过电位
制氢
氢
电解水
电解
抗坏血酸
氢经济
催化作用
电催化剂
高压电解
材料科学
析氧
阳极
化学工程
分解水
化学
无机化学
电极
电化学
有机化学
物理化学
工程类
电解质
光催化
食品科学
作者
Zheng-Jie Chen,Jiuyi Dong,Jiajing Wu,Qiting Shao,Na Luo,Minwei Xu,Yuanmiao Sun,Yongbing Tang,Jing Peng,Hui‐Ming Cheng
标识
DOI:10.1038/s41467-023-39848-w
摘要
Hydrogen production coupled with biomass upgrading is vital for future sustainable energy developments. However, most biomass electrooxidation reactions suffer from high working voltage and low current density, which substantially hinder large-scale industrial applications. Herein, we report an acidic hydrogen production system that combined anodic ascorbic acid electrooxidation with cathodic hydrogen evolution. Unlike C-H and O-H bonds cleavage with slow kinetics in conventional organic oxidation, the highly active enol structure in ascorbic acid allows for an ultralow overpotential of only 12 mV@10 mA/cm2 using Fe single-atom catalysts, and reaches 1 A/cm2 at only 0.75 V (versus reversible hydrogen electrode) with approximately 100% Faraday efficiency for hydrogen production. Furthermore, the fabricated two-electrode membrane-free electrolyser delivers an industrial current density of 2 A/cm2@1.1 V at 60 °C (2.63 kWh/Nm3 H2), which requires half of the electricity consumption in conventional water electrolysis (~5 kWh/Nm3 H2). This work provides a new avenue for achieving industrial-scale hydrogen production from biomass.
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