用于肼氧化和节能制氢的功能性硫化镍铁/氢氧化物催化剂

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL
Pooja J. Sharma, Kinjal K. Joshi, Parikshit Sahatiya, C. K. Sumesh and Pratik M. Pataniya
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引用次数: 0

摘要

电催化水裂解是一种很有前途的绿色制氢技术,但其效率受到阳极析氧反应(OER)缓慢的影响。本研究提出了一种有效的策略来解决这一挑战,即通过一锅化学浴沉积技术开发一种直接在泡沫镍上生长的氢氧化铁/硫化物异质结构(NFS@NF)催化剂。优化后的氢氧化镍/硫化物具有明显的催化性能,在10 mA/cm2电流下需要150过电位才能析氢。此外,NFS@NF在100 mA/cm²下表现出低电位OER (1.45 V vs. RHE)、尿素氧化(1.35 V vs. RHE)和肼氧化(0.26 V vs. RHE)。这些特殊的催化活性归因于镍和铁之间的协同作用以及硫诱导的化学状态和局部结构的修饰。在全电池配置下,电解水产生的电流为10ma /cm²,电压为1.57 V,用电解尿素和肼代替传统的电解水,电流可进一步降低至1.44 V和0.37 V。电极具有优异的耐用性,在300 mA/cm²的水电解和100 mA/cm²的肼电解下保持稳定的催化性能70小时。此外,在Mg/海水电池中的应用表明,其功率密度为4.02 mW/cm²,可稳定放电16小时,为肼电解提供所需的功率。最后,该研究为可持续制氢和储能应用提供了一种高效、地球丰富的催化剂解决方案,推动了混合水分解和Mg/海水电池技术的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Functional nickel iron sulphide/hydroxide catalysts for hydrazine oxidation and energy saving hydrogen production†

Functional nickel iron sulphide/hydroxide catalysts for hydrazine oxidation and energy saving hydrogen production†

Electrocatalytic water splitting is a promising technique for green hydrogen production, yet its efficiency is hindered by the sluggish oxygen evolution reaction (OER) at the anode. This study advocates an efficient strategy to address this challenge by developing a NiFe-hydroxide/sulfide heterostructure (NFS@NF) catalyst directly grown on nickel foam via a one-pot chemical bath deposition technique. The optimized NiFe-hydroxide/sulfide shows obvious catalytic performance, requiring overpotentials of 150 mV at a current of 10 mA cm−2 for hydrogen evolution. Additionally, the NFS@NF exhibits low potentials for the OER (1.45 V vs. RHE), urea oxidation (1.35 V vs. RHE), and hydrazine oxidation (0.26 V vs. RHE) at 100 mA cm−2. These exceptional catalytic activities are attributed to the synergy between nickel and iron and sulfur-induced modifications in chemical states and the local structure. A full-cell configuration generates 10 mA cm−2 current at 1.57 V for water electrolysis, which can be further reduced to 1.44 V and 0.37 V by substituting conventional electrolysis of water with electrolysis of urea and hydrazine, respectively. The electrodes exhibit excellent durability, maintaining stable catalytic performance for 70 hours at 300 mA cm−2 for water electrolysis and 100 mA cm−2 for hydrazine electrolysis. Additionally, its application in an Mg/seawater battery shows stable discharge for 16 hours with a power density of 4.02 mW cm−2, which provides the required power for hydrazine electrolysis. Finally, this research offers an efficient, earth-abundant catalyst solution for sustainable hydrogen production and energy storage applications, advancing hybrid water-splitting and Mg/seawater battery technologies.

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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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