Decrease In Emission Intensity Research Articles

What is the Impact of Fiscal Technology Expenditure on Carbon Emission Reduction? Evidence from Guangdong Province in China

China has put forward the strategic goal of striving to achieve peak carbon by 2030 and carbon neutrality by 2060, and reducing carbon emission intensity is a top priority. This paper analyses the impact of local government fiscal science and technology expenditures on carbon emission intensity based on a fixed panel regression model using panel data of 21 cities in Guangdong Province from 2000 to 2019, and draws the following main conclusions: (1) Higher fiscal science and technology expenditures significantly promote the reduction of carbon emission intensity. Specifically, for every 1% increase in expenditures, the carbon emission intensity decreases by 0.221%; (2) The mechanism includes promoting the level of green innovation and promoting the level of new and high technology. Therefore, local governments should pay attention to the role of environment-friendly science and technology innovation on low-carbon development, help glow-carbon research and application transformation, strengthen the regulation of heavy polluting enterprises, and guide the capital to green industries, so as to embark a new road of high-quality economic development and carbon reduction.

Defect Induced high-color-rendering white light emissions from Ag-doped ZnO

It is crucial to find high-quality white-light phosphors that are simple to synthesize in order to create efficient lighting. In this pursuit, the focus has been on achieving the emission of white light in ZnO and Ag-doped ZnO emerging as a promising phosphor candidate. The optimized ZnO nano phosphors demonstrated visible-light emission with ideal Commission international de I E “Eclairage frequently abbreviated as coordinates (x = 0.33, y = 0.33 ) and a correlated color temperature of 6200 K, and a color rendering index of 100 for equivalent to day white light. Furthermore, under certain ideal processing conditions, neutral white-light emission (x = 0.33, y = 0.33 at λex = 280 and 370 nm) with a Color correlated temperature (CCT) of 5500 K(approx.) was achieved. The Color Rendering Index (CRI) of the ZnO and Ag:ZnO nanoparticles exceeded 90, with high values approaching 96%, which is necessary for accurately portraying object colors in comparison to natural sunshine. The research findings revealed a decrease in the FS emission intensity with all the UV excitation when Ag doped in ZnO, which aligns well with the principles of Stern-Volmer quenching. A reduction in intensity was observed which may be due to the Ag dopant interacting with the luminescent nanoparticles and causing a reduction in their emitted light. The study successfully develops and optimizes ZnO-based nano phosphors with tailored white-light emission characteristics, presenting a promising solution for achieving energy-efficient and high-quality white-light sources for various lighting applications.

Impacts of ultraviolet and photosynthetically active radiations on photosynthetic efficiency and antioxidant systems of the cyanobacterium Spirulina subsalsa HKAR-19.

This study summarizes the response of cyanobacterium Spirulina subsalsa HKAR-19 under simulated light conditions of photosynthetically active radiation (PAR), PAR+UV-A (PA), and PAR+UV-A+UV-B (PAB). Exposure to UV radiation caused a significant (P < 0.05) decrease in chlorophyll a, phycocyanin, and total protein. In contrast, total carotene content increased significantly (P < 0.05) under PA and PAB with increasing irradiation time. The photosynthetic efficiency of photosystem II also decreased significantly in PA and PAB radiation. We havealso recorded a decrease in the fluorescence emission intensity of phycocyanin under PA and PAB exposure. The phycocyanin fluorescence shifted towards shorter wavelengths (blue-shift) after 72h of PA and PAB exposure. Intracellular reactive oxygen species (ROS) levels increased significantly in PA and PAB. Fluorescence microscopic images showed an increase in green fluorescence, indicating ROS generation in UV radiation. We havealso quantified ROS generation using green and red fluorescence ratio represented as G/R ratio. A 2-6-foldincrease in antioxidative enzymes activity was observed to overcome the damaging effects caused by UV stress as compared to untreated control cultures. The lipid peroxidation was assessed in terms of malondialdehyde content which increases significantly (P < 0.05) as the duration of exposure increases. These results suggest that a combined effect of PAR, UV-A, and UV-B was more deleterious than an individual one.

The Impact of Industrial Added Value on Energy Consumption and Carbon Dioxide Emissions: A Case Study of China

China, as the world’s largest energy consumer, is faced with the growing pressure of carbon emission reduction. Promoting the sustainable transformation of the economy and society has become a major concern for all sectors of society. This paper assesses the potential impacts of industrial added value on energy consumption and carbon dioxide (CO2) emissions from 2010 to 2020 in China using a multi-objective, linear programming model. The results show that when the industrial energy consumption is 3695.17 Mtce and the industrial CO2 emission is 9364.16 Mt, the goal of energy saving and emission reduction can be achieved. This corresponds to an annual average growth rate limit of industrial added value of 7.8%. In addition, we find that when the annual average growth rate of industrial added value is greater than 9.9%, changes in the annual average growth rate of industrial added value have no impact on economic development. However, industrial energy consumption intensity and industrial carbon emission intensity decrease with the increase in the annual average growth rate of sub-sectors. This study proposes that energy conservation, emission reduction, and a realization of the sustainable transformation of industry scheme need to be achieved by the Chinese government in order to to continue to promote the development of several sectors with low industrial energy consumption intensity and low industrial carbon emission intensity through policy implications.

Analyzing long-term dynamics of agricultural greenhouse gas emissions in Austria, 1830–2018

Agriculture is an important contributor to greenhouse gas (GHG) emissions. While the development of agricultural GHG emissions on national and global scales is well studied for the last three to six decades, little is known about their trajectory and drivers over longer periods. In this article, we address this research gap by calculating and analyzing GHG emissions related to agriculture in Austria from 1830 to 2018. We calculate territorial emissions on an annual basis and include all GHG emissions from the processes directly involved in agricultural production. Based on this time series, we quantify the relative importance of major drivers of changes in GHG emissions across time and agricultural product categories, applying a structural decomposition analysis. We find that agricultural GHG emissions in Austria increased by 69 % over the total study period, from 4.6 Mt. CO2e/yr in 1830 to 7.7 Mt. CO2e/yr in 2018. While emissions increased only moderately from 1830 to 1945 (+22 % overall), with strong fluctuations between 1914 and 1945, they doubled from 1945 to 1985. In the most recent period from 1985 to 2018, emissions fell by one third, with decreases leveling off over time. Our decomposition analysis reveals that increases in agricultural production per capita most importantly contributed to the high growth in GHG emissions from 1945 to 1985. Conversely, decreasing emission intensities of products and a more climate friendly product mix were key drivers in the emissions reduction observed after 1985. We also contribute to the discussion around the global warming potential star (GWP*), by calculating GHG emissions based on this alternative metric, and contextualize our data within total socio-economic GHG emission trends. By providing insights into the historical trends and drivers of agricultural GHG emissions, our findings enhance the understanding of their long-term historical dynamics and adds to the knowledge base for future mitigation efforts.

How does government efficiency affect carbon emission intensity? A comprehensive empirical study.

This study utilized panel data from 132 countries spanning from 1996 to 2019 to examine the effect of government efficiency on carbon emission intensity. Using a fixed effect model, the study found that stronger government efficiency is associated with a significant decrease in carbon emission intensity. Robustness tests were performed, the results of which consistently supported the main findings. Additionally, the study investigated the mechanisms underlying the linkage between government efficiency and carbon emission intensity, revealing that improved government efficiency can inhibit carbon emission intensity by fostering environmental innovation and promoting renewable energy consumption. Finally, the study examined the moderating effects of national income level, economic freedom, democracy, and ruling party ideology on the nexus of government efficiency and carbon emission intensity, and found empirical evidence supporting these moderating effects. These results provide new insights for governments seeking to reduce carbon emission intensity.

The borophene quantum dots scaffolded TiO2 nanocomposite as an efficient photo electrocatalyst for water splitting application

Herein, we are scaffolding borophene quantum dots (BPQDs) on photoactive semiconductor nanomaterial such as TiO2 nanoparticle which shows enhanced photoelectrochemical (PEC) water splitting activity. The BPQDs are synthesized by sonochemical method and then scaffolded onto TiO2 nanoparticles by hydrothermal method. Further, the concentration of BPQDs on TiO2 nanoparticles is optimized for better photoelectrochemical water splitting application. The effective absorption edge is found to be less (2.51 eV) for 2.5 wt% BPQDs scaffolded TiO2 nanoparticles as studied by UV–Visible spectroscopic analysis. Transmission electron microscopic (TEM) images reveal the scaffolding of BPQDs of size (2–9) nm with TiO2 nanoparticles of having the size ∼25 nm. XRD results confirmed the anatase phase of TiO2 nanoparticles and b-rhombohedral boron structure for BPQDs. The FTIR and XPS results confirms the presence of boron functionalized groups in the nanocomposites. The photoluminescence (PL) spectroscopic results revealed the decrease in PL emission intensity for BPQDs/TiO2 nanocomposite indicating the decreased photogenerated charge carriers recombination time. The work function (ϕ) is found to be less for BPQDs/TiO2 nanocomposite signifying the easy release of electrons under the presence of visible light illumination. Further, BPQDs/TiO2 nanocomposite shows the improvement in photoelectrochemical (PEC) water splitting due to the synergistic effects of individual components.

Carbon pricing and firms’ GHG emissions: Firm-level empirical evidence from East Asia

This study investigates the impacts of carbon pricing policies on firms' greenhouse gas (GHG) emissions. We include two carbon pricing policies: carbon tax and emission trading scheme (ETS) at national and sub-national (province) levels, measured as policy existence (binary variable) and carbon price (continuous variable). Firms' GHG emissions are measured as total emissions and emission intensity. Using unique recent firm-level data from 2010 to 2021 from three East Asia countries (Japan, the Republic of Korea (ROK), and the People's Republic of China (PRC)), we obtain the following key findings. First, the national carbon pricing policy significantly reduced firms' GHG emissions and GHG emission intensity in Japan and the ROK. The greater the carbon price, the greater the impact. Second, the subnational carbon pricing policies implemented in two provinces of Japan (Saitama and Tokyo) decreased firms' GHG emissions. Third, heavy industry sectors such as energy, utilities, and industrials experienced a substantial decrease in GHG emission intensity due to the carbon pricing policy. Finally, our main results are robust to different model specifications and various measures of firms' GHG emissions. Although literature studying the ex-post impact of carbon pricing on emissions at country and sector-level is abundant, this paper contributes to the existing literature providing empirical evidence of the impact of carbon pricing policies on firms' emissions using firm-level data, which is highly limited especially in Asia.

Simulation study on influence of oxygen concentrations on atmospheric-pressure streamer in oxygen-rich nitrogen–oxygen mixture

This study aims to investigate the behaviour of positive streamer discharge in various mixtures with different concentrations via two-dimensional simulations. The proposed model considers the effects of photoionisation caused by the photons generated by excited oxygen atoms , which enables the simulation of streamers in oxygen rich conditions. The simulation results indicate that the propagation velocity and diameter of the streamer increase with the oxygen concentration, while the emission intensity decreases. The result conforms to the experimental results of our previous work. Moreover, the simulation results suggest that changes in the ionisation rate caused by variations in the oxygen concentration affect the streamer propagation, while the impact of photoionisation is limited.

Bimetallic Eu/Tb Complexes for Ratiometric Temperature Sensing with Unusual Enhancement of Eu Luminescence with Temperature

In this paper we describe the results of the influence of temperature in the range of 280–340 K on the luminescence of bimetallic Eu/Tb complexes with N-heterocyclic ligand L based on 2,2′-bipyridyldicarboxylic acid in acetonitrile. The experiments were carried out for systems with various Eu/Tb ratios. The stability of the complexes of the ligand L with metal M (Eu or Tb) was determined using spectrophotometric titration in acetonitrile solutions. The LM complexes’ stability constants were found to be typical for these systems; however, the stability of Eu complex is slightly higher than that for Tb. Along with rising temperature, we observed a decrease in Tb emission intensity and, at the same time, an enhancement in Eu luminescence. An explanation of Eu luminescence enhancement involves the appearance of charge transfer states, bands of which can be observed in the Eu luminescence excitation spectra as difference spectra measured with two close temperatures. The unusual Eu luminescence enhancement upon heating was observed for the first time for the complex with tetradentate O,N-type heterocyclic diamide ligand L, while an inverse phenomenon was observed with the Tb luminescence. The Eu luminescence enhancement was found earlier for various carboxylate complex salts, but not for heterocyclic coordination complexes. This allows the construction of a ratiometric luminescent thermometer in the range of 280–340 K using the ratio of luminescence intensities for Eu and Tb. The stability constants for the individual Eu and Tb complexes help us to understand the equilibrium in L:Tb:Eu complex system and shed light on plausible speciation in solution.

UV and blue excited tunable emission of thermally stable Bi3+ sensitized Eu3+ doped calcium aluminozincate phosphor for photonic applications

Bi3+/Eu3+ co-driven calcium aluminozincate (CAZ) phosphor prepared by sol–gel route. Structural analysis was conducted based on X-ray diffractogram. Scanning Electron Microscope images were recorded using Carl Zeiss microscope. Luminescent traits of the said phosphors were identified using excitation and emission spectroscopy at room temperature and elevated temperature. The emission spectra recorded at room temperature under different excitations exhibit variation in spectral behavior. The Commision Internationale de-lElcairage coordinates shown in chromaticity diagram indicate the change in emission hue as pure blue, bluish red and finally pure red by varying the excitation wavelengths. The temperature dependent emission spectra show decrease in emission intensity with temperature and activation energy found to be 0.280 eV. The decay curves were also recorded to determine lifetime and study energy transfer between Bi3+ and Eu3+ ions. Auzel’s fit conducted based on the decay lifetimes helps in evaluating quantum efficiency theoretically. All these investigations authorize the potential of Bi3+/Eu3+ doped CAZ phosphors for their utilization as color-tunable phosphor in photonic applications.

Spatiotemporal analysis of CO2 emissions and emission reduction potential of Beijing buses using smart card data

Human activities, primarily carbon dioxide emissions, have undeniably caused global warming. The transportation sector contributes about a quarter of global CO2 emissions. While replacing traditional buses with electric ones has reduced emissions, it is crucial to consider the indirect emissions resulting from electricity consumption. This study proposes a framework for modeling bus emissions using smart card data, integrating spatiotemporal distribution characteristics and emission reduction potentials. Our analysis reveals that routes spanning 10–30 km contribute to 81% of total bus emissions, with an average emission rate of 56.2 gCO2/per-km for residents traveling by bus. Bus emissions also exhibit cyclical variations during holidays, weekdays, and weekends, indicating spatial clustering and trends. Although the area within Beijing's 4th Ring Road constitutes only 13% of the total area within the 6th Ring Road, it generates almost half of the CO2 emissions. With urban expansion, total bus emissions increase gradually, but emission intensity decreases. This study emphasizes the potential for reducing emissions through improved public transportation operations. It recommends fully electrifying the bus fleet and employing low grid emission factors, which could reduce emissions by up to 71% compared to diesel options. Electrification of buses and optimizing power generation on the grid are essential priorities for emission reduction.

Efficient Photocatalytic CO2 Reduction with High Selectivity for Ethanol by Synergistically Coupled MXene-Ceria and the Charge Carrier Dynamics.

The primary factors that govern the selectivity and efficacy of CO2 photoreduction are the degree of activation of CO2 on the active surface sites of photocatalysts and charge separation/transfer kinetics. In this context, the rational synthesis of heterostructured MXene-coupled CeO2-based photocatalysts with different loading concentrations of Ti3C2MXene via a one-step hydrothermal approach has been undertaken. These photocatalysts exhibit a shift in X-ray diffraction peaks to higher 2θ values and changes in stretching vibrations of 5 wt % Ti3C2MXene/CeO2(5-TC/Ce) that indicate interaction between Ti3C2MXene and CeO2. Moreover, XPS analysis confirms the presence of the Ce3+/Ce4+ states. A sharp band at 2335 cm-1 observed during the CO2 photoreduction process corresponds to bidentate b-CO32-, which facilitates the adsorption of CO2 at the surface of the catalyst as revealed by the TPD analysis. Furthermore, the Schryvers test and NMR analysis were undertaken to confirm the formaldehyde intermediate formation during CO2 photoreduction to C2H5OH. The decrease in emission intensity, reduced lifetimes (2.68 ns), and lower interfacial resistance, as revealed by PL, TR-PL, and EIS analysis, imply an efficient charge separation and charge transfer in the case of the Ti3C2MXene/CeO2 heterojunction. The decrease in the intensity of peaks in the EPR spectrum in the case of 5-TC/Ce further confirms efficient charge transfer kinetics across the interface. The optimized 5-TC/Ce shows CO2 reduction with a drastically enhanced yield of ethanol on the order of 6127 μmol g-1 at 5 h with 98% selectivity and 7.54% apparent quantum efficiency, which is 6-fold higher than that of ethanol produced by bare CeO2. Herein, CeO2 that acts as a redox couple (Ce3+/Ce4+) when coupled with MXene having a metallic nature that reduces the electron transfer resistance is in unison, enabling an enhanced mobilization of electrons. Thereby, the synergistic coupling of Ti3C2MXene with CeO2 leads to an efficient photoreduction of CO2 under visible light illumination.

Indonesian capital city relocation and regional economy's transition toward less carbon-intensive economy: An inter-regional CGE analysis

Transitioning to a low-carbon economy can take various forms, one of which is structural change, particularly tertiarization. When the economic structure shifts from being dominated by sectors that rely heavily on fossil fuels to one that does not, the economy can become less carbon-intensive. The relocation of Indonesia's capital city from Jakarta to East Kalimantan is an example of how a traditionally resource-intensive regional economy may respond to the sudden emergence of a large-scale service sector, in this case, the government sector. This paper investigates how the capital city relocation may affect the destination region's economic structure using an inter-regional computable general equilibrium modeling. The model considers not only how different economic sectors are interconnected but also how sectors within one province are interconnected with sectors in other provinces. According to the findings, the relocation of the capital city increases the Gross Regional Domestic Product (GRDP) of the destination region (KalTim) by a massive amount (22%) while decreasing the GRDP of Jakarta (the old capital) by a moderate amount (7%). However, because the expanding sector is relatively high-skill intensive, it tends to produce skill-biased increases in real wages. As a result, the destination region (Kaltim) undergoes massive structural change as its service sector share increases by 12%, a change historically comparable in two decades. In addition, Kaltim's carbon emission intensity decreases by 18% due to this large-scale tertiarization. The analysis has demonstrated how and to what extent the relocation of Indonesia's capital city may help the province diversify from a natural resource-intensive economy to a more service-oriented and low-carbon economy.

Phonon‐Assisted Negative Thermal Quenching in a One‐Photon Up‐Conversion Phosphor for Thermometry

AbstractThermal disturbance deteriorates the radiative transitions of up‐conversion phosphor, leading to decreased emission intensity at high operation temperatures. In this work, a thermal‐favored Yb3+/Nd3+ co‐doped KGaGeO4 up‐conversion phosphor with a negative thermal quenching behavior is explored. The as‐developed phosphor performs a one‐photon anti‐Stokes emission and exhibits a remarkable enhancement for the rise of ambient temperature reaching 653 K. It is demonstrated that the fascinating thermal behavior of the up‐conversion procedure is attributed to the enhanced energy transfer from the corresponding sensitizers to the activators by phonon assistance. Moreover, the microscopic dynamical process of phonon assistance and annihilation is revealed by introducing Er3+ ions as a probe. These results not only shed light on the phonon‐assisted strategy to build a highly efficient anti‐Stokes emission system but also open prospects for constructing phonon‐favored transitions with nonthermally coupled emissions to realize luminescence thermometry for their distinct thermal responsivity.

Improved Thermal and Chemical Stability of Oxynitride Phosphor from Facile Chemical Synthesis for Vehicle Cornering Lights

AbstractOrange Eu2+‐doped phosphors are essential for light‐emitting diodes for cornering lights to prevent fatal road accidents at night, but such phosphors require features of high thermal, chemical stability and facile synthesis. This study reports a series of yellow‐orange‐red emitting SrAl2Si3ON6:Eu2+ oxynitride phosphors, derived from the SrAlSi4N7 nitride iso‐structure by replacing Si4+−N3− with Al3+−O2−. The introduction of a certain amount of oxygen enabled the facile synthesis under atmospheric pressure using the air‐stable raw materials SrCO3, Eu2O3, AlN and Si3N4. SrAl2Si3ON6 has a smaller band gap and lower structure rigidity than SrAlSi4N7 (5.19 eV vs 5.50 eV, Debye temperature 719 K vs 760 K), but exhibits higher thermal stability with 100 % of room temperature intensity remaining at 150 °C compared to 85 % for SrAlSi4N7. Electron paramagnetic resonance, thermoluminescence and density functional theory revealed that the oxygen vacancy electron traps compensated the thermal loss. Additionally, no decrease in emission intensity was found after either being heated at 500 °C for 2 hours or being immersed in water for 20 days, implying both of the thermal and chemical stability of SrAl2Si3ON6:Eu2+ phosphors. The strategy of oxynitride‐introduction from nitride promotes the development of low‐cost thermally and chemically stable luminescent materials.

Improved Thermal and Chemical Stability of Oxynitride Phosphor from Facile Chemical Synthesis for Vehicle Cornering Lights.

Orange Eu2+ -doped phosphors are essential for light-emitting diodes for cornering lights to prevent fatal road accidents at night, but such phosphors require features of high thermal, chemical stability and facile synthesis. This study reports a series of yellow-orange-red emitting SrAl2 Si3 ON6 :Eu2+ oxynitride phosphors, derived from the SrAlSi4 N7 nitride iso-structure by replacing Si4+ -N3- with Al3+ -O2- . The introduction of a certain amount of oxygen enabled the facile synthesis under atmospheric pressure using the air-stable raw materials SrCO3 , Eu2 O3 , AlN and Si3 N4 . SrAl2 Si3 ON6 has a smaller band gap and lower structure rigidity than SrAlSi4 N7 (5.19 eV vs 5.50 eV, Debye temperature 719 K vs 760 K), but exhibits higher thermal stability with 100 % of room temperature intensity remaining at 150 °C compared to 85 % for SrAlSi4 N7 . Electron paramagnetic resonance, thermoluminescence and density functional theory revealed that the oxygen vacancy electron traps compensated the thermal loss. Additionally, no decrease in emission intensity was found after either being heated at 500 °C for 2 hours or being immersed in water for 20 days, implying both of the thermal and chemical stability of SrAl2 Si3 ON6 :Eu2+ phosphors. The strategy of oxynitride-introduction from nitride promotes the development of low-cost thermally and chemically stable luminescent materials.

Private Shareholder Engagements on Material ESG Issues

We study private shareholder engagements with 2,465 listed firms about environmental, social, and governance (ESG) issues from 2007 to 2020. We examine the extent to which private engagements address financially material ESG issues and contribute to firm performance. We find that material engagements succeed more often than immaterial engagements and that the targets of successful material engagements significantly outperform their peers by 2.5% over the next 14 months. Further, we find that material engagements are more often associated with improvements in profitability and cost ratios than immaterial engagements. Finally, our evidence indicates that a decrease in CO2e emission intensity accompanies environmental engagements.

Spectroscopic behavior differences between lumazine and alloxazine in the DMSO-water mixture

The absorption and emission spectra were investigated for lumazine, alloxazine and their cyanated or fluorinated derivatives, respectively. The spectroscopic properties were modulated by varying water concentration in dimethyl sulfoxide (DMSO). Some intriguing experimental results were found for the samples containing 65 % of water and 35% of DMSO. This finding is consistent with previously published molecular dynamics (MD) simulations confirming the concept of the ‘local bulk’ model. In this case, a notable decrease in absorption and emission intensities was registered, even larger than the water quenching observed in other cases. The changes in midrange DMSO concentrations could be explained by the formation of local solvents structures as predicted by MD, specifically the formation of DMSO·2H2O dimers. Experimentally, the cyano-substituted lumazine has shown a remarkable sensitivity to DMSO concentration. The spectroscopic measurements were interpreted using the density functional theory where the implicit DMSO solvent model was combined with explicit water molecules. Together with its enhanced water solubility, the cyanated lumazine derivate could be used for non-destructive DMSO detection in vitro for applications such as drug uptake monitoring, since DMSO is often used in pharmaceutical practice.

Effect of the local energy distribution of x-ray beams generated through inverse Compton scattering in dual-energy imaging applications.

X-ray sources based on the inverse Compton interaction between a laser and a relativistic electron beam are emerging as a promising compact alternative to synchrotron for the production of intense monochromatic and tunable radiation. The emission characteristics enable several innovative imaging techniques, including dual-energy K-edge subtraction (KES) imaging. The performance of these techniques is optimal in the case of perfectly monochromatic x-ray beams, and the implementation of KES was proven to be very effective with synchrotron radiation. Nonetheless, the features of inverse Compton scattering (ICS) sources make them good candidates for a more compact implementation of KES techniques. The energy and intensity distribution of the emitted radiation is related to the emission direction, which means different beam qualities in different spatial positions. In fact, as the polar angle increases, the average energy decreases, while the local energy bandwidth increases and the emission intensity decreases. The scope of this work is to describe the impact of the local energy distribution variations on KES imaging performance. By means of analytical simulations, the reconstructed signal, signal-to-noise ratio, and background contamination were evaluated as a function of the position of each detector pixel. The results show that KES imaging is possible with ICS x-ray beams, even if the image quality slightly degrades at the detector borders for a fixed collimation angle and, in general, as the beam divergence increases. Finally, an approach for the optimization of specific imaging tasks is proposed by considering the characteristics of a given source.