Efficient Hydrogen Production from Seawater via Fe-EL-Modified Catalysts: A Biomass-Coupled Approach for Sustainable Energy Storage.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2025-03-28 DOI:10.1002/cssc.202500070
Xiaoqian Liu, Mengyi Xu, Linqin Wang, Xuanyue Cui, Weikang Nie, Ziyi Wang, Xue Li, Meirong Song, Yanjie Huang, Ning Li, Yurong Su, Min Wei, Yifeng He, Xia Sheng
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Abstract

Hydrogen production from seawater electrolysis holds significant promise for future energy crisis. However, various ions in the seawater disrupt the electrolysis process, impelling the discovery of efficient oxygen evolution reaction (OER) catalysts coupling with organic small molecules to accelerate the hydrogen generation efficiency. Herein, an easy method is presented for loading Fe electrodepositon layer (EL) onto carbonized wood (CW) via a straightforward electrodeposition process. Fe-EL enriches the active sites on the hierarchical pores natural carbon materials, resulting in exceptional hydrogen evolution reaction (HER) performance. In KOH and artificial seawater, Fe-CW demonstrates overpotentials of merely 38 and 94 mV at 10 mA cm-2, accompanied with excellent stability. For the anodic counterpart, OER is replaced with the 5-hydroxyfurfural oxidation reaction (HMFOR) using Fe/NiB/CF catalyst. It achieves an oxidation potential of 1.46 V to attain 100 mA cm-2 for HMFOR and convertes 5-hydroxyfurfural to 2,5-furandicarboxylic acid with a remarkable conversion rate of approximately 100%. When coupled HER with HMFOR in the seawater, the Fe-CW‖Fe/NiB/CF cell achieves 100 mA cm-2 at an ultralow voltage of 1.47 V. This approach not only addresses the challenges posed by seawater electrolysis but also paves ways for the industrial application of biomass-coupled hydrogen production.

通过fe - el改性催化剂从海水中高效制氢:可持续能源存储的生物质耦合方法。
海水电解制氢对解决未来能源危机具有重要意义。然而,海水中的各种离子干扰了电解过程,促使人们发现了与有机小分子偶联的高效析氧反应(OER)催化剂,以加快制氢效率。在此,我们提出了一种简单的方法,通过简单的电沉积过程将铁电沉积层(EL)加载到碳化木材(CW)上。Fe-EL富集了层次化孔天然碳材料上的活性位点,使其具有优异的析氢反应性能。在KOH和人工海水中,Fe-CW在10 mA cm-2下的过电位仅为38 mV和94 mV,并具有良好的稳定性。对于阳极反应,我们使用Fe/NiB/CF催化剂将OER替换为5-羟基糠醛氧化反应(HMFOR)。在1.46 V的氧化电位下,HMFOR得到了100 mA cm-2,并将HMF转化为2,5 -呋喃二羧酸,转化率接近100%。当HER与HMFOR在海水中耦合时,Fe- cw‖Fe/NiB/CF电池在1.47 V的超低电压下达到100 mA cm-2。这种方法不仅解决了海水电解带来的挑战,而且为生物质偶联制氢的工业应用铺平了道路。
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
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
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