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DNA 辅助非晶态钴氢氧化物表面修饰作为无粘结剂电极用于电化学氧气析出反应。

Surface Decoration of DNA-Aided Amorphous Cobalt Hydroxide Ag Ions as Binder-Free Electrodes toward Electrochemical Oxygen Evolution Reaction.

机构信息

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.

Electrochemical Process Engineering (EPE) Division, CSIR-Central Electrochemical Research Institute (CECRI), Karaikudi 630003, Tamil Nadu, India.

出版信息

Inorg Chem. 2021 Feb 15;60(4):2680-2693. doi: 10.1021/acs.inorgchem.0c03569. Epub 2021 Feb 3.

Abstract

Out of various available methods, generation of hydrogen by electrocatalytic water splitting is the most accepted one which consists of two half-cell reactions, , oxygen evolution reaction (OER) at the anode and hydrogen evolution reaction at the cathode. OER is a complex four-electron transfer process, and to sustain the spontaneous generation of hydrogen at the cathode, it is urgent to develop some earth-abundant, low-cost electrode materials. Recently, use of cobalt-based hydroxide as the electrode substrate has taken much consideration and has been fabricated over various substrates. Because of various structural disorders, internal resistance, and dependence on the electrode, the binder substrate makes their applications limited. Here, in this work, to remove structural disorder and to increase electrical conductivity, we have incorporated silver ions into amorphous Co(OH), which turns to be a highly active OER electrocatalyst. Also, for the first time, we have developed hydroxide-based materials by using DNA as a stabilizer, and most importantly, using DNA gives an immense opportunity to run long-term OER applications without using an external binder such as nafion. Moreover, for the first time, these DNA-based materials were coated on nickel foam mainly to eliminate the low conductive nature of AgO. The synthesized catalyst showed a very high OER activity, and to reach 50 mA/cm current density, it needs only 260 mV as overpotential. The amorphous nature of hydroxide-based materials gives a higher opportunity toward the electrolyte to bind on the surface of a catalyst to run the OER with less applied overpotentials.

摘要

在各种可用的方法中,通过电催化水分解生成氢气是最被接受的方法,它由两个半反应组成,阳极的析氧反应(OER)和阴极的析氢反应。OER 是一个复杂的四电子转移过程,为了在阴极自发地产生氢气,迫切需要开发一些丰富、低成本的电极材料。最近,使用钴基氢氧化物作为电极基底得到了很多关注,并在各种基底上进行了制备。由于各种结构无序、内阻和对电极的依赖性,粘结剂基底使其应用受到限制。在这项工作中,为了消除结构无序并提高电导率,我们将银离子掺入非晶态 Co(OH)2 中,使其成为一种高活性的 OER 电催化剂。此外,我们首次使用 DNA 作为稳定剂来开发基于氢氧化物的材料,最重要的是,使用 DNA 为无需使用外部粘结剂(如 Nafion)运行长期 OER 应用提供了巨大的机会。此外,这些基于 DNA 的材料首次被涂覆在镍泡沫上,主要是为了消除 AgO 的低导电性。合成的催化剂表现出非常高的 OER 活性,为了达到 50 mA/cm 的电流密度,仅需要 260 mV 的过电势。基于氢氧化物的材料的非晶态为电解质提供了更高的机会,使其能够在催化剂表面结合,以较低的应用过电势进行 OER。

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