Ex Situ X-ray Photoelectron Spectroscopy Study of the Interface between a Ag(111) Electrode and an Alkaline Electrolyte. 1. Influence of the Electrode Potential on the Adsorption of Oxygen Species

Langmuir ◽  
1999 ◽  
Vol 15 (19) ◽  
pp. 6546-6551 ◽  
Author(s):  
E. R. Savinova ◽  
D. Zemlyanov ◽  
A. Scheybal ◽  
Th. Schedel-Niedrig ◽  
K. Doblhofer ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Electrode Potential ◽  
Ex Situ ◽  
Alkaline Electrolyte ◽  
Oxygen Species ◽  
Spectroscopy Study ◽  
X Ray

Ex Situ X-ray Photoelectron Spectroscopy Study of the Interface between a Ag(111) Electrode and an Alkaline Electrolyte. 2. Structure of the Double Layer

Langmuir ◽  
1999 ◽  
Vol 15 (19) ◽  
pp. 6552-6556 ◽  
Author(s):  
E. R. Savinova ◽  
D. Y. Zemlyanov ◽  
A. Scheybal ◽  
R. Schlögl ◽  
K. Doblhofer
Keyword(s):  
Double Layer ◽  
Photoelectron Spectroscopy ◽  
Ex Situ ◽  
Alkaline Electrolyte ◽  
Spectroscopy Study ◽  
X Ray

Oxygen Species in HfO2 Films: An in Situ X-Ray Photoelectron Spectroscopy Study

2019 ◽  
Vol 11 (4) ◽  
pp. 91-102 ◽  
Author(s):  
Carlos Driemeier ◽  
Robert Wallace ◽  
Israel Baumvol
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxygen Species ◽  
Spectroscopy Study ◽  
X Ray

Oxygen species in HfO2 films: An in situ x-ray photoelectron spectroscopy study

2007 ◽  
Vol 102 (2) ◽  
pp. 024112 ◽  
Author(s):  
C. Driemeier ◽  
R. M. Wallace ◽  
I. J. R. Baumvol
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxygen Species ◽  
Spectroscopy Study ◽  
X Ray

CO2 Reduction to Propanol by Copper Foams: A Pre- and Post-Catalysis Study

2020 ◽  
Author(s):  
Jennifer A. Rudd ◽  
Ewa Kazimierska ◽  
Louise B. Hamdy ◽  
Odin Bain ◽  
Sunyhik Ahn ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Photoelectron Spectroscopy ◽  
Carbon Capture ◽  
Surface Composition ◽  
Co2 Reduction ◽  
Structural Rearrangement ◽  
Copper Electrode ◽  
Ex Situ ◽  
X Ray ◽  
Copper Electrodes

The utilization of carbon dioxide is a major incentive for the growing field of carbon capture. Carbon dioxide could be an abundant building block to generate higher value products. Herein, we describe the use of porous copper electrodes to catalyze the reduction of carbon dioxide into higher value products such as ethylene, ethanol and, notably, propanol. For <i>n</i>-propanol production, faradaic efficiencies reach 4.93% at -0.83 V <i>vs</i> RHE, with a geometric partial current density of -1.85 mA/cm<sup>2</sup>. We have documented the performance of the catalyst in both pristine and urea-modified foams pre- and post-electrolysis. Before electrolysis, the copper electrode consisted of a mixture of cuboctahedra and dendrites. After 35-minute electrolysis, the cuboctahedra and dendrites have undergone structural rearrangement. Changes in the interaction of urea with the catalyst surface have also been observed. These transformations were characterized <i>ex-situ</i> using scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. We found that alterations in the morphology, crystallinity, and surface composition of the catalyst led to the deactivation of the copper foams.

scholarly journals Electrochemical study on nickel aluminum layered double hydroxides as high-performance electrode material for lithium-ion batteries based on sodium alginate binder

2021 ◽  
Author(s):  
Xinyue Li ◽  
Marco Fortunato ◽  
Anna Maria Cardinale ◽  
Angelina Sarapulova ◽  
Christian Njel ◽  
...  
Keyword(s):  
Lithium Ion Batteries ◽  
Electrode Material ◽  
Photoelectron Spectroscopy ◽  
Negative Electrode ◽  
Lithium Ion ◽  
Electrochemical Study ◽  
Ex Situ ◽  
Potential Range ◽  
X Ray ◽  
Storage Mechanism

AbstractNickel aluminum layered double hydroxide (NiAl LDH) with nitrate in its interlayer is investigated as a negative electrode material for lithium-ion batteries (LIBs). The effect of the potential range (i.e., 0.01–3.0 V and 0.4–3.0 V vs. Li+/Li) and of the binder on the performance of the material is investigated in 1 M LiPF6 in EC/DMC vs. Li. The NiAl LDH electrode based on sodium alginate (SA) binder shows a high initial discharge specific capacity of 2586 mAh g−1 at 0.05 A g−1 and good stability in the potential range of 0.01–3.0 V vs. Li+/Li, which is better than what obtained with a polyvinylidene difluoride (PVDF)-based electrode. The NiAl LDH electrode with SA binder shows, after 400 cycles at 0.5 A g−1, a cycling retention of 42.2% with a capacity of 697 mAh g−1 and at a high current density of 1.0 A g−1 shows a retention of 27.6% with a capacity of 388 mAh g−1 over 1400 cycles. In the same conditions, the PVDF-based electrode retains only 15.6% with a capacity of 182 mAh g−1 and 8.5% with a capacity of 121 mAh g−1, respectively. Ex situ X-ray photoelectron spectroscopy (XPS) and ex situ X-ray absorption spectroscopy (XAS) reveal a conversion reaction mechanism during Li+ insertion into the NiAl LDH material. X-ray diffraction (XRD) and XPS have been combined with the electrochemical study to understand the effect of different cutoff potentials on the Li-ion storage mechanism. Graphical abstract The as-prepared NiAl-NO3−-LDH with the rhombohedral R-3 m space group is investigated as a negative electrode material for lithium-ion batteries (LIBs). The effect of the potential range (i.e., 0.01–3.0 V and 0.4–3.0 V vs. Li+/Li) and of the binder on the material’s performance is investigated in 1 M LiPF6 in EC/DMC vs. Li. Ex situ X-ray photoelectron spectroscopy (XPS) and ex situ X-ray absorption spectroscopy (XAS) reveal a conversion reaction mechanism during Li+ insertion into the NiAl LDH material. X-ray diffraction (XRD) and XPS have been combined with the electrochemical study to understand the effect of different cutoff potentials on the Li-ion storage mechanism. This work highlights the possibility of the direct application of NiAl LDH materials as negative electrodes for LIBs.

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