Catalyst-free photochemical CO2 hydrogenation to CO and CH4 conversion to C2H6

被引:0
|
作者
Zhai, Jianxin [1 ,3 ]
Zhou, Baowen [2 ]
Wu, Haihong [1 ,3 ]
Chen, Xiao [1 ,3 ]
Xia, Zhanghui [1 ,3 ]
Chen, Chunjun [1 ,3 ]
Xue, Cheng [1 ,3 ]
Dong, Mengke [1 ,3 ]
Deng, Ting [1 ,3 ]
Jia, Shuaiqiang [1 ,3 ]
He, Mingyuan [1 ,3 ]
Han, Buxing [1 ,3 ,4 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, State Key Lab Petr Mol & Proc Engn, Shanghai 200062, Peoples R China
[2] Shanghai Jiao Tong Univ, Res Ctr Renewable Synthet Fuel, Sch Mech Engn, Key Lab Power Machinery & Engn,Minist Educ, Shanghai 200240, Peoples R China
[3] Inst Ecochongming, Shanghai 202162, Peoples R China
[4] Chinese Acad Sci, CAS Key Lab Colloid & Interface & Thermodynam, Beijing Natl Lab Mol Sci,Ctr Carbon Neutral Chem, CAS Res Educ Ctr Excellence Mol Sci,Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
METHANE; ADSORPTION; REDUCTION; NM;
D O I
10.1039/d4gc01820f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Direct utilization of high-energy photons to drive chemical reactions presents a promising approach for the achievement of green reaction process. Herein, we developed a simple photochemical route that utilized 172 nm vacuum ultraviolet (VUV) photons as drivers for CO2 hydrogenation to CO and transformation of CH4 to H-2 and C2H6. It was demonstrated that the reactions could proceed efficiently at catalyst-free and ambient conditions, and water could further promote the transformation of CH4. The reaction mechanism was proposed on the basis of control experiments. This study provides a green alternative to conventional catalytic processes for important reactions, i.e., CO2 hydrogenation or CH4 conversions triggered by high-energy photons under ambient conditions, which have promising potential in applications due to some obvious advantages.
引用
收藏
页码:8872 / 8876
页数:5
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