Kinetic Analysis of the Photochemical Paths in Asymmetric Diarylethene Dimer.

An asymmetric diarylethene dimer composed of 2- and 3-thienylethene units linked by m-phenylene developed various colors upon UV irradiation via an independent photochromic reaction on each unit. The change in contents and the other photoresponses of the photogenerated four isomers were analyzed using quantum yield for all the possible photochemical paths, i. e., photoisomerization, fluorescence, energy transfer, and the other non-radiative paths. Almost all the rate constants of photochemical paths were calculated using measurable quantum yields and lifetimes. It was found that a significant contribution on photoresponse was the competition between photoisomerization and intramolecular energy transfer. The clear difference was observed in the photoresponses of the dimer and the 1 : 1 mixture solution of the model compounds. The m-phenylene spacer appropriately regulated the rate of energy transfer in the asymmetric dimer, and the spacer enabled isolation of the excited state of the dimer, making the above quantitative analysis possible.

Contribution of Carbonyl Chromophores in Secondary Brown Carbon from Nighttime Oxidation of Unsaturated Heterocyclic Volatile Organic Compounds.

The light absorption properties of brown carbon (BrC), which are linked to molecular chromophores, may play a significant role in the Earth's energy budget. While nitroaromatic compounds have been identified as strong chromophores in wildfire-driven BrC, other types of chromophores remain to be investigated. Given the electron-withdrawing nature of carbonyls ubiquitous in the atmosphere, we characterized carbonyl chromophores in BrC samples from the nighttime oxidation of furan and pyrrole derivatives, which are important but understudied precursors of secondary organic aerosols primarily found in wildfire emissions. Various carbonyl chromophores were characterized and quantified in BrC samples, and their ultraviolet-visible spectra were simulated by using time-dependent density functional theory. Our findings suggest that chromophores with carbonyls bonded to nitrogen (i.e., imides and amides) derived from N-containing heterocyclic precursors substantially contribute to BrC light absorption. The quantified N-containing carbonyl chromophores contributed to over 40% of the total light absorption at wavelengths below 350 nm and above 430 nm in pyrrole BrC. The contributions of chromophores to total light absorption differed significantly by wavelength, highlighting their divergent importance in different wavelength ranges. Overall, our findings highlight the significance of carbonyl chromophores in secondary BrC and underscore the need for further investigation.

Wavelength-dependent error minimization for quantitative spectroscopic photoacoustic tomography with a ring-array system.

PURPOSE: Photoacoustic tomography (PAT) is a non-invasive and high-resolution imaging technique that can provide functional and molecular information from the optical properties of pathological tissues, such as cancer. Spectroscopic PAT (sPAT) is capable of supplying information such as oxygen saturation (sO2), which is an important biological indicator for diseases such as cancer. However, the wavelength dependent nature of sPAT makes it challenging to provide accurate quantitative measurements of tissue oxygenation beyond shallow depths. We have previously reported the utility of combined ultrasound tomography and PAT to achieve optical and acoustic compensated PAT images at a single wavelength and for enhanced PAT images at larger depths. In this work we further explore the utility of the optical and acoustic compensation PAT algorithm to minimize the wavelength dependency in sPAT by showcasing improvements in spectral unmixing. MATERIALS AND METHODS: Two optically and acoustically characterized heterogenous phantoms were manufactured to test the ability of the system and developed algorithm to minimize the wavelength-dependence driven error in sPAT spectral unmixing. The PA inclusions within each phantom were composed of a mixture of two sulfate dyes, copper sulfate (CuSO4) and nickel sulfate (NiSO4), with known optical spectra. Improvements between uncompensated and optically and acoustically compensated PAT (OAcPAT) were quantified as the relative percent error between the measured results and the ground truth. RESULTS: The results of our phantom studies demonstrate that OAcPAT can significantly improve the accuracy of sPAT measurements in a heterogenous medium and especially at larger inclusions depths which can reach to up to 12% improvement in measurement errors. This significant improvement can play a vital role in reliability of future in-vivo biomarker quantifications. CONCLUSIONS: Utilizing UST for model-based optical and acoustic compensation of PAT images was proposed by our group previously. In this work, we further demonstrated the efficacy of the developed algorithm in sPAT by minimizing the error caused by the tissue's optical heterogeneity on improving spectral unmixing, which is a major limiting factor in reliability of sPAT measurements. Such synergistic combination of UST and PAT provides a window of opportunity to achieve bias-free quantitative sPAT measurements, which plays an important role in future pre-clinical and clinical utility of PAT.

Revisiting the protocol for determining submicromolar concentrations of ozone in the water treated by advanced oxidation processes.

Ozone is formed at submicromolar concentrations from photolysis of many oxyanions and oxidants in water and contributes importantly to the degradation of emerging contaminants and inactivation of pathogenic microorganisms in the natural and engineered aquatic systems. In this study, we identified and discussed the critical limitations of the commonly-used protocols using cinnamic acid (CNA) as a probe compound to determine the submicromolar-level ozone and proposed a modified protocol that overcomes those limitations. Our experimental investigation demonstrated that the radicals (e.g., HO•) formed from photolysis of oxyanions and oxidants, other than ozone, could also oxidize CNA and form benzaldehyde, resulting in the overestimation of ozone concentrations by using the commonly-used protocols. Moreover, the benzaldehyde formed from ozone-CNA reactions could be degraded by the radicals, leading to the underestimation of ozone concentrations by using the commonly-used protocols. A new protocol with high accuracy and precision was proposed and the rationales for each operational step of the new protocol were explained in detail and supported with justifications. The new protocol was compared with two commonly-used protocols in determining the concentration of ozone in the same water sample treated by the UV/chlorine process at three different UV wavelengths. The wavelength-dependent overestimation/underestimation of the ozone concentrations by using the two commonly-used protocols was well demonstrated and explained by the overlooked interferences of radicals in the protocols.

Underwater light climate and wavelength dependence of microalgae photosynthetic parameters in a temperate sea.

Studying how natural phytoplankton adjust their photosynthetic properties to the quantity and quality of underwater light (i.e. light climate) is essential to understand primary production. A wavelength-dependent photoacclimation strategy was assessed using a multi-color pulse-amplitude-modulation chlorophyll fluorometer for phytoplankton samples collected in the spring at 19 locations across the English Channel. The functional absorption cross section of photosystem II, photosynthetic electron transport (PETλ) parameters and non-photochemical quenching were analyzed using an original approach with a sequence of three statistical analyses. Linear mixed-effects models using wavelength as a longitudinal variable were first applied to distinguish the fixed effect of the population from the random effect of individuals. Population and individual trends of wavelength-dependent PETλ parameters were consistent with photosynthesis and photoacclimation theories. The natural phytoplankton communities studied were in a photoprotective state for blue wavelengths (440 and 480 nm), but not for other wavelengths (green (540 nm), amber (590 nm) and light red (625 nm)). Population-detrended PETλ values were then used in multivariate analyses (partial triadic analysis and redundancy analysis) to study ecological implications of PETλ dynamics among water masses. Two wavelength ratios based on the microalgae saturation parameter Ek (in relative and absolute units), related to the hydrodynamic regime and underwater light climate, clearly confirmed the physiological state of microalgae. They also illustrate more accurately that natural phytoplankton communities can implement photoacclimation processes that are influenced by in situ light quality during the daylight cycle in temporarily and weakly stratified water. Ecological implications and consequences of PETλ are discussed in the context of turbulent coastal ecosystems.

Wavelength-dependent chlorine photolysis and subsequent radical production using UV-LEDs as light sources.

UV-LEDs are considered as the most promising UV light sources, because it has the potential to replace conventional UV lamps in some water treatment applications in the foreseeable future. In this study, UV-LEDs at four wavelengths in the UV-C or near UV-C range (i.e., 257.7, 268, 282.3, and 301.2 nm) were used to investigate the wavelength-dependency on chlorine photolysis and its subsequent radical formation. The fluence-based photodecay rates of hypochlorous acid (HOCl) and hypochlorite (OCl-) were monotonically correlated to their molar absorption coefficients and quantum yields, and the chlorine photodecay rates were much more significantly affected by molar absorption coefficients (ß â€¯= 0.949) than quantum yields (ß â€¯= 0.055). An empirical model that incorporated the chlorine photodecay rate constants, quantum yields, and molar absorption coefficients of HOCl and OCl- was established, validated and then used to predict the chlorine photodecay rate at any wavelength (257.7-301.2 nm) and pH (5-10). The modelling results suggested that the maximum fluence-based rate constant (1.46 × 10-4 m2 J-1) was obtained at 289.7 nm and pH 9.95. The wavelength dependency was larger at alkaline pH than at acidic pH, and the pH dependency was the largest at the longest wavelength. The formation of hydroxyl radicals (HO·) and reactive chlorine species (RCS) decreased with increasing wavelength at pH 6, and increased with increasing wavelength at pH 7. More HO· was formed at pH 6 than pH 7, but RCS showed the opposite pH-dependency. The findings in this study provide the fundamental information in selecting UV-LEDs with specific wavelength for enhancing/optimizing chlorine photodecay and/or its radical generation at different pHs in real-world applications.