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Cathodic H_2 Evolution from Molten HF,H_2O and H_O~+ Solvates,and the Nature of the Catalytic Surface for H_2 Formation

机译:来自熔融HF,H_2O和H_O〜+溶剂化物的阴极H_2进化,以及H_2形成的催化表面的性质

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The cathodic H_2 evolution reaction (the HER) has been studied primarily from aqueous solutions though significant works have reported results on the kinetics of the HER from alcoholic [1] and some other [2] solvents with the purpose of examining proton solvation effects in the initial discharge step [1,2] and the role of proton-tunneling [3] in that step.On the other hand,rather little work has been done on studies of the HER from proton sources at low activity,e.g.in KF-2HF and its aqueous analogue,K or NaOHcentre dot2H_2O.In the former case the anion is FHF with solvation of K~+ and the F~- anion by the second HF molecule.
机译:虽然重大作用据报道了来自酒精[1]的动力学的显着作用,但虽然有重大作用,但是虽然显着的作品,但是含有含酒精的动力学的结果,但是在含酒精[1]和一些其他[2]溶剂的目的中的目的是检查质子溶剂化效应的结果,还研究了阴极的H_2的进化反应初始排放步骤[1,2]和质子隧道的作用[3]在该步骤中。另一方面,在低活性的质子源的研究中,对她的研究已经完成了相反的工作,EGIN KF-2HF及其水性类似物,K或Naohcentre Dot2H_2O.在前一种情况下,阴离子是具有k〜+和第二次HF分子的F〜阴离子的FHF。

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