Changes In Light Absorption Research Articles

Proposal for Low-Cost Optical Sensor for Measuring Flow Velocities in Aquatic Environments.

The ocean, with its intricate processes, plays a pivotal role in shaping marine life, habitats, and the Earth's climate. This study addresses issues such as beach erosion, the survival of propagules from species like Posidonia oceanica, and nutrient distribution. To tackle these challenges, we propose an innovative sensor that quantifies hydrodynamic velocity by measuring the output voltage derived from detecting changes in light absorption and scattering using LEDs and LDRs. Our results not only demonstrate the effectiveness of the sensor but also the accuracy of the processing algorithm. Notably, the blue LED exhibited the lowest mean relative error of 7.59% in freshwater, while the yellow LED was most precise in chlorophyll-containing water, with a mean relative error of 6.80%. In a runoff simulation, we observed similar velocities with the blue, green, and white LEDs, 6.89 cm/s, 6.99 cm/s, and 7.05 cm/s, respectively, for nearly identical time intervals. It is important to highlight that our proposed sensor is not only effective but also highly cost-efficient, representing less than 0.43% of the cost of a Nortek Vector 6 MHz and 0.18% of the Teledyne Workhorse II 300 kHz Marine. This makes it a key tool for managing marine ecosystems sustainably.

Impacts of elevated anthropogenic emissions on physicochemical characteristics of black-carbon-containing particles over the Tibetan Plateau

Abstract. Black carbon (BC) in the Tibetan Plateau (TP) region has distinct climate effects that strongly depend on its mixing state. The aging processes of BC in the TP are subject to emissions from various regions, resulting in considerable variability of its mixing state and physicochemical properties. However, the mechanism and magnitude of this effect are not yet clear. In this study, field observations on physicochemical properties of BC-containing particles (PMBC) were conducted in the northeast (Xihai) and southeast (Lulang) regions of the TP to investigate the impacts of transported emissions from lower-altitude areas on BC characteristics in the TP. Large spatial discrepancies were found in the chemical composition of PMBC. Both sites showed higher concentrations of PMBC when they were affected by transported air masses outside the TP but with diverse chemical composition. Source apportionment for organic aerosol (OA) suggested that primary OA in the northeastern TP was attributed to hydrocarbon OA (HOA) from anthropogenic emissions, while it was dominated by biomass burning OA (BBOA) in the southeastern TP. Regarding secondary aerosol, a marked enhancement in nitrate fraction was observed on aged BC coating in Xihai when the air masses were brought by updrafts and easterly winds from lower-altitude areas. With the development of boundary layer, the enhanced turbulent mixing promoted the elevation of anthropogenic pollutants. In contrast to Xihai, the thickly coated BC in Lulang was mainly caused by elevation and transportation of biomass burning plumes from south Asia, showing a large contribution of secondary organic aerosol (SOA). The distinct transported emissions lead to substantial variations of both chemical composition and light absorption ability of BC across the TP. The thicker coating and higher mass absorption cross-section (MAC) of PMBC in air masses elevated from lower-altitude regions reveal the promoted BC aging processes and their impacts on the mixing state and light absorption of BC in the TP. These findings emphasize the vulnerability of plateau regions to influences of elevated emissions, leading to significant changes in BC concentration, mixing states and light absorption across the TP, all of which need to be considered in the evaluation of BC radiative effects for the TP region.

Electric Polarization-Dependent Absorption and Photocurrent Generation in Limnospira indica Immobilized on Boron-Doped Diamond.

We present the change of light absorption of cyanobacteria in response to externally applied electrical polarization. Specifically, we studied the relation between electrical polarization and changes in light absorbance for a biophotoelectrode assembly comprising boron-doped diamond as semiconducting electrode and live Limnospira indicaPCC 8005 trichomes embedded in either polysaccharide (agar) or conductive conjugated polymer (PEDOT-PSS) matrices. Our study involves the monitoring of cyanobacterial absorbance and the measurement of photocurrents at varying wavelengths of illumination for switched electric fields, i.e., using the bioelectrode either as an anode or as cathode. We observed changes in the absorbance characteristics, indicating a direct causal relationship between electrical polarization and absorbing properties of L. indica. Our finding opens up a potential avenue for optimization of the performance of biophotovoltaic devices through controlled polarization. Furthermore, our results provide fundamental insights into the wavelength-dependent behavior of a bio photovoltaic system using live cyanobacteria.

Study of Electrochromic Properties of PEDOT:PSS for Tunable Filter Optics with Lithium Salt Electrolyte

Nowadays, conductive polymers based on poly(3,4-ethylenedioxythiophene), poly(styrene sulfonic acid), or PEDOT:PSS, have been employed as a flexible and transparent coating in various significant electronic applications. With the demand for electrochromic properties, such as in electronic displays, further research into its electrooptic properties is required, especially the systematic understanding to obtain the optimized switching. Our research investigates the electrooptic properties of the PEDOT:PSS film, particularly the refractive index changing under various applied biases. The electrochromic device is prepared in a simple fashion, and the electroactive layer of PEDOT:PSS thickness is defined via spin-coating between two indium tin oxide (ITO) substrates. To increase the switching properties of PEDOT:PSS, lithium perchlorate (LiClO4) was prepared in acetonitrile, as the electrolyte in varied concentrations of 1.195 M, 1.5 M, and 2.0 M, respectively. A potential voltage of -4.0 V to 0.0 V is utilized to study the device's electrochromic properties with the step 5 mV/s continuously. Finally, the optical properties are characterized using the spectroscopy method based on real-time measurement of the transmission spectrum and transmission matrix calculations. The change in visible light absorption, transmission, and film color is recorded under a switching cycle that shows consistent behavior. This allows the further utilization of such a hybrid structure for possible tunable filter applications. Keywords: Electrochromic, PEDOT:PSS, Optical, Lithium salt, Electrolyte

Nanocellulose-based cobalt(II) coordinated malonic acid hybrid aerogels exhibiting reversible thermochromism and moisture sensor properties

The emergence of sustainable polymers and technologies has led to the development of innovative materials with minimal carbon emissions which find extensive applications in wearable electronics, biomedical sensors, and Internet of Things (IoT)-based monitoring systems. Nanocellulose which can be generated from abundant biomass materials has been widely recognized as a sustainable alternative for a diverse range of applications due to its remarkable properties and eco-friendly nature. By making use of the unique and easily accessible coordination transformation property of Co(II) ions and associated visible light absorption changes, we report a novel Co(II) cation-incorporated nanocellulose/malonic acid hybrid aerogel material that exhibits reversible thermochromism induced by thermal stimulus in the presence of atmospheric moisture. This effect is accentuated by the highly porous nature of the nanocellulose aerogel material we have developed. Besides the reversible thermochromic property which Co(II) ions exhibit, the metal ions act as very efficient reinforcing units contributing significantly to the structural stability and rigidity of the hierarchical aerogels by coordinative cross-linking through carboxylate moieties present in the TEMPO-oxidized cellulose nanofibers (TCNF) and additionally adding malonic acid to provide sufficient COO− for cross-linking. Thorough characterization and detailed investigation of as-prepared hybrid aerogels was conducted to evaluate their overall properties including reversible thermochromism and moisture sensor behaviour. Further, an Android mobile-based application was developed to demonstrate the real-world application of the aerogels for atmospheric humidity sensing.

Optical properties and radiative forcing of carbonaceous aerosols in a valley city under persistent high temperature

Carbonaceous aerosols were collected in the valley city of Baoji city in Northern China in August 2022. The light absorption characteristics and influencing factors of black carbon (BC) and brown carbon (BrC) were analyzed, and their radiative forcing was estimated. The results showed that the light absorption of secondary brown carbon [AbsBrC,sec (370)] was 7.5 ± 2.4 Mm−1, which was 2.5 times that of primary brown carbon [AbsBrC,pri (370), 3.0 ± 1.2 Mm−1]. During the study period, the absorption Ångström exponent (AAE) of aerosol was 1.6, indicating that there was obvious secondary aerosol formation or carbonaceous aerosol aging in the valley city of Baoji. Except for secondary BrC (BrCsec), the light absorption coefficient (Abs) and mass absorption efficiency (MAE) of BC and primary BrC (BrCpri) during the persistent high temperature period (PHT) were higher than those during the normal temperature period (NT) and the precipitation period (PP), which indicated that the light absorption capacity of black carbon and primary brown carbon increased, while the light absorption capacity of secondary brown carbon decreased under persistent high temperature period. Secondary aerosols sulfide (SO42−), nitrate (NO3−) and secondary organic carbon (SOC) are important factors for promoting the light absorption enhancemen of BC and BrCpri and photobleaching of BrCsec during persistent high temperature period. The Principal Component Analysis-Multiple Linear Regression (PCA-MLR) model showed that traffic emissions was the most important source of pollution in Baoji City. Based on this, the secondary source accelerates the aging of BC and BrC, causing changes in light absorption. During PHT, the radiative forcing of BC and BrCpri were enhanced, while the radiative forcing of BrCsec was weakened, but the positive radiative forcing generated by them may aggravate the high-temperature disaster.

In Vivo Biosynthesis of Au and Ag NPs Using Two Medicago sativa L. Genotypes

The nano size as well as physical and chemical properties of Au and Ag nanoparticles (NPs) allow them to be used in medicine or plant protection, but chemical solvents used during synthesis makes them toxic and pose a threat to the environment. Chemical NP synthesis can be replaced by in vivo synthesis in which independently growing plants such as alfalfa take up and then split the precursor in their cells down to nano size using synthesis-promoting solvent-biomolecules, which can break down materials without free radicals and have anti-inflammatory, antioxidant effects, making NPs environmentally benign. In this study, two-week-old seedlings of two Medicago sativa L. genotypes, ‘Kometa’ and ‘la Bella’, were exposed to two precursors (AgNO3, HAuCl4) for 24 and 48 h to determine whether in vivo synthesis is possible. Two-beam and certain wavelength spectrophotometry and confocal microscopy confirmed statistically significant (p < 0.05) changes in light absorption and light fluorescence compared to the control. Confocal microscopy showed both precursors visible in the roots of both genotypes. Currently, NP synthesis and visualisation methods require a complex, expensive, and time-consuming sequence of methods. It is important to find an effective, environmentally friendly, and as cheap and simple as possible method for the biosynthesis of NPs.

The Franz–Keldysh effect in the optical absorption spectrum of a TlGaSe2 layered semiconductor caused by charged native defects

The Franz–Keldysh effect in the optical absorption edge of a bulk TlGaSe2 layered semiconductor poled under an external electric field was investigated in the present work. The Franz–Keldysh shift below the optical bandgap absorption region, as well as the quasi-periodic oscillations above the fundamental bandgap of TlGaSe2, were observed. The measured changes in optical light absorption of the TlGaSe2 sample were revealed after poling processing. The poling technique is used to produce the built-in internal electric field within the TlGaSe2 semiconductor. The frozen-in internal electric field in TlGaSe2 was experimentally monitored through changes in the lineshape of the absorption spectra at the fundamental band edge. The observed results are accurately fitted with the theoretical lineshape function of the Franz–Keldysh absorption tail below the bandgap of TlGaSe2 and quasi-periodic oscillations above the bandgap. A good agreement between the theoretical and experimental results was observed. The present study demonstrated that the Franz–Keldysh effect can be used to identify and characterize the localized internal electric fields originating from electrically active native imperfections in the TlGaSe2 crystals.

Investigating Ultraviolet-Visible Absorption of Pure Water and Normal Saline under the Treatment of Taheri Consciousness Fields

UV-Vis spectroscopy is a spectrophotometric technique that relies on the absorption of light by species within the ultraviolet to visible range (200 to 700 nanometers). The study of water absorption has been conducted over the decades from the 1930s to the 1980s to investigate electron transfer levels in various studies. The investigation of the absorptive properties of solutions provides significant information about changes in their internal environment, reactions, and molecular interactions. In this study, with the aim of investigating the effectiveness of T-Consciousness Fields on water molecules and examining the potential changes in the physical properties of water, we have focused on the changes in light absorption in the ultraviolet-visible range by water molecules in the presence of T-Consciousness Fields 1, 2, and 3. Additionally, alongside observing the effects of T-Consciousness Fields on the absorptive properties of pure water, the absorptive properties of normal saline are investigated to provide a valuable basis for comparison. In this study, absorptive properties of normal saline are also examined using UV-Vis absorption spectroscopy. Changes in absorption between the control and samples subjected to T-Consciousness Fields 1, 2, and 3 are obtained compared to the standard deviations of changes caused by the control for each wavelength. According to the results obtained for pure water, T-Consciousness Field 1 has led to significant changes in the visible region, exceeding the standard deviation. In the case of normal saline samples, the absorption resulting from the samples in the visible region in the case of T-Consciousness Field 1 shows a decreasing trend, and in the case of T-Consciousness Field 2, it exhibits an increasing trend. Furthermore, the changes in absorption in the sample treated with T-Consciousness Field 3 fall within the range of the average standard deviation of absorption values for the sample and control. A detailed analysis of absorption regions and a comparison of the effectiveness of the three applied T-Consciousness Fields on pure water and normal saline are in the authors' agenda.

Determining light absorption changes in multilayered turbid media through analytically computed photon mean partial pathlengths

Determining light absorption changes in multilayered turbid media through analytically computed photon mean partial pathlengths

Investigation of Electrochromic, Combinatorial TiO2-SnO2 Mixed Layers by Spectroscopic Ellipsometry Using Different Optical Models.

We determined the optimal composition of reactive magnetron-sputtered mixed layers of Titanium oxide and Tin oxide (TiO2-SnO2) for electrochromic purposes. We determined and mapped the composition and optical parameters using Spectroscopic Ellipsometry (SE). Ti and Sn targets were put separately from each other, and the Si-wafers on a glass substrate (30 cm × 30 cm) were moved under the two separated targets (Ti and Sn) in a reactive Argon-Oxygen (Ar-O2) gas mixture. Different optical models, such as the Bruggeman Effective Medium Approximation (BEMA) or the 2-Tauc-Lorentz multiple oscillator model (2T-L), were used to obtain the thickness and composition maps of the sample. Scanning Electron Microscopy (SEM) with Energy-Dispersive X-ray Spectroscopy (EDS) has been used to check the SE results. The performance of diverse optical models has been compared. We show that in the case of molecular-level mixed layers, 2T-L is better than EMA. The electrochromic effectiveness (the change of light absorption for the same electric charge) of mixed metal oxides (TiO2-SnO2) that are deposited by reactive sputtering has been mapped too.

Reconstruction of light absorption changes in the human head using analytically computed photon partial pathlengths in layered media.

Functional near infrared spectroscopy has been used in recent decades to sense and quantify changes in hemoglobin concentrations in the human brain. This noninvasive technique can deliver useful information concerning brain cortex activation associated with different motor/cognitive tasks or external stimuli. This is usually accomplished by considering the human head as a homogeneous medium; however, this approach does not explicitly take into account the detailed layered structure of the head, and thus, extracerebral signals can mask those arising at the cortex level. This work improves this situation by considering layered models of the human head during reconstruction of the absorption changes in layered media. To this end, analytically calculated mean partial pathlengths of photons are used, which guarantees fast and simple implementation in real-time applications. Results obtained from synthetic data generated by Monte Carlo simulations in two- and four-layered turbid media suggest that a layered description of the human head greatly outperforms typical homogeneous reconstructions, with errors, in the first case, bounded up to ∼20% maximum, while in the second case, the error is usually larger than 75%. Experimental measurements on dynamic phantoms support this conclusion.

Nonanal Gas Sensors Using Porous Glass as a Reaction Field for Ammonia-Catalyzed Aldol Condensation.

Transmittance in porous-glass gas sensors, which use aldol condensation of vanillin and nonanal as the detection mechanism for nonanal, decreases because of the production of carbonates by the sodium hydroxide catalyst. In this study, the reasons for the decrease in transmittance and the measures to overcome this issue were investigated. Alkali-resistant porous glass with nanoscale porosity and light transparency was employed as a reaction field in a nonanal gas sensor using ammonia-catalyzed aldol condensation. In this sensor, the gas detection mechanism involves measuring the changes in light absorption of vanillin arising from aldol condensation with nonanal. Furthermore, the problem of carbonate precipitation was solved with the use of ammonia as the catalyst, which effectively resolves the issue of reduced transmittance that occurs when a strong base, such as sodium hydroxide, is used as a catalyst. Additionally, the alkali-resistant glass exhibited solid acidity because of the incorporated SiO2 and ZrO2 additives, which supported approximately 50 times more ammonia on the glass surface for a longer duration than a conventional sensor. Moreover, the detection limit obtained from multiple measurements was approximately 0.66 ppm. In summary, the developed sensor exhibits a high sensitivity to minute changes in the absorbance spectrum because of the reduction in the baseline noise of the matrix transmittance.

Measurement report: Changes in light absorption and molecular composition of water-soluble humic-like substances during a winter haze bloom-decay process in Guangzhou, China

Abstract. Water-soluble humic-like substances (HULIS) absorb light in near-UV and visible wavelengths and exert significant influence on the atmospheric environment and climate. However, knowledge on HULIS evolution during haze bloom-decay process is limited. Herein, PM2.5 samples were obtained during a winter haze event in Guangzhou, China, and the light absorption and molecular composition of HULIS were investigated by UV–Vis spectrophotometry and ultrahigh-resolution mass spectrometry. Compared with HULIS on clean days, the absorption coefficients (Abs365) of HULIS on haze days were significantly higher but the mass absorption efficiencies (MAE365) were relatively low, suggesting diverse and dynamic absorption properties of HULIS during haze episodes. The CHO and CHON compounds were the most abundant components in HULIS, followed by CHOS, CHONS, and CHN. Haze HULIS presented comparatively high molecular weight; a lower aromaticity index (AImod); and higher O/Cw, O/Nw, and O/Sw ratios, indicating that HULIS fractions undergo relatively high oxidation during haze days compared to clean days. Moreover, CHON and CHO compounds with high AImod were the major potential chromophores in HULIS and significantly contributed to HULIS light absorption. It is worth noting that the proportions of these chromophores decreased during haze events, mainly owing to their higher oxidation during haze episodes. Besides, accumulated contribution of organic compounds emitted from vehicles and formed from reactions of biogenic volatile organic compounds (bio-VOCs) also diluted light-absorbing compounds in haze HULIS. These findings help us to understand HULIS evolution during haze bloom-decay processes in the subtropic region of China.

Effects of Atypical Hydrogen Bonds and π-π Interactions on Nonlinear Optical Properties: Dimers of Triangular Structures Based on Perylene, Naphthalene, and Pyromellitic Diimides.

Nonlinear optical (NLO) materials have become important materials in the field of high-speed optical devices due to the changes in light absorption and refraction caused by the photoelectric field. Compounds tend to exist as aggregates rather than single molecules, so intermolecular interactions are crucial to the nature of aggregates. Therefore, to study the effects of intermolecular interactions on nonlinear optical properties, we use a dimer simplified model and adopt the methods of controlling variables, which are the different intermolecular interactions resulting from the different stacking patterns of dimers based on the same monomer structures (2PMDI-1NDI and 2NDI-1PDI). It is found that compared with dimers involving π-π interactions, dimers involving C-H···O interactions have shorter intermolecular distances, larger intermolecular interaction energies, and smaller highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO) energy gaps. Moreover, the C-H···O interactions are more conducive to the intermolecular charge transfers and more beneficial for increasing the nonlinear optical response values of aggregates with respect to π-π interactions. This work provides an important basis for the influence of intermolecular interactions on nonlinear optical properties.

Vegetation clumping modulates global photosynthesis through adjusting canopy light environment.

The spatial dispersion of photoelements within a vegetation canopy, quantified by the clumping index (CI), directly regulates the within-canopy light environment and photosynthesis rate, but is not commonly implemented in terrestrial biosphere models to estimate the ecosystem carbon cycle. A few global CI products have been developed recently with remote sensing measurements, making it possible to examine the global impacts of CI. This study deployed CI in the radiative transfer scheme of the Community Land Model version 5 (CLM5) and used the revised CLM5 to quantitatively evaluate the extent to which CI can affect canopy absorbed radiation and gross primary production (GPP), and for the first time, considering the uncertainty and seasonal variation of CI with multiple remote sensing products. Compared to the results without considering the CI impact, the revised CLM5 estimated that sunlit canopy absorbed up to 9%-15% and 23%-34% less direct and diffuse radiation, respectively, while shaded canopy absorbed 3%-18% more diffuse radiation across different biome types. The CI impacts on canopy light conditions included changes in canopy light absorption, and sunlit-shaded leaf area fraction related to nitrogen distribution and thus the maximum rate of Rubisco carboxylase activity (Vcmax ), which together decreased photosynthesis in sunlit canopy by 5.9-7.2PgC year-1 while enhanced photosynthesis by 6.9-8.2PgC year-1 in shaded canopy. With higher light use efficiency of shaded leaves, shaded canopy increased photosynthesis compensated and exceeded the lost photosynthesis in sunlit canopy, resulting in 1.0 ± 0.12 PgC year-1 net increase in GPP. The uncertainty of GPP due to the different input CI datasets was much larger than that caused by CI seasonal variations, and was up to 50% of the magnitude of GPP interannual variations in the tropical regions. This study highlights the necessity of considering the impacts of CI and its uncertainty in terrestrial biosphere models.

Dispersion-assisted tunable fluorescence from carbon dots

In this study, carbon dots (CDs) synthesized by hydrothermal method with amino-rich surface exhibit tunable fluorescence across entire visible range by simply controlling the concentration. A comprehensive comparison has been performed for the first time between concentration-induced aggregation of the single-type CDs and electrostatic-induced agglomeration of opposite-charged CDs in terms of their fluorescence properties. Experimental results show that both the aggregation of CDs and internal absorption filtration are possible causes of the concentration-dependent fluorescence emission. Subsequently, the inter distance of adjacent CDs in their aggregates was enlarged by forming rigid double-stranded DNA (dsDNA) between adjacent CDs through base pairing. It is clear that the contact of CDs induces the changes of fluorescence emission and light absorption. Through a better understanding of the mechanisms behind concentration-induced multicolor emission, this work can provide a novel strategy to develop the advanced applications of CDs.

Changes in light absorption and composition of chromophoric marine-dissolved organic matter across a microbial bloom.

Marine chromophoric dissolved organic matter (m-CDOM) mediates many vital photochemical processes at the ocean's surface. Isolating m-CDOM within the chemical complexity of marine dissolved organic matter has remained an analytical challenge. The SeaSCAPE campaign, a large-scale mesocosm experiment, provided a unique opportunity to probe the in situ production of m-CDOM across phytoplankton and microbial blooms. Results from mass spectrometry coupled with UV-VIS spectroscopy reveal production of a chemodiverse set of compounds well-correlated with increases in absorbance after a bacterial bloom, indicative of autochthonous m-CDOM production. Notably, many of the absorbing compounds were found to be enriched in nitrogen, which may be essential to chromophore function. From these results, quinoids, porphyrins, flavones, and amide-like compounds were identified via structural analysis and may serve as important photosensitizers in the marine boundary layer. Overall, this study demonstrates a step forward in identifying and characterizing m-CDOM using temporal mesocosm data and integrated UV-VIS spectroscopy and mass spectrometry analyses.

Inorganic-organic derivatives of layered perovskite-like titanates HLnTiO4 (Ln = La, Nd) with n-amines and n-alcohols: Synthesis, thermal, vacuum and hydrolytic stability

Protonated Ruddlesden-Popper phases HLnTiO4 (Ln = La, Nd) have been used to yield two series of inorganic-organic derivatives containing non-covalently intercalated n-alkylamines and covalently grafted n-alkoxy groups with a various hydrocarbon chain length. Synthesis was carried out according to multistage schemes using both conventional benchtop and solvothermal methods. It was shown that inorganic-organic derivatives obtained contain approximately 0.4–0.5 interlayer organic molecules or groups per proton of the initial titanate as well as some amount of intercalated water. The introduction of organic components into the interlayer space of the titanates leads to its significant expansion and formation of a paraffin-like bilayer possessing an average tilting angle of 75.5°. At the same time, the organic modification does not result in noticeable changes in light absorption of the samples in near-ultraviolet and visible regions. Their thermal stability strongly depends on the nature of the organic component bonding. While non-covalent amine derivatives are stable only at low temperatures <50 °C, covalent alkoxy ones can withstand heating up to 250 °C without perceptible decomposition. While most of the products demonstrate good stability under reduced pressure, some of them undergo phase composition changes upon prolonged exposure to water.

Fabrication of ZnO Ceramics with Defects by Spark Plasma Sintering Method and Investigations of Their Photoelectrochemical Properties

ZnO, as an important semiconductor material, has attracted much attention due to its excellent physical properties, which can be widely used in many fields. Notably, the defects concentration and type greatly affect the intrinsic properties of ZnO. Thus, controllable adjustment of ZnO defects is particularly important for studying its photoelectric properties. In this work, we fabricated ZnO ceramics (ZnO(C)) with different defects through spark plasma sintering (SPS) process by varying sintering temperature and using reduction environment. The experimental results indicate that the changes of color and light absorption in as-prepared ZnO originate from the different kinds of defects, i.e., oxygen vacancies (VO), interstitial zinc (Zni), and Zinc vacancies (VZn). Moreover, with the increase in calcination temperature, the concentration of oxygen defects and interstitial zinc defects in the ceramics increases gradually, and the conductivity of the ceramics is also improved. However, too many defects are harmful to the photoelectrochemical properties of the ceramics, and the appropriate oxygen defects can improve the utilization of visible light.