scholarly journals Tuning Local Proton Flux in Yolk-Shell Cu@Cu2Se Nanoreactors to Enable Efficient Electrochemical Nitrate-Ammonia Conversion

Author(s):  
Qi Hu ◽  
Hongju Zheng ◽  
Xiaodeng Wang ◽  
Keru Gao ◽  
Lingren Mi ◽  
...  

Abstract Electrochemical nitrate (NO3−) reduction reaction (NO3−RR) represents an ideal alternative for ammonia (NH3) generation. Despite recent success on the synthesis of Cu-based electrocatalysts, the kinetics of Cu-catalyzed NO3−RR is still greatly limited by the slow proton transfer rate since the large energy barrier for water dissociation. Here, we report the construction of a yolk-shell structure, comprising a Cu core and Cu2Se shell that functions like the tandem nanoreactor. Specific, the Cu2Se shell with strong water dissociation ability can easily produce protons and then transfer to the Cu core for driving the reduction of NO3−. Intriguingly, the proton flux arriving to the Cu core can be well tuned by altering the void size of the yolk-structure, thereby enabling rapid proton transfer yet hindering the competitive hydrogen evolution. More importantly, operando Raman spectra reveal that the rapid proton transfer significantly promotes the hydrogenation of key intermediates for reducing the overall energy barrier of the NO3−RR. Consequently, the optimized yolk-shell structure enables highly selective and efficient NO3−RR with a large NH3 yield rate of 0.94 mmol cm−2 h−1. This work offers a fresh concept to boost the NO3−RR by tuning proton transfer rate.

2017 ◽  
Vol 121 (37) ◽  
pp. 6917-6924 ◽  
Author(s):  
Oren Gajst ◽  
Ron Simkovitch ◽  
Dan Huppert

2005 ◽  
Vol 109 (21) ◽  
pp. 4852-4861 ◽  
Author(s):  
Liat Genosar ◽  
Tatiana Lasitza ◽  
Rinat Gepshtein ◽  
Pavel Leiderman ◽  
Nahum Koifman ◽  
...  

1980 ◽  
Vol 35 (10) ◽  
pp. 1286-1288 ◽  
Author(s):  
K. C. Dash ◽  
A. Schmidpeter ◽  
H. Schmidbaur

Abstract Contrary to the reports on the coordination oi copper (I) to N/P-ambidentate cyclotri-phosphazenes, gold (I), gold (III) and dimethylgoldf 111) chloride are found to become exclusively P-coordinated to the prototype ligand 2-methyl-4,4,6,6-tetraphenylcyclotri-phosphazene (1). The P-H proton is transferred to an adjacent nitrogen atom of the heterocycle. According to temperature dependent NMR spectra, the AuCl and the AuCl3 complexes are fluxional molecules or ions, resp., with a rapid proton transfer between P-NH-P and P = N-P functions. The behaviour is similar to that of related palladium and platinum complexes, reported previously.


2010 ◽  
Vol 11 (5) ◽  
pp. 434-437 ◽  
Author(s):  
Yuanwei Ma ◽  
Huamin Zhang ◽  
Hexiang Zhong ◽  
Ting Xu ◽  
Hong Jin ◽  
...  

1984 ◽  
Vol 81 (12) ◽  
pp. 5596-5600 ◽  
Author(s):  
D. H. Huppert ◽  
A. Jayaraman ◽  
R. G. Maines ◽  
D. W. Steyert ◽  
P. M. Rentzepis

Sign in / Sign up

Export Citation Format

Share Document