In situ decorated Cu2FeSnS4 nanosheet arrays for low voltage hydrogen production through the ammonia oxidation reaction†

IF 6 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Materials Chemistry Frontiers Pub Date : 2023-08-30 DOI:10.1039/D3QM00291H
Yoongu Lim, Subramani Surendran, Won So, Sathyanarayanan Shanmugapriya, Chanmin Jo, Gnanaprakasam Janani, Hyeonuk Choi, Hyun Soo Han, Heechae Choi, Young-Hoon Yun, Tae-Hoon Kim, Myeong-Jin Kim, Kyoungsuk Jin, Jung Kyu Kim and Uk Sim
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Abstract

Water electrolysis is a possible method for producing ultrapure hydrogen (H2). However, the typical water electrolysis process has significant overpotential, mostly because of the slow kinetics in the oxygen evolution reaction (OER). The OER that produces reactive oxygen species weakens the proton exchange membrane in the water electrolyzer. Besides, oxygen can interact with cathodic H2 to create explosive gaseous mixtures. These issues can be solved using the hybrid water electrolysis (HWE) method, replacing the OER with an alternative oxidation reaction. The oxidizing chemical agent helps in electrochemical hydrogen production at extremely low voltage while oxidizing the substance to value-added products in the HWE process. Electrocatalysts are used to power the chemical species-assisted hydrogen generation in the HWE process. Quaternary metal sulfide, a highly electrochemically active material, has attracted attention as a promising platform for effective application in various redox reactions. In this work, we reported quaternary copper–iron–tin sulfide with the chemical formula Cu2FeSnS4 (CFTS) in the form of nanosheets and evaluated the HWE with the ammonia oxidation reaction at the anode. The CFTS nanosheets were synthesized by a facile one-step solvothermal method using carbon cloth (CC) as the substrate. To evaluate the effect of solvents used in the synthesis process on the morphology and electrochemical performance of the material, deionized water (DI), ethanol (EtOH), and ethylene glycol (EG) were applied, and their effects were studied thoroughly. A feasible formation mechanism has been presented in which the viscosity and dielectric constants of the solvents play key roles in determining the morphology of CFTS nanosheets. The CFTS nanosheets synthesized in EG showed a porous and rougher surface than those produced using other solvents. As expected, the EG-mediated CFTS exhibited remarkable H2 production with ammonia oxidation at the anode due to better electron and electrolyte ion transmission. Our results describe the effect of solvents used for solvothermal reactions and that the CFTS material can be deliberated as a potential alternative for divergent energy conversion device applications.

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原位修饰的Cu2FeSnS4纳米片阵列用于通过氨氧化反应生产低压氢气†
水电解是一种生产超纯氢气(H2)的可能方法。然而,典型的水电解过程具有显著的过电位,主要是因为析氧反应(OER)的动力学缓慢。产生活性氧的OER削弱了水电解槽中的质子交换膜。此外,氧气可以与阴极H2相互作用,产生爆炸性气体混合物。这些问题可以使用混合水电解(HWE)方法来解决,用替代氧化反应代替OER。氧化化学剂有助于在极低电压下进行电化学制氢,同时在HWE过程中将物质氧化为增值产品。在HWE过程中,电催化剂用于为化学物质辅助的氢气生成提供动力。四元金属硫化物是一种高度电化学活性的材料,作为一种很有前途的平台,在各种氧化还原反应中得到了广泛的应用。在这项工作中,我们报道了化学式为Cu2FeSnS4(CFTS)的纳米片形式的季铜-铁-锡硫化物,并评估了在阳极进行氨氧化反应的HWE。以碳布(CC)为基体,采用一步溶剂热法合成了CFTS纳米片。为了评估合成过程中使用的溶剂对材料形态和电化学性能的影响,使用了去离子水(DI)、乙醇(EtOH)和乙二醇(EG),并对它们的影响进行了深入研究。提出了一种可行的形成机制,其中溶剂的粘度和介电常数在决定CFTS纳米片的形态方面起着关键作用。在EG中合成的CFTS纳米片显示出比使用其他溶剂生产的CFTS更多孔、更粗糙的表面。正如预期的那样,由于更好的电子和电解质离子传输,EG介导的CFTS在阳极氨氧化的情况下表现出显著的H2生成。我们的结果描述了用于溶剂热反应的溶剂的影响,并且CFTS材料可以作为发散能量转换装置应用的潜在替代品。
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来源期刊
Materials Chemistry Frontiers
Materials Chemistry Frontiers Materials Science-Materials Chemistry
CiteScore
12.00
自引率
2.90%
发文量
313
期刊介绍: Materials Chemistry Frontiers focuses on the synthesis and chemistry of exciting new materials, and the development of improved fabrication techniques. Characterisation and fundamental studies that are of broad appeal are also welcome. This is the ideal home for studies of a significant nature that further the development of organic, inorganic, composite and nano-materials.
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