一种分子(NCS2)Ni(II)电催化剂类似于[NiFe]氢化酶的氢演化途径

Soumalya Sinha, Giang N Tran, Hanah Na, Liviu M. Mirica
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引用次数: 0

摘要

电化学析氢反应(HER)被认为是推进燃料电池技术的可持续能源途径,而类似于[NiFe]氢化酶的HER电催化剂是非常需要的。在此,我们报道了一种生物激发的Ni(II)配合物(NCHS2)Ni(OTf)2,其中NCHS2为3,7-二硫-1(2,6)-吡啶-5(1,3)-苯并环己烷,它是一种高效的HER电催化剂,在低酸浓度存在下的周转率高达400,000 s-1,与其他已报道的Ni HER电催化剂相比具有优势。重要的是,在该配合物中,合理设计的NCHS2配体经历了C-H键激活,由此产生的有机金属Ni-芳基配合物限制了Ni(0)的形成,这类似于半胱氨酸配体在[NiFe]氢化酶中的作用。此外,这种电催化剂通过可检测的Ni(I)/Ni(III)中间体遵循独特的HER机制,这些中间体也被提出用于[NiFe]氢化酶,但迄今为止尚未在模型系统中观察到这种机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A molecular (NCS2)Ni(II) electrocatalyst resembles [NiFe]hydrogenase pathway for H2 evolution
The electrochemical hydrogen evolution reaction (HER) is considered a sustainable energy approach to advance fuel-cell technologies, and HER electrocatalysts that resembles the [NiFe] hydrogenases are highly desired. Herein, we report a bioinspired Ni(II) complex (NCHS2)Ni(OTf)2, where NCHS2 is 3,7-dithia-1(2,6)-pyridina-5(1,3)-benzenacyclooctaphane, that is an efficient electrocatalyst for HER with turnover frequencies up to 400,000 s–1 in the presence of low acid concentration, and compares favorably with the other reported Ni HER electrocatalysts. Importantly, in this complex the rationally designed NCHS2 ligand undergoes C-H bond activation and the resulting organometallic Ni-aryl complex restricts the formation of a Ni(0) species, which resembles the role of the cysteine ligands in [NiFe] hydrogenases. In addition, this electrocatalyst follows a unique HER mechanism via detectable Ni(I)/Ni(III) intermediates that are also proposed for [NiFe] hydrogenases, yet such a mechanism has not been observed to date in model systems.
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