuO, which provides more reaction sites, thereby enhancing spatial utilization and heat release efficiency. This study provides new insights for the design and application of highly active nanoenergetic materials.

Estimating nutrient stoichiometry and cascading influences on plankton in thermokarst lakes on the Qinghai-Tibet Plateau

Thermokarst lakes play a critical role in global biogeochemistry. Here we delved into nutrient stoichiometry and its cascading effects on plankton communities across thermokarst lakes on the Qinghai-Tibet Plateau. Our findings revealed significant variability in nutrient concentrations and stoichiometric ratios in both water and seston, indicating heterogeneous nature of thermokarst lakes. Phytoplankton communities were dominated by cyanobacteria. Zooplankton communities, though simple, varied significantly and responded distinctly to the prevailing nutrient stoichiometry, and particularly shown competitive interactions between copepods and Cladocera. Structural Equation Modeling revealed a complex web of interactions, underscoring the bottom-up influences from nutrient stoichiometry in water to phytoplankton/seston, and finally to zooplankton, although there were no direct relationships between phytoplankton and zooplankton communities. Water nutrient stoichiometry positively affected eukaryotic algae but negatively impacted seston stoichiometry, which. had a negative influence on copepods. Our study highlighted the intertwined relationships between nutrient stoichiometry and plankton communities within thermokarst lakes.

Patterns and Driving Mechanisms of Soil Organic Carbon, Nitrogen, and Phosphorus, and Their Stoichiometry in Limestone Mines of Anhui Province, China

Active vegetation restoration plays an important role in the improvement in soil organic matter (SOM), including the carbon (C), nitrogen (N) and phosphorus (P) sequestration of degraded mining ecosystems. However, there is still a lack of understanding of the key drivers of SOM pool size and dynamics in active vegetation restoration. For this study, soil was collected from five different sites (Xiaoxian, Dingyuan, Chaohu, Tongling and Dongzhi), four habitats (platforms, slopes, steps and native areas) and two soil layers (0–20 cm and 20–40 cm) in limestone mines of Anhui province to quantify the spatial distribution of SOM contents and their stoichiometric characteristics and influential factors. It was found that the top soil in Chaohu had the highest significant C, N and P contents in the ranges of 14.95–17.97, 1.74–2.21 and 0.80–1.24 g/kg, respectively. Comparing the stoichiometric ratios of the different sites revealed significant differences in C:N and N:P ratios, but C:P ratios were relatively consistent. In particular, the C:N and C:P ratios in deep soil were higher than those in top soil, whereas the N:P ratio in deep soil was lower than that in top soil, suggesting that soil N is a major limiting factor in the top soil. The SOM content did not differ significantly between the three reclaimed habitats, but was significantly higher than that in the native habitat, suggesting that mine restoration has significantly enhanced SOM accumulation. Further analysis showed that nutrient availability and enzyme activity are important factors affecting soil C, N and P content in top soil, while the relationship gradually weakens in deep soil. This was attributed to active anthropogenic management and conservation measures during the early stages of reclamation. This study shows that the ecological recovery of the mining area can be enhanced by implementing differentiated vegetation planting strategies and anthropogenic management on different habitats in the mining area.

Change in the Chemical State of Phosphorus Sulfide Molecules Inside Single‐Walled Carbon Nanotubes

This article presents the first experiments on filling single‐walled carbon nanotubes (SWCNTs) with the phosphorus sulfides P4S3 and P4S10 using the ampoule method. Transmission electron microscopy examination reveals the encapsulation of phosphorus and sulfur species inside the cavities of SWCNTs without the formation of any regular structures. X‐ray photoelectron spectroscopy observes different oxidation states of P and S atoms, depending on the P/S ratio in the initial mixture used to fill the nanotubes. The Raman signals associated with the encapsulated species are low in intensity, and the vibrational modes are shifted and broadened as compared to those in crystalline P4S3 and P4S10. The proposed models for the arrangement of sulfur and phosphorus inside SWCNTs suggest the formation of 1D amorphous glassy phosphorus sulfides with stoichiometric ratios close to those of elemental phosphorus and sulfur in the initial mixtures.

Enhancing soil ecosystem multifunctionality through combined conservation tillage and legume-based crop rotation in the North China Plain

Conservation agriculture (CA), based on principles of conservation tillage (CT) and crop rotations, has been adopted as a solution to global climate change. However, interactions between these principles and their cumulative effects on soil functions and crop productivity are not yet fully understood. Herein, a 4-year filed experiment was conducted to assess the impact of CA on soil ecosystem multifunctionality (EMF) in the North China Plain (NCP). The results showed that CA improved EMF by up to 532 % compared to traditional agriculture (rotary tillage under wheat and maize rotation system). This enhancement is mainly driven by a 12.3 % increase in soil organic carbon (SOC) storage, an 8.3 % reduction in soil carbon to nitrogen ratio (C: N), a 68.3 % boost in soil enzyme activities index (SEI), and a 59.7 % increase in available phosphorus (AP) under legume-based crop rotations (LBCR) compared to maize-wheat-maize-wheat (MWMW). The principle of CT improved soil physical structure, enhancing soil aggregate stability by up to 38.1 % compared to rotary tillage (RT). Although, the benefits of CT on crop yield were not always observed, positive interactions on crop yield occurred under LBCR combined with CT. For instance, the soybean-wheat-soybean-wheat (SWSW) rotation produced 40.8 % higher yields than the MWMW rotation under CT. Overall, benefits of CT in improving soil structure, along with the increased diversity crop residues, adjustments in soil nutrient stoichiometric ratios, and enhanced soil enzyme activity under LBCR, led to improved SOC sequestration, crop yield and EMF under CA. The positive interactions between the principles of CA demonstrate its ability to enhance ecosystem multifunctionality. As a result, the combination of CT and LBCR within CA is recommended to sustain the productivity in NCP and other regions with similar conditions.

A Li-Rich Fluorinated Lithium Zirconium Chloride Solid Electrolyte for 4.8 V-Class All-Solid-State Batteries.

Chloride solid-state electrolytes (SEs) represent an important advance for applications in all-solid-state batteries (ASSBs). Among various chloride SEs, lithium zirconium chloride (Li2ZrCl6) is an attractive candidate considering the high natural abundance of Zr. However, Li2ZrCl6 meets the challenge in practical ASSBs because of its limited ionic conductivity and instability when paired with high-voltage cathodes. This is a major drawback, which can result in a high internal resistance, a low capacity utilization of cathode, and poor cycle stability, especially at high voltage. Existing methods cannot achieve simultaneous enhancement on both ionic conductivity and high-voltage stability due to a trade-off between lithium-ion migration and structural stability. Here a two-pronged strategy based on partial fluorination and incorporation of lithium ions in excess of stoichiometric ratios is introduced that enables high-voltage stability while increasing ionic conductivity concurrently. The Li-rich fluorinated halide SE (Li2.3ZrCl6.1F0.2) exhibits a significant advancement in performance, with an ionic conductivity that is double that of the pristine Li2ZrCl6 and much better high-voltage stability. By leveraging Li2.3ZrCl6.1F0.2 with the LiCoO2 cathode and the Li-In anode, the all-solid-state cell exhibits a remarkable initial specific capacity (198.0 mAh g-1 at 0.1 C) and a high capacity retention (78.5% after 150 cycles) within 3.0-4.8V.

Optimization of Thermoelectric Performance of Ag2Te Films via a Co-Sputtering Method.

Providing self-powered energy for wearable electronic devices is currently an important research direction in the field of thermoelectric (TE) thin films. In this study, a simple dual-source magnetron sputtering method was used to prepare Ag2Te thin films, which exhibit good TE properties at room temperature, and the growth temperature and subsequent annealing process were optimized to obtain high-quality films. The experimental results show that films grown at a substrate temperature of 280 °C exhibit a high power factor (PF) of ~3.95 μW/cm·K2 at room temperature, which is further improved to 4.79 μW/cm·K2 after optimal annealing treatment, and a highest PF of ~7.85 μW/cm·K2 was observed at 200 °C. Appropriate annealing temperature effectively increases the carrier mobility of the Ag2Te films and adjusts the Ag/Te ratio to make the composition closer to the stoichiometric ratio, thus promoting the enhancement of electrical transport properties. A TE device with five legs was assembled using as-fabricated Ag2Te thin films. With a temperature difference of 40 K, the device was able to generate an output voltage of approximately 14.43 mV and a corresponding power of about 50.52 nW. This work not only prepared a high-performance Ag2Te film but also demonstrated its application prospects in the field of self-powered electronic devices.

Renewable syngas production and technoeconomic validation in a pilot-scale reactor of air and air-steam gasification of biomass

Optimal conditions for the gasification at the pilot scale of pine chips biomass feedstock with two different gasifying agents (air and an air/steam mixture) are determined. Ten experimental tests were performed at a fixed temperature, air stoichiometric ratio, and steam-to-biomass ratio. Results showed cold gas efficiencies circa 75 % (air) and 95 % (air/steam), yielding ∼3 Nm3syngas/kgbiomass, in both cases, and lower heating values of 7.6 and 8.5 MJ/Nm3, respectively. Hydrogen production and process performance were assessed and compared to those found in literature, showing a good performance considering biomass, ca. 35 g H2/kg biomass. A techno-economic model fed with the experimental results obtained was validated. The model established that air gasification could be more profitable for energy than air/steam gasification, especially at higher scales. The internal return rate was less than 1.5 years; nevertheless, air/steam mixture as a gasifying agent more adequate for H2/biofuel production.

Probing host guest inclusion complex and its applications by biophysical approach subsequently optimized by molecular docking

Herein, we explored the construction of a supramolecular encapsulated complex between Nile blue (NB) and p-sulfonatothiacalix[4]arene (TSC4X). The developed inclusion complex (NB-TSC4X) was established by fluorescence spectroscopy, TGA, FTIR, 1H NMR, and DFT studies. Benesi-Hildebrand calculation showed a linear plot that indicated a 1:1 stoichiometric ratio having a fairly high stability constant of 2720 M−1 in the solution phase. DFT analysis helps us to find out the optimized structure of the inclusion complex. Finally, the binding interaction of the inclusion complex with bovine serum albumin (BSA) was evaluated. In brief, this work uncloses a new strategy to enhance the performance of fluorescent dye.

Computational and experimental investigation on functional monomer selection for a novel molecularly imprinting polymer of remdesivir

Molecularly-imprinted polymers (MIPs) are a sample preparation technique with a functional cavity that can rebind the same or similar analyte to the template. It also can increase the selectivity of the analytical method. Computational approaches are capable of making predictions about the most optimal synthesis conditions, including the most appropriate monomers and solvents. This study used the DFT method, GFN2-xTB, and molecular dynamics simulation to predict MIP synthesis’s best functional monomer, solvent, and stoichiometric ratio. Remdesivir (RMD), used as a template, has also never been developed to be made as MIP. The monomers were acrylic acid (AA), 2-hydroxyethyl methacrylate (HEMA), and acrylamide (AM). Laboratory testing, association constant, and Job plot analysis are carried out to confirm the results of computational tests. The polymer was synthesized using precipitation and characterized using SEM, FTIR, and TGA. The adsorption capacity was evaluated in two different solvents, i.e. acetonitrile (ACN) and water: ACN=9: 1 (v/v). Computational study results identified acrylamide as the most interactive ligand with RMD as a template. The results of molecular dynamics simulations identify that the RMD: AM=1: 1 complex is the most stable in terms of the radial distribution function, hydrogen bond occupancy, and Gibbs bond free energy. The adsorption ability test results show that MIP 1 and MIP 2 have imprinting factor values of 1.36 and 1.15, respectively.

Future Technological Directions for Hydrogen Internal Combustion Engines in Transport Applications

The paper discusses some of the requirements, drivers, and resulting technological paths for manufacturers to develop hydrogen combustion engines for use in two types of market application – on-road heavy- and light-duty. One of the main requirements is legislative certainty, and this has now been afforded – at least in the major market of Europe – by the European Union's recent adoption into law of tailpipe emissions limits specifically designed to encourage the uptake of hydrogen engines in heavy-duty vehicles, giving manufacturers the confidence they need to invest in productionized solutions to offer to customers.It then discusses combustion systems and boosting systems for the two market types, emphasizing that heavy-duty vehicles need best efficiency throughout their operating map while light-duty ones, since they are rarely operated at full load, will mainly primarily need efficiency in the part-load region. This difference will likely cause a divergence in solutions, with heavy-duty engines running very lean everywhere and light-duty ones likely operating at the stoichiometric air-fuel ratio, at least for most of the map. The impacts of the strategies on engine systems and vehicle integration are discussed.It is postulated that due to reasons of preignition avoidance and efficiency hydrogen engines will rapidly adopt direct injection and that the long-term heavy-duty types will migrate towards the typical current spark-ignition-type cylinder head architecture where tumble, rather than swirl, will ultimately be needed for air motion in the cylinder for these reasons. They may also adopt active pre-chamber technology to ignite extremely lean mixtures for maximum efficiency and minimum emissions of oxides of nitrogen.It is suggested that light-duty engines will evolve less from their current gasoline architectural norm since they already contain all of the necessary fundamentals for hydrogen combustion. However, since part-load efficiency will be important, some new strategies may become desirable. Developing dual-fuel light-duty engines could accelerate their uptake as the heavy-duty market simultaneously accelerates the creation of the fuel supply infrastructure.The likely technological evolution suggests that variable valve trains, and specifically cam profile switching technology, would be extremely useful for all types of hydrogen engine, especially since they are readily available in different gasoline engines now. New operating strategies afforded by variable valve trains would benefit both heavy- and light-duty engines, and these strategies will become more sophisticated. There will therefore likely be a convergence of technologies for the two markets, albeit with some key differences maintained due to their vehicle applications and their differing operation in the field.

Tracking and measuring local protein synthesis in vivo.

Detecting when and how much of a protein molecule is synthesized is important for understanding cell function, but current methods either cannot be performed in vivo or have poor temporal resolution. Here, we developed a technique to detect and quantify subcellular protein synthesis events in real time in vivo. This Protein Translation Reporting (PTR) technique uses a genetic tag that produces a stoichiometric ratio of a small peptide portion of a split fluorescent protein and the protein of interest during protein synthesis. We show that the split fluorescent protein peptide can generate fluorescence within milliseconds upon binding the larger portion of the fluorescent protein, and that the fluorescence intensity is directly proportional to the number of molecules of the protein of interest synthesized. Using PTR, we tracked and measured protein synthesis events in single cells over time in vivo. We use different color split fluorescent proteins to detect multiple genes or alleles in single cells simultaneously. We also split a photoswitchable fluorescent protein to photoconvert the reconstituted fluorescent protein to a different channel to continually reset the time of detection of synthesis events.

Quantum yield, energy transfer, and x-ray induced study of Sm3+ ions doped oxide glasses for intense orange-red photo-emitting optoelectronic device applications

The work elucidates detailed analysis of X-ray near edge structure of Gd3+ ions using Synchrotron studies and deciphers the energy transfer mechanism involved in the stoichiometric ratio of (79-x)B2O3 + 10ZnO + 10BaO + xGd2O3 + 1Sm2O3 (BZBGS; x = 0, 5, 10, 15, 20 mol.%) glasses. A detailed analysis of the glasses’ optical, structural, and luminescence properties were instigated to understand light emitting behaviour. The oxidation state of Gd atom inside the glass found to be + 3. Stimulated emission cross section, radiative transition probability and branching of the metastable state of rare-earth ions were evaluated using Judd-Ofelt model and compared with other reported literature. Photo-Emission spectra were monitored at the UV-C band and X-rays. Luminescence was analysed with various excitation wavelengths and sources. Photoluminescence quantum yield show more than 22 % efficiency and show more than 15 % compared with other reported glasses. Luminescence intensity ratio was analysed and found that the Sm3+-ions do not occupy the inversion-symmetry which enhances the luminescence intensity in the present glass system. The CIE and CCT values were evaluated and discussed.

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 306V, current of 4.71µA, and maximum power density of 3.48µW/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 12000 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.