Isolated single-atom Pt sites for highly selective electrocatalytic hydrogenation of formaldehyde to methanol

被引:34
|
作者
Zhao, Shunzheng [1 ]
Wen, Yanfeng [1 ]
Peng, Xianyun [2 ]
Mi, Yuying [2 ]
Liu, Xijun [2 ]
Liu, Yifan [3 ]
Zhuo, Longchao [4 ]
Hu, Guangzhi [5 ]
Luo, Jun [2 ]
Tang, Xiaolong [1 ]
机构
[1] Univ Sci & Technol Beijing, Dept Environm Engn, Beijing 100083, Peoples R China
[2] Tianjin Univ Technol, Sch Mat Sci & Engn, Inst New Energy Mat & Low Carbon Technol, Ctr Electron Microscopy,Tianjin Key Lab Adv Funct, Tianjin 300384, Peoples R China
[3] Shenzhen Univ, Coll Phys & Optoelect Engn, Key Lab Optoelect Devices & Syst, Minist Educ & Guangdong Prov, Shenzhen 518060, Peoples R China
[4] Xian Univ Technol, Sch Mat Sci & Engn, Xian 710048, Peoples R China
[5] Yunnan Univ, Sch Chem Sci & Technol, Kunming 650091, Yunnan, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
OXIDATION; EVOLUTION; CATALYST; FIXATION; REMOVAL; CO;
D O I
10.1039/d0ta00190b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The direct electrochemical conversion of noxious formaldehyde into value-added chemicals is a quite promising technique for resolving the increasingly serious environmental issue arising from industrial formaldehyde-containing wastewater. However, thus far, it has not been examined, to the best of our knowledge. This study reports the electrocatalytic hydrogenation of formaldehyde to methanol in a neutral aqueous medium under ambient conditions over a Pt single-atom catalyst, and this catalyst exhibits a favorable methanol yield rate and a high faradaic efficiency of 30.7 mg h(-1) mg(cat.)(-1) and 95.8% at -0.8 V versus the reversible hydrogen electrode in 0.1 M Na2SO4. Also, it exhibits excellent durability. Atomic-scale structural characterization and theoretical calculations revealed that the above-mentioned efficient performance is related to atomically dispersed Pt-O sites, which could lower the free-energy change for the chemisorption of formaldehyde and activate the C-H bond.
引用
收藏
页码:8913 / 8919
页数:7
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