Nitration-Promoted Vanadate Catalysts for Low-Temperature Selective Catalytic Reduction of NOX with NH3.

Vanadium-based catalysts have been commercially used in selective catalytic reduction (SCR), owing to their high catalytic activity and effectiveness across a wide temperature range; however, their catalytic efficiency decreases at lower temperatures under exposure to SOX. This decrease is largely due to ammonium sulfate generation on the catalyst surface. To overcome this limitation, we added ammonium nitrate to the V2O5-WO3/TiO2 catalyst, producing a V2O5-WO3/TiO2 catalyst with nitrate functional groups. With this approach, we found that it was possible to adjust the amount of these functional groups by varying the amount of ammonium nitrate. Overall, the resultant nitrate V2O5-WO3/TiO2 catalyst has large quantities of NO3- and chemisorbed oxygen, which improves the density of Brønsted and Lewis acid sites on the catalyst surface. Furthermore, the nitrated V2O5-WO3/TiO2 catalyst has a high NOX removal efficiency and N2 selectivity at low temperatures (i.e., 300 °C); this is because NO3- and chemisorbed oxygen, generated by nitrate treatment, facilitated the occurrence of a fast SCR reaction. The approach outlined in this study can be applied to a wide range of SCR catalysts, allowing for the development of more, low-temperature SCR catalysts.

Cl- and Al-Doped Argyrodite Solid Electrolyte Li6PS5Cl for All-Solid-State Lithium Batteries with Improved Ionic Conductivity.

Argyrodite solid electrolytes such as lithium phosphorus sulfur chloride (Li6PS5Cl) have recently attracted great attention due to their excellent lithium-ion transport properties, which are applicable to all-solid-state lithium batteries. In this study, we report the improved ionic conductivity of an argyrodite solid electrolyte, Li6PS5Cl, in all-solid-state lithium batteries via the co-doping of chlorine (Cl) and aluminum (Al) elements. Electrochemical analysis was conducted on the doped argyrodite structure of Li6PS5Cl, which revealed that the substitution of cations and anions greatly improved the ionic conductivity of solid electrolytes. The ionic conductivity of the Cl- and Al-doped Li6PS5Cl (Li5.4Al0.1PS4.7Cl1.3) electrolyte was 7.29 × 10-3 S cm-1 at room temperature, which is 4.7 times higher than that of Li6PS5Cl. The Arrhenius plot of the Li5.4Al0.1PS4.7Cl1.3 electrolyte further elucidated its low activation energy at 0.09 eV.

Hybrid Carbon Supports Composed of Small Reduced Graphene Oxide and Carbon Nanotubes for Durable Oxygen Reduction Catalysts in Proton Exchange Membrane Fuel Cells.

We demonstrated highly active and durable hybrid catalysts (HCs) composed of small reduced graphene oxide (srGO) and carbon nanotubes (CNTs) for use as oxygen reduction reaction (ORR) catalysts in proton exchange membrane fuel cells. Pt/srGO and Pt/CNTs were prepared by loading Pt nanoparticles onto srGO and CNTs using a polyol process, and HCs with different Pt/CNT and Pt/srGO ratios were prepared by mechanically mixing the two components. The prepared HCs consisted of Pt/CNTs well dispersed on Pt/srGO, with catalyst HC55, which was prepared using Pt/srGO and Pt/CNTs in a 5:5 ratio, exhibiting excellent oxygen reduction performance and high stability over 1000 cycles of the accelerated durability test (ADT). In particular, after 1000 cycles of the ADT, the normalized electrochemically active surface area of Pt/HC55 decreased by 11.9%, while those of Pt/srGO and Pt/C decreased by 21.2% and 57.6%, respectively. CNTs have strong corrosion resistance because there are fewer defect sites on the surface, and the addition of CNTs in rGO further improved the durability and the electrical conductivity of the catalyst. A detailed analysis of the structural and electrochemical properties of the synthesized catalysts suggested that the synergetic effects of the high specific surface area of srGO and the excellent electrical conductivity of CNTs were responsible for the enhanced efficiency and durability of the catalysts.

Bi-functional 3D-NiCu-Double Hydroxide@Partially Etched 3D-NiCu Catalysts for Non-Enzymatic Glucose Detection and the Hydrogen Evolution Reaction.

Hydrogen production, which is in the spotlight as a promising eco-friendly fuel, and the need for inexpensive and accurate electronic devices in the biochemistry field are important emerging technologies. However, the use of electrocatalytic devices based on expensive noble metal catalysts limits commercial applications. In recent years, to improve performance and reduce cost, electrocatalysts based on cheaper copper or nickel materials have been investigated for the non-enzymatic glucose oxidation reaction (GOR) and hydrogen evolution reaction (HER). In this study, we demonstrate a facile and easy electrochemical method of forming a cheap nickel copper double hydroxide (NiCu-DH) electrocatalyst deposited onto a three-dimensional (3D) CuNi current collector, which can effectively handle two different reactions due to its high activity for both the GOR and the HER. The as-prepared electrode has a structure comprising abundant 3D-interconnected porous dendritic walls for easy access of the electrolyte ions and highly conductive networks for fast electron transfer; additionally, it provides numerous electroactive sites. The synergistic combination of the dendritic 3D-CuNi with its abundant active sites and the self-made NiCu-DH with its excellent electrocatalytic activity toward the oxidation of glucose and HER enables use of the catalyst for both reactions. The as-prepared electrode as a glucose sensor exhibits an outstanding glucose detection limit value (0.4 µM) and a wide detection range (from 0.4 µM to 1.4 mM) with an excellent sensitivity of 1452.5 µA/cm2/mM. The electrode is independent of the oxygen content and free from chloride poisoning. Furthermore, the as-prepared electrode also requires a low overpotential of -180 mV versus reversible hydrogen electrode to yield a current density of 10 mA/cm2 with a Tafel slope of 73 mV/dec for the HER. Based on this performance, this work introduces a new paradigm for exploring cost-effective bi-functional catalysts for the GOR and HER.

Small Reduced Graphene Oxides for Highly Efficient Oxygen Reduction Catalysts.

We demonstrated highly efficient oxygen reduction catalysts composed of uniform Pt nanoparticles on small, reduced graphene oxides (srGO). The reduced graphene oxide (rGO) size was controlled by applying ultrasonication, and the resultant srGO enabled the morphological control of the Pt nanoparticles. The prepared catalysts provided efficient surface reactions and exhibited large surface areas and high metal dispersions. The resulting Pt/srGO samples exhibited excellent oxygen reduction performance and high stability over 1000 cycles of accelerated durability tests, especially the sample treated with 2 h of sonication. Detailed investigations of the structural and electrochemical properties of the resulting catalysts suggested that both the chemical functionality and electrical conductivity of these samples greatly influence their enhanced oxygen reduction efficiency.

Ammonium Ion Enhanced V2O5-WO3/TiO2 Catalysts for Selective Catalytic Reduction with Ammonia.

Selective catalytic reduction (SCR) is the most efficient NOX removal technology, and the vanadium-based catalyst is mainly used in SCR technology. The vanadium-based catalyst showed higher NOX removal performance in the high-temperature range but catalytic efficiency decreased at lower temperatures, following exposure to SOX because of the generation of ammonium sulfate on the catalyst surface. To overcome these limitations, we coated an NH4+ layer on a vanadium-based catalyst. After silane coating the V2O5-WO3/TiO2 catalyst by vapor evaporation, the silanized catalyst was heat treated under NH3 gas. By decomposing the silane on the surface, an NH4+ layer was formed on the catalyst surface through a substitution reaction. We observed high NOX removal efficiency over a wide temperature range by coating an NH4+ layer on a vanadium-based catalyst. This layer shows high proton conductivity, which leads to the reduction of vanadium oxides and tungsten oxide; additionally, the NOX removal performance was improved over a wide temperature range. These findings provide a new mothed to develop SCR catalyst with high efficiency at a wide temperature range.

Effect of Catalyst Crystallinity on V-Based Selective Catalytic Reduction with Ammonia.

In this study, we synthesized V2O5-WO3/TiO2 catalysts with different crystallinities via one-sided and isotropic heating methods. We then investigated the effects of the catalysts' crystallinity on their acidity, surface species, and catalytic performance through various analysis techniques and a fixed-bed reactor experiment. The isotropic heating method produced crystalline V2O5 and WO3, increasing the availability of both Brønsted and Lewis acid sites, while the one-sided method produced amorphous V2O5 and WO3. The crystalline structure of the two species significantly enhanced NO2 formation, causing more rapid selective catalytic reduction (SCR) reactions and greater catalyst reducibility for NOX decomposition. This improved NOX removal efficiency and N2 selectivity for a wider temperature range of 200 °C-450 °C. Additionally, the synthesized, crystalline catalysts exhibited good resistance to SO2, which is common in industrial flue gases. Through the results reported herein, this study may contribute to future studies on SCR catalysts and other catalyst systems.

Selective Wettability Membrane for Continuous Oil-Water Separation and In Situ Visible Light-Driven Photocatalytic Purification of Water.

Membrane-based technologies are attractive for remediating oily wastewater because they are relatively energy-efficient and are applicable to a wide range of industrial effluents. For complete treatment of oily wastewater, removing dissolved contaminants from the water phase is typically followed by adsorption onto an adsorbent, which complicates the process. Here, an in-air superhydrophilic and underwater superoleophobic membrane-based continuous separation of surfactant-stabilized oil-in-water emulsions and in situ decontamination of water by visible-light-driven photocatalytic degradation of dissolved organic contaminants is reported. The membrane is fabricated by utilizing a thermally sensitized stainless steel mesh coated with visible light absorbing iron-doped titania nanoparticles. Post annealing of the membrane can enhance the adhesion of nanoparticles to the membrane surface by formation of a bridge between them. An apparatus that enables continuous separation of surfactant-stabilized oil-in-water emulsion and in situ photocatalytic degradation of dissolved organic matter in the water-rich permeate upon irradiation of visible light on the membrane surface with greater than 99% photocatalytic degradation is developed. The membrane demonstrates the recovery of its intrinsic water-rich permeate flux upon continuous irradiation of light after being contaminated with oil. Finally, continuous oil-water separation and in situ water decontamination is demonstrated by photocatalytically degrading model toxins in water-rich permeate.

Synthesis of oxygen functionalized carbon nanotubes and their application for selective catalytic reduction of NO x with NH3.

Oxygen functionalized carbon nanotubes synthesized by surface acid treatment were used to improve the dispersion properties of active materials for catalysis. Carbon nanotubes have gained attention as a support for active materials due to their high specific surface areas (400-700 m2 g-1) and chemical stability. However, the lack of surface functionality causes poor dispersion of active materials on carbon nanotube supports. In this study, oxygen functional groups were prepared on the surface of carbon nanotubes as anchoring sites for decoration with catalytic nanoparticles. The oxygen functional groups were prepared through a chemical acid treatment using sulfuric acid and nitric acid, and the amount of functional groups was controlled by the reaction time. Vanadium, tungsten, and titanium oxides as catalytic materials were dispersed using an impregnation method on the synthesized carbon nanotube surfaces. Due to the high density of oxygen functional groups, the catalytic nanoparticles were well dispersed and reduced in size on the surface of the carbon nanotube supports. The selective catalytic reduction catalyst with the oxygen functionalized carbon nanotube support exhibited enhanced NO x removal efficiency of over 90% at 350-380 °C which is the general operating temperature range of catalysis in power plants.

Differences in theta coherence between spatial and nonspatial attention using intracranial electroencephalographic signals in humans.

A number of previous studies revealed the importance of the frontoparietal network for attention and preparatory top-down control. Here, we investigated the theta (7-9 Hz) coherence of the right frontoparietal networks to explore the differences in connectivity changes for the right frontoparietal regions during spatial attention (i.e., attention to a specific location rather than a specific feature) and nonspatial attention (i.e., attention to a specific feature rather than a specific location) tasks. The theta coherence in both tasks was primarily maintained at a preparatory state, decreases after stimulus onset, and recovers to the level of the preparatory state after the response time. However, the theta coherence of the frontoparietal network during spatial attention was immediately maintained after cue-onset, whereas for the case of nonspatial attention, it was immediately decreased after cue-onset. In addition, the connectivity of the right frontoparietal network, including the middle frontal gyrus and superior parietal lobe, were significantly higher for spatial attention rather than for nonspatial attention, suggesting that the dorsal parts of right frontoparietal network are more engaged in spatial-specific attention from the preparatory state. These findings also suggest that these two attention systems involve the use of different regional connectivity patterns, not only in the cognitive state, but in the preparatory state as well.

Highly Active Bifunctional Electrocatalysts for Oxygen Evolution and Reduction in Zn-Air Batteries.

To realize the full performance of Zn-air batteries, the co-presence of a highly efficient oxygen reduction reaction (ORR) and an oxygen evolution reaction (OER) in the system is critical. Although copper and nickel are known to be bifunctional catalysts for ORR and OER, sluggish reactions as a result of the exceptionally strong O=O bond on the metal surface make it difficult to achieve high system efficiency. In this study, a metal carbide layer (CuCx and NiCx ) on dendritic copper and nickel is fabricated by a facile electrodeposition process to provide efficient catalytic active sites with moderate binding energy for easy electron transfer in both the OER and the ORR. The dendritic structure provides an enriched catalytic surface and the protective metal carbide layer offers an appropriate O binding energy and durability of Zn-air batteries. Owing to the presence of the stable metal carbide surface on the dendritic metal, the CuCx /Cu and NiCx /Ni catalysts exhibited well-defined limiting current densities of -5.19 and -5.11 mA cm-2 , respectively, and improved ORR and OER activities with lower polarization than the corresponding metal catalysts. Density functional theory revealed a 0.74 eV decrease in the overpotential of NiCx /Ni-catalyzed OER reactions compared with Ni-catalyzed OER reactions. The experimental and theoretical results prove that carbide layers on dendritic metal surfaces can greatly improve the activity of ORR and OER bifunctional electrocatalysts for Zn-air batteries.

Ultrathin nickel hydroxide on carbon coated 3D-porous copper structures for high performance supercapacitors.

An ultrathin nickel hydroxide layer electrodeposited on a carbon-coated three-dimensional porous copper structure (3D-C/Cu) is suggested as an additive and binder-free conductive electrode with short electron path distances, large electrochemical active sites, and improved structural stability, for high performance supercapacitors. The 3D-porous copper structure (3D-Cu) provides high electrical conductivity and facilitates electron transport between the Ni(OH)2 active materials and the current collector of the Ni-plate. A carbon coating was applied to the 3D-Cu to prevent the oxidation of Cu, without degrading the electron transport behavior of the 3D-Cu. The 3D-Ni(OH)2/C/Cu exhibited a high specific capacitance of 1860 F g-1 at 1 A g-1, and good cycling performance, with an 86.5% capacitance retention after 10 000 cycles. When tested in a two-electrode system, an asymmetric supercapacitor exhibited an energy density of 147.9 W h kg-1 and a power density of 37.0 kW kg-1. These results open a new area of ultrahigh-performance supercapacitors, supported by 3D-Cu electrodes.

Nickel Hydroxide Supercapacitor with a Theoretical Capacitance and High Rate Capability Based on Hollow Dendritic 3D-Nickel Current Collectors.

A straightforward way to attain the theoretical capacitance and high rate capability of nickel hydroxide supercapacitors, by utilizing a mesoporous hollow dendritic three-dimensional-nickel (3D-Ni) current collector is proposed. A facile electrodeposition method employing a hydrogen bubble template was chosen for rapid fabrication of the dendritic 3D-nickel structure. After nickel hydroxide was deposited on the hollow 3D-nickel current collector, it exhibited a highest capacitance of 3637 F g-1 at a current density of 1 A g-1 , and retained 97 % of capacitance at a high current density of 100 A g-1 with a cycle stability of over 80 % after 10 000 cycles. The enhanced performance could be attributed to the large surface area and high conductivity of the moss-like dendritic 3D-Ni current collector, which allowed direct contact between the active materials and the current collector, and reduced diffusion resistance between the surface of the active materials and the electrolyte. These results not only confirmed a facile fabrication method for high-performance 3D metal nanostructures, but also offer a promising solution for state-of-the-art energy storage systems.

Zinc-Reduced Mesoporous TiOx Li-Ion Battery Anodes with Exceptional Rate Capability and Cycling Stability.

We demonstrate a unique synthetic route for oxygen-deficient mesoporous TiOx by a redox-transmetalation process by using Zn metal as the reducing agent. The as-obtained materials have significantly enhanced electronic conductivity; 20 times higher than that of as-synthesized TiO2 material. Moreover, electrochemical impedance spectroscopy (EIS) and galvanostatic intermittent titration technique (GITT) measurements are performed to validate the low charge carrier resistance of the oxygen-deficient TiOx . The resulting oxygen-deficient TiOx battery anode exhibits a high reversible capacity (∼180 mA h g-1 at a discharge/charge rate of 1 C/1 C after 400 cycles) and an excellent rate capability (∼90 mA h g-1 even at a rate of 10 C). Also, the full cell, which is coupled with a LiCoO2 cathode material, exhibits an outstanding rate capability (>75 mA h g-1 at a rate of 3.0 C) and maintains a reversible capacity of over 100 mA h g-1 at a discharge/charge of 1 C/1 C for 300 cycles.

Frontostriatal Connectivity Changes in Major Depressive Disorder After Repetitive Transcranial Magnetic Stimulation: A Randomized Sham-Controlled Study.

OBJECTIVE: The aim of this randomized, sham-controlled study was to investigate the therapeutic effects of underlying neurobiological changes after 2-week repetitive transcranial magnetic stimulation (rTMS) treatment using functional connectivity magnetic resonance imaging in patients with major depression. METHODS: Twenty-four patients with major depressive disorder diagnosed with DSM-IV-TR criteria were randomly assigned to the active rTMS (n = 13) or sham (n = 11) groups from January 2009 to June 2011. rTMS was given for 2 weeks at 110% of the motor threshold for 10 minutes at 10 Hz over the left dorsolateral prefrontal cortex (DLPFC). Resting state functional connectivity was evaluated before and after rTMS. The 17-item Hamilton Depression Rating Scale (HDRS) was administered, and neurocognitive tasks were performed. We examined between-group differences in functional connectivity changes from the bilateral DLPFC. RESULTS: Participants in the active rTMS group showed significant clinical improvement in HDRS scores compared to those in the sham group (P < .001). After 2-week rTMS, there were significant differences in changes in DLPFC-left caudate connectivity (corrected P < .05): the active group showed a greater reduction of connectivity strength between the DLPFC and left caudate compared to the sham group. Reduced levels of DLPFC-left caudate connectivity predicted improvement in depressive symptoms (r = 0.58, P = .001). Additionally, a positive correlation between residual depressive symptoms and connectivity strength after 2-week rTMS was found (r = 0.46, P = .023). CONCLUSIONS: High-frequency rTMS over the left DLPFC showed therapeutic effects in patients with major depression. The therapeutic effect of rTMS is related to the modulation of functional connectivity in the frontostriatal network. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT01325831​.

Neural correlates of spatial and nonspatial attention determined using intracranial electroencephalographic signals in humans.

Few studies have directly compared the neural correlates of spatial attention (i.e., attention to a particular location) and nonspatial attention (i.e., attention to a feature in the visual scene) using well-controlled tasks. Here, we investigated the neural correlates of spatial and nonspatial attention in humans using intracranial electroencephalography. The topography and number of electrodes showing significant event-related desynchronization (ERD) or event-related synchronization (ERS) in different frequency bands were studied in 13 epileptic patients. Performance was not significantly different between the two conditions. In both conditions, ERD in the low-frequency bands and ERS in the high-frequency bands were present bilaterally in the parietal cortex (prominently on the right hemisphere) and frontal regions. In addition to these common changes, spatial attention involved right-lateralized activity that was maximal in the right superior parietal lobule (SPL), whereas nonspatial attention involved wider brain networks including the bilateral parietal, frontal, and temporal regions, but still had maximal activity in the right parietal lobe. Within the parietal lobe, spatial attention involved ERD or ERS in the right SPL, whereas nonspatial attention involved ERD or ERS in the right inferior parietal lobule. These findings reveal that common as well as different brain networks are engaged in spatial and nonspatial attention. Hum Brain Mapp 37:3041-3054, 2016. © 2016 The Authors Human Brain Mapping Published by Wiley Periodicals, Inc.

Asymmetric behaviours of brain oscillations in the human hippocampus during spatial navigation tasks.

Hippocampal-dependent memory functions may be lateralized to the right hippocampus during spatial navigation. However, direct electrophysiological evidence supporting these findings in the bilateral hippocampi during spatial navigation has not been well documented in humans. We studied changes in brain oscillations between the dominant and the nondominant hippocampi during encoding periods of environmental novelty using spatial navigation tasks. Results showed that brain oscillations during the encoding period of spatial navigation increased significantly in the nondominant hippocampus compared with the dominant hippocampus. These findings provide direct electrophysiological evidence that the nondominant hippocampus plays a predominant role in spatial navigation.

Hematite-based photoelectrochemical water splitting supported by inverse opal structures of graphene.

By coupling α-Fe2O3 with a 3D graphene inverse opal (3D-GIO) conducting electrode, the short diffusion length of carriers and low absorption coefficient in α-Fe2O3 for photoelectrochemical applications were successfully addressed. GIO was directly grown on FTO substrate under low temperature conditions, removing the need for a graphene transfer process. α-Fe2O3 nanoparticles (NPs) were hydrothermally deposited on the surface of GIO, creating α-Fe2O3/GIO. The photocurrent density of α-Fe2O3/GIO in water splitting reactions reached 1.62 mA/cm(2) at 1.5 V vs RHE, which is 1.4 times greater than that of optimized α-Fe2O3. The EIS and IPCE data confirm reduced electron-hole recombination and fast electron transfer processes due to the short distance between active materials and the conducting electrode in the α-Fe2O3/GIO system. Our result may pave the way for designing devices in advanced energy conversion applications as well as a high efficiency hematite-based PEC system.

Great improvement in pseudocapacitor properties of nickel hydroxide via simple gold deposition.

In this letter, we report a facile approach to improve the capacitor properties of nickel hydroxide (Ni(OH)2) by simply coating gold nanoparticles (Au NPs) on the surface of Ni(OH)2. Au NP-deposited Ni(OH)2 (Au/Ni(OH)2) has been prepared by application of a conventional colloidal coating of Au NPs on the surface of 3D-Ni(OH)2 synthesized via a hydrothermal method. Compared with pristine Ni(OH)2, Au/Ni(OH)2 shows a 41% enhanced capacitance value, excellent rate capacitance behavior at high current density conditions, and greatly improved cycling stability for supercapacitor applications. The specific capacitance of Au/Ni(OH)2 reached 1927 F g(-1) at 1 A g(-1), which is close to the theoretical capacitance and retained 66% and 80% of the maximum value at a high current density of 20 A g(-1) and 5000 cycles while that of pristine Ni(OH)2 was 1363 F g(-1) and significantly decreased to 48% and 30%, respectively, under the same conditions. The outstanding performance of Au/Ni(OH)2 as a supercapacitor is attributed to the presence of metal Au NPs on the surface of semiconductor Ni(OH)2; this permits the creation of virtual 3D conducting networks via metal/semiconductor contact, which induces fast electron and ion transport by acting as a bridge between Ni(OH)2 nanostructures, thus eventually leading to significantly improved electrochemical capacitive behaviors, as confirmed by the EIS and I-V characteristic data.

Role of low- and high-frequency oscillations in the human hippocampus for encoding environmental novelty during a spatial navigation task.

The hippocampus plays a key role in the encoding and retrieval of information related to novel environments during spatial navigation. However, the neural basis for these processes in the human hippocampus remains unknown because it is difficult to directly measure neural signals in the human hippocampus. This study investigated hippocampal neural oscillations involved in encoding novel environments during spatial navigation in a virtual environment. Seven epileptic patients with implanted intracranial hippocampal depth electrodes performed three sessions of virtual environment navigation. Each session consisted of a navigation task and a location-recall task. The navigation task consisted of eight blocks, and in each block, the participant navigated to the location of four different objects and was instructed to remember the location of the objects. After the eight blocks were completed, a location-recall task was performed for each of the four objects. Intracranial electroencephalography data were monitored during the navigation tasks. Theta (5-8 Hz) and delta (1-4 Hz) oscillations were lower in the first block (novel environment) than in the eighth block (familiar environment) of the navigation task, and significantly increased from block one to block eight. By contrast, low-gamma (31-50 Hz) oscillations were higher in the first block than in the eighth block of the navigation task, and significantly decreased from block one to block eight. Comparison of sessions with high recall performance (low error between identified and actual object location) and low recall performance revealed that high-gamma (51-100 Hz) oscillations significantly decreased from block one to block eight only in sessions with high recall performance. These findings suggest that delta, theta, and low-gamma oscillations were associated with encoding of environmental novelty and high-gamma oscillations were important for the successful encoding of environmental novelty.