电合成
催化作用
氢氧化物
合成气
法拉第效率
材料科学
氧化还原
电子转移
无机化学
剥离(纤维)
化学工程
甲烷化
氢
双层(生物学)
氧气
反应机理
电解
分解水
钝化
化学
原材料
层状双氢氧化物
锌
制氢
化学反应
解吸
作者
Peng Zhang,Wenxiong Shi,Hua-Qing Yin,Bao-Qin Sun,Yu‐Fei Song,Tong‐Bu Lu,Zhiming Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-10-14
卷期号:19 (42): 37206-37217
被引量:1
标识
DOI:10.1021/acsnano.5c11814
摘要
Syngas electrosynthesis stands as an energy-saving strategy for producing chemical raw materials, but it remains a great challenge in achieving a balance between the hydrogen evolution reaction (HER) and the CO2 reduction reaction (CO2RR). Herein, a series of single-cluster catalysts (SCCs) were constructed by uniformly dispersing different polyoxometalates (POMs) into ZnAl-layered double hydroxide (ZnAl-LDH) through a simple stripping self-assembly technique, forming single-sandwich-layer-based ZnAl-POM (POM = W10, PW12, and P2W18) with abundant oxygen vacancies and zinc vacancies. The well-defined monodispersed W10 clusters function as electron sponges for reversibly accepting and releasing electrons to boost the level of CO2 reduction. The ZnAl-W10-3 can efficiently adjust HER and CO2RR to achieve a total Faradaic efficiency (FE) of 96.9% for both H2 and CO production. A broad CO/H2 ratio (0.32-1.35) can be obtained over the optimized ZnAl-W10-3 within a wide potential window (-0.8 to -2.0 V vs RHE) via adjusting the W10 amount. Systematic investigations reveal that W10-mediated electron and proton transfer processes and abundant unsaturated sites in ultrathin ZnAl-LDH significantly enhance the tunability of the CO2RR and HER activities.
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