甲酸
催化作用
甲醛
氢
氧化还原
材料科学
制氢
化学工程
氢燃料
分子
选择性
无机化学
纳米技术
化学
有机化学
工程类
作者
Peiyuan Mao,Bingbing Chen,Rui Huang,Yang Jing,Long Xiao,Baihao Zhang,Chuan Shi
出处
期刊:Small
[Wiley]
日期:2024-09-18
卷期号:20 (48): e2405358-e2405358
被引量:9
标识
DOI:10.1002/smll.202405358
摘要
Abstract The replacement of oxygen evolution reactions with organic molecule oxidation reactions to enable energy‐efficient hydrogen production has been a subject of interest. However, further reducing reaction energy consumption and releasing hydrogen from organic molecules continue to pose significant challenges. Herein, a strategy is proposed to produce hydrogen and formic acid from formaldehyde using Ag/Co 3 O 4 interface catalysts at the anode. The key to improving the performance of Ag‐based catalysts for formaldehyde oxidation lies in the strong SMSI achieved through the well‐designed “spontaneous redox reaction” between Ag and Co 3 O 4 precursors. Nano‐sized Ag particles are uniformly dispersed on Co 3 O 4 nanosheets, and electron‐deficient Ag δ+ are formed by the SMSI between Ag and Co 3 O 4. Ag/Co 3 O 4 demonstrates exceptional formaldehyde oxidation activity at low potentials of 0.32 V versus RHE and 0.65 V versus RHE, achieving current densities of 10 and 100 mA cm −2 , respectively. The electrolyzer “Ag/Co 3 O 4 ||20% Pt/C” achieves over 195% hydrogen efficiency and over 98% formic acid selectivity, maintaining stable operation for 60 hours. This work not only presents a novel approach to precisely modulate Ag particle size and interface electronic structure via SMSI, but also provides a promising approach to efficient and energy‐saving hydrogen production and the transformation of harmful formaldehyde.
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