Lin Long, Liu Tianfu, Xiao Jianping, Li Hefei, Wei Pengfei, Gao Dunfeng, Nan Bing, Si Rui, Wang Guoxiong, Bao Xinhe
State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, 116023, China.
University of Chinese Academy of Sciences, Beijing, 100039, China.
Angew Chem Int Ed Engl. 2020 Dec 7;59(50):22408-22413. doi: 10.1002/anie.202009191. Epub 2020 Oct 7.
Developing copper-free catalysts for CO conversion into hydrocarbons and oxygenates is highly desirable for electrochemical CO reduction reaction (CO RR). Herein, we report a cobalt phthalocyanine (CoPc) and zinc-nitrogen-carbon (Zn-N-C) tandem catalyst for CO RR to CH . This tandem catalyst shows a more than 100 times enhancement of the CH /CO production rate ratio compared with CoPc or Zn-N-C alone. Density functional theory (DFT) calculations and electrochemical CO reduction reaction results suggest that CO is first reduced into CO over CoPc and then CO diffuses onto Zn-N-C for further conversion into CH over Zn-N site, decoupling complicated CO RR pathway on single active site into a two-step tandem reaction. Moreover, mechanistic analysis indicates that CoPc not only generates CO but also enhances the availability of *H over adjacent N sites in Zn-N , which is the key to achieve the high CH production rate and understand the intriguing electrocatalytic behavior which is distinctive to copper-based tandem catalysts.
开发用于将CO转化为碳氢化合物和含氧化合物的无铜催化剂对于电化学CO还原反应(CO RR)非常重要。在此,我们报道了一种用于CO RR制CH的钴酞菁(CoPc)和锌氮碳(Zn-N-C)串联催化剂。与单独的CoPc或Zn-N-C相比,这种串联催化剂的CH/CO生成速率比提高了100多倍。密度泛函理论(DFT)计算和电化学CO还原反应结果表明,CO首先在CoPc上还原为CO,然后CO扩散到Zn-N-C上,在Zn-N位点进一步转化为CH,将单活性位点上复杂的CO RR途径解耦为两步串联反应。此外,机理分析表明,CoPc不仅生成CO,还提高了Zn-N中相邻N位点上*H的可用性,这是实现高CH生成速率和理解与铜基串联催化剂不同的有趣电催化行为的关键。