Introduction
X-ray imaging is ubiquitous in clinical diagnosis and has common applications in digital radiography (DR) and computed tomography (CT). DR provides two-dimensional absorption imaging, whereas CT offers slices and three-dimensional absorption imaging. Compared with DR, CT effectively addresses the issue of overlapping projection information. Despite this, current X-ray absorption-contrast CT (XACT) performs exceptionally well for imaging highly absorbing objects, but still faces challenges in the imaging of weakly absorbing objects or those with similar absorption characteristics [1, 2], potentially leading to patients missing the optimal treatment period. To overcome the limitations of XACT, dual-energy CT (DECT) and X-ray phase-contrast CT (XPCT) have been proposed to address the issue [3-5]. The former utilizes two different X-ray energy spectra to distinguish materials, whereas the latter combines X-ray phase-contrast imaging (XPCI) and CT to extract the phase information of materials. The popular XPCI methods include crystal interference (CI) [6], propagation based imaging (PBI) [7-9], speckle imaging [10, 11], analyzer based imaging (ABI) [12-14], grating interference (GI) [15-20] and edge illumination (EI) [21-23]. ABI, GI, and EI can measure phase signals using conventional X-ray sources. However, ABI and GI face challenges due to low usable flux and high system stability requirements. EI offers advantages through lower coherence and alignment needs, and better stability. Compared to DECT, XPCT extracts more significant phase information and remains an emerging imaging technology. However, XPCT needs additional optical components to convert phase information into measurable intensity signals, requiring complex equipment, stringent optical components, and optimized system design. For details on XPCI methods’ benefits and challenges, see reference [1].Therefore, addressing these challenges is critical for the development of XPCT.
However, while DECT has gradually become more popular and has been applied in clinical diagnosis because of its excellent ability to identify components, the application of XPCT technology in medicine remains at the research stage because of the complexity of the device, which lags behind that of DECT in terms of medical implementation. Given the widespread use of DECT, the feasibility and necessity of XPCT in the medical field must be reconsidered. Both XPCT and DECT have advantages and disadvantages in medical applications. However, a systematic comparison of these two technologies is currently lacking. To compare the performance of XPCT in medical imaging with that of DECT, Zhang et al. [4] evaluated and compared the two techniques using the CHO model and theoretically analyzing the preferred order of application for XPCT and DECT in different CT spatial resolution scenarios. They employed the GI method in XPCT and noted that the XPCT relies on the spatial resolution of images and is more suitable for ultrahigh spatial resolution imaging tasks of small objects. In their distinguished work, some limitations of GI based XPCT imaging were observed. The size of the grating and detector devices limited the size of the imaged object. Furthermore, their work based on a numerical simulation was significantly different from the actual results, and the Monte Carlo-based simulation we used was closer to reality. Additionally, the precision of the displacement system is more challenging for actual GI scanning and data acquisition, particularly for imaging methods that use interference [24, 25]. This is also a challenge in current medical applications of XPCT technology, which utilizes the temporal coherence of radiation. In addition to the GI method, the EI method holds promise for the widespread application of XPCT technology. The EI-based XPCT method is a non-interference imaging technique with a simpler mask and detector configuration than GI, facilitating easier imaging of large objects [26]. Furthermore, the EI-based XPCT method can be simulated using GEANT4, a feat challenging to accomplish using interferometric methods. The results of the EI-based XPCT simulations in this study are different from theirs because of differences in the XPCT method and simulation tools. In addition, a more comprehensive and specific statistical evaluation is required to compare the advantages and disadvantages of DECT and EI-based XPCT imaging, which will be discussed in detail later.
XPCT is currently undergoing rapid development; however, matching the device simplicity of XACT or DECT remains challenging. Single-mask and single-shot (SMSS) EI stands out among XPCTs, adding an optical component to existing clinical CT devices to extract phase information efficiently.
Classical EI imaging uses two absorption masks - one before the object and one before the detector, requiring multiple exposures through mask displacement. Although displacement requirements are less stringent than GI, the double mask makes imaging cumbersome. This paper uses SMSS EI model [27], retaining only the object mask and using adjacent pixel pairs as detection units for single-exposure imaging. Considering practical applications, sacrificing some resolution for a simpler SMSS method is optimal. SMSS EI-based XPCT can be improved on existing medical CT equipment.
In this study, we built a complete set of SMSS EI imaging models and algorithms based on GEANT4 and MATLAB for quantitative evaluation using XACT and DECT at the same dose. To demonstrate the differences among the three techniques more intuitively, we directly used the physical quantities reconstructed using MATLAB as the reconstructed image contrast for evaluation. To assess the image quality of the three techniques, a statistical evaluation system was implemented, including absolute error (AE), mean absolute error (MAE), structure similarity index measure (SSIM), peak signal-to-noise ratio (PSNR), and contrast-to-noise ratio (CNR). Through this work, we not only quantitatively compared the differences between XACT, DECT, and XPCT, confirming the superiority of XPCT, but also provided an alternative and fast solution for XPCT medical applications.
Methods and materials
Imaging Technologies
In theory, as X-rays pass through an object, not only do their intensity attenuate, but their phase also shifts. This can be explained well by the refractive index formula n=1 - δ + iβ, where β represents the absorption factor and δ represents the phase-shift factor. Both XACT and DECT extract the intensity attenuation of X-rays, whereas XPCT focuses on extracting the phase-shift of the X-rays. Considering that the emission energy spectrum of the X-ray is Ω (E) and the spatial position of the object under test is (x, y, z), where the direction of _2026_05/1001-8042-2026-05-91/alternativeImage/1001-8042-2026-05-91-M001.png)
DECT employs a widely used basis material decomposition model that leveraging the distinct absorption coefficient μ characteristics of objects under varying X-ray energies. Through mathematical modeling, the imaging data were decomposed on different bases. In this process, the linear attenuation coefficient μ (x, y, z) is transformed into μL (x, y, z) + μH (x, y, z), where the subscripts L and H represent the conditions of low and high X-ray tube voltages, respectively. Correspondingly, the projection quantity P that describes DECT-based absorption projection formula is transformed as follows:_2026_05/1001-8042-2026-05-91/alternativeImage/1001-8042-2026-05-91-M002.png)
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Unlike the first two techniques, XPCT extracts phase-shift information from X-rays. The double-mask EI method requires the illumination curve (IC) to be read by moving the two masks laterally relative to each other. IC acquisition required at least three exposures. Absorption, refraction, and scattering information can be obtained in the presence and absence of an object, which means that the imaging process requires the positional alignment of the two optics and multiple exposures, and the accuracy and stability requirements of the system are challenging for clinical conditions. The SMSS EI method utilizes two adjacent pixels to detect the offset of beamlets in a single exposure, thereby quantitatively extracting refraction information, as shown in Eq. 5 [28]._2026_05/1001-8042-2026-05-91/alternativeImage/1001-8042-2026-05-91-M005.png)
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Simulation Model
We used GEANT4 version 11.1.0, with Ubuntu 20.04.02, for all the simulations. The GEANT4 simulations were run on a desktop machine with an Intel Core i7-13700KF 5.40 GHz CPU processor. The simulations involve the physical principles of electromagnetism and X-ray refraction, adhering to the Beer–Lambert law (considering photon-matter interactions such as the photoelectric effect and Compton effect, but excluding electron pair effects as photon energies are below 1.02 MeV in our setup) and Snell’s law (refracting X-rays when transitioning between media based on their refractive indexes). G4ElectromagneticPhysics is used to make X-ray follow the absorption process, and G4MaterialPropertiesTable is used to define the RINDEX of an object to make X-ray follow the refraction process. The emitted particles employ the G4GeneralParticleSource module using the command /gps/hist/point to weigh the energy of each emitted photon based on the corresponding energy spectrum intensity.
The GEANT4 configurations of the three systems are presented in Fig. 1. Zso is the distance from the source to the object and Zsd is the distance from the source to the detector, with values of 80 and 100 cm, respectively. The XACT system is a basic device consisting of an X-ray source, an object, and a detector, where the energy of the X-ray source corresponds only to the low-energy option. The DECT system adds a high-energy X-ray source to the XACT system. The XPCT system utilizes the SMSS EI method by adding a coded-aperture module to the XACT system as a mask.
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The specific parameters for CT imaging are listed in Table 1. Based on Handschuh et al. [32], X-ray tubes with 40 and 80 kVp voltages were selected for DECT imaging. The X-ray energy spectrum, generated by Spekpy simulation [33], is shown in Fig. 2. XACT and XPCT used a 40 kVp X-ray source, whereas DECT used 40 and 80 kVp sources. Glass filter (1.1 mm) and aluminum filter (0.5 mm) were placed before the 40 and 80 kVp tubes to reduce beamline hardening. Source and detector pixels were 40 and 62 μm, respectively, with the detector having 200 single-row pixels. The system’s magnification factor was 1.25, yielding a reconstructed voxel size of 49.6 μm. Projection data were acquired at 1-degree intervals, obtaining 360 images per rotation. XACT emitted 4×107 photons per angle, whereas DECT emitted 2×107 photons due to dual voltage requirements. In XPCT, the y-direction resolution was halved per Eq. 5; however, linear interpolation achieved 49.6 μm voxel size for comparison. The mask’s projected size doubled the pixel size, with beamlets hitting the pixel midpoints. The mask thickness ensured that the X-rays passed only through the apertures, enabling the absorption of almost all 40 kVp X-rays elsewhere. XPCT photon count was increased tenfold to offset the 90% mask loss (i.e., 4×108).
| X-ray Energy (LE) | X-ray Energy (HE) | X-ray Focus Size | Zsd | M (Magnification) | Projections per rotation | Number of photons physically emitted per projection |
| 40 kVp | 80 kVp | 40 μm | 100 cm | 1.25 | 360 | 4×107 |
| Projection Mask Aperture | Projection Mask Period | Pixels Number | Pixel | Voxel | Mask Material | Mask Thickness |
| 12.4 μm | 124 μm | 1×200 | 62 μm | 49.6 μm | Gold | 80 μm |
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The simulated soft-tissue phantom is shown in Fig. 3, and the corresponding tissue material information is presented in Table 2. The radius of the phantom was 4 mm, whereas those of the other plugs were 0.6 mm. The phantom height was 2 mm. Tissue material data were obtained from CIRS 062M phantom and International Commission on Radiological Protection. The μ(E) of the phantom was obtained from the database of the National Institute of Standards and Technology and δ was calculated as δ = 4.15×104 ρZ/(AE2) [27].
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| Position | Plug | Material | Elemental Composition | |||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| density | H | C | N | O | Na | P | S | Cl | K | Ca | ||
| Right | Lung (Inhale) | 0.20 | 8.8 | 67.5 | 3.5 | 18.6 | - | - | - | 1.6 | - | - |
| Left | Lung (Exhale) | 0.50 | 9.8 | 70.2 | 2.3 | 15.1 | - | - | - | 1.0 | - | 1.6 |
| Top | Adipose | 0.96 | 9.4 | 72.4 | 2.3 | 15.5 | - | - | - | 0.2 | - | 0.3 |
| Bottom | Water (liquid) | 1.00 | 66.0 | - | - | 34.0 | - | - | - | - | - | - |
| Background | Soft tissue | 1.03 | 10.5 | 25.6 | 2.7 | 60.2 | 0.1 | 0.2 | 0.3 | 0.2 | 0.2 | - |
The system setup in GEANT4 corresponds to that shown in Fig. 1. The GEANT4 simulation program for SMSS EI-based XPCT is optimized by Brombal et al. [34, 35]. The energy spectrum is input into the source module, generating photons with the same distribution as in Fig. 2. In the SMSS EI system, photons must pass through the mask and hit the center of two pixels precisely, making mask position calibration essential. The mask must meet requirements in both y and z directions. For y-direction calibration, the normalized intensity position of 0.5 is determined by extracting the single-mask IC curve [36], as shown in Fig. 4(a), ensuring the photon reaches the detection unit’s middle position. For z-direction calibration, the mask is moved until achieving a uniform image. The refractive angle signal at this z-position, shown in Fig. 4(b), confirms z-direction requirements are met. Table 2 and δ containing phantom information are input into the object module. The soft-tissue phantom has five solid parts. We add an object rotation module to adjust positions and rotations during scanning, as the original program lacks direct phantom rotation. Using Python scripting, the program enables simultaneous multitasking and multithreading for efficient simulation.
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The data read by the detector are imported into MATLAB for processing and imaging, as shown in Fig. 5. Projection images are presented by moving the object in the x-direction to show the projected image with a larger field of view, with CT imaging only imaging a certain height. The simulated profiles in Fig. 5(b), (g), (h) and (q) closely match theoretical profiles. For XACT imaging, 360-degree projections are acquired, and the projection sinogram is obtained using the fanbeam function, followed by ifanbeam for the sliced image. Hamming filters are used in all back-projection (BP) procedures except Fig. 5(w). The XACT image contrast in Fig. 5(d) originates from linear absorption coefficient μ. DECT imaging is based on XACT, with material decomposition performed on low-energy (Fig. 5(k)) and high-energy (Fig. 5(l)) images. Figure 5(k) appears sharper due to decreased X-ray interaction cross-section at higher energies. Using calcium and water as basis materials (μ values: (calcium) 8.31 and 1.47 cm-1; (water) 0.69 and 0.25 cm-1 at 40 and 80 kVp, respectively), Eqs. 2, 3 and 4 yield relative electron density Zeff and effective atomic number images in Fig. 5(m) and (n). The DECT image contrast in Fig. 5(o) combines normalized Zeff values. XPCT imaging requires complex fanbeam transformation due to non-constant
_2026_05/1001-8042-2026-05-91/alternativeImage/1001-8042-2026-05-91-F005.jpg)
For a better comparison with the simulation results, we additionally built theoretical CT images of XACT, DECT and XPCT of the phantom with the same voxel based on MATLAB. After modeling in MATLAB, the same process was performed, as shown in Fig. 5. The next step involves the development of methods to evaluate these results.
Evaluation System
In this study, the performance of DECT, XPCT and XACT was assessed through a comprehensive evaluation system based on four aspects: error evaluation metrics, image quality evaluation metrics, contrast and noise evaluation metrics, and data distribution and dispersion evaluation metrics. The error evaluation metrics include the absolute error (AE) and mean absolute error (MAE), which are calculated using Eqs. 7 and 8 respectively, to assess the difference between the measured and theoretical values for different tissues. The image quality evaluation metrics consist of the structural similarity index (SSIM) and peak signal-to-noise ratio (PSNR), where the former compares the similarity between two images, and the latter measures the noise level and distortion of the image, as indicated by Eqs. 9 and 10. The contrast and noise evaluation metrics, represented by the contrast-to-noise ratio (CNR) defined in Eq. 11, assess the clarity and noise level of the reconstructed images. The data distribution and dispersion evaluation metrics were represented by boxplots that visually displayed the distribution and dispersion of the data, including the minimum, lower, median, upper, and maximum values. This method helps visualize the distribution and dispersion of the measurement data, aiding in the identification of outliers and the shape of the data distribution._2026_05/1001-8042-2026-05-91/alternativeImage/1001-8042-2026-05-91-M007.png)
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Results and discussion
CT Images
Following the reconstruction algorithms described in Sect. 2.2, we obtained slice images for the three techniques as shown in Fig. 6. All the images share identical ROIs, with normalized image intensities. To reveal hidden textures, we use pseudo-color representation, mapping grayscale values to the RGB color range. The colorbar indicates normalized intensity. The lung (inhale) region appears blue, lung (exhale) appears green, adipose appears orange, and water and soft-tissue regions appear in varying shades of red. The similar colors for water and soft tissue reflect their comparable densities. In subsequent analyses, the distinction between water and soft tissue serves as a reference for imaging technology resolution - clearer distinction indicates better discriminatory ability. From the theoretical images in Fig. 6(a) and 6(c), XACT and DECT show similar image contrasts due to their shared principle of intensity attenuation. While the performance of XPCT differs from that of absorption imaging techniques, advantages and disadvantages cannot be determined through simple observations.
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For simulated images, XACT and DECT show similar characteristics, both struggling with water detection, with DECT showing higher noise due to emitting half the photons as XACT in two emissions. In XPCT, we selected Fig. 5(w) for comparison. The XPCT noise differs from Gaussian noise in absorption images, showing slight ringing artifacts [38], but edges remain clearly visible in all five materials..
For quantitative analysis, we extracted information from each image, as shown by white boxes in Fig. 6(a), with results depicted in Fig. 7. Panels (a), (b) and (c) in Fig. 7 show the intensity profiles of XACT, DECT, and XPCT images, respectively, against soft-tissue background. XPCT demonstrates the best profile smoothing and shows water’s signal intensity, which is not reflected by absorption-contrast imaging. The statistical evaluation process is detailed in the next section.
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Statistical Evaluation
The physical quantities reconstructed from the simulated images and the AE results are compared with the theoretical values in Table 3. Among these, DECT exhibited the largest deviation, which was due to the halving of the dose per emission, leading to relatively poor performance in the simulated images. Conversely, XPCT had the smallest AE, indicating a closer alignment with the theoretical values.
| Lung (inhale) | Lung (exhale) | Adipose | Water (liquid) | Soft-tissue (background) | ||
|---|---|---|---|---|---|---|
| XACT | μ (cm-1) | 0.12 ± 8.03% | 0.35 ± 7.30% | 0.49 ± 11.21% | 0.71 ± 4.33% | 0.69 ± 1.51% |
| DECT | ρe (×1022 cm-3) | 0.65 ± 3.26% | 1.58 ± 5.82% | 3.29 ± 10.55% | 2.97 ± 11.33% | 3.27 ± 6.03% |
| Zeff | 7.89 ± 1.33% | 10.76 ± 17.49% | 7.31 ± 14.55% | 11.41 ± 14.09% | 10.58 ± 11.58% | |
| XPCT | δ (×10-8) | 2.09 ± 1.32% | 5.12 ± 0.56% | 9.89 ± 0.35% | 11.44 ± 0.50% | 10.61 ± 0.17% |
Furthermore, we compare the SSIM and PSNR values of the images shown in Fig. 6, and the results are listed in Table 4. These two metrics are calculated using the simulated and theoretical images. Larger SSIM and PSNR values indicate better-simulated images. Evidently, XPCT is the closest to the theoretical image and exhibits the least noise effect. XACT and DECT do not perform well on image quality assessment metrics because of the effect of Gaussian noise.
Table 5 displays the theoretical and simulated CNR results of the images in Fig. 7. The theoretical CNR shows XACT and DECT have similar resolving power. XACT performs better for tissues with large density differences, while DECT excels for tissues with small density differences. XPCT shows the highest CNR for large density differences, with resolving power between DECT and XACT for small density differences. In simulated results, DECT performs the worst overall, while XACT surpasses XPCT for tissues with large density differences, and XPCT excels for similar-density tissues. The theoretical CNR values are on the order of 1014, approaching infinity; however, reconstruction algorithm noise prevents infinite values. Simulated CNR values are lower due to noise impact. Comparing both on the same scale reveals XACT maintains excellent resolution for high density differences, XPCT performs the best for smaller differences, while DECT shows weakest performance, primarily due to photon statistical fluctuations proportional to the square root of emitted particles. In the DECT simulated results, increased statistical fluctuation from halving the photon emission affects both low-energy and high-energy slice images. Both projections deviate from true values due to statistical fluctuations. When performing material decomposition using Eq. 2, this deviation amplifies errors in calculating b1 and b2 [39]. Boxplots from Fig. 6 are shown in Fig. 8. White lines indicate median position, while white dots show mean position. Box height shows data dispersion, with bottom and top edges at 25th and 75th percentiles. The whiskers extend to the remaining data range. The boxplots show that XPCT has better data distribution than do DECT and XACT, indicating better phase information reconstruction and extraction.
| Lung (Inhale) | Lung (Exhale) | Adipose | Water (liquid) | ||
|---|---|---|---|---|---|
| XACT | Theoretical (×1014) | 23.10 | 15.52 | 7.47 | 2.36 |
| Simulated | 36.60 | 22.61 | 10.07 | 1.05 | |
| DECT | Theoretical (×1014) | 22.88 | 12.33 | 8.10 | 3.03 |
| Simulated | 17.05 | 16.34 | 0.83 | 0.57 | |
| XPCT | Theoretical (×1014) | 30.11 | 18.78 | 2.54 | 2.57 |
| Simulated | 14.63 | 8.68 | 1.26 | 3.92 |
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In brief, this section provides a quantitative evaluation of DECT and XPCT compared to XACT. Results show XPCT performs relatively better in several performance metrics.
While the SMSS EI-based XPCT method is easier to implement, misalignments in mask position during gantry movement can invalidate calibration, requiring more precise equipment. Radiation safety is crucial in medical applications. Though radiation dose is comparable, exposure time is significantly longer due to reduced X-ray efficiency. Research shows optimizing the mask [40] and reducing exposure through low-dose irradiation [31] can address this. The method requires specific detector capabilities, as pixel crosstalk affects detection sensitivity, making direct-conversion or photon-counting detectors more suitable.
In this study, soft-tissue models with low-density and similar tissues are used owing to limited data on other tissues, and such tissue differentiation remains challenging in clinical diagnosis. XPCT offers a new technique for this, though complex situations require further biological experiments for resolution.
Conclusion
In this study, we performed a systematic comparative evaluation of DECT and SMSS EI-based XPCT for soft-tissue phantoms using a comprehensive evaluation system. Multiple metrics demonstrate that XPCT outperformed DECT, due to XPCT’s sensitivity to low-density objects and excessive statistical fluctuations in DECT. The SMSS EI-based XPCT shows potential for fast, accurate imaging through its simple, robust setup. This system provides a reliable method for evaluating imaging technology advancements and comparing algorithms, enabling efficient quantitative analysis for non-specialists. These findings confirm XPCT’s significance in medical research and its sensitivity to low-density objects.
For objects with similar densities, XPCT shows clear advantages, whereas XACT excels with small densities and large differences, and DECT has optimization potential in algorithms and absorbed dose. In XPCT, SMSS EI method optimally balances device complexity and phase information extraction accuracy. The SMSS EI method’s noise resistance and simple setup enable practical low-dose, large field XPCT applications. The widespread adoption of XPCI technology in medical fields like lung, breast, musculoskeletal, and dental imaging is inevitable [41]. Challenges remain in radiation dose, acquisition time, field restrictions, and stability. Due to dose limitations, DECT requires more focus on dose restrictions, making radiation dose reduction a key research area, with dual-layer or photon-counting detectors showing promise [42-45]. XPCI development will advance through sources, absorption masks, phase gratings, and detectors, with hardware and hybrid upgrades impacting XPCT information extraction [46].
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