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Haoyuan Chemexpress Co Ltd x ray diffraction xrd patterns
X Ray Diffraction Xrd Patterns, supplied by Haoyuan Chemexpress Co Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Article Title: Preparation of quinone modified graphene-based fiber electrodes and its application in flexible asymmetrical supercapacitor
Article Snippet: The flexible graphene fiber-based symmetic supercapacitors are usually greatly expected to power small wearable electronics because of their many potential applications.. In the present work, the organic electrochemically active material of quinone for asymmetric supercapacitors has been introduced to decorate graphene oxide nanosheets as negative electrodes via a facile hydrothermal self-assembly method.. Fortunately, 1,4-naphthoquinone (NQ) is a suitable choice for functionalizing graphene-based materials through noncovalent interactions.

Extraction:

Article Title: Preparation of quinone modified graphene-based fiber electrodes and its application in flexible asymmetrical supercapacitor
Article Snippet: The flexible graphene fiber-based symmetic supercapacitors are usually greatly expected to power small wearable electronics because of their many potential applications.. In the present work, the organic electrochemically active material of quinone for asymmetric supercapacitors has been introduced to decorate graphene oxide nanosheets as negative electrodes via a facile hydrothermal self-assembly method.. Fortunately, 1,4-naphthoquinone (NQ) is a suitable choice for functionalizing graphene-based materials through noncovalent interactions.

Spectrophotometry:

Article Title: Preparation of quinone modified graphene-based fiber electrodes and its application in flexible asymmetrical supercapacitor
Article Snippet: The flexible graphene fiber-based symmetic supercapacitors are usually greatly expected to power small wearable electronics because of their many potential applications.. In the present work, the organic electrochemically active material of quinone for asymmetric supercapacitors has been introduced to decorate graphene oxide nanosheets as negative electrodes via a facile hydrothermal self-assembly method.. Fortunately, 1,4-naphthoquinone (NQ) is a suitable choice for functionalizing graphene-based materials through noncovalent interactions.



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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) <t>Energy-dispersive</t> <t>X-ray</t> spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) <t>XRD</t> analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).
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Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) Energy-dispersive X-ray spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).

Journal: Bioactive Materials

Article Title: Smart microenvironment-adaptive nanocatalytic hydrogel for sequential antibacterial, anti-inflammatory, and regenerative therapy of biofilm-infected wounds

doi: 10.1016/j.bioactmat.2026.02.043

Figure Lengend Snippet: Structural characterization of HC. (A) Schematic illustration of the synthesis of HC. (B, C) TEM images of Cu 5.4 O and HC. (D) Energy-dispersive X-ray spectroscopy (EDS) mapping images of C, N, Cu and O for HC. (E) Zeta potentials and hydrodynamic size distribution, and (F) XRD analysis of Cu 5.4 O, HAs and HC. (G, H) XPS spectra of Cu 2p of Cu 5.4 O and HC. (I) X-ray-induced Auger electron spectroscopy (XAES) spectra of the Cu 5.4 O. (J) Size stability of HC in different solvents (Water, PBS, FBS, DMEM) on days 3, 5, and 7 at a concentration of 200 μg/mL, with a sample size of n = 3 (mean ± SD). (∗P < 0.05, ∗∗P < 0.01, ∗∗∗P < 0.001).

Article Snippet: X-ray diffraction (XRD) patterns were conducted on a Bruker D8 ADVANCE X-ray diffractometer using Cu-Kα radiation (λ = 1.5418 Å).

Techniques: Spectroscopy, Concentration Assay