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Ni-oxide-based thin films, prepared by sputtering, are investigated by electrochemical impedance spectroscopy in a KOH electrolyte. The films are electrochromic, and an increase of the applied potential leads to a variation from a bleached to a colored state as a result of proton (H+) extraction together with extraction of electrons from the valence band. The complex frequency-dependent impedance displays different features in different potential ranges. At low potentials, where coloration is weak, the spectra give evidence for a constant-phase element in parallel with a leak resistance. At intermediate and high potentials, the impedance spectra indicate the presence of a diffusion process, and a model for anomalous diffusion gives excellent fits to the spectra except in a crossover region. The applicability of this model in a significant part of the studied potential range suggests the presence of a multiple-trapping process for the ions. The potential dependence of the chemical capacitance, as well as the diffusion coefficient of un-trapped ions, are analyzed. The electrochemical density-of-states of the chargecompensating electrons gives indications of the top of the valence band and of a band tail extending into the band gap. Diffusion coefficients are found to increase steeply in the crossover potential region to very high values at high potentials. These features are discussed and related to the electrochromic behavior of Ni-oxide-based thin films.

Ni-oxide-based thin films, prepared by sputtering, are investigated by electrochemical impedance spectroscopy in a KOH electrolyte. The films are electrochromic, and an increase of the applied potential leads to a variation from a bleached to a colored state as a result of proton (H+) extraction together with extraction of electrons from the valence band. The complex frequency-dependent impedance displays different features in different potential ranges. At low potentials, where coloration is weak, the spectra give evidence for a constant-phase element in parallel with a leak resistance. At intermediate and high potentials, the impedance spectra indicate the presence of a diffusion process, and a model for anomalous diffusion gives excellent fits to the spectra except in a crossover region. The applicability of this model in a significant part of the studied potential range suggests the presence of a multiple-trapping process for the ions. The potential dependence of the chemical capacitance, as well as the diffusion coefficient of un-trapped ions, are analyzed. The electrochemical density-of-states of the chargecompensating electrons gives indications of the top of the valence band and of a band tail extending into the band gap. Diffusion coefficients are found to increase steeply in the crossover potential region to very high values at high potentials. These features are discussed and related to the electrochromic behavior of Ni-oxide-based thin films.

Ni-oxide-based thin films, prepared by sputtering, are investigated by electrochemical impedance spectroscopy in a KOH electrolyte. The films are electrochromic, and an increase of the applied potential leads to a variation from a bleached to a colored state as a result of proton (H+) extraction together with extraction of electrons from the valence band. The complex frequency-dependent impedance displays different features in different potential ranges. At low potentials, where coloration is weak, the spectra give evidence for a constant-phase element in parallel with a leak resistance. At intermediate and high potentials, the impedance spectra indicate the presence of a diffusion process, and a model for anomalous diffusion gives excellent fits to the spectra except in a crossover region. The applicability of this model in a significant part of the studied potential range suggests the presence of a multiple-trapping process for the ions. The potential dependence of the chemical capacitance, as well as the diffusion coefficient of un-trapped ions, are analyzed. The electrochemical density-of-states of the chargecompensating electrons gives indications of the top of the valence band and of a band tail extending into the band gap. Diffusion coefficients are found to increase steeply in the crossover potential region to very high values at high potentials. These features are discussed and related to the electrochromic behavior of Ni-oxide-based thin films.

Ni-oxide-based thin films, prepared by sputtering, are investigated by electrochemical impedance spectroscopy in a KOH electrolyte. The films are electrochromic, and an increase of the applied potential leads to a variation from a bleached to a colored state as a result of proton (H+) extraction together with extraction of electrons from the valence band. The complex frequency-dependent impedance displays different features in different potential ranges. At low potentials, where coloration is weak, the spectra give evidence for a constant-phase element in parallel with a leak resistance. At intermediate and high potentials, the impedance spectra indicate the presence of a diffusion process, and a model for anomalous diffusion gives excellent fits to the spectra except in a crossover region. The applicability of this model in a significant part of the studied potential range suggests the presence of a multiple-trapping process for the ions. The potential dependence of the chemical capacitance, as well as the diffusion coefficient of un-trapped ions, are analyzed. The electrochemical density-of-states of the chargecompensating electrons gives indications of the top of the valence band and of a band tail extending into the band gap. Diffusion coefficients are found to increase steeply in the crossover potential region to very high values at high potentials. These features are discussed and related to the electrochromic behavior of Ni-oxide-based thin films.

Ni-oxide-based thin films, prepared by sputtering, are investigated by electrochemical impedance spectroscopy in a KOH electrolyte. The films are electrochromic, and an increase of the applied potential leads to a variation from a bleached to a colored state as a result of proton (H+) extraction together with extraction of electrons from the valence band. The complex frequency-dependent impedance displays different features in different potential ranges. At low potentials, where coloration is weak, the spectra give evidence for a constant-phase element in parallel with a leak resistance. At intermediate and high potentials, the impedance spectra indicate the presence of a diffusion process, and a model for anomalous diffusion gives excellent fits to the spectra except in a crossover region. The applicability of this model in a significant part of the studied potential range suggests the presence of a multiple-trapping process for the ions. The potential dependence of the chemical capacitance, as well as the diffusion coefficient of un-trapped ions, are analyzed. The electrochemical density-of-states of the chargecompensating electrons gives indications of the top of the valence band and of a band tail extending into the band gap. Diffusion coefficients are found to increase steeply in the crossover potential region to very high values at high potentials. These features are discussed and related to the electrochromic behavior of Ni-oxide-based thin films.

Tungsten oxide and titanium doped tungsten oxide thin films, deposited by sputtering, were immersed in a viscous electrolyte comprised of LiClO4 in propylene carbonate and 2.0 wt% of polyethylene oxide (PEO). Electrochromic properties of the films were investigated by electrochemical techniques and in situ transmittance measurements. Cyclic voltammetry data were taken in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs Li/Li+ for up to 500 cycles. A potentiostatic rejuvenation treatment was then performed on the degraded electrochromic films, at 6.0 V for 20 h, which was subsequently followed by another cyclic voltammetry measurement. Titanium incorporation into tungsten oxide resulted in a small cyclic stability improvement in the 2.0–4.0-V range, whereas less pronounced effects were observed for cycling in the 1.5–4.0-V range. Combining the results of the present study with our previous work, we are able to assess the relative merits of titanium incorporation and PEO addition to the electrolyte for the durability of electrochromic tungsten oxide thin films. Titanium addition was found advantageous for electrochemical durability in the 2.0–4.0-V range, but no clear benefits of PEO in the electrolyte were seen. On the other hand, in the wider 1.5–4.0-V range, tungsten oxide exhibited better durability than titanium-containing films, and this was especially so after rejuvenation in the PEO-containing electrolyte.

Electrochromic (EC) technology allows control of the transmission of visible light and solar radiation through thin-film devices. When applied to “smart” windows, EC technology can significantly diminish energy use for cooling and air conditioning of buildings and simultaneously provide good indoor comfort for the buildings’ occupants through reduced glare. EC “smart” windows are available on the market, but it is nevertheless important that their degradation under operating conditions be better understood and, ideally, prevented. In the present work, we investigated EC properties, voltammetric cycling durability, and potentiostatic rejuvenation of sputter-deposited WO3 thin films immersed in LiClO4–propylene carbonate electrolytes containing up to 3.0 wt% of ∼7-nm-diameter SiO2 nanoparticles. Adding about 1 wt% SiO2 led to a significant improvement in cycling durability in the commonly used potential range of 2.0–4.0 V vs. Li/Li+. Furthermore, X-ray photoemission spectroscopy indicated that O–Si bonds were associated with enhanced durability in the presence of SiO2 nanoparticles.

Electrochromic (EC) technology allows control of the transmission of visible light and solar radiation through thin-film devices. When applied to “smart” windows, EC technology can significantly diminish energy use for cooling and air conditioning of buildings and simultaneously provide good indoor comfort for the buildings’ occupants through reduced glare. EC “smart” windows are available on the market, but it is nevertheless important that their degradation under operating conditions be better understood and, ideally, prevented. In the present work, we investigated EC properties, voltammetric cycling durability, and potentiostatic rejuvenation of sputter-deposited WO3 thin films immersed in LiClO4–propylene carbonate electrolytes containing up to 3.0 wt% of ∼7-nm-diameter SiO2 nanoparticles. Adding about 1 wt% SiO2 led to a significant improvement in cycling durability in the commonly used potential range of 2.0–4.0 V vs. Li/Li+. Furthermore, X-ray photoemission spectroscopy indicated that O–Si bonds were associated with enhanced durability in the presence of SiO2 nanoparticles.

Electrochromic (EC) technology allows control of the transmission of visible light and solar radiation through thin-film devices. When applied to “smart” windows, EC technology can significantly diminish energy use for cooling and air conditioning of buildings and simultaneously provide good indoor comfort for the buildings’ occupants through reduced glare. EC “smart” windows are available on the market, but it is nevertheless important that their degradation under operating conditions be better understood and, ideally, prevented. In the present work, we investigated EC properties, voltammetric cycling durability, and potentiostatic rejuvenation of sputter-deposited WO3 thin films immersed in LiClO4–propylene carbonate electrolytes containing up to 3.0 wt% of ∼7-nm-diameter SiO2 nanoparticles. Adding about 1 wt% SiO2 led to a significant improvement in cycling durability in the commonly used potential range of 2.0–4.0 V vs. Li/Li+. Furthermore, X-ray photoemission spectroscopy indicated that O–Si bonds were associated with enhanced durability in the presence of SiO2 nanoparticles.

Electrochromic (EC) technology allows control of the transmission of visible light and solar radiation through thin-film devices. When applied to “smart” windows, EC technology can significantly diminish energy use for cooling and air conditioning of buildings and simultaneously provide good indoor comfort for the buildings’ occupants through reduced glare. EC “smart” windows are available on the market, but it is nevertheless important that their degradation under operating conditions be better understood and, ideally, prevented. In the present work, we investigated EC properties, voltammetric cycling durability, and potentiostatic rejuvenation of sputter-deposited WO3 thin films immersed in LiClO4–propylene carbonate electrolytes containing up to 3.0 wt% of ∼7-nm-diameter SiO2 nanoparticles. Adding about 1 wt% SiO2 led to a significant improvement in cycling durability in the commonly used potential range of 2.0–4.0 V vs. Li/Li+. Furthermore, X-ray photoemission spectroscopy indicated that O–Si bonds were associated with enhanced durability in the presence of SiO2 nanoparticles.

Tungsten oxide and titanium doped tungsten oxide thin films, deposited by sputtering, were immersed in a viscous electrolyte comprised of LiClO4 in propylene carbonate and 2.0 wt% of polyethylene oxide (PEO). Electrochromic properties of the films were investigated by electrochemical techniques and in situ transmittance measurements. Cyclic voltammetry data were taken in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs Li/Li+ for up to 500 cycles. A potentiostatic rejuvenation treatment was then performed on the degraded electrochromic films, at 6.0 V for 20 h, which was subsequently followed by another cyclic voltammetry measurement. Titanium incorporation into tungsten oxide resulted in a small cyclic stability improvement in the 2.0–4.0-V range, whereas less pronounced effects were observed for cycling in the 1.5–4.0-V range. Combining the results of the present study with our previous work, we are able to assess the relative merits of titanium incorporation and PEO addition to the electrolyte for the durability of electrochromic tungsten oxide thin films. Titanium addition was found advantageous for electrochemical durability in the 2.0–4.0-V range, but no clear benefits of PEO in the electrolyte were seen. On the other hand, in the wider 1.5–4.0-V range, tungsten oxide exhibited better durability than titanium-containing films, and this was especially so after rejuvenation in the PEO-containing electrolyte.

Tungsten oxide and titanium doped tungsten oxide thin films, deposited by sputtering, were immersed in a viscous electrolyte comprised of LiClO4 in propylene carbonate and 2.0 wt% of polyethylene oxide (PEO). Electrochromic properties of the films were investigated by electrochemical techniques and in situ transmittance measurements. Cyclic voltammetry data were taken in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs Li/Li+ for up to 500 cycles. A potentiostatic rejuvenation treatment was then performed on the degraded electrochromic films, at 6.0 V for 20 h, which was subsequently followed by another cyclic voltammetry measurement. Titanium incorporation into tungsten oxide resulted in a small cyclic stability improvement in the 2.0–4.0-V range, whereas less pronounced effects were observed for cycling in the 1.5–4.0-V range. Combining the results of the present study with our previous work, we are able to assess the relative merits of titanium incorporation and PEO addition to the electrolyte for the durability of electrochromic tungsten oxide thin films. Titanium addition was found advantageous for electrochemical durability in the 2.0–4.0-V range, but no clear benefits of PEO in the electrolyte were seen. On the other hand, in the wider 1.5–4.0-V range, tungsten oxide exhibited better durability than titanium-containing films, and this was especially so after rejuvenation in the PEO-containing electrolyte.

Tungsten oxide and titanium doped tungsten oxide thin films, deposited by sputtering, were immersed in a viscous electrolyte comprised of LiClO4 in propylene carbonate and 2.0 wt% of polyethylene oxide (PEO). Electrochromic properties of the films were investigated by electrochemical techniques and in situ transmittance measurements. Cyclic voltammetry data were taken in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs Li/Li+ for up to 500 cycles. A potentiostatic rejuvenation treatment was then performed on the degraded electrochromic films, at 6.0 V for 20 h, which was subsequently followed by another cyclic voltammetry measurement. Titanium incorporation into tungsten oxide resulted in a small cyclic stability improvement in the 2.0–4.0-V range, whereas less pronounced effects were observed for cycling in the 1.5–4.0-V range. Combining the results of the present study with our previous work, we are able to assess the relative merits of titanium incorporation and PEO addition to the electrolyte for the durability of electrochromic tungsten oxide thin films. Titanium addition was found advantageous for electrochemical durability in the 2.0–4.0-V range, but no clear benefits of PEO in the electrolyte were seen. On the other hand, in the wider 1.5–4.0-V range, tungsten oxide exhibited better durability than titanium-containing films, and this was especially so after rejuvenation in the PEO-containing electrolyte.

BACKGROUND: The definition of partial resuscitative endovascular balloon occlusion of the aorta (pREBOA) is not yet determined and clinical markers of the degree of occlusion, metabolic effects and end-organ injury that are clinically monitored in real time are lacking. The aim of the study was to test the hypothesis that end-tidal carbon dioxide (ETCO2) targeted pREBOA causes less metabolic disturbance compared to proximal systolic blood pressure (SBP) targeted pREBOA in a porcine model of hemorrhagic shock. MATERIALS AND METHODS: Twenty anesthetized pigs (26-35 kg) were randomized to 45 min of either ETCO2 targeted pREBOA (pREBOAETCO2, ETCO2 90-110% of values before start of occlusion, n = 10) or proximal SBP targeted pREBOA (pREBOASBP, SBP 80-100 mmHg, n = 10), during controlled grade IV hemorrhagic shock. Autotransfusion and reperfusion over 3 h followed. Hemodynamic and respiratory parameters, blood samples and jejunal specimens were analyzed. RESULTS: ETCO2 was significantly higher in the pREBOAETCO2 group during the occlusion compared to the pREBOASBP group, whereas SBP, femoral arterial mean pressure and abdominal aortic blood flow were similar. During reperfusion, arterial and mesenteric lactate, plasma creatinine and plasma troponin concentrations were higher in the pREBOASBP group. CONCLUSIONS: In a porcine model of hemorrhagic shock, ETCO2 targeted pREBOA caused less metabolic disturbance and end-organ damage compared to proximal SBP targeted pREBOA, with no disadvantageous hemodynamic impact. End-tidal CO2 should be investigated in clinical studies as a complementary clinical tool for mitigating ischemic-reperfusion injury when using pREBOA.

Tungsten oxide and titanium doped tungsten oxide thin films, deposited by sputtering, were immersed in a viscous electrolyte comprised of LiClO4 in propylene carbonate and 2.0 wt% of polyethylene oxide (PEO). Electrochromic properties of the films were investigated by electrochemical techniques and in situ transmittance measurements. Cyclic voltammetry data were taken in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs Li/Li+ for up to 500 cycles. A potentiostatic rejuvenation treatment was then performed on the degraded electrochromic films, at 6.0 V for 20 h, which was subsequently followed by another cyclic voltammetry measurement. Titanium incorporation into tungsten oxide resulted in a small cyclic stability improvement in the 2.0–4.0-V range, whereas less pronounced effects were observed for cycling in the 1.5–4.0-V range. Combining the results of the present study with our previous work, we are able to assess the relative merits of titanium incorporation and PEO addition to the electrolyte for the durability of electrochromic tungsten oxide thin films. Titanium addition was found advantageous for electrochemical durability in the 2.0–4.0-V range, but no clear benefits of PEO in the electrolyte were seen. On the other hand, in the wider 1.5–4.0-V range, tungsten oxide exhibited better durability than titanium-containing films, and this was especially so after rejuvenation in the PEO-containing electrolyte.

Electrochromic (EC) technology allows control of the transmission of visible light and solar radiation through thin-film devices. When applied to “smart” windows, EC technology can significantly diminish energy use for cooling and air conditioning of buildings and simultaneously provide good indoor comfort for the buildings’ occupants through reduced glare. EC “smart” windows are available on the market, but it is nevertheless important that their degradation under operating conditions be better understood and, ideally, prevented. In the present work, we investigated EC properties, voltammetric cycling durability, and potentiostatic rejuvenation of sputter-deposited WO3 thin films immersed in LiClO4–propylene carbonate electrolytes containing up to 3.0 wt% of ∼7-nm-diameter SiO2 nanoparticles. Adding about 1 wt% SiO2 led to a significant improvement in cycling durability in the commonly used potential range of 2.0–4.0 V vs. Li/Li+. Furthermore, X-ray photoemission spectroscopy indicated that O–Si bonds were associated with enhanced durability in the presence of SiO2 nanoparticles.

Tungsten oxide is a widely used electrochromic material with important applications in variable-transmittance smart windows as well as in other optoelectronic devices. Here we report on electrochemical impedance spectroscopy applied to hydrous electrochromic tungsten oxide films in a wide range of applied potentials. The films were able to reversibly bleach and color upon electrochemical cycling. Interestingly, the bleaching potential was found to be significantly higher than in conventional non-hydrous tungsten oxide films. Impedance spectra at low potentials showed good agreement with anomalous diffusion models for ion transport in the films. At high potentials,where little ion intercalation takes place, it seems that parasitic side reactions influence the spectra. The potential dependence of the chemical capacitance, as well as the ion diffusion coefficient, were analyzed. The chemical capacitance is discussed in terms of the electron density of states in the films and evidence was found for a band tail extending below the conduction band edge.

From an enforcement point of view, the revocation of the European Commission’s two adequacy decisions on the federal US system of data protection raises many questions regarding the interrelations between the EU data protection regime and the Union’s legal frameworks for data ‘transfers’. Whereas data uploaded in the Union was once upon a time wired over the Atlantic to be downloaded in the US and vice versa, data packets are nowadays often exchanged over various radio spectra. As online resources around the world can be used to store data, and the data is made available and retrieved from domains rather than ‘exported’ and ‘imported’, the idea that the EU data protection regime would no longer apply when data is ‘transferred’ from the Union easily leads astray. In fact, the location of data or data processing equipment is irrelevant for the applicability of EU law as its territorial scope is determined by the location of the data subjects or undertakings concerned. Whereas the EU legislation applies with regard to legal entities overseas with affiliated undertakings in the Union, the Union seeks to guarantee the EU data subjects an adequate level of protection also in cases of onward transfers of data to non-affiliated organisations and unwarranted interceptions. Furthermore, the European Commission promotes a level of protection in non-EU Member States that is essentially equivalent to that enjoyed under the EU data protection regime since the authorities and courts may refrain from applying EU law pursuant to private international law. However, the Cases which resulted in the revocation of the two adequacy decisions concerned an Austrian citizen filing complaints against an undertaking established in Ireland and its US parent company. Hence, it must be called into question whether the EU data protection regime should at all have been substituted by the US system irrespective of whether it provided an adequate level of data protection. An argument could be made th, Online platform trade and EU privacy law

Tungsten oxide is a widely used electrochromic material with important applications in variable-transmittance smart windows as well as in other optoelectronic devices. Here we report on electrochemical impedance spectroscopy applied to hydrous electrochromic tungsten oxide films in a wide range of applied potentials. The films were able to reversibly bleach and color upon electrochemical cycling. Interestingly, the bleaching potential was found to be significantly higher than in conventional non-hydrous tungsten oxide films. Impedance spectra at low potentials showed good agreement with anomalous diffusion models for ion transport in the films. At high potentials,where little ion intercalation takes place, it seems that parasitic side reactions influence the spectra. The potential dependence of the chemical capacitance, as well as the ion diffusion coefficient, were analyzed. The chemical capacitance is discussed in terms of the electron density of states in the films and evidence was found for a band tail extending below the conduction band edge.

From an enforcement point of view, the revocation of the European Commission’s two adequacy decisions on the federal US system of data protection raises many questions regarding the interrelations between the EU data protection regime and the Union’s legal frameworks for data ‘transfers’. Whereas data uploaded in the Union was once upon a time wired over the Atlantic to be downloaded in the US and vice versa, data packets are nowadays often exchanged over various radio spectra. As online resources around the world can be used to store data, and the data is made available and retrieved from domains rather than ‘exported’ and ‘imported’, the idea that the EU data protection regime would no longer apply when data is ‘transferred’ from the Union easily leads astray. In fact, the location of data or data processing equipment is irrelevant for the applicability of EU law as its territorial scope is determined by the location of the data subjects or undertakings concerned. Whereas the EU legislation applies with regard to legal entities overseas with affiliated undertakings in the Union, the Union seeks to guarantee the EU data subjects an adequate level of protection also in cases of onward transfers of data to non-affiliated organisations and unwarranted interceptions. Furthermore, the European Commission promotes a level of protection in non-EU Member States that is essentially equivalent to that enjoyed under the EU data protection regime since the authorities and courts may refrain from applying EU law pursuant to private international law. However, the Cases which resulted in the revocation of the two adequacy decisions concerned an Austrian citizen filing complaints against an undertaking established in Ireland and its US parent company. Hence, it must be called into question whether the EU data protection regime should at all have been substituted by the US system irrespective of whether it provided an adequate level of data protection. An argument could be made th, Online platform trade and EU privacy law

Tungsten oxide is a widely used electrochromic material with important applications in variable-transmittance smart windows as well as in other optoelectronic devices. Here we report on electrochemical impedance spectroscopy applied to hydrous electrochromic tungsten oxide films in a wide range of applied potentials. The films were able to reversibly bleach and color upon electrochemical cycling. Interestingly, the bleaching potential was found to be significantly higher than in conventional non-hydrous tungsten oxide films. Impedance spectra at low potentials showed good agreement with anomalous diffusion models for ion transport in the films. At high potentials,where little ion intercalation takes place, it seems that parasitic side reactions influence the spectra. The potential dependence of the chemical capacitance, as well as the ion diffusion coefficient, were analyzed. The chemical capacitance is discussed in terms of the electron density of states in the films and evidence was found for a band tail extending below the conduction band edge.

From an enforcement point of view, the revocation of the European Commission’s two adequacy decisions on the federal US system of data protection raises many questions regarding the interrelations between the EU data protection regime and the Union’s legal frameworks for data ‘transfers’. Whereas data uploaded in the Union was once upon a time wired over the Atlantic to be downloaded in the US and vice versa, data packets are nowadays often exchanged over various radio spectra. As online resources around the world can be used to store data, and the data is made available and retrieved from domains rather than ‘exported’ and ‘imported’, the idea that the EU data protection regime would no longer apply when data is ‘transferred’ from the Union easily leads astray. In fact, the location of data or data processing equipment is irrelevant for the applicability of EU law as its territorial scope is determined by the location of the data subjects or undertakings concerned. Whereas the EU legislation applies with regard to legal entities overseas with affiliated undertakings in the Union, the Union seeks to guarantee the EU data subjects an adequate level of protection also in cases of onward transfers of data to non-affiliated organisations and unwarranted interceptions. Furthermore, the European Commission promotes a level of protection in non-EU Member States that is essentially equivalent to that enjoyed under the EU data protection regime since the authorities and courts may refrain from applying EU law pursuant to private international law. However, the Cases which resulted in the revocation of the two adequacy decisions concerned an Austrian citizen filing complaints against an undertaking established in Ireland and its US parent company. Hence, it must be called into question whether the EU data protection regime should at all have been substituted by the US system irrespective of whether it provided an adequate level of data protection. An argument could be made th, Online platform trade and EU privacy law

Nitric oxide (NO) for inhalation has been a clinical option in the ICU since the early 1990s. Much has been written and claimed after the initial enthusiasm over an acutely improved arterial oxygenation in adult patients with ARDS. A few years ago, a meta-analysis (1) concluded that the regular use of inhaled NO (iNO) in patients with ARDS outside a clinical trial could not be recommended, as no benefit such as reduced mortality or time on the ventilator could be identified in published randomized studies.

Tungsten oxide is a widely used electrochromic material with important applications in variable-transmittance smart windows as well as in other optoelectronic devices. Here we report on electrochemical impedance spectroscopy applied to hydrous electrochromic tungsten oxide films in a wide range of applied potentials. The films were able to reversibly bleach and color upon electrochemical cycling. Interestingly, the bleaching potential was found to be significantly higher than in conventional non-hydrous tungsten oxide films. Impedance spectra at low potentials showed good agreement with anomalous diffusion models for ion transport in the films. At high potentials,where little ion intercalation takes place, it seems that parasitic side reactions influence the spectra. The potential dependence of the chemical capacitance, as well as the ion diffusion coefficient, were analyzed. The chemical capacitance is discussed in terms of the electron density of states in the films and evidence was found for a band tail extending below the conduction band edge.

From an enforcement point of view, the revocation of the European Commission’s two adequacy decisions on the federal US system of data protection raises many questions regarding the interrelations between the EU data protection regime and the Union’s legal frameworks for data ‘transfers’. Whereas data uploaded in the Union was once upon a time wired over the Atlantic to be downloaded in the US and vice versa, data packets are nowadays often exchanged over various radio spectra. As online resources around the world can be used to store data, and the data is made available and retrieved from domains rather than ‘exported’ and ‘imported’, the idea that the EU data protection regime would no longer apply when data is ‘transferred’ from the Union easily leads astray. In fact, the location of data or data processing equipment is irrelevant for the applicability of EU law as its territorial scope is determined by the location of the data subjects or undertakings concerned. Whereas the EU legislation applies with regard to legal entities overseas with affiliated undertakings in the Union, the Union seeks to guarantee the EU data subjects an adequate level of protection also in cases of onward transfers of data to non-affiliated organisations and unwarranted interceptions. Furthermore, the European Commission promotes a level of protection in non-EU Member States that is essentially equivalent to that enjoyed under the EU data protection regime since the authorities and courts may refrain from applying EU law pursuant to private international law. However, the Cases which resulted in the revocation of the two adequacy decisions concerned an Austrian citizen filing complaints against an undertaking established in Ireland and its US parent company. Hence, it must be called into question whether the EU data protection regime should at all have been substituted by the US system irrespective of whether it provided an adequate level of data protection. An argument could be made th, Online platform trade and EU privacy law

Tungsten oxide is a widely used electrochromic material with important applications in variable-transmittance smart windows as well as in other optoelectronic devices. Here we report on electrochemical impedance spectroscopy applied to hydrous electrochromic tungsten oxide films in a wide range of applied potentials. The films were able to reversibly bleach and color upon electrochemical cycling. Interestingly, the bleaching potential was found to be significantly higher than in conventional non-hydrous tungsten oxide films. Impedance spectra at low potentials showed good agreement with anomalous diffusion models for ion transport in the films. At high potentials,where little ion intercalation takes place, it seems that parasitic side reactions influence the spectra. The potential dependence of the chemical capacitance, as well as the ion diffusion coefficient, were analyzed. The chemical capacitance is discussed in terms of the electron density of states in the films and evidence was found for a band tail extending below the conduction band edge.

Tungsten-oxide-based thin films were prepared by reactive DC magnetron sputtering in the presence ofoxygen and nitrogen. Nitrogen contents up to 12 at.% were documented by Rutherford backscattering spectrometry and time-of-flight elastic recoil detection analysis. Optical and electrochemical measurements showed that films with up to 4 at.% of nitrogen were as transparent as undoped tungsten oxide films and displayed enhanced electrochromic properties manifested in an increase in the coloration efficiency by as much as 20%.

Thin films of electrochromic (EC) W oxide were prepared by reactive DC magnetron sputtering and were immersed in electrolytes of LiClO4 in propylene carbonate with 0.5–3.0 wt% of added polyethylene oxide (PEO). Charge density and optical modulation range were found to diminish monotonically upon prolonged voltammetric cycling with concurrent optical transmittance measurements for up to 500 and 200 cycles in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs. Li/Li+, respectively. Rejuvenation of the degraded EC films was then accomplished by potentiostatic treatment at 6.0 V vs. Li/Li+ for 20 h and has been ascribed to expulsion of trapped Li ions. Importantly, degradation subsequent to rejuvenation was found to progress at a significantly lowered pace than for as-deposited films—in proportion with the amount of PEO—especially for harsh voltammetric cycling in the voltage range 1.5–4.0 V vs. Li/Li+. The results of this explorative study are of considerable value for the development of highly durable EC devices such as polymer-laminated smart glazing for energy efficient buildings with excellent indoor comfort., De två första författarna delar förstaförfattarskapetTitle in Web of Science: Potentiostatic rejuvenation of electrochromic WO3 thin films: Exploring the effect of polyethylene oxide in LiClO4-Propylene carbonate electrolytes

Films of electrochromic Ni oxide, with thickness in the ∼100–1000-nm range, were prepared by reactive advanced gas deposition (AGD) and, for comparison, also by reactive DC magnetron sputtering (MS). Voltammetric cycling was performed in an electrolyte of lithium perchlorate in propylene carbonate in the voltage range 2.0–4.1 V vs Li/Li+, and concurrent optical transmittance modulation was studied at a wavelength of 530 nm. For the thickest films, the optical modulation range was as large as ∼54% and the maximum transmittance was ∼82% for deposition by AGD, whereas the corresponding numbers were ∼45% and ∼87% for MS. Rutherford backscattering spectrometry together with measurements of film thickness demonstrated that the porosity of 400–500-nm-thick films made by AGD and MS were ∼84% and ∼45%, respectively. The charge exchange per mass unit was as high as 48–67 C g–1 for samples made by AGD. The corresponding number was much lower for MS, namely 13–18 C g–1. These results lend convincing support to the view that the electrochromism of Ni-oxide-based films in Li-ion-conducting electrolytes is dominated by surface effects., De två första författarna delar förstaförfattarskapet

Electrochemical degradation of electrochromic W oxide and W–Ti oxide thin films, prepared by reactive DC magnetron sputtering, was studied by voltammetric cycling in potential intervals from 1.5–4.0 to 2.0–4.0 V vs Li/Li+ in an electrolyte of lithium perchlorate in propylene carbonate. Cycling-dependent evolution of the upper and lower limits for the optical modulation range was critically dependent on potential interval. This phenomenon was analyzed through an extension of a previously formulated model for power-law dynamics; it was discovered that the upper and lower limits for the optical modulation range varied in distinctly different ways, and that only data acquired in the interval 2.0–4.0 V vs Li/Li+ could be reconciled with dispersive chemical kinetics. We thus find that our data on optical transmittance degradation lends strong support to the existence of dual degradation modes for electrochromism upon extended electrochemical cycling. This result is of great importance for the development of highly durable electrochromic devices such as smart windows for energy-efficient buildings. The present article is a sequel to a recent publication of ours [J. Electrochem. Soc., 166, H795 (2019)].

Electrochromic W oxide and W–In oxide thin films were prepared by dual-target reactive DC magnetron sputtering and were cycled voltammetrically in an electrolyte of lithium perchlorate in propylene carbonate. Film degradation was investigated for up to 500 cycles in the voltage ranges 1.5–4.0, 1.7–4.0 and 2.0–4.0 V vs. Li/Li+, and optical transmittance was recorded concurrently. Indium doping was found to be unambiguously detrimental to electrochromic cycling durability, which resolves an outstanding issue related to recently discovered unprecedented durability of potentiostatically pretreated W oxide films backed by In2O3:Sn and gives strong support in favor of beneficial effects of solid-electrolyte interfacial layers.

Filamin C (FLNC) variants are associated with cardiac and muscular phenotypes. Originally, FLNC variants were described in myofibrillar myopathy (MFM) patients. Later, high-throughput screening in cardiomyopathy cohorts determined a prominent role for FLNC in isolated hypertrophic and dilated cardiomyopathies (HCM and DCM). FLNC variants are now among the more prevalent causes of genetic DCM. FLNC-associated DCM is associated with a malignant clinical course and a high risk of sudden cardiac death. The clinical spectrum of FLNC suggests different pathomechanisms related to variant types and their location in the gene. The appropriate functioning of FLNC is crucial for structural integrity and cell signaling of the sarcomere. The secondary protein structure of FLNC is critical to ensure this function. Truncating variants with subsequent haploinsufficiency are associated with DCM and cardiac arrhythmias. Interference with the dimerization and folding of the protein leads to aggregate formation detrime

Thin films of electrochromic (EC) W oxide were prepared by reactive DC magnetron sputtering and were immersed in electrolytes of LiClO4 in propylene carbonate with 0.5–3.0 wt% of added polyethylene oxide (PEO). Charge density and optical modulation range were found to diminish monotonically upon prolonged voltammetric cycling with concurrent optical transmittance measurements for up to 500 and 200 cycles in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs. Li/Li+, respectively. Rejuvenation of the degraded EC films was then accomplished by potentiostatic treatment at 6.0 V vs. Li/Li+ for 20 h and has been ascribed to expulsion of trapped Li ions. Importantly, degradation subsequent to rejuvenation was found to progress at a significantly lowered pace than for as-deposited films—in proportion with the amount of PEO—especially for harsh voltammetric cycling in the voltage range 1.5–4.0 V vs. Li/Li+. The results of this explorative study are of considerable value for the development of highly durable EC devices such as polymer-laminated smart glazing for energy efficient buildings with excellent indoor comfort., De två första författarna delar förstaförfattarskapetTitle in Web of Science: Potentiostatic rejuvenation of electrochromic WO3 thin films: Exploring the effect of polyethylene oxide in LiClO4-Propylene carbonate electrolytes

Thin films of electrochromic (EC) W oxide were prepared by reactive DC magnetron sputtering and were immersed in electrolytes of LiClO4 in propylene carbonate with 0.5–3.0 wt% of added polyethylene oxide (PEO). Charge density and optical modulation range were found to diminish monotonically upon prolonged voltammetric cycling with concurrent optical transmittance measurements for up to 500 and 200 cycles in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs. Li/Li+, respectively. Rejuvenation of the degraded EC films was then accomplished by potentiostatic treatment at 6.0 V vs. Li/Li+ for 20 h and has been ascribed to expulsion of trapped Li ions. Importantly, degradation subsequent to rejuvenation was found to progress at a significantly lowered pace than for as-deposited films—in proportion with the amount of PEO—especially for harsh voltammetric cycling in the voltage range 1.5–4.0 V vs. Li/Li+. The results of this explorative study are of considerable value for the development of highly durable EC devices such as polymer-laminated smart glazing for energy efficient buildings with excellent indoor comfort., De två första författarna delar förstaförfattarskapetTitle in Web of Science: Potentiostatic rejuvenation of electrochromic WO3 thin films: Exploring the effect of polyethylene oxide in LiClO4-Propylene carbonate electrolytes

Electrochromic W oxide and W–In oxide thin films were prepared by dual-target reactive DC magnetron sputtering and were cycled voltammetrically in an electrolyte of lithium perchlorate in propylene carbonate. Film degradation was investigated for up to 500 cycles in the voltage ranges 1.5–4.0, 1.7–4.0 and 2.0–4.0 V vs. Li/Li+, and optical transmittance was recorded concurrently. Indium doping was found to be unambiguously detrimental to electrochromic cycling durability, which resolves an outstanding issue related to recently discovered unprecedented durability of potentiostatically pretreated W oxide films backed by In2O3:Sn and gives strong support in favor of beneficial effects of solid-electrolyte interfacial layers.

Films of electrochromic Ni oxide, with thickness in the ∼100–1000-nm range, were prepared by reactive advanced gas deposition (AGD) and, for comparison, also by reactive DC magnetron sputtering (MS). Voltammetric cycling was performed in an electrolyte of lithium perchlorate in propylene carbonate in the voltage range 2.0–4.1 V vs Li/Li+, and concurrent optical transmittance modulation was studied at a wavelength of 530 nm. For the thickest films, the optical modulation range was as large as ∼54% and the maximum transmittance was ∼82% for deposition by AGD, whereas the corresponding numbers were ∼45% and ∼87% for MS. Rutherford backscattering spectrometry together with measurements of film thickness demonstrated that the porosity of 400–500-nm-thick films made by AGD and MS were ∼84% and ∼45%, respectively. The charge exchange per mass unit was as high as 48–67 C g–1 for samples made by AGD. The corresponding number was much lower for MS, namely 13–18 C g–1. These results lend convincing support to the view that the electrochromism of Ni-oxide-based films in Li-ion-conducting electrolytes is dominated by surface effects., De två första författarna delar förstaförfattarskapet

Electrochemical degradation of electrochromic W oxide and W–Ti oxide thin films, prepared by reactive DC magnetron sputtering, was studied by voltammetric cycling in potential intervals from 1.5–4.0 to 2.0–4.0 V vs Li/Li+ in an electrolyte of lithium perchlorate in propylene carbonate. Cycling-dependent evolution of the upper and lower limits for the optical modulation range was critically dependent on potential interval. This phenomenon was analyzed through an extension of a previously formulated model for power-law dynamics; it was discovered that the upper and lower limits for the optical modulation range varied in distinctly different ways, and that only data acquired in the interval 2.0–4.0 V vs Li/Li+ could be reconciled with dispersive chemical kinetics. We thus find that our data on optical transmittance degradation lends strong support to the existence of dual degradation modes for electrochromism upon extended electrochemical cycling. This result is of great importance for the development of highly durable electrochromic devices such as smart windows for energy-efficient buildings. The present article is a sequel to a recent publication of ours [J. Electrochem. Soc., 166, H795 (2019)].

Electrochromic W oxide and W–In oxide thin films were prepared by dual-target reactive DC magnetron sputtering and were cycled voltammetrically in an electrolyte of lithium perchlorate in propylene carbonate. Film degradation was investigated for up to 500 cycles in the voltage ranges 1.5–4.0, 1.7–4.0 and 2.0–4.0 V vs. Li/Li+, and optical transmittance was recorded concurrently. Indium doping was found to be unambiguously detrimental to electrochromic cycling durability, which resolves an outstanding issue related to recently discovered unprecedented durability of potentiostatically pretreated W oxide films backed by In2O3:Sn and gives strong support in favor of beneficial effects of solid-electrolyte interfacial layers.

Films of electrochromic Ni oxide, with thickness in the ∼100–1000-nm range, were prepared by reactive advanced gas deposition (AGD) and, for comparison, also by reactive DC magnetron sputtering (MS). Voltammetric cycling was performed in an electrolyte of lithium perchlorate in propylene carbonate in the voltage range 2.0–4.1 V vs Li/Li+, and concurrent optical transmittance modulation was studied at a wavelength of 530 nm. For the thickest films, the optical modulation range was as large as ∼54% and the maximum transmittance was ∼82% for deposition by AGD, whereas the corresponding numbers were ∼45% and ∼87% for MS. Rutherford backscattering spectrometry together with measurements of film thickness demonstrated that the porosity of 400–500-nm-thick films made by AGD and MS were ∼84% and ∼45%, respectively. The charge exchange per mass unit was as high as 48–67 C g–1 for samples made by AGD. The corresponding number was much lower for MS, namely 13–18 C g–1. These results lend convincing support to the view that the electrochromism of Ni-oxide-based films in Li-ion-conducting electrolytes is dominated by surface effects., De två första författarna delar förstaförfattarskapet

Electrochemical degradation of electrochromic W oxide and W–Ti oxide thin films, prepared by reactive DC magnetron sputtering, was studied by voltammetric cycling in potential intervals from 1.5–4.0 to 2.0–4.0 V vs Li/Li+ in an electrolyte of lithium perchlorate in propylene carbonate. Cycling-dependent evolution of the upper and lower limits for the optical modulation range was critically dependent on potential interval. This phenomenon was analyzed through an extension of a previously formulated model for power-law dynamics; it was discovered that the upper and lower limits for the optical modulation range varied in distinctly different ways, and that only data acquired in the interval 2.0–4.0 V vs Li/Li+ could be reconciled with dispersive chemical kinetics. We thus find that our data on optical transmittance degradation lends strong support to the existence of dual degradation modes for electrochromism upon extended electrochemical cycling. This result is of great importance for the development of highly durable electrochromic devices such as smart windows for energy-efficient buildings. The present article is a sequel to a recent publication of ours [J. Electrochem. Soc., 166, H795 (2019)].

Thin films of electrochromic (EC) W oxide were prepared by reactive DC magnetron sputtering and were immersed in electrolytes of LiClO4 in propylene carbonate with 0.5–3.0 wt% of added polyethylene oxide (PEO). Charge density and optical modulation range were found to diminish monotonically upon prolonged voltammetric cycling with concurrent optical transmittance measurements for up to 500 and 200 cycles in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs. Li/Li+, respectively. Rejuvenation of the degraded EC films was then accomplished by potentiostatic treatment at 6.0 V vs. Li/Li+ for 20 h and has been ascribed to expulsion of trapped Li ions. Importantly, degradation subsequent to rejuvenation was found to progress at a significantly lowered pace than for as-deposited films—in proportion with the amount of PEO—especially for harsh voltammetric cycling in the voltage range 1.5–4.0 V vs. Li/Li+. The results of this explorative study are of considerable value for the development of highly durable EC devices such as polymer-laminated smart glazing for energy efficient buildings with excellent indoor comfort., De två första författarna delar förstaförfattarskapetTitle in Web of Science: Potentiostatic rejuvenation of electrochromic WO3 thin films: Exploring the effect of polyethylene oxide in LiClO4-Propylene carbonate electrolytes

Electrochromic W oxide and W–In oxide thin films were prepared by dual-target reactive DC magnetron sputtering and were cycled voltammetrically in an electrolyte of lithium perchlorate in propylene carbonate. Film degradation was investigated for up to 500 cycles in the voltage ranges 1.5–4.0, 1.7–4.0 and 2.0–4.0 V vs. Li/Li+, and optical transmittance was recorded concurrently. Indium doping was found to be unambiguously detrimental to electrochromic cycling durability, which resolves an outstanding issue related to recently discovered unprecedented durability of potentiostatically pretreated W oxide films backed by In2O3:Sn and gives strong support in favor of beneficial effects of solid-electrolyte interfacial layers.

Films of electrochromic Ni oxide, with thickness in the ∼100–1000-nm range, were prepared by reactive advanced gas deposition (AGD) and, for comparison, also by reactive DC magnetron sputtering (MS). Voltammetric cycling was performed in an electrolyte of lithium perchlorate in propylene carbonate in the voltage range 2.0–4.1 V vs Li/Li+, and concurrent optical transmittance modulation was studied at a wavelength of 530 nm. For the thickest films, the optical modulation range was as large as ∼54% and the maximum transmittance was ∼82% for deposition by AGD, whereas the corresponding numbers were ∼45% and ∼87% for MS. Rutherford backscattering spectrometry together with measurements of film thickness demonstrated that the porosity of 400–500-nm-thick films made by AGD and MS were ∼84% and ∼45%, respectively. The charge exchange per mass unit was as high as 48–67 C g–1 for samples made by AGD. The corresponding number was much lower for MS, namely 13–18 C g–1. These results lend convincing support to the view that the electrochromism of Ni-oxide-based films in Li-ion-conducting electrolytes is dominated by surface effects., De två första författarna delar förstaförfattarskapet

Electrochemical degradation of electrochromic W oxide and W–Ti oxide thin films, prepared by reactive DC magnetron sputtering, was studied by voltammetric cycling in potential intervals from 1.5–4.0 to 2.0–4.0 V vs Li/Li+ in an electrolyte of lithium perchlorate in propylene carbonate. Cycling-dependent evolution of the upper and lower limits for the optical modulation range was critically dependent on potential interval. This phenomenon was analyzed through an extension of a previously formulated model for power-law dynamics; it was discovered that the upper and lower limits for the optical modulation range varied in distinctly different ways, and that only data acquired in the interval 2.0–4.0 V vs Li/Li+ could be reconciled with dispersive chemical kinetics. We thus find that our data on optical transmittance degradation lends strong support to the existence of dual degradation modes for electrochromism upon extended electrochemical cycling. This result is of great importance for the development of highly durable electrochromic devices such as smart windows for energy-efficient buildings. The present article is a sequel to a recent publication of ours [J. Electrochem. Soc., 166, H795 (2019)].

Thin films of electrochromic (EC) W oxide were prepared by reactive DC magnetron sputtering and were immersed in electrolytes of LiClO4 in propylene carbonate with 0.5–3.0 wt% of added polyethylene oxide (PEO). Charge density and optical modulation range were found to diminish monotonically upon prolonged voltammetric cycling with concurrent optical transmittance measurements for up to 500 and 200 cycles in the voltage ranges 2.0–4.0 and 1.5–4.0 V vs. Li/Li+, respectively. Rejuvenation of the degraded EC films was then accomplished by potentiostatic treatment at 6.0 V vs. Li/Li+ for 20 h and has been ascribed to expulsion of trapped Li ions. Importantly, degradation subsequent to rejuvenation was found to progress at a significantly lowered pace than for as-deposited films—in proportion with the amount of PEO—especially for harsh voltammetric cycling in the voltage range 1.5–4.0 V vs. Li/Li+. The results of this explorative study are of considerable value for the development of highly durable EC devices such as polymer-laminated smart glazing for energy efficient buildings with excellent indoor comfort., De två första författarna delar förstaförfattarskapetTitle in Web of Science: Potentiostatic rejuvenation of electrochromic WO3 thin films: Exploring the effect of polyethylene oxide in LiClO4-Propylene carbonate electrolytes

Electrochemical degradation of electrochromic W oxide and W–Ti oxide thin films, prepared by reactive DC magnetron sputtering, was studied by voltammetric cycling in potential intervals from 1.5–4.0 to 2.0–4.0 V vs Li/Li+ in an electrolyte of lithium perchlorate in propylene carbonate. Cycling-dependent evolution of the upper and lower limits for the optical modulation range was critically dependent on potential interval. This phenomenon was analyzed through an extension of a previously formulated model for power-law dynamics; it was discovered that the upper and lower limits for the optical modulation range varied in distinctly different ways, and that only data acquired in the interval 2.0–4.0 V vs Li/Li+ could be reconciled with dispersive chemical kinetics. We thus find that our data on optical transmittance degradation lends strong support to the existence of dual degradation modes for electrochromism upon extended electrochemical cycling. This result is of great importance for the development of highly durable electrochromic devices such as smart windows for energy-efficient buildings. The present article is a sequel to a recent publication of ours [J. Electrochem. Soc., 166, H795 (2019)].

Films of electrochromic Ni oxide, with thickness in the ∼100–1000-nm range, were prepared by reactive advanced gas deposition (AGD) and, for comparison, also by reactive DC magnetron sputtering (MS). Voltammetric cycling was performed in an electrolyte of lithium perchlorate in propylene carbonate in the voltage range 2.0–4.1 V vs Li/Li+, and concurrent optical transmittance modulation was studied at a wavelength of 530 nm. For the thickest films, the optical modulation range was as large as ∼54% and the maximum transmittance was ∼82% for deposition by AGD, whereas the corresponding numbers were ∼45% and ∼87% for MS. Rutherford backscattering spectrometry together with measurements of film thickness demonstrated that the porosity of 400–500-nm-thick films made by AGD and MS were ∼84% and ∼45%, respectively. The charge exchange per mass unit was as high as 48–67 C g–1 for samples made by AGD. The corresponding number was much lower for MS, namely 13–18 C g–1. These results lend convincing support to the view that the electrochromism of Ni-oxide-based films in Li-ion-conducting electrolytes is dominated by surface effects., De två första författarna delar förstaförfattarskapet

Electrochromic W oxide and W–In oxide thin films were prepared by dual-target reactive DC magnetron sputtering and were cycled voltammetrically in an electrolyte of lithium perchlorate in propylene carbonate. Film degradation was investigated for up to 500 cycles in the voltage ranges 1.5–4.0, 1.7–4.0 and 2.0–4.0 V vs. Li/Li+, and optical transmittance was recorded concurrently. Indium doping was found to be unambiguously detrimental to electrochromic cycling durability, which resolves an outstanding issue related to recently discovered unprecedented durability of potentiostatically pretreated W oxide films backed by In2O3:Sn and gives strong support in favor of beneficial effects of solid-electrolyte interfacial layers.

Thin films of electrochromic W oxide and W–Ti oxide were prepared by reactive DC magnetron sputtering and were cycled voltammetrically in an electrolyte of lithium perchlorate in propylene carbonate. Film degradation was studied for up to 500 voltammetric cycles in voltage ranges between 1.5–4.0 and 2.0–4.0 V vs. Li/Li+. Optically and electrochemically degraded films were subjected to potentiostatic posttreatment at 6.0 V vs. Li/Li+ to achieve ion de-trapping and rejuvenation so that the films partly regained their original properties. Ti incorporation and potentiostatic posttreatment jointly yielded superior electrochromic properties provided the lower limit of the voltage range was above 1.6–1.7 V vs. Li/Li+. Degradation dynamics for as-deposited and rejuvenated thin films was modeled successfully by power-law kinetics; this analysis indicated coexistence of two degradation mechanisms, one based on dispersive chemical kinetics and operating universally and another, of unknown origin, rendered inactive by rejuvenation. The results of the present study are of large interest for the development of electrochromic devices with exceptional durability.