Subjects -> CHEMISTRY (Total: 928 journals)
    - ANALYTICAL CHEMISTRY (59 journals)
    - CHEMISTRY (661 journals)
    - CRYSTALLOGRAPHY (23 journals)
    - ELECTROCHEMISTRY (28 journals)
    - INORGANIC CHEMISTRY (45 journals)
    - ORGANIC CHEMISTRY (47 journals)
    - PHYSICAL CHEMISTRY (65 journals)

ELECTROCHEMISTRY (28 journals)

Showing 1 - 25 of 25 Journals sorted alphabetically
Anti-Corrosion Methods and Materials     Hybrid Journal   (Followers: 11)
Batteries     Open Access   (Followers: 10)
Batteries & Supercaps     Hybrid Journal   (Followers: 5)
ChemElectroChem     Hybrid Journal   (Followers: 9)
Chemistry of Heterocyclic Compounds     Hybrid Journal   (Followers: 5)
Corrosion Engineering, Science and Technology     Hybrid Journal   (Followers: 36)
Current Opinion in Electrochemistry     Hybrid Journal   (Followers: 4)
ECS Journal of Solid State Science and Technology     Hybrid Journal   (Followers: 7)
Electrocatalysis     Hybrid Journal   (Followers: 4)
Electrochemical Science Advances     Open Access   (Followers: 4)
Electrochemistry Communications     Open Access   (Followers: 15)
Electrochimica Acta     Hybrid Journal   (Followers: 28)
IEEE Journal of Photovoltaics     Hybrid Journal   (Followers: 16)
International Journal of Electrochemistry     Open Access   (Followers: 10)
International Journal of Electronics Letters     Hybrid Journal   (Followers: 1)
Journal of Applied Electrochemistry     Hybrid Journal   (Followers: 12)
Journal of Electrochemical Science and Engineering     Open Access   (Followers: 4)
Journal of New Materials for Electrochemical Systems     Free   (Followers: 7)
Journal of Solid State Electrochemistry     Hybrid Journal   (Followers: 7)
Journal of The Electrochemical Society     Hybrid Journal   (Followers: 22)
Materials and Corrosion     Hybrid Journal   (Followers: 14)
Portugaliae Electrochimica Acta     Open Access  
Reports in Electrochemistry     Open Access   (Followers: 5)
Russian Journal of Electrochemistry     Hybrid Journal   (Followers: 4)
Surface Engineering and Applied Electrochemistry     Hybrid Journal   (Followers: 7)
Similar Journals
Journal Cover
International Journal of Electrochemistry
Number of Followers: 10  

  This is an Open Access Journal Open Access journal
ISSN (Print) 2090-3529 - ISSN (Online) 2090-3537
Published by Hindawi Homepage  [339 journals]
  • Enabling the Electrochemical Performance of Maricite-NaMnPO4 and
           Maricite-NaFePO4 Cathode Materials in Sodium-Ion Batteries

    • Abstract: NaMnPO4 and NaFePO4, polyanion cathode materials, exist in two different phases maricite/natrophilite and maricite/olivine, respectively. Both natrophilite NaMnPO4 and olivine NaFePO4 are electrochemically active and possess a one-dimensional tunnel for sodium-ion migration; however, these two phases are thermodynamically unstable. Therefore, they can be synthesized through an electrochemical route. On the contrary, maricite (m)-NaMnPO4 and maricite (m)-NaFePO4 are thermodynamically stable forms but have a huge activation energy of their diffusion pathways for sodium extraction and insertion in the crystal structure, which hinders electrochemical reactions. Therefore, the electrochemical behaviour of commercial m-NaMnPO4 and m-NaFePO4 has been studied to find a way for enabling them electrochemically. Ball milling and thermal/mechanical carbon coating are employed to reduce the particle size to enhance the electrochemical performance and shorten the diffusion pathway. Moreover, ball milling leads to defects and partial phase transformation. The electrochemical performance of milled-coated NaMnPO4 and NaFePO4 has been thoroughly investigated and compared. The phase transition of NaFePO4 is revealed by a differential scanning calorimeter. As a result, the achievable capacities of both cathode materials are significantly enhanced up to ∼50 mAh.g−1 via the particle size reduction as well as by carbon coating. However, the side reactions and agglomeration problems in such materials need to be minimized and must be considered to enable them for applications.
      PubDate: Fri, 27 Jan 2023 07:50:01 +000
       
  • Electrooxidation and Development of a Highly Sensitive Electrochemical
           Probe for Trace Determination of the Steroid 11-Desoxycorticosterone Drug
           Residues in Water

    • Abstract: Anabolic-androgenic steroids (AASs), a class of compounds frequently misused by competitors and unfortunately by the general population, have lately attracted international attention. Thus, extraordinary demands for developing low cost, precise, rapid, and facile protocols for detection and/or determination of AAS have arisen. Hence, the current strategy explores for the first time the redox features of 21-hydroxypregn-4-ene-3, 20-dione, namely, 11-desoxycorticosterone (DCS) AA drug steroid at a glassy-carbon electrode (GCE) in a wide pH range (pH 2.0–10.0) by adsorptive differential pulse-anodic stripping voltammetry (DP- ASV) and cyclic voltammetry (CV). At pH 2, DP-ASV and CV at the optimized pH 2–3 displayed an irreversible anodic peak at 0.4 V versus Ag/AgCl electrode. The dependency of the anodic peak current of the CV at 0.4 V at various concentrations and scan rate of the DCS drug was characteristic of an electrode-coupled electron transfer of EE type mechanism. At the optimized parameters, the proposed strategy allowed quantification of DCS in the concentration range 2.5 -13.19 nM (0.83-4.36 ng mL−1) with satisfactory limits of detection (LOD) and quantization (LOQ) of 9.3 × 10−1 nM (3.1 × 10−1 ng mL−1) and 3.1 nM (1.02 ng mL−1), respectively. A relative standard deviation (RSD) of ±3.93% (n = 5) at 4.0 ng mL−1 DCS was achieved. The established probe was fruitfully employed and validated for trace determination of DCS residues in environmental water. The interference of several common diverse species on DCS sensing was insignificant revealing good selectivity. The established probe exhibited good sensitivity, selectivity, precision, and accuracy, short analytical time, and low cost compared with the reported methods, for DCS determination.
      PubDate: Wed, 04 May 2022 16:35:00 +000
       
 
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