Electrocatalytic activity of tungsten carbide hybrids with two different MOFs for water splitting: a comparative analysis

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY Nanoscale Advances Pub Date : 2024-08-19 DOI:10.1039/D4NA00289J
Umair Sohail, Erum Pervaiz, Rafiq Khosa and Maryum Ali
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Abstract

Conventional energy resources are diminishing, and environmental pollution is constantly increasing because of the excessive use of fossil fuels to sustain the ever-increasing population and industrialization. This has raised concerns regarding a sustainable future. In the pursuit of addressing sustainability in industrial processes and energy systems, the production of green hydrogen is considered a promising and crucial solution to meet the growing energy demands. Water-splitting is one of the most effective technologies for producing clean and carbon-neutral hydrogen. Water-splitting is a scientifically emerging application, but it is commercially limited due to its economic non-viability. The sluggish kinetics and the high overpotential needed for the water-splitting reactions (HER and OER) have encouraged the scientific community to design electrocatalysts that address the concerns of low activity, efficiency and stability. Designing a hybrid catalyst using metal–organic frameworks (MOFs) with transition metal carbides can be a suitable approach to address the deficiencies of conventional water-splitting catalysts. In this study, we have designed and fabricated an electrocatalyst of tungsten carbide (WC) with two different MOFs (Zr-based and Fe-based) and explored their electrocatalytic activity for hydrogen generation in an alkaline medium. It should be noted that hybrids of tungsten carbide with a zirconia MOF (UiO-66) showed better electrocatalytic activity with low overpotentials of 104 mV (HER) and 152 mV (OER) at a current density of 10 mA cm−2. This superior activity of WC with the Zr-MOF in comparison to the Fe-MOF is due to the synergistic effect of Zr present in UiO-66 grown on the WC matrix. Moreover, UiO-66 provides a larger electrocatalytic active surface area, so available active sites are more in UiO-66 as compared to the Fe-MOF. These findings set the stage for the systematic development and production of bi-functional hybrid catalysts with the potential to be utilized in water-splitting processes.

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碳化钨混合物与两种不同 MOFs 在水分离方面的电催化活性:对比分析。
由于过度使用化石燃料来维持不断增长的人口和工业化进程,传统能源资源日益减少,环境污染不断加剧。这引发了人们对可持续未来的担忧。为了解决工业流程和能源系统的可持续发展问题,生产绿色氢气被认为是满足日益增长的能源需求的一个前景广阔的重要解决方案。分水制氢是生产清洁和碳中和氢气的最有效技术之一。水分离在科学上是一种新兴应用,但由于其经济上的不可行性而在商业上受到限制。水分离反应(HER 和 OER)所需的缓慢动力学和高过电位促使科学界设计电催化剂,以解决低活性、高效率和稳定性等问题。利用金属有机框架(MOFs)和过渡金属碳化物设计混合催化剂是解决传统水分离催化剂缺陷的合适方法。在本研究中,我们设计并制造了一种碳化钨(WC)与两种不同 MOFs(Zr 基和 Fe 基)的电催化剂,并探索了它们在碱性介质中产生氢气的电催化活性。值得注意的是,碳化钨与氧化锆 MOF(UiO-66)的混合物显示出更好的电催化活性,在电流密度为 10 mA cm-2 时,过电位较低,分别为 104 mV(HER)和 152 mV(OER)。与 Fe-MOF 相比,含有 Zr-MOF 的 WC 具有更高的活性,这是因为生长在 WC 基体上的 UiO-66 中的 Zr 具有协同效应。此外,UiO-66 提供了更大的电催化活性表面积,因此与 Fe-MOF 相比,UiO-66 中的可用活性位点更多。这些发现为系统开发和生产双功能混合催化剂奠定了基础,这种催化剂有望用于水分离过程。
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来源期刊
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
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