海水
制氢
催化作用
电解
析氧
氢
电解水
阳极
化学工程
碳纤维
化学
分解水
无机化学
材料科学
电化学
电解质
电极
有机化学
物理化学
生态学
光催化
工程类
复合材料
复合数
生物
作者
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
出处
期刊:Chemsuschem
[Wiley]
日期:2025-03-28
卷期号:18 (12): e202500070-e202500070
被引量:4
标识
DOI:10.1002/cssc.202500070
摘要
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.
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