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electrochemical analyzer vertex eis  (Ivium Technologies USA)

 
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    Ivium Technologies USA electrochemical analyzer vertex eis
    Molecular‐ and microscale characterizations of heterophilic CNT yarns a) Visualization of the surface property in CNT yarn during half‐immersion <t>electrochemical</t> oxidation (HECO) treatment. Optical photographs of a homophobic (left panel) and a heterophilic (right panel) CNT yarn, and a false color mapping representing the contact angle along the CNT yarn length during HECO (middle panel). Deconvoluted C1s X‐ray photoelectron spectroscopy (XPS) spectra of the b) HPB and c) HPL regions. d) Time dependence of the sprayed water amount and e) the spray rate of an ultrasonic humidifier calculated at 1‐second intervals (the number of samples = 4). f) Time dependence of yarn weight% of the HPB and HPL regions during a single hydration/dehydration cycle (inset: optical photographs of the HPL region at initial and fully hydrated states, scale bar = 100 µm). g) Schematic illustration depicting hydration‐induced volume expansion affecting the yarn radius ( r ), individual CNT bundle length ( L s ), and the number of twists ( n ) of one‐chiral McKibben structure. h) Scanning electron microscopy (SEM) images of the microscale structure of the HPB region at low (upper panel) (scale bar = 30 µm) and high magnifications (lower panel) (scale bar = 2 µm). i) 3D atomic force microscopy (AFM) mapping (upper panel) and height profile (lower panel) of the HPB region (size = 2.5 × 1.5 µm 2 ). Corresponding j) SEM images and k) AFM mapping and height profile of the HPL region.
    Electrochemical Analyzer Vertex Eis, supplied by Ivium Technologies USA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/electrochemical+analyzer+vertex+eis/electrochemical+analyzer+vertex+eis/pmc12272001-257-8-12
    Average 90 stars, based on 1 article reviews
    electrochemical analyzer vertex eis - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Dual‐Scale Hydration‐Induced Electrical and Mechanical Torsional Energy Harvesting in Heterophilically Designed CNT Yarns"

    Article Title: Dual‐Scale Hydration‐Induced Electrical and Mechanical Torsional Energy Harvesting in Heterophilically Designed CNT Yarns

    Journal: Advanced Materials (Deerfield Beach, Fla.)

    doi: 10.1002/adma.202501111

    Molecular‐ and microscale characterizations of heterophilic CNT yarns a) Visualization of the surface property in CNT yarn during half‐immersion electrochemical oxidation (HECO) treatment. Optical photographs of a homophobic (left panel) and a heterophilic (right panel) CNT yarn, and a false color mapping representing the contact angle along the CNT yarn length during HECO (middle panel). Deconvoluted C1s X‐ray photoelectron spectroscopy (XPS) spectra of the b) HPB and c) HPL regions. d) Time dependence of the sprayed water amount and e) the spray rate of an ultrasonic humidifier calculated at 1‐second intervals (the number of samples = 4). f) Time dependence of yarn weight% of the HPB and HPL regions during a single hydration/dehydration cycle (inset: optical photographs of the HPL region at initial and fully hydrated states, scale bar = 100 µm). g) Schematic illustration depicting hydration‐induced volume expansion affecting the yarn radius ( r ), individual CNT bundle length ( L s ), and the number of twists ( n ) of one‐chiral McKibben structure. h) Scanning electron microscopy (SEM) images of the microscale structure of the HPB region at low (upper panel) (scale bar = 30 µm) and high magnifications (lower panel) (scale bar = 2 µm). i) 3D atomic force microscopy (AFM) mapping (upper panel) and height profile (lower panel) of the HPB region (size = 2.5 × 1.5 µm 2 ). Corresponding j) SEM images and k) AFM mapping and height profile of the HPL region.
    Figure Legend Snippet: Molecular‐ and microscale characterizations of heterophilic CNT yarns a) Visualization of the surface property in CNT yarn during half‐immersion electrochemical oxidation (HECO) treatment. Optical photographs of a homophobic (left panel) and a heterophilic (right panel) CNT yarn, and a false color mapping representing the contact angle along the CNT yarn length during HECO (middle panel). Deconvoluted C1s X‐ray photoelectron spectroscopy (XPS) spectra of the b) HPB and c) HPL regions. d) Time dependence of the sprayed water amount and e) the spray rate of an ultrasonic humidifier calculated at 1‐second intervals (the number of samples = 4). f) Time dependence of yarn weight% of the HPB and HPL regions during a single hydration/dehydration cycle (inset: optical photographs of the HPL region at initial and fully hydrated states, scale bar = 100 µm). g) Schematic illustration depicting hydration‐induced volume expansion affecting the yarn radius ( r ), individual CNT bundle length ( L s ), and the number of twists ( n ) of one‐chiral McKibben structure. h) Scanning electron microscopy (SEM) images of the microscale structure of the HPB region at low (upper panel) (scale bar = 30 µm) and high magnifications (lower panel) (scale bar = 2 µm). i) 3D atomic force microscopy (AFM) mapping (upper panel) and height profile (lower panel) of the HPB region (size = 2.5 × 1.5 µm 2 ). Corresponding j) SEM images and k) AFM mapping and height profile of the HPL region.

    Techniques Used: Spectroscopy, Electron Microscopy, Microscopy

    Related Articles

    Impedance Spectroscopy:

    Article Title: Enhanced Hydro-Actuation and Capacitance of Electrochemically Inner-Bundle-Activated Carbon Nanotube Yarns.
    Article Snippet: Recently, several attempts have been made to activate or functionalize macroscopic carbon nanotube (CNT) yarns to enhance their innate abilities.. However, a more homogeneous and holistic activation approach that reflects the individual nanotubes constituting the yarns is crucial.. Herein, a facile strategy is reported to maximize the intrinsic properties of CNTs assembled in yarns through an electrochemical inner-bundle activation (EIBA) process.

    Article Title: Transition of Carbon Nanotube Sheets from Hydrophobicity to Hydrophilicity by Facile Electrochemical Wetting.
    Article Snippet: .. In addition, the electrochemical performances of the CNT/PET films were evaluated using an electrochemical analyzer (Vertex EIS, Ivium, Eindhoven, The Netherlands). .. The chemical composition and features of the CNT sheets were determined via XPS measurements performed (Versaprobe II, ULVAC–PHI, Kazaki, Kanagawa, Japan).

    Article Title: Dual‐Scale Hydration‐Induced Electrical and Mechanical Torsional Energy Harvesting in Heterophilically Designed CNT Yarns
    Article Snippet: Thermal images were captured using a near‐infrared camera (XI400, Optris) to assess heat distribution. .. All electrochemical performance evaluations were conducted using an electrochemical analyzer (Vertex EIS, Ivium). .. The mechanical properties of the yarn were measured using a universal testing machine (Instron 5966, Instron, Norwood, USA) at a strain rate of 0.5 mm min −1 .

    Article Title: Highly Elastically Deformable Coiled CNT/Polymer Fibers for Wearable Strain Sensors and Stretchable Supercapacitors.
    Article Snippet: While both ends of the coiled fiber are fixed and mounted onto digital Vernier calipers (Mitutoyo, Kawasaki, Japan), The electrical measurements were performed using multimeter probes (Fluke). .. The electrochemical measurements used an electrochemical analyzer (Vertex EIS, Ivium Soft 4.1100). ..

    Article Title: Electrochemically Oxidized Carbon Nanotube Sheets for High-Performance and Flexible-Film Supercapacitors.
    Article Snippet: Scanning electron microscopy (SEM) images of the CNT and EOT CNT sheet supercapacitors were captured using an S-4600 instrument (Hitachi, Tokyo, Japan). .. Their electrochemical performances were evaluated using an electrochemical analyzer (Vertex EIS, Ivium, Noord-Brabant, The Netherlands). .. In addition, multi-meter probes (Model 187, Fluke Corporation, Washington, USA) were employed to measure resistance.

    Article Title: Wearable and Washable MnO 2 −Zn Battery Packaged by Vacuum Sealing
    Article Snippet: Scanning electron microscope (SEM) images of the battery yarn electrodes were obtained (S−4600, Hitachi, Japan), along with optical images of the textile battery using an optical camera (D750, Nikon, Dokyo, Japan). .. In addition, the electrochemical performances of the nonpackaged and packaged textile batteries were evaluated using an electrochemical analyzer (Vertex EIS, Ivium, Eindhoven, Netherland). ..

    Article Title: Transition of Carbon Nanotube Sheets from Hydrophobicity to Hydrophilicity by Facile Electrochemical Wetting.
    Article Snippet: .. Then, a potentiostatic voltage (vs. Ag/AgCl) was applied using an electrochemical analyzer (Vertex EIS, Ivium, Eindhoven, The Netherlands). .. Scanning electron microscope (SEM) images of the CNT and ECW treated CNT sheets/PET film were obtained (S−4600, Hitachi, Tokyo, Japan), along with optical images of the film using an optical camera (D750, Nikon, Tokyo, Japan).

    Article Title: High–Performance Biscrolled Ni–Fe Yarn Battery with Outer Buffer Layer
    Article Snippet: The morphological information was obtained with SEM (S–4600, Hitachi, Japan) and optical microscopy (D750, Nikon, Japan). .. In addition, an electrochemical analyzer (Vertex EIS, Ivium) was used for all the electrochemical measurements. ..



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    electrochemical analyzer vertex eis  (Ivium Technologies USA)
    90
    Ivium Technologies USA electrochemical analyzer vertex eis
    Molecular‐ and microscale characterizations of heterophilic CNT yarns a) Visualization of the surface property in CNT yarn during half‐immersion <t>electrochemical</t> oxidation (HECO) treatment. Optical photographs of a homophobic (left panel) and a heterophilic (right panel) CNT yarn, and a false color mapping representing the contact angle along the CNT yarn length during HECO (middle panel). Deconvoluted C1s X‐ray photoelectron spectroscopy (XPS) spectra of the b) HPB and c) HPL regions. d) Time dependence of the sprayed water amount and e) the spray rate of an ultrasonic humidifier calculated at 1‐second intervals (the number of samples = 4). f) Time dependence of yarn weight% of the HPB and HPL regions during a single hydration/dehydration cycle (inset: optical photographs of the HPL region at initial and fully hydrated states, scale bar = 100 µm). g) Schematic illustration depicting hydration‐induced volume expansion affecting the yarn radius ( r ), individual CNT bundle length ( L s ), and the number of twists ( n ) of one‐chiral McKibben structure. h) Scanning electron microscopy (SEM) images of the microscale structure of the HPB region at low (upper panel) (scale bar = 30 µm) and high magnifications (lower panel) (scale bar = 2 µm). i) 3D atomic force microscopy (AFM) mapping (upper panel) and height profile (lower panel) of the HPB region (size = 2.5 × 1.5 µm 2 ). Corresponding j) SEM images and k) AFM mapping and height profile of the HPL region.
    Electrochemical Analyzer Vertex Eis, supplied by Ivium Technologies USA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/electrochemical+analyzer+vertex+eis/electrochemical+analyzer+vertex+eis/pmc12272001-257-8-12
    Average 90 stars, based on 1 article reviews
    electrochemical analyzer vertex eis - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier
    electrochemical analyzer (vertex eis  (Ivium Technologies USA)
    90
    Ivium Technologies USA electrochemical analyzer (vertex eis
    Molecular‐ and microscale characterizations of heterophilic CNT yarns a) Visualization of the surface property in CNT yarn during half‐immersion <t>electrochemical</t> oxidation (HECO) treatment. Optical photographs of a homophobic (left panel) and a heterophilic (right panel) CNT yarn, and a false color mapping representing the contact angle along the CNT yarn length during HECO (middle panel). Deconvoluted C1s X‐ray photoelectron spectroscopy (XPS) spectra of the b) HPB and c) HPL regions. d) Time dependence of the sprayed water amount and e) the spray rate of an ultrasonic humidifier calculated at 1‐second intervals (the number of samples = 4). f) Time dependence of yarn weight% of the HPB and HPL regions during a single hydration/dehydration cycle (inset: optical photographs of the HPL region at initial and fully hydrated states, scale bar = 100 µm). g) Schematic illustration depicting hydration‐induced volume expansion affecting the yarn radius ( r ), individual CNT bundle length ( L s ), and the number of twists ( n ) of one‐chiral McKibben structure. h) Scanning electron microscopy (SEM) images of the microscale structure of the HPB region at low (upper panel) (scale bar = 30 µm) and high magnifications (lower panel) (scale bar = 2 µm). i) 3D atomic force microscopy (AFM) mapping (upper panel) and height profile (lower panel) of the HPB region (size = 2.5 × 1.5 µm 2 ). Corresponding j) SEM images and k) AFM mapping and height profile of the HPL region.
    Electrochemical Analyzer (Vertex Eis, supplied by Ivium Technologies USA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/electrochemical+analyzer+vertex+eis/electrochemical+analyzer/pmc10650619-38-13-17
    Average 90 stars, based on 1 article reviews
    electrochemical analyzer (vertex eis - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Molecular‐ and microscale characterizations of heterophilic CNT yarns a) Visualization of the surface property in CNT yarn during half‐immersion electrochemical oxidation (HECO) treatment. Optical photographs of a homophobic (left panel) and a heterophilic (right panel) CNT yarn, and a false color mapping representing the contact angle along the CNT yarn length during HECO (middle panel). Deconvoluted C1s X‐ray photoelectron spectroscopy (XPS) spectra of the b) HPB and c) HPL regions. d) Time dependence of the sprayed water amount and e) the spray rate of an ultrasonic humidifier calculated at 1‐second intervals (the number of samples = 4). f) Time dependence of yarn weight% of the HPB and HPL regions during a single hydration/dehydration cycle (inset: optical photographs of the HPL region at initial and fully hydrated states, scale bar = 100 µm). g) Schematic illustration depicting hydration‐induced volume expansion affecting the yarn radius ( r ), individual CNT bundle length ( L s ), and the number of twists ( n ) of one‐chiral McKibben structure. h) Scanning electron microscopy (SEM) images of the microscale structure of the HPB region at low (upper panel) (scale bar = 30 µm) and high magnifications (lower panel) (scale bar = 2 µm). i) 3D atomic force microscopy (AFM) mapping (upper panel) and height profile (lower panel) of the HPB region (size = 2.5 × 1.5 µm 2 ). Corresponding j) SEM images and k) AFM mapping and height profile of the HPL region.

    Journal: Advanced Materials (Deerfield Beach, Fla.)

    Article Title: Dual‐Scale Hydration‐Induced Electrical and Mechanical Torsional Energy Harvesting in Heterophilically Designed CNT Yarns

    doi: 10.1002/adma.202501111

    Figure Lengend Snippet: Molecular‐ and microscale characterizations of heterophilic CNT yarns a) Visualization of the surface property in CNT yarn during half‐immersion electrochemical oxidation (HECO) treatment. Optical photographs of a homophobic (left panel) and a heterophilic (right panel) CNT yarn, and a false color mapping representing the contact angle along the CNT yarn length during HECO (middle panel). Deconvoluted C1s X‐ray photoelectron spectroscopy (XPS) spectra of the b) HPB and c) HPL regions. d) Time dependence of the sprayed water amount and e) the spray rate of an ultrasonic humidifier calculated at 1‐second intervals (the number of samples = 4). f) Time dependence of yarn weight% of the HPB and HPL regions during a single hydration/dehydration cycle (inset: optical photographs of the HPL region at initial and fully hydrated states, scale bar = 100 µm). g) Schematic illustration depicting hydration‐induced volume expansion affecting the yarn radius ( r ), individual CNT bundle length ( L s ), and the number of twists ( n ) of one‐chiral McKibben structure. h) Scanning electron microscopy (SEM) images of the microscale structure of the HPB region at low (upper panel) (scale bar = 30 µm) and high magnifications (lower panel) (scale bar = 2 µm). i) 3D atomic force microscopy (AFM) mapping (upper panel) and height profile (lower panel) of the HPB region (size = 2.5 × 1.5 µm 2 ). Corresponding j) SEM images and k) AFM mapping and height profile of the HPL region.

    Article Snippet: All electrochemical performance evaluations were conducted using an electrochemical analyzer (Vertex EIS, Ivium).

    Techniques: Spectroscopy, Electron Microscopy, Microscopy