Alkyl Ammonium Research Articles

Tunable Magnetism in 2D Organic‐Ion‐Intercalated MnPS3 via Molecule‐Dependent Vacancy Generation

AbstractThe magnetic properties of van der Waals materials are profoundly influenced by structural defects. The layered antiferromagnet MnPS3 offers a unique opportunity to explore defect‐related magnetism, as Mn2+ vacancies can be generated by the intercalation of specific guest molecules. However, the effectiveness of this process in atomically thin flakes and the extent of the magnetic tunability remain unclear. Here, it is shown that the magnetic properties of MnPS3 can be tailored through the intercalation of different guest molecules. Notably, the insertion of four alkylammonium ions introduces different populations of Mn2+ vacancies, leading to a transition from the pristine antiferromagnetic state to more complex magnetic textures, including a ferrimagnetic state displaying a magnetic saturation of 1 µB per atom. Moreover, it is shown that the intercalation of few‐nm‐thick flakes also leads to the emergence of a ferrimagnetic response. This in‐flake intercalation, which can be monitored in real time using optical microscopy, can be interrupted before completion, generating lateral heterostructures between pristine and intercalated areas. This approach opens the way to the use of partial intercalation to define regions with distinct magnetic properties within a single flake.

All‐Aromatic Polymer‐Based Anion Conductive Ionomers with Different Ion Exchange Capacities for Water Electrolysis

Anion exchange membrane water electrolysis (AEMWE) is vital for efficient, environmentally friendly, and cost‐effective hydrogen production. Herein, fluorene‐based polymers containing alkyl ammonium groups with different ion exchange capacities (IECs) for use in anion exchange membranes (AEMs) and anion exchange ionomers (AEIs) are investigated. Among the AEMs tested, the AEM with an IEC of 2.2 meq g−1 shows the highest anion conductivity because of its efficient water uptake characteristics. The anode catalyst layers utilize AEIs and iridium oxide catalyst particles. It is essential to select AEIs with appropriate IEC and suitable solvents for high‐performance anodes in water electrolyzers. Morphological and physical property evaluations reveal that moderate hydrophilicity and suppression of water swelling of AEIs improve water electrolysis performance. The optimized catalyst layer achieves better water electrolysis performance (2.64 V, 1.8 A cm−2 at 30 °C) than the conventional catalyst layer (3.83 V, 1.8 A cm−2 at 30 °C). Although the water electrolysis performance in this study falls short of the final targets, further research on anion conductive polymers and catalyst layers, based on this study's findings, is expected to promote practical applications of AEMWEs.

Theory of Turing pattern formation and its experimental realization in the CIMA reaction system in the presence of materials lowering the diffusivity of activators

In 1952, Alan Turing accomplished a pioneering theoretical study to show that the coupling of nonlinear chemical reactions and diffusion leads to the instability of spatially homogeneous states. The activator and inhibitor are synthesized as intermediates of the reaction system in the Turing model. Turing found that spatially periodic stationary concentration patterns are spontaneously generated when the diffusion coefficient of the activator is lower than that of the inhibitor. The first experimental realization of the Turing pattern was achieved in 1990 in a chlorite–iodide–malonic acid (CIMA) reaction system. Iodide and chlorite anions act as the activator and inhibitor of this reaction system, respectively. Although there is no significant difference in the diffusion coefficient of iodide and chlorite anions, the Turing pattern was generated because starch was added to the gel reactor to enhance the color tone. This formed a complex with iodide to inhibit its diffusion to satisfy the condition for the Turing instability. Several examples were found after this finding. We focused on the high affinity of quaternary alkyl ammonium cations to iodide. The CIMA reaction was performed in an open gel reactor by adding a quaternary alkyl ammonium cationic surfactant. In addition, the polymer gel consists of the quaternary alkyl ammonium group as the side chain was utilized for the open gel reactor. The micelles of the surfactants and the polymer gels trapped iodide in their vicinity as a counter anion to lower the effective diffusivity to satisfy the condition for the Turing instability.

Synthesis and Evaluation of Ph and Temperature Stimuli-Responsive Magnetic Nanohydrogels for Gene Delivery

The offer of gene delivery technologies as a promising approach to treating diverse diseases has revolutionized human medicine during the last two decades. So, the application of suitable vectors, particularly polymers with substrates with unique physicochemical properties for the transfer of targeted genes to logical sites for effective treatment, plays an indispensable role for more personalized medicine and improves the safety profile in response to continuing to use new medical technologies. For this purpose, we synthesized nanocarriers with a two-block cationic hydrogel, magnetic and non-magnetic, based on N-isopropyl acrylamide (NIPAM) and quaternary alkyl ammonium halide salts of DMAEMA (DMAEMAQ) with pH and temperature responsiveness via the free radical polymerization technique. The bulk properties of these co-polymers were characterized by using Fourier transform infrared spectroscopy, 1H NMR spectroscopy, Zeta potential, lower critical solution temperature (LCST), and gel electrophoresis to show the loading of nanoparticles with the gene. In the results, magnetic P[NIPAM-DMAEMAQ] hydrogel showed controllable responsive properties determined by the nature of the cationic charge +24.7 mV incorporated, nanosize around 86.95 and 91.22 nm, and efficiency loaded with the gene more than 95%. As well, the synthesized nanohydrogel exhibited a sharp volume-phase transition in water at a LCST of ∼40 °C. So, the combination of both monomers yielded an interesting system with high transfection efficiency and compliant biocompatibility characteristics, which could effectively achieve gene loading. Also, the magnetic potential of nanohydrogel was determined as a vector to deliver genes to localized sites. Notably, the synthesized combination P[NIPAM-DMAEMAQ] nanohydrogel has been considered a transfection of the biodegradable and biocompatible magnetic nanoparticle sensitive to tunable pH and temperature responsiveness, demonstrating that it will hold a promising approach as a potential carrier to improve gene delivery therapeutic efficacy in cancer and different disease treatments.

Mo7O246- and alkyl ammonium based metal organic ionic framework and their protein conjugates: Adsorbent for removal of cationic/ anionic dyes

Herein, we report the removal of organic dyes by metal–organic ionic frameworks (MOIFs) incorporating Mo7O246- and alkyl ammonium ions synthesized via an ion-exchange process in aqueous medium, [CnH2n+1)nN(CH3)3][Mo7O24], where n = 12, 14, 16. These were characterized using powder X-ray diffraction (XRD), UV/Visible spectroscopy, and Fourier-transform infrared (FTIR) spectroscopy techniques. A thermal transition occurring at 300–400 °C attributed to the decomposition of organic moieties analyzed through thermal gravimetric analysis (TGA). Coats-Redfern analysis revealed an activation energy of approximately −1.32763 kJ/mol, suggesting rapid interaction capability of MOIFs with pollutants. The heat capacity found approximately 135 J/K, indicating thermal stability investigated using differential scanning calorimetry (DSC). MOIFs exhibited remarkable adsorption of organic dyes demonstrated through complete removal (100 %) of anionic congo red dye and 88 % of cationic safranin dye. MOIFs functionalized with protein conjugates (MOIF@BSA) were evaluated for their adsorption efficiency on mix dye compared to MOIFs, displaying superior performance with up to 95 % removal of mixed dyes. Kinetic studies employing pseudo-first-order kinetics indicated that the adsorption process is primarily governed by the diffusion of dye molecules within the MOIFs structure. Desorption analysis demonstrated complete recovery of MOIFs, dyes, and solvent, highlighting the environmentally friendly nature of the approach employed, consistent with green chemistry principles.

Surface engineering of FAPbI3 based organic–inorganic hybrid perovskite for memristors

Organic–inorganic hybrid perovskites (OIHPs) have been spotlighted as emerging solution-processed electronics and show promise as economical, flexible, and stretchable emerging memristors. However, OIHPs suffer from considerable defects derived from solution processing; thus, post-processing is often required to alleviate such shortcomings. Treating alkyl ammonium organic salt on OIHP films is a representative approach to efficiently mediate the defect density. Here, we adopted n-octyl ammonium chloride (OACl) in our post-processing agent for organometal perovskite memristors (OPMs). The OACl-incorporated OPM showed an enlarged ON/OFF resistance ratio of 520 compared to OPM without passivation (3.91). Thin film analysis revealed that the synergistic insulating/passivating layer from OACl post-treatment retarded the interaction with the electroactive electrode (Ag). Additionally, the combined effects from the lower-dimensional OIHP induced by OA, including the p-doping of lead by chloride, enhanced the energetic barrier with Ag electrode to reduce the parasitic current at the high resistance state. This study offers deeper insights into the surface passivation of OIHPs and its effects on memristic performance.

A comparative study of alkylammonium halide interface modification for high efficiency and ion migration stability perovskite solar cells

Constructing 2D/3D perovskite heterostructures with organic molecules is key to improving the power conversion efficiency (PCE) and stability of perovskite solar cells (PSCs). However, a comprehensive understanding of the inhibitory relationship between the 2D perovskite layer and ion migration at the interface is still lacking. In this study, we use different alkyl ammonium iodides to build 2D/3D perovskite heterostructures. The research results show that both the chain length of alkyl and amino group count in alkyl ammonium iodide can significantly affect the crystal structure orientation of the 2D perovskite layer. A Dion-Jacobson (DJ) 2D/3D structure treated with ODADI shows superior defect passivation and carrier extraction, leading to PSCs with a 24.51 % PCE. Furthermore, the perovskite based on ODA cations eliminates the influence of Van der Waals interaction in perovskite based on BA or OA cations, which improves the stability of the lattice structure, and significantly inhibits ion migration. Therefore, after a maximum power point stability test of 1500 h, devices retain approximately 88 % of their initial PCE. This work offers fresh insights into optimizing interfaces in 2D/3D PSCs by selecting suitable organic molecules.

Functionalization and Structural Evolution of Conducting Quasi-One-Dimensional Chevrel-Type Telluride Nanocrystals.

Interfacing organic molecular groups with well-defined inorganic lattices, especially in low dimensions, enables synthetic routes for the rational manipulation of both their local or extended lattice structures and physical properties. While appreciably studied in two-dimensional systems, the influence of surface organic substituents on many known and emergent one-dimensional (1D) and quasi-1D (q-1D) crystals has remained underexplored. Herein, we demonstrate the surface functionalization of bulk and nanoscale Chevrel-like q-1D ionic crystals using In2Mo6Te6, a predicted q-1D Dirac semimetal, as the model phase. Using a series of alkyl ammonium (-NR4+; R = H, methyl, ethyl, butyl, and octyl) substituents with varying chain lengths, we demonstrate the systematic expansion of the intrachain c-axis direction and the contraction of the interchain a/b-axis direction with longer chain substituents. Additionally, we demonstrate the systematic expansion of the intrachain c-axis direction and the contraction of the interchain a/b-axis direction as the alkyl chain substituents become longer using a combination of powder X-ray diffraction and Raman experiments. Beyond the structural modulation that the substituted groups can impose on the lattice, we also found that the substitution of ammonium-based groups on the surface of the nanocrystals resulted in selective suspension in aqueous (NH4+-functionalized) or organic solvents (NOc4+-functionalized), imparted fluorescent character (Rhodamine B-functionalized), and modulated the electrical conductivity of the nanocrystal ensemble. Altogether, our results underscore the potential of organic-inorganic interfacing strategies to tune the structural and physical properties of rediscovered Chevrel-type q-1D ionic solids and open opportunities for the development of surface-addressable building blocks for hybrid electronic and optoelectronic devices at the nanoscale.

Influence of titanium dioxide nanotubes with alkyl ammonium alkyl bromide on the physicochemical properties and adhesion of experimental adhesive resins to dentin

ObjectiveThis study evaluated the effect of the incorporation of titanium dioxide nanotubes with alkyl trimethyl ammonium bromide (ntTiO2/ATAB) into experimental adhesive resins on their physicochemical properties and adhesion to dentin. Materials & methodsThe experimental adhesive resins were formulated with 66.66 wt% Bis-GMA and 33.33 wt% HEMA, photoinitiator with addition of ntTiO2/ATAB (1:1) in different concentrations: G1%, G2.5%, and G5%. One groups with no ntTiO2/ATAB addition was used as control (G0%). An optical tensiometer was used to analyze the contact angle (COA) by the sessile drop method (distilled water and α-bromonaphthalene) (n = 5), while the surface free energy (SFE) was calculated using Owens-Wendt-Rabel-Kaelble method. Flexural strength (FS) test (three-point bending) of polymerized adhesive samples was performed according to ISO 4049:2019 (n = 10) after 24 h or one year of water storage at 37 °C, as well as for the microtensile bond strength (μTBS) test, in which a commercial adhesive (GSBMP) was also used as control (n = 10). The adhesive-dentin interfaces were evaluated by scanning electron microscopy and X-ray spectrometry (n = 5). Data were analyzed by one-way (COA and SFE), two-way (FLE and μTBS) ANOVA and Tukey's test (α = 0.05). ResultsG5% showed the highest COA with nonpolar liquid and higher SFE than G0%. The G5% showed decreased FS compared to G0%. The μTBS of both controls (G0% and GSBMP) decreased after one year. TiO2/ATAB-containing adhesives to dentin showed no significant decrease after one year. All adhesives formed hybrid layer and the resin tags inside the dentinal tubules. ConclusionsThe incorporation of 1 and 2.5% of ntTiO2/ATAB into experimental adhesive resins did not impar the SFE. After one year, any concentration of ntTiO2/ATAB reduced the FS compared with control, but did not impair the μTBS.

Alkyl ammonium hydrogen sulfate immobilized on Fe3O4@SiO2 nanoparticles: a highly efficient catalyst for the multi-component preparation of novel tetrazolo[1,5-a]pyrimidine-6-carboxamide derivatives

In this, a three-component reaction for the preparation of novel tetrazolo[1,5-a]pyrimidine-6-carboxamide derivatives from N,N′-(sulfonylbis(1,4-phenylene))bis(3-oxobutanamide), aldehydes and 1H-tetrazol-5-amine is reported. The application of Fe3O4@SiO2-(PP)(HSO4)2 (A) as a catalyst afforded the desired products (a1–a18) in high yields in DMF as solvent as well as under solvent-free conditions.

Reducing Ice Adhesion to Polyelectrolyte Surfaces by Counterion-Mediated Nonfrozen Hydration Water.

Hydrophilic anti-icing coatings can be energy-effective passive solutions for combating ice accretion and reducing ice adhesion. However, their underlying mechanisms of action remain inferential and are ill-defined from a molecular perspective. Here, we systematically investigate the influence of the counterion identity on the shear ice adhesion strength to cationic polymer coatings having quaternary alkyl ammonium moieties as chargeable groups. Temperature-dependent molecular information on the hydrated polymer films is obtained using total internal reflection (TIR) Raman spectroscopy, complemented with differential scanning calorimetry (DSC) and ellipsometry. Ice adhesion measurements show a pronounced counterion-specific behavior with a sharp increase in adhesion at temperatures that depend on the anion identity, following the order Cl- < F- < SCN- < Br- < I-. Linked to the freezing of hydration water, the specific ordering results from differences in ion pairing and the amount of water present within the polymer film. Moreover, similar effects can be promoted by varying the cross-linking density in the coating while keeping the anion identity fixed. These findings shed new light on low ice adhesion mechanisms and may inspire novel approaches for improved anti-icing coatings.

PREPARATION AND CHARACTERIZATION OF PERFLUOROETHYLSUBSTITUTED ALKYLAMMONIUM OLIGOFLUOROPHOSPHATES

Mono-, di-, triperfluoroethyl substituted fluorophosphate anions are building blocks in the molecular design of salts with onium cations, and are used to increase hydrophobicity, modify surfactant properties and electrical conductivity. The work proposes methods for the synthesis of superacid H+[PF3(C2F5)3]- by the reaction of tri(pentafluoroethyl)difluorophosphorane with a solution of hydrofluoric acid, as well as superacids H+[PF4(C2F5)2]- and H+[PF5C2F5]- by step-by-step removal of the pentafluoroethyl substituent by hydrolysis with subsequent treatment with HF solution. Ionic compounds were synthesized by metathesis of anions at 0 °C from the corresponding quaternary ammonium chloride based on the obtained superacids. The article presents NR4FAP-class ionic compounds with the tributylmethylammonium (TBMA) cation of the general formula [(C4H9)3NCH3]+[PF6-n(C2F5)n]-, where n = 1, 2, 3. The square bipyramidal structure of the three studied anions was confirmed by nuclear magnetic resonance (NMR) spectroscopy and X-ray diffraction (XRD) data. The study shows, the synthesized compounds are characterized by extremely low vapor pressure up to 300 °C, a wide range of the liquid state with a width of up to 310 K by the methods of differential scanning calorimetry (DSC) and synchronous thermal analysis (STA). Melting temperatures and enthalpies were determined. The TBMA salts belong to ionic liquids (IL's), including one type liquid at room temperature (RT-IL). The general patterns of compounds decomposition were analyzed by the analysis of evolved gases (STA-EGA); it was shown that in all cases, the decomposition of the studied ionic liquids begins with the destruction of the anion. The electrical resistance of a pure ionic liquid at room temperature was studied. The described characteristics of perfluoroethylsubstituted alkyl ammonium oligofluorophosphates open up prospects for their use as electro conducting and antistatic additives for petrochemicals, fuels and polymers. For citation: Mokrushin I.G., Pinegina O.A., Krasnovskikh M.P., Dmitriev M.V., Markin I.V., Kozen A.L. Preparation and characterization of perfluoroethylsubstituted alkylammonium oligofluorophosphates. ChemChemTech [Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol.]. 2024. V. 67. N 5. P. 54-61. DOI: 10.6060/ivkkt.20246705.6916.

On the dependence of electrical mobility on temperature, humidity and structure of alkylammonium ions

Insights into the effect of temperature (T) and relative humidity (RH) as well as structure and polarisation on ion mobility help the comparison and interpretation of mobility and mass-based data. We measured alkylammonium ions in air under different T (14 °C, 24 °C, 34 °C and 41 °C) and RH (0 %, 20 %, 40 %) conditions using two individual setups (in both cases a planar differential mobility analyser coupled with a time-of-flight mass spectrometer) and the results are in excellent agreement. Mobility increases with rising T and decreases with water vapour loading. When separating the measurement mobility by structures, clear mass dependence was observed. The measured mobilities exhibited large deviations from theoretically calculated results in dry conditions, which are possibly caused by adduct formation on the monomer ions via clustering (or reactions). This phenomenon seems to be unavoidably associated with light ions under atmospheric pressures, which is worth further exploration and bearing in mind when comparing measurements to calculations. Both methanol and oxygen (occasionally nitrogen or alkyl chain elongation) are possible candidates of the adduct. Under spherical assumption, we used the modified Mason–Schamp's approximation to link the measured mobility to the mobility equivalent diameter. The drag enhancement factor ξ and the effective gas-molecule collision diameter dg derived from our measurement data are comparable to literature values. Our data also exposed a non-linear dependence on the polarisation parameter ε*. Polarisation, ξ and dg were parameterised using linear models against ion structures, T, and RH for primary, secondary and tertiary alkylammonium ions with identical alkyl groups. Our model parametrisations predict mobilities within ±10 % deviation from the measured data. The model also has satisfying predicting power for alkylammonium ions with unidentical alkyl structures.

Monolayer Modification of Spherical Amorphous Silica by Clay Nanosheets.

Clay-silica nanocomposite materials (CSiN) were prepared by an electrostatic interaction between negatively charged clay nanosheets and positively charged spherical silica, which was modified with an alkyl ammonium group by silane coupling. By optimization of the preparation conditions, 84% coverage of the silica surface by the clay nanosheets was achieved. Adsorption experiments using cationic porphyrin dyes on the CSiN revealed that the clay nanosheet covers the spherical silica as a single layer and does not detach from the silica surface under aqueous conditions. In addition, it turned out that the cationic porphyrin dye did not penetrate the space between the silica surface and the clay nanosheet. Porphyrin molecules were adsorbed only at the outer surface of the clay nanosheet without molecular aggregation even under the high-density adsorption conditions. By combining spherical silica and clay nanosheets, it is possible to prepare novel hybrid materials where the surface can act as a unique adsorption field for dyes.

Structure and properties of ZnO‐organobentonite‐filled natural rubber composites

AbstractThis study involved the preparation of composites consisting of zinc oxide (ZnO) nanoparticles deposited within the structure of organophilic bentonite. These composites were subsequently utilized as fillers in natural rubber (NR). The organobentonites were initially prepared via a cation exchange reaction using alkylammonium ions with different chain lengths (C8N−C18N) and later deposited by ZnO nanoparticles. The identification of the ZnO‐organobentonites was conducted using various techniques, including powder X‐ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), UV‐Vis spectroscopy, etc. The findings demonstrate the successful deposition of ZnO nanoparticles within the organobentonite's structure. The basal space between the silicate layers increased with the increasing chain length of alkylammonium ions. When added to NR, the ZnO‐organoclays mutually acted as a cure activator and filler. As expected, the ZnO‐organoclay modified by octadecylammonium ions (C18N) showed the greatest reinforcement due to its highest capability to enlarge the basal space between the silicate layers.

Alkyl ammonium iodide-based ligand exchange strategy for high-efficiency organic-cation perovskite quantum dot solar cells

Alkyl ammonium iodide-based ligand exchange strategy for high-efficiency organic-cation perovskite quantum dot solar cells

Enhanced azeotropic C2ClF5/C3F8 separation by TMA+ exchanged MFI zeolites for ultrapure fluorine electronic gas

AbstractThe demand for the azeotropic C2ClF5/C3F8 separation continues to rise owing to the significance of ultrapure fluoride gases for the electronic industry. With a boiling point differential of 1.1 K, separating an azeotropic mixture of C2ClF5/C3F8 through sorption‐based processes under ambient conditions is a preferable alternative to the current energy‐intensive cryogenic separation method. Here, we report the highly efficient C2ClF5/C3F8 adsorption separation in quaternary alkylammonium ions modified MFI type zeolites with interlaced channels which provide a cooperative effect conferred by specific interaction sites and optimal pore size. A path‐regulatory mechanism was proposed, whereby TMA+ cations located at intersections resembling “train turnouts” force gas molecules to switch traffic channels to confined sinusoidal channels affecting the C2ClF5/C3F8 recognition sites and diffusion behavior. Molecular simulations were conducted to reveal the separation mechanism, and the breakthrough experiment validated the effectiveness of this adsorbent at 298 K outperforming conventional adsorbents for the challenging azeotropic separation.

Proton transport in oxalate compounds of iron(iii) containing (alkyl)ammonium cations: the influence of the density of hydrogen bonds on conductivity

The proton conductivity of novel mononuclear and 1D oxalate-based compounds of iron(iii) containing (alkyl)ammonium cations was investigated: the discrete compound shows remarkable humidity sensing properties and very high proton conductivity.

Scalable and adaptable two-ligand co-solvent transfer methodology for gold bipyramids to organic solvents.

Large and faceted nanoparticles, such as gold bipyramids, presently require synthesis using alkyl ammonium halide ligands in aqueous conditions to stabilize the structure, which impedes subsequent transfer and suspension of such nanoparticles in low polarity solvents despite success with few nanometer gold nanoparticles of shapes such as spheres. Phase transfer methodologies present a feasible avenue to maintain colloidal stability of suspensions and move high surface energy particles into organic solvent environments. Here, we present a method to yield stable suspensions of gold bipyramids in low-polarity solvents, including methanol, dimethylformamide, chloroform, and toluene, through the requisite combination of two capping agents and the presence of a co-solvent. By utilizing PEG-SH functionalization for stability, dodecanethiol (DDT) as the organic-soluble capping agent, and methanol to aid in the phase transfer, gold bipyramids with a wide-range of aspect ratios and sizes can be transferred between water and chloroform readily and maintain colloidal stability. Subsequent transfer to various organic and low-polarity solvents is then demonstrated for the first time.

Unveiling the role of linear alkyl organic cations in 2D layered tin halide perovskite field-effect transistors.

Two-dimensional (2D) tin halide perovskites are promising semiconductors for field-effect transistors (FETs) owing to their fascinating electronic properties. However, the correlation between the chemical nature of organic cations and charge carrier transport is still far from understanding. In this study, the influence of chain length of linear alkyl ammonium cations on film morphology, crystallinity, and charge transport in 2D tin halide perovskites is investigated. The carbon chain lengths of the organic spacers vary from propylammonium to heptanammonium. The increase of alkyl chain length leads to enhanced local charge carrier transport in the perovskite film with mobilities of up to 8 cm2 V-1 s-1, as confirmed by optical-pump terahertz spectroscopy. A similar improved macroscopic charge transport is also observed in FETs, only to the chain length of HA, due to the synergistic enhancement of film morphology and molecular organization. While the mobility increases with the temperature rise from 100 K to 200 K due to the thermally activated transport mechanism, the device performance decreases in the temperature range of 200 K to 295 K because of ion migration. These results provide guidelines on rational design principles of organic spacer cations for 2D tin halide perovskites and contribute to other optoelectronic applications.