过电位
材料科学
多金属氧酸盐
电化学
X射线光电子能谱
逐层
催化作用
化学工程
聚合物
吸附
极化(电化学)
电极
图层(电子)
无机化学
纳米技术
物理化学
有机化学
复合材料
化学
工程类
作者
Indherjith Sakthinathan,Jonas Köhling,Veit Wagner,Timothy McCormac
标识
DOI:10.1021/acsami.2c17397
摘要
In this contribution, a nanoarchitectural approach was employed to produce a nanolayer of polyoxometalate (POM) on the surface of a glassy carbon electrode (GCE) to achieve a higher surface area with higher electrocatalytic activity toward the electrochemical hydrogen evolution reaction (HER). To accomplish this, the well-known layer-by-layer (LbL) technique was employed, which involved the alternate adsorption of the POM, Na0.3[N(C4H9)4]7.7 [(Mo3O8)4(O3PC(O)(C3H6NH2CH2C4H3S)PO3)4], abbreviated as [(TBA)Mo12(AleThio)4], and polyethyleneimine (PEI) polymer. This nanolayered electrode exhibited catalytic properties toward the HER in 0.5 M H2SO4 with the resulting polarization curves indicating an increase in the HER activity with the increasing number of POM layers, and the overpotential required for this reaction was lowered by 0.83 V when compared with a bare GCE. The eighth PEI/[(TBA)Mo12(AleThio)4] bilayer exhibited a significantly lower HER overpotential of -0.077 V at a current density of 10 mA cm-2. Surface characterization of the LbL-assembled nanolayers was carried out using X-ray photoelectron spectroscopy, atomic force microscopy, and scanning electron microscopy. We believe that the synergetic effect of the positively charged PEI polymer and the catalytically active molybdate POM is the cause for the successful response to the electrochemical HER.
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