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    <loc>https://www.unityvoltsolutions.com/blog/cell-kpi-summary</loc>
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    <loc>https://www.unityvoltsolutions.com/blog/afm-xas-nmr-advanced-characterization-li-ion</loc>
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    <loc>https://www.unityvoltsolutions.com/blog/bet-dsc-tga-physical-thermal-properties-li-ion-cathodes</loc>
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      <image:title>Blog - 1.6. Physical &amp;amp; Thermal Properties (BET &amp;amp; DSC/TGA) - Make it stand out</image:title>
      <image:caption>Figure 1. Nitrogen adsorption–desorption isotherms and calculated pore-size distributions of different LFP/C powders (see article 1.3, Fig. 1 for info on these powders). In the main graph, the x-axis shows relative nitrogen pressure while the y-axis shows the amount of nitrogen adsorbed by the powder. Nitrogen uptake across a range of pressures is recorded, and the resulting data is analysed mathematically to calculate specific surface area, accessible pore volume and pore-size distribution. Image Source: Peng et al. 2023</image:caption>
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    <image:image>
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      <image:title>Blog - 1.6. Physical &amp;amp; Thermal Properties (BET &amp;amp; DSC/TGA) - Make it stand out</image:title>
      <image:caption>Figure 2. Simultaneous DSC–TGA analysis of the carbon-coated LFP/C-0 powder. The sample was heated from 25 to 700°C at 10°C min⁻¹ in flowing air. The black TGA curve, read against the left axis, shows changes in sample mass, while the red DSC curve, read against the right axis, shows heat absorbed or released during heating. The upward direction is exothermic.</image:caption>
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    <loc>https://www.unityvoltsolutions.com/blog/tem-hrtem-nanostructure-imaging-li-ion-cathodes</loc>
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      <image:title>Blog - 1.5. Nanostructure Imaging (TEM &amp;amp; HRTEM) - Make it stand out</image:title>
      <image:caption>Figure 1. TEM (g) and HRTEM (h) images of the carbon-coated LFP/C-60 sample from Peng et al. 2023.</image:caption>
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    <loc>https://www.unityvoltsolutions.com/blog/raman-ftir-lattice-vibrations-li-ion-materials</loc>
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    <lastmod>2026-07-15</lastmod>
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      <image:title>Blog - 1.4. Vibrational Spectroscopy (Raman &amp;amp; FTIR) - Figure 1. Raman spectrum of carbon-coated LiFePO₄/C prepared using urea-assisted combustion, with sucrose used as the carbon source, followed by heat treatment at 600°C. The x-axis, Raman shift (cm⁻¹), identifies different vibrational modes, while the y-axis, intensity (a.u.), shows their relative signal strength.</image:title>
      <image:caption>Raman spectrum of carbon-coated LiFePO₄/C prepared using urea-assisted combustion, with sucrose used as the carbon source, followed by heat treatment at 600°C. The x-axis, Raman shift (cm⁻¹), identifies different vibrational modes, while the y-axis, intensity (a.u.), shows their relative signal strength.</image:caption>
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    <image:image>
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      <image:title>Blog - 1.4. Vibrational Spectroscopy (Raman &amp;amp; FTIR) - Figure 2. FTIR spectrum of the same carbon-coated LiFePO₄/C material after heat treatment at 600°C. The x-axis, wavenumber (cm⁻¹), identifies the vibrational energy, while the y-axis, transmittance (%), shows how much infrared light passes through the sample. Because this is a transmittance spectrum, the downward features represent infrared absorption bands.</image:title>
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  <url>
    <loc>https://www.unityvoltsolutions.com/blog/xrd-xps-structural-surface-chemistry-li-ion-cathodes</loc>
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    <priority>0.5</priority>
    <lastmod>2026-07-15</lastmod>
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      <image:title>Blog - 1.3. Structural &amp;amp; Surface Chemistry (XRD &amp;amp; XPS) - Make it stand out</image:title>
      <image:caption>Figure 1. XRD patterns of three carbon-coated LFP samples prepared using different mixtures of phytic acid and phosphoric acid as the phosphorus source. LFP/C-0, LFP/C-60 and LFP/C-100 used 0%, 60% and 100% phytic acid, respectively; the remainder was phosphoric acid. These names describe the synthesis route and do not indicate carbon content or material grade. Image Source: Peng et al. 2023</image:caption>
    </image:image>
    <image:image>
      <image:loc>https://images.squarespace-cdn.com/content/v1/6870a61da3af0b47861cbcf1/4b216cda-432d-4e4f-9811-a4adf17caf1a/lfp-xps-surface-chemistry-spectra.png</image:loc>
      <image:title>Blog - 1.3. Structural &amp;amp; Surface Chemistry (XRD &amp;amp; XPS) - Make it stand out</image:title>
      <image:caption>Figure 2. XPS survey and high-resolution spectra of the carbon-coated LFP/C-60 sample. Panel (a) is a broad survey scan showing the elements detected at the particle surface. Panels (b)–(e) examine the Fe 2p, P 2p, C 1s and O 1s regions in more detail. The The x-axis, binding energy (eV), indicates how strongly an electron is bound to an atom, and helps identify the element and its chemical state, while the y-axis, intensity (a.u.), shows the relative strength of the detected signal. Image Source: Peng et al. 2023</image:caption>
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  <url>
    <loc>https://www.unityvoltsolutions.com/blog/fe-sem-eds-morphology-composition-li-ion-cathodes</loc>
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    <lastmod>2026-07-15</lastmod>
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      <image:title>Blog - 1.2. Morphology &amp;amp; Composition (FE-SEM &amp;amp; EDS) - Make it stand out</image:title>
      <image:caption>Figure 1. FE-SEM images of three LiFePO₄/C samples showing differences in particle morphology, surface texture, carbon distribution and agglomeration, together with corresponding EDS elemental maps for Fe, C, O and P. Panel (b) shows the most regular secondary-particle morphology and uniform distribution, while panel (a) contains visible amorphous-carbon-rich regions and panel (c) shows substantial agglomeration. Note: Conventional SEM–EDS does not reliably detect lithium and cannot independently confirm LFP phase purity, elemental stoichiometry or carbon-coating thickness. XRD, XPS and TEM provide complementary information. Image Source: Peng et al. 2023</image:caption>
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