一般注記Anodic stripping voltammetry was made in AgNO3 solution, here Ag was deposited under long term potentiostatic conditions to evaluate the reduction charge, qr, and then was stripped by linear sweep voltammetry to determine the oxidation charge, qo. The charges were unbalanced, satisfying ca. qo=0.7|qr|, where other possible reduction charge such as by dioxygen and dichlorosilver were subtracted. The 30 % loss of the anodic charge can be ascribed to the negative capacitance by the potential sweep generation of Ag+. The generated Ag+ forms a dipole with a counter ion, of which orientation is the same as the direction of the externally applied electric field and opposite to the dipoles of solvent. The redox dipole decreases the conventional double layer capacitance caused by solvent dipoles, and high concentrations of Ag+ takes the capacitance to be negative values. The unbalanced charge, however, has no influence on quantitative determination of concentrations Ag+ by use of a calibration line.
一次資料へのリンクURLhttps://u-fukui.repo.nii.ac.jp/?action=repository_action_common_download&item_id=24517&item_no=1&attribute_id=22&file_no=1
連携機関・データベース国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）