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铁电极化与铁取代协同增强氯氧化铋纳米片中的电催化析氧反应

Ferroelectric Polarization and Iron Substitution Synergistically Boost Electrocatalytic Oxygen Evolution Reaction in Bismuth Oxychloride Nanosheets.

作者信息

Singh Dinesh, Joshi Bhavana, Poddar Pankaj

机构信息

Physical & Materials Chemistry Division, CSIR-National Chemical Laboratory, Pune 411008, India.

Academy of Scientific and Innovative Research (AcSIR), Sector 19, Kamla Nehru Nagar, Ghaziabad 201002, Uttar Pradesh, India.

出版信息

Langmuir. 2023 Aug 15;39(32):11414-11425. doi: 10.1021/acs.langmuir.3c01272. Epub 2023 Aug 1.

Abstract

Ferroelectric materials have gained significant interest in various kinds of water splitting, but the study of ferroelectric materials for electrocatalytic water splitting is in its infancy. Ferroelectric materials have spontaneous polarization below their Curie temperature due to dipolar alignment, which results in surface charges. In 2D ferroelectric materials, spontaneous polarization depends on thickness. Herein, we report that thickness-dependent ferroelectric polarization in 2D nanosheets can also accelerate the oxygen evolution reaction (OER) along with the tailored active surface area of exposed crystalline facets, which improves the electrocatalytic activity relatively. Iron-substituted BiOCl nanosheets of varying thickness are fabricated by varying the pH using a facile coprecipitation method. The substituted iron enhances polarization and electrochemical active sites on the surface. The findings in this study show that the exposed (001) facet and higher thickness of the nanosheets have high ferroelectric polarization and, in turn, superior electrocatalytic activity and remarkable stability, requiring low overpotentials (348 mV and 270 mV at 100 mA/cm and 10 mA/cm) in alkaline (1.0 M KOH) electrolyte. As the thickness of the nanosheets is decreased from 140 to 34 nm, the electrocatalytic performance of iron-substituted BiOCl nanosheets starts to reduce due to the lower Coulomb-Coulomb interaction and the increasing depolarization.

摘要

铁电材料在各种水分解反应中引起了广泛关注,但用于电催化水分解的铁电材料研究尚处于起步阶段。由于偶极排列,铁电材料在其居里温度以下具有自发极化,这导致了表面电荷。在二维铁电材料中,自发极化取决于厚度。在此,我们报道二维纳米片中与厚度相关的铁电极化,连同暴露晶面的定制活性表面积,也能加速析氧反应(OER),从而相对提高电催化活性。通过使用简便的共沉淀法改变pH值,制备了不同厚度的铁取代BiOCl纳米片。取代的铁增强了表面的极化和电化学活性位点。本研究结果表明,纳米片暴露的(001)晶面和较大的厚度具有高铁电极化,进而具有优异的电催化活性和显著的稳定性,在碱性(1.0 M KOH)电解液中,在100 mA/cm²和10 mA/cm²时所需的过电位较低(分别为348 mV和270 mV)。随着纳米片厚度从140 nm减小到34 nm,由于较低的库仑-库仑相互作用和去极化增加,铁取代BiOCl纳米片的电催化性能开始降低。

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