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用于制备面向析氧反应和甲醇氧化反应的自支撑CoFe@PANI双功能电催化剂的层间连接策略

Layer interfacing strategy to derive free standing CoFe@PANI bifunctional electrocatalyst towards oxygen evolution reaction and methanol oxidation reaction.

作者信息

Rajpure Manoj M, Jadhav Harsharaj S, Kim Hern

机构信息

Department of Energy Science and Technology, Environmental Waste Recycle Institute, Myongji University, Yongin, Gyeonggi-do 17058, Republic of Korea.

Centre for Materials for Electronics Technology (C-MET), Pune 411 008, India.

出版信息

J Colloid Interface Sci. 2024 Jan;653(Pt A):949-959. doi: 10.1016/j.jcis.2023.09.123. Epub 2023 Sep 24.

DOI:10.1016/j.jcis.2023.09.123
PMID:37776722
Abstract

Developing inexpensive, highly electrochemically active, and stable catalysts towards electrochemical studies remains challenge for researchers. In this regard, binder-free CoFe@PANI composite electrocatalyst is deposited on nickel foam (NF) substrate via successive electrodeposition of polyaniline (PANI) and CoFe-LDH at Room temperature (RT). As deposited binder-free CoFe@PANI electrocatalyst displays high electrocatalytic activity towards oxygen evolution reaction (OER) and methanol oxidation reaction (MOR) in alkaline media. In CoFe@PANI structure, interfacing of high-electron conducting PANI establishes strong interconnection with CoFe-LDH by tuning electronic structures, which accelerates the electrochemical performance towards OER and MOR. For OER, CoFe@PANI requires low overpotential (η) of 237 mV to reach current density (I) of 10 mA cm and displays low Tafel slope value of 46 mV dec in 1 M KOH solution. Also, it displayed specific I of 120 mA cm, when it was tested for MOR in 1 M KOH with 0.5 M methanol solution. The superior electrocatalytic activity of CoFe@PANI is mainly ascribed to high electrochemical active surface area (ECSA), abundant active sites and fast electron transfer between electrocatalyst and electrode surface. Of note, the current work may open new era for design and development of non-precious highly active and stable hybrid electrocatalysts at RT for various applications.

摘要

开发价格低廉、具有高电化学活性且稳定的用于电化学研究的催化剂,对研究人员来说仍然是一项挑战。在这方面,通过在室温下依次电沉积聚苯胺(PANI)和CoFe-LDH,将无粘结剂的CoFe@PANI复合电催化剂沉积在泡沫镍(NF)基底上。所沉积的无粘结剂CoFe@PANI电催化剂在碱性介质中对析氧反应(OER)和甲醇氧化反应(MOR)显示出高电催化活性。在CoFe@PANI结构中,高电子传导性的PANI通过调节电子结构与CoFe-LDH建立了强相互连接,这加速了对OER和MOR的电化学性能。对于OER,CoFe@PANI在1 M KOH溶液中达到10 mA cm的电流密度(I)时需要237 mV的低过电位(η),并且显示出46 mV dec的低塔菲尔斜率值。此外,当在含有0.5 M甲醇溶液的1 M KOH中对其进行MOR测试时,它显示出120 mA cm的比电流(I)。CoFe@PANI优异的电催化活性主要归因于高电化学活性表面积(ECSA)、丰富的活性位点以及电催化剂与电极表面之间快速的电子转移。值得注意的是,当前的工作可能为室温下设计和开发用于各种应用的非贵金属高活性和稳定的混合电催化剂开启新的时代。

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