In Situ STM Investigation of Gold Reconstruction and of Silicon Electrodeposition on Au(111) in the Room Temperature Ionic Liquid 1-Butyl-1-methylpyrrolidinium Bis(trifluoromethylsulfonyl)imide

2006 ◽  
Vol 110 (12) ◽  
pp. 6250-6256 ◽  
Author(s):  
N. Borisenko ◽  
S. Zein El Abedin ◽  
F. Endres
2013 ◽  
Vol 15 (4) ◽  
pp. 1188-1197 ◽  
Author(s):  
Benjamin C. M. Martindale ◽  
Dzianis Menshykau ◽  
Sven Ernst ◽  
Richard G. Compton

2003 ◽  
Vol 2003 (9) ◽  
pp. 549-551 ◽  
Author(s):  
Tao Jiang ◽  
Buxing Han ◽  
Guoying Zhao ◽  
Yanhong Chang ◽  
Liang Gao ◽  
...  

The synthesis of dimethyl carbonate (DMC) by oxidative carbonylation of methanol with PdCl2 as a catalyst was investigated in the room temperature ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]). The products were recovered in situ using supercritical carbon dioxide. Enhanced selectivity of DMC over this catalyst was observed in the synthesis in [bmim][PF6] compared with the situation without the ionic liquid (IL). The mixture of catalyst and [bmim][PF6] could be recycled.


Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1315
Author(s):  
Jaanus Kruusma ◽  
Arvo Tõnisoo ◽  
Rainer Pärna ◽  
Thomas Thomberg ◽  
Mati Kook ◽  
...  

In this study, we used the in situ X-ray photoelectron spectroscopy (XPS), in situ mass spectroscopy, cyclic voltammetry and electrochemical impedance spectroscopy methods, for the first time, in a detailed exploration of the electrochemical behaviour of a quaternary amine cation-based room-temperature ionic liquid, butyl-trimethyl-ammonium bis(trifluoromethylsulfonyl)imide (N4111(TFSI)), at the negatively and positively polarised molybdenum carbide-derived micro-mesoporous carbon (mmp-C(Mo2C)) electrodes that can be used as high surface area supporting material for electrocatalysts. The shapes of the C 1s, N 1s, O 1s, F 1s and S 2p XPS spectra were stable for N4111(TFSI) within a very wide potential range. The XPS data indicated the non-specific adsorption character of the cations and anions in the potential range from −2.00 V to 0.00 V. Thus, this region can be used for the detailed analysis of catalytic reaction mechanisms. We observed strong adsorption from 0.00 V to 1.80 V, and at E > 1.80 V, very strong adsorption of the N4111(TFSI) at the mmp-C(Mo2C) took place. At more negative potentials than −2.00 V, the formation of a surface layer containing both N4111+ cations and TFSI− anions was established with the formation of various gaseous compounds. Collected data indicated the electrochemical instability of the N4111+ cation at E < −2.00 V.


2019 ◽  
Vol 16 (24) ◽  
pp. 1-6 ◽  
Author(s):  
Yusaku Nishimura ◽  
Yasuhiro Fukunaka ◽  
Caetano R. Miranda ◽  
Tetsuo Nishida ◽  
Toshiyuki Nohira ◽  
...  

2011 ◽  
Vol 13 (17) ◽  
pp. 7968 ◽  
Author(s):  
Benedetto Bozzini ◽  
Alessandra Gianoncelli ◽  
Burkhard Kaulich ◽  
Maya Kiskinova ◽  
Claudio Mele ◽  
...  

2005 ◽  
Vol 73 (8) ◽  
pp. 610-613 ◽  
Author(s):  
Noritoshi NANBU ◽  
Tomonori KATO ◽  
Yukio SASAKI ◽  
Fusao KITAMURA

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