Au Cluster-derived Electrocatalysts for CO2 Reduction

被引:8
|
作者
Sharma, Shailendra Kumar [1 ,2 ]
Ahangari, Hani Taleshi [2 ]
Johannessen, Bernt [3 ]
Golovko, Vladimir B. [1 ]
Marshall, Aaron T. [2 ]
机构
[1] Univ Canterbury, MacDiarmid Inst Adv Mat & Nanotechnol, Sch Phys & Chem Sci, Christchurch, New Zealand
[2] Univ Canterbury, MacDiarmid Inst Adv Mat & Nanotechnol, Dept Chem & Proc Engn, Christchurch, New Zealand
[3] Australian Synchrotron, 800 Blackburn Rd, Clayton, Vic 3168, Australia
关键词
Cluster chemistry; Electrochemical CO2 reduction; Nanocatalyst; Selectivity;
D O I
10.1007/s12678-023-00821-2
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
Metal clusters often exhibit superior chemical, electronic, and geometrical properties and can show exciting catalytic performance. The catalytic behaviour of the clusters is strongly affected by their size and composition, offering unique opportunities to fine-tune such materials for a specific application. In this study, atomically precise [Au-6(dppp)(4)](NO3)(2), [Au-9(PPh3)(8)](NO3)(3), [Au-13(dppe)(5)Cl-2]Cl-3 and Au-101(PPPh3)(21)Cl-5 clusters were synthesised, characterised and their activity for electrocatalytic CO2 reduction is compared. These Au clusters were deposited onto carbon paper to serve as the cathode for the electrochemical reduction of CO2. The experimental studies suggest that the clusters remain intact upon deposition on the carbon paper but undergo agglomeration during CO2 electrolysis. The cluster-based catalysts demonstrated high selectivity (75%-90%) for CO production over hydrogen evolution reaction. Upon calcination, the activity of the cluster-based electrodes decreases, which can be attributed to the agglomeration of small clusters into larger bulk-like nanoparticles, as suggested by XPS, XAS and SEM.
引用
收藏
页码:611 / 623
页数:13
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