Emission Band Research Articles

Spectroscopic assessments on Sm3+ ions doped phospho-borate glasses mixed with fluoride modifiers for the applications of reddish-orange visible light

Sm3+ions doped Phospho-Borate glasses were synthesized and their physical and spectroscopic parameters were studied to evaluate its potential reddish-orange emission for photonic applications. Structural investigation made through XRD analysis confirms the amorphous nature. The evaluated bonding parameters from the absorption spectral analysis confirm the ionic bonding of the Sm–O network in the prepared glasses. Four emission bands were observed from the luminescence spectra, and the HT 4G5/2 → 6H7/2 is observed at 601 nm. The oscillator strength values elucidate the intensity of the absorption bands, and the PBKZnF:Sm sample exhibits a higher oscillator strength value. The Judd-Ofelt intensity parameters were observed to trail the trend Ω4 > Ω6. > Ω2 for the majority of the samples. The CIE 1931 color chromaticity investigation confirms that the present glass samples are suitable for reddish-orange media. Barium and strontium-incorporated glasses exhibit outstanding lasing potential, which was confirmed through the efficiency of the quantum yield and some of the radiative parameters like effective bandwidth, transition probability and stimulated emission cross-section. Radiative parameters have been calculated from the luminescence spectra. Amid all transitions, 4G5/2 →6H7/2 transition has higher transition probability and higher stimulated emission cross-section values for all the prepared glass samples. Barium-incorporated glass exhibits a higher emission cross-section of 30.55 × 10−22 cm2 and a transition probability of 30.89 s−1 compared to all other glasses. The non-exponential decay profiles of the fabricated samples were plotted by examining the excitation wavelength at 402 nm and emission wavelength at 600 nm. Of all the prepared glasses, the quantum efficiency is found to be higher for the glass sample PBKSrF:Sm (65 %).

Spinel-Type Structured Phosphor Near-Infrared-II Emission: Intervalence Charge Transfer and Hetero-Valent Chromium Pairs.

Near-infrared (NIR) emitting phosphors draw much attention because they show great applicability and development prospects in many fields. Herein, a series of inverse spinel-type structured LiGa5O8 phosphors with a high concentration of Cr3+ activators is reported with a dual emission band covering NIR-I and II regions. Except for strong ionic exchange interactions such as Cr3+-Cr3+ and Cr3+ clusters, an intervalence charge transfer (IVCT) process between aggregated Cr ion pairs is proposed as the mechanism for the ~1210 nm NIR-II emission. Comprehensive structural and luminescence characterization points to IVCT between two Cr3+ being induced by structural distortion and further enhanced by irradiation. Construction of the configurational energy level diagram enabled elucidation of this transition within the IVCT process. Therefore, this work provides insight into the emission mechanism within the high Cr3+ concentration system, revealing a new design strategy for NIR-II emitting phosphors to promote its response.

Ultrafast Near‐Infrared Luminescence from Cyclometalated Iridium(III) Complexes with Indirubin as Ancillary Ligand

AbstractBeing a constitutional isomer of the indigo dye, indirubin has been known as a purple colourant for a long time. On the other hand, its structural and photophysical properties as ligand in metal complexes are virtually unexplored. Herein, for the first time, we utilized indirubin as ancillary chelator to develop two new heteroleptic iridium(III) complexes equipped with two 2‐phenylpyridine units as archetypical cyclometalating ligands. These new complexes display fully reversible oxidation and reduction processes, and show a panchromatic absorption extending up to 900 nm in acetonitrile solution at 298 K. Moreover, an unexpected broad and unstructured emission band is detected for both complexes in the near‐infrared region, peaking at approx. 1100 nm and having a lifetime of approx. 60 ps; such an emission is attributed to a ligand‐centred triplet excited state (3LC) located on the indirubin ligand itself, as proved by DFT calculations. These findings may pave the way for further exploration of the indirubin dye as a ligand for different types of metal centres to create efficient near‐infrared triplet emitters without the need for difficult synthetic procedures.

Nonadiabatic Molecular Dynamics Simulations Provide Evidence for Coexistence of Planar and Nonplanar Intramolecular Charge Transfer Structures in Fluorazene.

Fluorazene is a model compound for photoinduced intramolecular charge transfer (ICT) between aromatic moieties. Despite intensive studies, both spectroscopic and theoretical, a complete model of its photophysics is still lacking. Especially controversial is the geometry of its ICT structure, or structures. In order to fill in the gaps in the state of knowledge on this important model system, in the present study I report the results of nonadiabatic molecular dynamics (NAMD) simulations of its photorelaxation process in acetonitrile solution. To afford a direct comparison to spectroscopic data, I use the simulation results as the basis for the calculation of the transient absorption (TA) spectrum. The NAMD simulations provide detailed information on the sequence of events during the excited-state relaxation of the title compound. Following initial photoexcitation into the bright S2 state, the molecule undergoes rapid internal conversion into the S1 state, leading to the locally excited (LE) structure. The LE structure, in turn, undergoes isomerization into a population of ICT structures, with geometries ranging from near-planar to markedly nonplanar. The LE → ICT isomerization reaction is accompanied by the decay of the characteristic excited-state absorption band of the LE structure near 2 eV. The anomalous fluorescence emission band of fluorazene is found to originate mainly from the near-planar ICT structures, in part because they dominate the overall population of ICT structures. Thus, the planar ICT (PICT) model appears to be the most appropriate description of the geometry of the ICT structure of fluorazene.

Thermally induced Modulation of optoelectronic characteristics In (ZrO2)0.8 doped (CuO) 0.2 screen printed thick films: An Innovative approach to enhanced materials

The Zirconium Dioxide (ZrO2) dopedCopper Oxide (CuO) thick films were fabricated on a glass substrate using the screen printing method, employing sintering temperatures of 500 °C, 550 °C, and 600 °C. The structural characteristics of the doped films were analyzed through Scanning Electron Microscopy (SEM), X-Ray Powder Diffraction (XRD), and Fourier Transform Infrared Spectroscopy (FTIR). Additionally, the optical properties were assessed via UV–Vis spectroscopy and Photoluminescence (PL) spectroscopy. SEM investigations revealed an increase in nanoparticle grain size and agglomeration as the sintering temperature was raised. XRD results exhibited the polycrystalline nature of the films and an augmented intensity of the monoclinic phase of ZrO2, with a noticeable preferred orientation along the (111) plane, which increased with higher sintering temperatures. FTIR analysis demonstrated slight peak shifts and increased sharpness as the sintering temperature was elevated. UV–Vis spectroscopy indicated a redshift in the reflectance edge, with the band gap transitioning from 3.81 eV (at 500 °C) to 3.65 eV (at 600 °C). These findings were corroborated by PL spectroscopy, which exhibited a redshift in the band emission as the sintering temperature increased. Electrical conductivity displayed semiconducting behavior of the sample. These investigations collectively indicate that elevating the sintering temperature leads to enhanced crystallinity in the films and a reduction in lattice deformations within the composite materials which is crucial for applications in large-area and flexible electronics.

Tuning of structure, surface morphology and optical properties of spray-coated nickel tin oxide thin films by heat treatment

In this work, nickel tin oxide (NiSnO3) in a 1:1 ratio was synthesized using a simple spray pyrolysis technique followed by annealing at 450 °C for different time durations. The X-ray diffraction (XRD) revealed the polycrystalline nature with perovskite structure of NiSnO3 without the formation of any secondary phases. Annealing improved the crystallinity of the films. The annealed films exhibited a preference for orientation along the (310) plane. The largest crystallite size was obtained for 4 h of annealed film. The scanning electron microscopy (SEM) images of the films distinctly illustrate enhanced crystallinity following the annealing process. Energy-dispersive X-ray spectroscopy (EDS or EDX) indicates that the film possesses a near-stoichiometric composition. All the films resulted in more than 70 % transmittance in the visible region except for 8 h annealed. The gradual reduction of energy bandgap was observed for the sample. The four peaks at 358 nm, 415 nm, 436 nm, and 460 nm were observed in photoluminescence (PL) spectra corresponding to near band emission and defects related emissions respectively. The determined optical parameters from the present study indicate that the 4-h annealed film holds promise as a favourable option for optoelectronic and photonic devices.

Effect of Isopropanol on Optical Properties of Fe3O4/ZnO/Graphene Quantum Dots (GQDs) Nanocomposite

This study aims to investigate the impact of isopropanol on the optical properties of the Fe₃O₄/ZnO/GQDs nanocomposite. The synthesis of Fe₃O₄ and ZnO nanoparticles was conducted using the coprecipitation method, followed by the synthesis of GQDs using the hydrothermal method with varying concentrations of isopropanol. Subsequently, the Fe₃O₄/ZnO nanocomposite was combined with GQDs synthesized using the sonication method. The amalgamation of magnetic and luminescent materials holds promise for applications in the biomedical field, particularly in bioimaging. XRD data analysis revealed crystal structure alterations attributed to the incorporation of carbon elements in both ZnO and Fe₃O₄. The TEM results indicated a particle size of 16.2 nm for the Fe₃O₄/ZnO/GQDs nanocomposite with a 10 ml isopropanol variation. Identified phases from the XRD analysis include Fe₃O₄, ZnO, and GQDs. UV-Vis spectroscopy detected distinctive absorbance peaks at wavelengths of 323.7 nm, 333.0 nm, 329.9 nm, and 323.9 nm. Moreover, the energy gap exhibited an increase with escalating concentrations of isopropanol in the GQDs. Photoluminescence analysis yielded robust, broad emission bands characterized by orange and red luminescence.

Solvent effect on the excited state photophysics of Imiquimod: A DFT/TD-DFT and spectroscopic study

Solvation plays an important role in chemistry and biology. The role of the solvent is crucial in any chemical processes such as tautomerization that controls the structure and function of biomolecules. The current study aims to explore how different solvent medium affects the tautomeric forms of an antitumor drug, Imiquimod (IMQ). We have used several spectroscopical methods, including UV–Vis absorption spectroscopy, steady-state and time-resolved fluorescence spectroscopy, and quantum mechanical (QM) calculations. Our results revealed that solvent, indeed, plays a significant role in the modulation of the photophysics of the drug. IMQ has three emission bands in protic and aprotic solvents and two bands in non-polar medium associated with different forms of the drug. Using time-resolved technique, and comparing with the predicted lifetimes from QM calculations, we succeed to assign these three forms as cation, tautomer and neutral of IMQ with 1.6 ns, 2.0 ns and 4.0 ns lifetime values, respectively. Since IMQ is a nucleobase analogue and one of the most effective medications for skin tumors; these findings about which specie of IMQ is present in a given medium, and beyond, how the medium alters the photophysics of the molecule may provide deeper insights into its structure and function.

Multiple pathways for lanthanide sensitization in self-assembled aqueous complexes

Lanthanide photoluminescence (PL) emission has attracted much attention for technological and bioimaging applications because of its particularly interesting features, such as narrow emission bands and very long PL lifetimes. However, this emission process necessitates a preceding step of energy transfer from suitable antennas. While biocompatible applications require luminophores that are stable in aqueous media, most lanthanide-based emitters are quenched by water molecules. Previously, we described a small luminophore, 8-methoxy-2-oxo-1,2,4,5-tetrahydrocyclopenta[de]quinoline-3-phosphonic acid (PAnt), which is capable of dynamically coordinating with Tb(III) and Eu(III), and its exchangeable behavior improved their performance in PL lifetime imaging microscopy (PLIM) compared with conventional lanthanide cryptate imaging agents. Herein, we report an in-depth photophysical and time-dependent density functional theory (TD–DFT) computational study that reveals different sensitization mechanisms for Eu(III) and Tb(III) in stable complexes formed in water. Understanding this unique behavior in aqueous media enables the exploration of different applications in bioimaging or novel emitting materials.

Visible light activated time dependent phosphorescence colors from carbon dots based materials

To endow carbon dots (CDs)-based materials with time dependent phosphorescence colors (TDPCs) activated by visible light will benefit high-level data encryption and anticounterfeiting. It needs multiple emission centers of triplet state stabilized by noncovalent bonds. In this work, levofloxacin and ethanolamine were applied to synthesize CDs (LEE-CDs), in which, aromatic moieties and multiple emissive centers were formed by the reaction between fluorinated quinolone moieties and ethanolamine. Melamine (MA) and cyanuric acid (CA) with large π systems were selected as matrices, and urea and biuret without π systems were selected as the comparison matrices. Interestingly, LEE-CDs encapsulated in MA (LEE-CDs@MA) exhibited visible-light-activated TDPCs varying from red to yellow green, while LEE-CDs@CA displayed TDPCs from red to yellow green after excited by visible light, yellow to green after excited by UV light. However, LEE-CDs@Urea and LEE-CDs@Biuret could only generate a single color RTP after excited by visible or UV light. It can be inferred that π-π stacking interactions combining with hydrogen bonds activated the O-related triplet state with a short lifetime, and hydrogen bonds only retained the N-related triplet state in LEE-CDs with a long lifetime and the emissive center of matrices with an intermediate lifetime. Therefore, the dynamic ratio of the RTP emissive bands from the three centers changing over time resulted in TDPCs.

On the properties of ZnO nanorods (ZnO NRs)/NiO heterostructure prepared by double chemical bath deposition

We report on the ZnONRs and ZnONRs/NiO heterostructure synthesized by the chemical bath deposition technique. The samples were characterized using x-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence (PL) spectroscopy, Raman spectroscopy, and UV–vis spectroscopy techniques. XRD, Raman spectroscopy, and SEM analysis revealed the formation of ZnONRs/NiO heterostructure. Raman spectra showed a decrease in intensity of low-frequency non-polar and active (E 2 (low)) vibrational mode when NiO is deposited onto ZnONRs. The PL spectra revealed ultraviolet and visible emission bands, whose intensities decreased when NiO grew onto ZnONRs. The Au/NiO/ZnONRs/FTO heterostructure Schottky diode performed better than the Au/ZnONRs/FTO Schottky diode. The Au/NiO/ZnONRs/FTO heterojunction demonstrated a current rectification ratio of 3.03 × 102 at ± 2 V and a forward current of 1.51 × 10−3 A, which is higher than that of Au/ZnONRs/FTO having a rectification ratio of 6.79 × 101 at ± 2 V and a forward current of 1.651 × 10−5 A.

Antimicrobial photodynamic therapy against Escherichia coli by exploiting endogenously produced Protoporphyrin IX- In vitro study.

Due to antimicrobial drug resistance, there is a growing interest in the development of light based alternative antibacterial therapies. This research work is focused on the inactivation of Escherichia coli (E. coli) by exploiting the absorption bands 405, 505, 542, 580 and 631nm of its indigenously produced Protoporphyrin IX (PpIX) excited by three LEDs with broad emission bands at 418, 522 and 630nm and two laser diodes with narrow emission bands at 405 and 635nm. Fluorescence spectroscopy and plate count method have been employed for studying the inactivation rate of E. coli strain in autoclaved water suspension. It has been found that LEDs at 418, 522 and 630nm produced pronounced antimicrobial photodynamic effect on E. coli strain comparing laser diodes at 405 and 635nm, which might be attributed to the overlapping of broad emission bands of LEDs with the absorption bands of PpIX than narrow emission bands of laser diodes. Particular effect of LED at 522nm has been noticed because its broad emission band overlaps three absorption bands 505, 542 and 580nm of PpIX. The gold standard plate count method strongly correlates with Fluorescence spectroscopy, making it an innovative tool to administer bacterial inactivation. The experimental results suggested the development of a light source that entirely overlap absorption bands of PpIx to produce a pronounced antimicrobial photodynamic effect, which might become an effective modality for in vivo disinfection of antibiotic resistant microbes in wounds and lesions.

Investigating Optical Variability of the Blazar S5 0716+714 on Diverse Timescales

We present the results of the observational study of the blazar S5 0716+716 in the optical bands B, V, R, and I between 2019 March and 2023 August to investigate its variability on diverse timescales. The blazar was followed up by the T60 robotic telescope in Türkiye for 416 nights to obtain long-term variability during this period. In order to search for the intraday variability of the object, we have carried out 21 nights of observations with the T100 telescope for at least 1 hr. The blazar showed a ∼2.47 mag variation in the optical R band during our monitoring period, the brightest state on 2020 January 18 (MJD 58866) as R = 12.109 ± 0.011 mag and the faintest state on 2019 March 23 (MJD 58565) as R = 14.580 ± 0.013 mag. We employed the nested ANOVA test and the power-enhanced F-test to quantify intraday variability, which showed that the blazar was significantly variable in the R band on 12 out of 21 nights. Correlation analysis of the light curves shows that the emission in the BVRI optical bands was strongly correlated both in the short and long term without any time lag. The blazar has likely quasiperiods of 186 ± 30 and 532 ± 76 days in the optical R-band light curve according to the weighted wavelet Z-transform and Lomb–Scargle periodogram. The intraday variation and long-term variation features are discussed within the frame of prospective scenarios.

Ruthenium-doped ZnO nanostructures: Growth, characterization, and applications in waveguides and light-emitting devices

ZnO based materials are gaining importance due to its potential applications. In many of these applications, the size, shape and dopability of the structures grown play a determinant role. In the present work, ZnO nano- and microstructures doped with Ru have been grown using the Vapour-Solid (VS) method. Among the different growth parameters, gas flux and initial dopant content seem to play the major role to determine both shape and size of the structures. The main morphologies obtained are self-arranged triangular grids and elongated structures. Based on microscopic observations a simplified growth model is proposed for the grids. An exhaustive characterization has been performed. X-Ray diffraction (XRD) investigations demonstrate good crystallinity and texturing related to preferential growth direction changes due to doping. Luminescence characterization through photo- and cathodoluminescence (PL and CL) techniques reveals typical ZnO near band edge and deep level emission bands at 3.2 and 2.3 eV, respectively. The potential use of elongated structures as waveguides and optical cavities, Fabry-Pèrot resonators, is explored.

Impacts of Eu2+ -doped K3LuSi2O7 phosphor and a scattering particle on conventional white light emitting diodes

The K<sub>3</sub>LuSi<sub>2</sub>O<sub>7</sub> phosphor doping Eu2+ rare-earth ions (KLS:Eu) was reported to possess broad emission band from near-ultraviolet to nearinfrared. Additionally, this phosphor showed a wide absorption band of 250-600 nm, allowing it to be excited by blue-light chip of 460 nm, making it one of the suitable phosphor materials for a light emitting diode (LED). Besides, the scattering particle material CaCO<sub>3</sub> is incorporated into the yellow phosphor layer to serve the scattering-enhancement purpose. The combination of both materials aims at accomplishing improvements in performance of commercial LED package. The concentration of KLS:Eu is constant while that of CaCO3 is modified. As a result, the scattering factor is regulated and become the key factor influencing the optical outputs of the simulated LED. The increasing CaCO<sub>3</sub> concentration enhances the phosphor scattering efficiency of light, helping to improve the lumen output and color-temperature consistency of the LED. However, the color rendering performance declines as a function of the CaCO3 growing amount, despite the presence of a KLS:Eu phosphor layer. Further works should be done to optimize the application of KLS:Eu in cooperation with scattering particles for a higher-quality LED device.

A novel material for radiation detection application of zinc bismuth lithium borotellurite glass doped with Dy2O3

Radiation detection glass with the following chemical composition B2O3–TeO2–Li2O3–Bi2O3–ZnO doped with Dy2O3 where x = 0.00, 0.10, 0.50, 1.00, 1.50 and 2.00 mol%, was developed for the characterization of physical properties such as density, molar volume (Vm), and refractive index, optical absorption, luminescence, CIE's diagram, and radiation detection properties. The density and refractive index of glass samples increase with the increase of Dy2O3 composition. The optical property of glass shows eight strongest peaks from 6H15/2 centering at 263 nm (4I13/2 + 4F7/2), 298 nm (4G11/2), 357 nm (4I15/2), 803 nm (6F5/2), 897 nm (6F7/2), 1090 nm (6H7/2 + 6F9/2), 1272 nm (6F11/2 + 6H9/2) and 1671 nm (6H11/2), respectively. The emission peaks are r (4F9/2), 481 nm (6H15/2), 575 nm (6H13/2), 664 nm (6H11/2), and 751 nm (6H9/2) under excited at 453 nm (4F9/2), respectively. The excitation peaks under emission at 575 nm from 6H15/2 centering at 350 nm (6P7/2), 365 nm (4P3/2), 388 nm (4K17/2), 425 nm (4G11/2), 453 nm (4I15/2), and 471 nm (4F9/2) respectively. The study of luminescence characteristics, which includes emission, excitation, and CIE diagrams, reveals white emission bands that coincide with the CIE diagram. Furthermore, measuring the parameters of the thermoluminescence dosimeter (TLD) recorded with a heating rate of 5 °C/s in the temperature up to a maximum of 400 °C yields good results in low dose radiation detection. Based on all the results, it was determined that this glass can be a candidate for radiation detection materials in the future.

Peripheral carbazole units-decorated MR emitter containing B−N covalent bond for highly efficient green OLEDs with low roll-off

Boron−nitrogen doped multiple resonance (BN-MR) emitters, characterized by B−N covalent bonds, offer distinctive advantages as pivotal building blocks for facile access to novel MR emitters featuring narrowband spectra and high efficiency. However, there remains a scarcity of exploration concerning synthetic methods and structural derivations to expand the library of novel BN-MR emitters. Herein, we present the synthesis of a BN-MR emitter, tCz[B−N]N, through a one-pot borylation reaction directed by the amine group, achieving an impressive yield of 94%. The emitter is decorated by incorporating two 3,6-di-t-butylcarbazole (tCz) units into a B−N covalent bond doped BN-MR parent molecule via para-C−π−D and para-N−π−D conjugations. This peripheral decoration strategy enhances the reverse intersystem crossing process and shifts the emission band towards the pure green region, peaking at 526 nm with a narrowband full-width at half maximum (FWHM) of 41 nm. Consequently, organic light emitting diodes (OLEDs) employing this emitter achieved a maximum external quantum efficiency (EQEmax) value of 27.7%, with minimal efficiency roll-off. Even at a practical luminance of 1000 cd∙m−2, the device maintains a high EQE value of 24.6%.

Room temperature luminescence of 1,N2-etheno-2-aminopurine in poly (vinyl alcohol) films.

We studied spectral properties of 1,N2-etheno-2-aminopurine after immobilization in poly (vinyl alcohol) films. The absorption spectrum of 1,N2-ε2APu consists of two peaks centered at 300 and 370 nm, and the fluorescence spectrum has maximum at about 460 nm. The fluorescence quantum efficiency is 62%. The fluorescence anisotropy reaches a value of 0.3 at longer wavelengths, while it is low at shorter wavelengths (corresponding to the second single excited state). The 1,N2-ε2APu has a relatively long fluorescence lifetime of about 16 ns and a noticeable room temperature phosphorescence with a lifetime of about 220 ms. A broad phosphorescence emission band (425-675 nm) is centered at about 530 nm and markedly overlaps with fluorescence at shorter wavelengths. Surprisingly, the phosphorescence excitation spectrum of 1,N2-ε2APu-doped poly (vinyl alcohol) film differs from the absorption and fluorescence excitation spectra. The strongest room temperature phosphorescence excitation is about 335 nm. At longer excitation wavelengths, above 450 nm, where fluorescence cannot be excited, a triplet excitation is still possible. The 1,N2-ε2APu phosphorescence anisotropy spectra confirm direct triplet state excitation. The ability to excite molecules at long wavelengths can find applications in the study of biological molecules that are unstable when excited at high energies.

Promising deep-red emitting Cr3+-doped SrAl12O19 phosphors for plant growth LEDs.

Recently, deep-red-emitting phosphors that can be excited by ultraviolet (UV) and near-ultraviolet (NUV) light have been extensively investigated for plant growth LED applications. However, due to the harmful effects of these high-energy rays on plants, violet- or blue-excited deep-red-emitting phosphors are considered a more appropriate solution. In this work, SrAl12O19:Cr3+ phosphors were synthesized using a simple solid-state reaction, revealing a strikingly sharp deep-red emission band centered at 694 nm and effective excitation by violet light. The optimal SrAl12O19:1.0%Cr3+ phosphor, annealed at 1500°C, exhibits an extended lifetime of 0.549 ms, an energy activation level of 0.239 eV, a good quantum efficiency (QE) of 36.2%, and superior color purity at 100%. Further, an LED prototype with a precise absorption spectrum for far-red phytochrome (Pfr) has been demonstrated. These results indicate that the synthesized SrAl12O19:1.0%Cr3+ phosphors could be used as a promising deep-red-emitting phosphor for plant growth LED.

FEAST: Feedback in Emerging extragAlactic Star ClusTers: JWST Spots Polycyclic Aromatic Hydrocarbon Destruction in NGC 628 during the Emerging Phase of Star Formation

We investigate the emergence phase of young star clusters in the nearby spiral galaxy NGC 628. We use JWST NIRCam and MIRI observations to create spatially resolved maps of the Paα 1.87 μm and Brα 4.05 μm hydrogen recombination lines, as well as 3.3 and 7.7 μm emission from polycyclic aromatic hydrocarbons (PAHs). We extract 953 compact H ii regions and analyze the PAH emission and morphology at ∼10 pc scales in the associated photodissociation regions. While H ii regions remain compact, radial profiles help us to define three PAH morphological classes: compact (∼42%), extended (∼34%), and open (∼24%). The majority of compact and extended PAH morphologies are associated with very young star clusters (<5 Myr), while open PAH morphologies are mainly associated with star clusters older than 3 Myr. We observe a general decrease in the 3.3 and 7.7 μm PAH band emission as a function of cluster age, while their ratio remains constant with age out to 10 Myr and morphological class. The recovered PAH3.3μm/PAH7.7μm ratio is lower than values reported in the literature for reference models that consider neutral and ionized PAH populations and analyses conducted at galactic physical scales. The 3.3 and 7.7 μm bands are typically associated with neutral and ionized PAHs, respectively. While we expected neutral PAHs to be suppressed in proximity to an ionizing source, the constant PAH3.3μm/PAH7.7μm ratio would indicate that both families of molecules disrupt at similar rates in proximity to H ii regions.