Atomically Engineered Cobalt-doped Boron Nitride Nanosheets for Water Oxidation Reaction

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL
Arunmuthukumar Pugalendhi, Suprobhat Singha Roy, Suganthi Periyadurai, Amuthan Dekshinamoorthy, Saranyan Vijayaraghavan, Gosipathala Sreedhar, Subrata Kundu
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引用次数: 0

Abstract

Hexagonal boron nitride (h-BN) is a fascinating two-dimensional material with a wide range of potential applications. However, its application in electrocatalysis is limited due to the lack of proper active sites and poor electrical conductivity. Herein, we introduce cobalt as a dopant into h-BN nanosheets using a controlled molten salt technique at elevated temperature. The structural and morphological analysis confirms the successful formation of h-BN and cobalt-doped BN nanosheets. The presence of cobalt in the h-BN nanosheets disrupts the extended π conjugation of h-BN by electronically interacting with B and N. While bare h-BN exhibits poor catalytic activity towards the oxygen evolution reaction (OER), cobalt doping significantly enhances its performance. The Cobalt centers serve as the active sites for OER, with the material containing 2.5 weight% Cobalt (Co2.5-BN) demonstrating optimized catalytic performance, demanding only 322 mV overpotential at 10 mA/cm2 current density along with a robust stability of 20 hours. A turnover frequency (TOF) of 1.0 s-1 at 400 mV overpotential highlights the high intrinsic activity of Co2.5-BN. The in-situ EIS analysis reveals the fast kinetics and supports the proposed equivalent electrical circuit model at the electrode/electrolyte interface. This study utilizes the structural features of h-BN material via cobalt doping towards enhanced OER catalysis.
用于水氧化反应的原子工程钴掺杂氮化硼纳米片
六方氮化硼(h-BN)是一种具有广泛应用潜力的二维材料。然而,由于缺乏合适的活性位点和导电性差,其在电催化中的应用受到限制。在此,我们使用受控熔盐技术在高温下将钴作为掺杂剂引入h-BN纳米片。结构和形态分析证实了h-BN和钴掺杂BN纳米片的成功形成。h-BN纳米片中钴的存在通过与B和n的电子相互作用破坏了h-BN的扩展π共轭,而裸h-BN对析氧反应(OER)的催化活性较差,钴掺杂可显著提高其性能。钴中心作为OER的活性位点,含有2.5重量%钴(Co2.5-BN)的材料显示出优化的催化性能,在10 mA/cm2电流密度下仅需322 mV过电位,并具有20小时的稳定性能。在400mv过电位下,转换频率(TOF)为1.0 s-1,表明co25 - bn具有较高的固有活性。原位EIS分析显示了快速动力学,并支持所提出的电极/电解质界面等效电路模型。本研究利用氢氮化硼材料的结构特点,通过钴掺杂来增强OER催化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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