甲醇
甲醛
催化作用
光催化
制氢
纳米点
氢
水溶液
材料科学
光化学
化学工程
电子转移
化学
纳米技术
物理化学
有机化学
工程类
作者
Hui Wang,Haifeng Qi,Xiao Sun,Shuya Jia,Xiyi Li,Tina Jingyan Miao,Lunqiao Xiong,Shihao Wang,Xiaolei Zhang,H. Liu,Aiqin Wang,Tao Zhang,Weixin Huang,Junwang Tang
出处
期刊:Nature Materials
[Springer Nature]
日期:2023-04-10
卷期号:22 (5): 619-626
被引量:108
标识
DOI:10.1038/s41563-023-01519-y
摘要
Methanol with 12.5 wt% H2 content is widely considered a liquid hydrogen medium. Taking into account water with 11.1 wt% H2 content, H2 synthesis from the mixture of water and methanol is a promising method for on-demand hydrogen production. We demonstrate an atomic-level catalyst design strategy using the synergy between single atoms and nanodots for H2 production. The PtCu-TiO2 sandwich photocatalyst achieves a remarkable H2 formation rate (2,383.9 µmol h-1) with a high apparent quantum efficiency (99.2%). Furthermore, the oxidation product is a high-value chemical formaldehyde with 98.6% selectivity instead of CO2, leading to a nearly zero-carbon-emission process. Detailed investigations indicate a dual role of the copper atoms: an electron acceptor to facilitate photoelectron transfer to Pt, and a hole acceptor for the selective oxidation of methanol to formaldehyde, thus avoiding over-oxidation to CO2. The synergy between Pt nanodots and Cu single atoms together reduces the activation energy of this process to 13.2 kJ mol-1.
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