共 50 条
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
相关论文