电催化剂
介孔材料
析氧
电极
氧气
材料科学
电荷(物理)
无机化学
氧还原反应
化学
催化作用
物理化学
电化学
物理
生物化学
有机化学
量子力学
作者
Assel Amirzhanova Katırcı,Irmak Karakaya Durukan,Ömer Dag
标识
DOI:10.1021/acsaem.4c03305
摘要
Stable electroactive mesoporous Ni1–xMnxO thin-film electrodes are fabricated over FTO and graphite rods using the molten-salt-assisted self-assembly (MASA) method. Ethanol solutions of two salts ([Mn(H2O)4](NO3)2 and [Ni(H2O)6](NO3)2 with varying Ni(II)/Mn(II) mole ratios, 1.0 to 0.1) and two surfactants (C12H25(OCH2CH2)10OH, C12E10 and C16H33N(CH3)3Br, CTAB) are coated over a conducting substrate (FTO and graphite rod) to assemble the salt–surfactant lyotropic liquid crystalline (LLC) mesophase that is calcined to obtain a mesoporous Ni1–xMnxO thin-film electrode. Ni1–xMnxO is a solid solution up to x of 0.7, but it transforms the NiMnO3, Mn3O4, and Mn2O3 phases in the samples with x values of 0.5 and higher at higher annealing temperatures. FTO and graphite-coated (F-Ni1–xMnxO and G-Ni1–xMnxO) electrodes have a high charge capacity, but the FTO-coated electrodes are unstable and undergo degradation. They display an increasing charge capacity during early CV cycles (or consecutive GCD measurements) but decay in capacity over long-term experiments. The G-Ni1–xMnxO electrodes are more robust and display high charge capacities (958 C/g in pure NiO and 720 C/g in Ni0.9Mn0.1O, close to the theoretical values). During the electrochemical tests, both pure NiO and Ni1–xMnxO electrodes transform to core-NiO/shell-Ni(OH)2 and core-Ni1–xMnxO/shell-Ni(OH)2 structures on the pore walls, respectively. The shell thickness decreases from 2.0 nm in pure NiO to 1.1 nm with 10% Mn(II) addition in Ni0.9Mn0.1O at 350 °C. Moreover, the shell thickness is also dependent on the pore-wall thickness that increases exponentially with annealing temperature (from 4.4 to 27.1 nm in pure NiO and 4.0 to 12 nm in Ni0.9Mn0.1O by increasing the temperature from 350 to 500 °C, respectively). It increases from 2.0 to 4.5 nm in pure NiO and 1.1 to 1.5 nm in the Ni0.9Mn0.1O electrodes at those temperatures, respectively, and determines the charge capacity of the electrodes. The addition of manganese significantly improves the stabilities of the electrodes but almost has no effect on the overpotential of the electrodes. Even though the charge capacity depends on the annealing temperature, OER performance almost shows no effect on the annealing temperature.
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