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A SERS Investigation of Cyanide Adsorption and Reactivity during the Electrodeposition of Gold, Silver and Copper from Aqueous Cyanocomplexes Solutions

机译:sERs对氰化物吸附和反应活性的研究   从含水氰基复合物中电沉积金,银和铜   解决方案

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摘要

In this paper we report on the reactivity of adsorbed cyanide deriving fromligand release during metal electrodeposition from cyanocomplex solutions ofAu(I), Au(III), Ag(I) and Cu(I) in H2O and D2O. When CN is adsorbed at cathodicpotentials in excess of the HER threshold, metal-dependent reactivity can bedetected by SERS. Finite surface coverages with adsorbed CN at such cathodicpotentials can be obtained only if CN is delivered directly to the cathodesurface as by decomplexing of the cyanocomplexes of the metals undergoingcathodic reduction. In Au(I) and Au(III) baths, Au-CN reacts with Au-H and ishydrogenated to adsorbed CH2=NH and CH3-NH2. In Ag(I) baths, Ag-CN reacts withAg-H giving rise to polycyanogens. No reactivity of Cu-CN was found, underotherwise identical conditions. Our conclusions are supported also by dedicatedDFT molecular computations.
机译:在本文中,我们报告了金属电沉积过程中,Au(I),Au(III),Ag(I)和Cu(I)在H2O和D2O中的氰基络合物溶液在金属电沉积过程中源自配体释放的吸附氰化物的反应性。当CN在超过HER阈值的阴极电位上吸附时,可以通过SERS检测到金属依赖性反应性。只有在CN直接传递到阴极表面的情况下,如通过阴极还原金属的氰基络合物的分解,才能获得在这种阴极电位吸附有CN的有限表面覆盖率。在Au(I)和Au(III)浴中,Au-CN与Au-H反应并氢化成吸附的CH2 = NH和CH3-NH2。在Ag(I)浴中,Ag-CN与Ag-H反应生成多氰。在其他相同条件下,未发现Cu-CN的反应性。专用DFT分子计算也支持我们的结论。

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