Correction to "Band Gap and Morphology Engineering of Hematite Nanoflakes from an Ex Situ Sn Doping for Enhanced Photoelectrochemical Water Splitting".

[This corrects the article DOI: 10.1021/acsomega.2c04028.].

MOF-Derived Co Nanoparticles Catalyst Assisted by F- and N-Doped Carbon Quantum Dots for Oxygen Reduction.

The oxygen reduction reaction is crucial in the cathode of fuel cells and metal-air batteries. Consequently, designing robust and durable ORR catalysts is vital to developing metal-air batteries and fuel cells. Metal-organic frameworks feature an adjustable structure, a periodic porosity, and a large specific surface area, endowing their derivative materials with a unique structure. In this study, F and N co-doped on the carbon support surface (Co/FN-C) via the pyrolysis of ZIF-67 as a sacrificial template while using Co/FN-C as the non-noble metal catalysts. The Co/FN-C displays excellent long-term durability and electrochemical catalytic performance in acidic solutions. These performance improvements are achieved because the CQDs alleviate the structural collapse during the pyrolysis of ZIF-67, which increases the active sites in the Co nanoparticles. Moreover, F- and N-doping improves the catalytic activity of the carbon support by providing additional electrons and active sites. Furthermore, F anions are redox-stable ligands that exhibit long-term operational stability. Therefore, the well-dispersed Co NPs on the surface of the Co/FN-C are promising as the non-noble metal catalysts for ORR.

Band gap and Morphology Engineering of Hematite Nanoflakes from an Ex Situ Sn Doping for Enhanced Photoelectrochemical Water Splitting.

In this article, we report a simple ex situ Sn-doping method on hematite nanoflakes (coded as MSnO2-H) that can protect the nanoflake (NF) morphology against the 800 °C high-temperature annealing process and activate the photoresponse of hematite until 800 nm wavelength excitation. MSnO2-H has been fabricated by dropping SnCl4 ethanol solution on hematite nanoflakes homogeneously grown over the conductive FTO glass substrate and annealed at 500 °C to synthesize the SnO2 nanoparticles on hematite NFs. The Sn-treated samples were then placed in a furnace again, and the sintering process was conducted at 800 °C for 15 min. During this step, structure deformation of hematite occurs normally due to the grain boundary motion and oriented attachment. However, in the case of MSnO2-H, the outer SnO2 nanoparticles efficiently prevented a shape deformation and maintained the nanoflake shape owing to the encapsulation of hematite NFs. Furthermore, the interface of hematite/SnO2 nanoparticles became the spots for a heavy Sn ion doping. We demonstrated the generation of the newly localized states, resulting in an extension of the photoresponse of hematite until 800 nm wavelength light irradiation. Furthermore, we demonstrated that SnO2 nanoparticles can effectively act as a passivation layer, which can reduce the onset potential of hematite for water splitting redox reactions. The optimized MSnO2-H nanostructures showed a 2.84 times higher photocurrent density and 300 mV reduced onset potential compared with a pristine hematite nanoflake photoanode.

Well-dispersed Pt/RuO2-decorated mesoporous N-doped carbon as a hybrid electrocatalyst for Li-O2 batteries.

Despite their high energy density, the poor cycling performance of lithium-oxygen (Li-O2) batteries limits their practical application. Therefore, to improve cycling performance, considerable attention has been paid to the development of an efficient electrocatalyst for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). Catalysts that can more effectively reduce the overpotential and improve the cycling performance for the OER during charging are of particular interest. In this study, porous carbon derived from protein-based tofu was investigated as a catalyst support for the oxygen electrode (O2-electrode) of Li-O2 batteries, wherein ORR and OER occur. The porous carbon was synthesized using carbonization and KOH activation, and RuO2 and Pt electrocatalysts were introduced to improve the electrical conductivity and catalytic performance. The well-dispersed Pt/RuO2 electrocatalysts on the porous N-doped carbon support (Pt/RuO2@ACT) showed excellent ORR and OER catalytic activity. When incorporated into a Li-O2 battery, the Pt/RuO2@ACT O2-electrode exhibited a high specific discharge capacity (5724.1 mA h g-1 at 100 mA g-1), a low discharge-charge voltage gap (0.64 V at 2000 mA h g-1), and excellent cycling stability (43 cycles with a limit capacity of 1000 mA h g-1). We believe that the excellent performance of the Pt/RuO2@ACT electrocatalyst is promising for accelerating the commercialization of Li-O2 batteries.

Interfacial Engineering of a Heteroatom-Doped Graphene Layer on Patterned Aluminum Foil for Ultrafast Lithium Storage Kinetics.

The design of the interfacial architecture between the electrode and the current collector in lithium-ion batteries (LIB) plays a key role in achieving ultrafast lithium storage kinetics with respect to efficient charge transfer and cycle stability. However, in recent years, despite considerable efforts in the structural and chemical engineering of active materials (anode and cathode materials), interfacial architectures between the electrode and the current collector have received relatively insufficient attention in the case of ultrafast LIBs. Here, the interface architecture of a micropatterned Al current collector with a heteroatom-doped graphene interfacial layer is developed using roll pressing and dip coating processes. The cathode electrode fabricated with the resultant current collector offers increased contact area with enhanced interfacial stability between the electrode and the current collector because of micropatterns with heteroatom-doped graphene formed on the current collector, leading to outstanding ultrafast cycling capacity (105.8 mA h g-1) at 20 C. Furthermore, at extremely high rate and long-term cycling performance, significant ultrafast cycling stability (specific capacity of 87.1 mA h g-1 with capacity retention of 82.3% at 20 C after 1000 cycles) is noted. These improved ultrafast and ultra-stable performances are explained in terms of the increased electron collection/provision site with a high contact area between the electrode and the current collector for enhanced ultrafast cycling capacity and the effective corrosion prevention of the current collector with fast charge transfer for ultrafast cycling stability.

Activation of α-Fe2 O3 for Photoelectrochemical Water Splitting Strongly Enhanced by Low Temperature Annealing in Low Oxygen Containing Ambient.

Photoelectrochemical (PEC) water splitting is a promising method for the conversion of solar energy into chemical energy stored in the form of hydrogen. Nanostructured hematite (α-Fe2 O3 ) is one of the most attractive materials for a highly efficient charge carrier generation and collection due to its large specific surface area and the short minority carrier diffusion length. In the present work, the PEC water splitting performance of nanostructured α-Fe2 O3 is investigated which was prepared by anodization followed by annealing in a low oxygen ambient (0.03 % O2 in Ar). It was found that low oxygen annealing can activate a significant PEC response of α-Fe2 O3 even at a low temperature of 400 °C and provide an excellent PEC performance compared with classic air annealing. The photocurrent of the α-Fe2 O3 annealed in the low oxygen at 1.5 V vs. RHE results as 0.5 mA cm-2 , being 20 times higher than that of annealing in air. The obtained results show that the α-Fe2 O3 annealed in low oxygen contains beneficial defects and promotes the transport of holes; it can be attributed to the improvement of conductivity due to the introduction of suitable oxygen vacancies in the α-Fe2 O3 . Additionally, we demonstrate the photocurrent of α-Fe2 O3 annealed in low oxygen ambient can be further enhanced by Zn-Co LDH, which is a co-catalyst of oxygen evolution reaction. This indicates low oxygen annealing generates a promising method to obtain an excellent PEC water splitting performance from α-Fe2 O3 photoanodes.

Effects of Trauma Center Establishment on the Clinical Characteristics and Outcomes of Patients with Traumatic Brain Injury : A Retrospective Analysis from a Single Trauma Center in Korea.

OBJECTIVE: To investigate the effects of trauma center establishment on the clinical characteristics and outcomes of trauma patients with traumatic brain injury (TBI). METHODS: We enrolled 322 patients with severe trauma and TBI from January 2015 to December 2016. Clinical factors, indexes, and outcomes were compared before and after trauma center establishment (September 2015). The outcome was the Glasgow outcome scale classification at 3 months post-trauma. RESULTS: Of the 322 patients, 120 (37.3%) and 202 (62.7%) were admitted before and after trauma center establishment, respectively. The two groups were significantly different in age (p=0.038), the trauma location within the city (p=0.010), the proportion of intensive care unit (ICU) admissions (p=0.001), and the emergency room stay time (p<0.001). Mortality occurred in 37 patients (11.5%). Although the preventable death rate decreased from before to after center establishment (23.1% vs. 12.5%), the difference was not significant. None of the clinical factors, indexes, or outcomes were different from before to after center establishment for patients with severe TBI (Glasgow coma scale score ≤8). However, the proportion of inter-hospital transfers increased and the time to emergency room arrival was longer in both the entire cohort and patients with severe TBI after versus before trauma center establishment. CONCLUSION: We confirmed that for patients with severe trauma and TBI, establishing a trauma center increased the proportion of ICU admissions and decreased the emergency room stay time and preventable death rate. However, management strategies for handling the high proportion of inter-hospital transfers and long times to emergency room arrival will be necessary.

Novel tunneled phosphorus-doped WO3 films achieved using ignited red phosphorus for stable and fast switching electrochromic performances.

Simultaneous improvement of both the performance and stability of electrochromic devices (ECDs) to encourage their practical use in various applications, such as commercialized smart windows, electronic displays, and adjustable mirrors, by tuning the film structure and the electronic structure of transition metal oxides remains a challenging issue. In the present study, we developed novel tunneled phosphorus (P)-doped WO3 films via the ignition reaction of red P. The ignited red P, which can generate exothermic energy, was used as an attractive factor to create a tunneled structure and P-doping on the WO3 films. Therefore, by optimizing the effect of ignited red P on the WO3 films, tunneled P-doped WO3 films fabricated by using 1 wt% red P demonstrated a striking improvement of the EC performances, including both a fast switching speed (6.1 s for the colouration speed and 2.5 s for the bleaching speed) caused by the improvement of Li ion diffusion by the tunneled structure and electrical conductivity by P-doping WO3 and a superb colouration efficiency (CE, 55.9 cm2 C-1) as a result of increased electrochemical activity by the elaborate formation of the tunneled structure. Simultaneously, this film displayed a noticeable long-cycling stability due to a higher retention (91.5%) of transmittance modulation after 1000 electrochromic (EC) cycles as compared to bare WO3 films, which can mainly be attributed to the optimizing effect of the tunneled structure to generate an efficient charge transfer and an alleviated structural variation during the insertion-extraction of Li ions. Therefore, our results suggest a valuable and well-designed strategy to manufacture stable fast-switching EC materials that are fit for various practical applications of the ECDs.

Hematite Photoanode with Complex Nanoarchitecture Providing Tunable Gradient Doping and Low Onset Potential for Photoelectrochemical Water Splitting.

Over the past years, α-Fe2 O3 (hematite) has re-emerged as a promising photoanode material in photoelectrochemical (PEC) water splitting. In spite of considerable success in obtaining relatively high solar conversion efficiency, the main drawbacks hindering practical application of hematite are its intrinsically hampered charge transport and sluggish oxygen evolution reaction (OER) kinetics on the photoelectrode surface. In the present work, we report a strategy that synergistically addresses both of these critical limitations. Our approach is based on three key features that are applied simultaneously: i) a careful nanostructuring of the hematite photoanode in the form of nanorods, ii) doping of hematite by Sn4+ ions using a controlled gradient, and iii) surface decoration of hematite by a new class of layered double hydroxide (LDH) OER co-catalysts based on Zn-Co LDH. All three interconnected forms of functionalization result in an extraordinary cathodic shift of the photocurrent onset potential by more than 300 mV and a PEC performance that reaches a photocurrent density of 2.00 mA cm-2 at 1.50 V vs. the reversible hydrogen electrode.

Improved Ionic Diffusion through the Mesoporous Carbon Skin on Silicon Nanoparticles Embedded in Carbon for Ultrafast Lithium Storage.

Because of their combined effects of outstanding mechanical stability, high electrical conductivity, and high theoretical capacity, silicon (Si) nanoparticles embedded in carbon are a promising candidate as electrode material for practical utilization in Li-ion batteries (LIBs) to replace the conventional graphite. However, because of the poor ionic diffusion of electrode materials, the low-grade ultrafast cycling performance at high current densities remains a considerable challenge. In the present study, seeking to improve the ionic diffusion, we propose a novel design of mesoporous carbon skin on the Si nanoparticles embedded in carbon by hydrothermal reaction, poly(methyl methacrylate) coating process, and carbonization. The resultant electrode offers a high specific discharge capacity with excellent cycling stability (1140 mA h g-1 at 100 mA g-1 after 100 cycles), superb high-rate performance (969 mA h g-1 at 2000 mA g-1), and outstanding ultrafast cycling stability (532 mA h g-1 at 2000 mA g-1 after 500 cycles). The battery performances are surpassing the previously reported results for carbon and Si composite-based electrodes on LIBs. Therefore, this novel approach provides multiple benefits in terms of the effective accommodation of large volume expansions of the Si nanoparticles, a shorter Li-ion diffusion pathway, and stable electrochemical conditions from a faster ionic diffusion during cycling.

Improvement of Transparent Conducting Performance on Oxygen-Activated Fluorine-Doped Tin Oxide Electrodes Formed by Horizontal Ultrasonic Spray Pyrolysis Deposition.

In this study, highly transparent conducting fluorine-doped tin oxide (FTO) electrodes were fabricated using the horizontal ultrasonic spray pyrolysis deposition. In order to improve their transparent conducting performances, we carried out oxygen activation by adjusting the ratio of O2/(O2+N2) in the carrier gas (0%, 20%, and 50%) used during the deposition process. The oxygen activation on the FTO electrodes accelerated the substitution concentration of F (FO•) into the oxygen sites in the FTO electrode while the oxygen vacancy (VO••) concentration was reduced. In addition, due to growth of pyramid-shaped crystallites with (200) preferred orientations, this oxygen activation caused the formation of a uniform surface structure. As a result, compared to others, the FTO electrode prepared at 50% O2 showed excellent electrical and optical properties (sheet resistance of ∼4.0 ± 0.14 Ω/□, optical transmittance of ∼85.3%, and figure of merit of ∼5.09 ± 0.19 × 10-2 Ω-1). This led to a superb photoconversion efficiency (∼7.03 ± 0.20%) as a result of the improved short-circuit current density. The photovoltaic performance improvement can be defined by the decreased sheet resistance of FTO used as a transparent conducting electrode in dye-sensitized solar cells (DSSCs), which is due to the combined effect of the high carrier concentration by the improved FO• concentration on the FTO electrodes and the fasted Hall mobility by the formation of a uniform FTO surface structure and distortion relaxation on the FTO lattices resulting from the reduced VO••• concentration.

Fast-switching electrochromic properties of mesoporous WO3 films with oxygen vacancy defects.

In this study, mesoporous WO3 films with oxygen vacancy defects have been fabricated using the camphene-assisted sol-gel method. By controlling the optimized weight ratio of camphene on the WO3 films, we developed a unique film structure of the WO3 phase with both mesoporous morphology and oxygen vacancy defects due to the distinctive effect of camphene. The mesoporous WO3 films with oxygen vacancy defects fabricated using 10 wt% camphene showed superb multifunctional electrochromic (EC) properties with both fast switching speeds (5.8 s for coloration speed and 1.0 s for bleaching speed) and high coloration efficiency (CE, 51.4 cm2 C-1), which include the most prominent properties, particularly for switching speeds among WO3-based films reported so far. The attractive EC properties are due to the synergistic effects of the mesoporous morphology and oxygen vacancy defects on the WO3. The fast switching speeds are mainly caused by the reduced Li+ diffusion pathway due to the mesoporous morphology and increased electrical conductivity due to the oxygen vacancy defects. In addition, the increased CE value is due to the large transmittance modulation as a result of a more effective electrostatic contact of the mesoporous morphology and an increased optical bandgap of the oxygen vacancy defects on the WO3. Therefore, this unique film structure of the mesoporous WO3 films with oxygen vacancy defects can be potentially regarded as a novel EC material for high-performance EC devices.

Tunneled Mesoporous Carbon Nanofibers with Embedded ZnO Nanoparticles for Ultrafast Lithium Storage.

Carbon and metal oxide composites have received considerable attention as anode materials for Li-ion batteries (LIBs) owing to their excellent cycling stability and high specific capacity based on the chemical and physical stability of carbon and the high theoretical specific capacity of metal oxides. However, efforts to obtain ultrafast cycling stability in carbon and metal oxide composites at high current density for practical applications still face important challenges because of the longer Li-ion diffusion pathway, which leads to poor ultrafast performance during cycling. Here, tunneled mesoporous carbon nanofibers with embedded ZnO nanoparticles (TMCNF/ZnO) are synthesized by electrospinning, carbonization, and postcalcination. The optimized TMCNF/ZnO shows improved electrochemical performance, delivering outstanding ultrafast cycling stability, indicating a higher specific capacity than previously reported ZnO-based anode materials in LIBs. Therefore, the unique architecture of TMCNF/ZnO has potential for use as an anode material in ultrafast LIBs.

Ultrafast Lithium Storage Using Antimony-Doped Tin Oxide Nanoparticles Sandwiched between Carbon Nanofibers and a Carbon Skin.

Metal oxides as anode materials for Li-ion batteries (LIBs) are of significant interest to many potential technologies because of their high theoretical capacity value, low price, and environmentally friendly features. In spite of these considerable benefits and ongoing progress in the field, momentous challenges exist, related with structural disintegration due to volume expansion of electrode materials. This leads to rapid capacity decline and must be resolved in order to progress for realistic utilization of LIBs with ultrafast cycling stability. This article proposes a novel architecture of Sb-doped SnO2 nanoparticles sandwiched between carbon nanofiber and carbon skin (CNF/ATO/C) using electrospinning and hydrothermal methods. The CNF/ATO/C exhibits superb electrochemical behavior such as high specific capacity and outstanding cycling stability (705 mA h g-1 after 100 cycles), outstanding high-rate performance (411 mA h g-1 at 2000 mA g-1), and ultrafast cycling stability (347 mA h g-1 at 2000 mA g-1 after 100 cycles), which is high compared to any reported value using SnO2-based anode materials. Thus, this unique architecture furnishes profitable effects, including electroactive sites, structural stability, and electrical conductivity, which can potentially be realizes for ultrafast LIBs.

Carbon-Encapsulated Hollow Porous Vanadium-Oxide Nanofibers for Improved Lithium Storage Properties.

Carbon-encapsulated hollow porous vanadium-oxide (C/HPV2O5) nanofibers have been fabricated using electrospinning and postcalcination. By optimized postcalcination of vanadium-nitride and carbon-nanofiber composites at 400 °C for 30 min, we synthesized a unique architecture electrode with interior void spaces and well-defined pores as well as a uniform carbon layer on the V2O5 nanofiber surface. The optimized C/HPV2O5 electrode postcalcined at 400 °C for 30 min showed improved lithium storage properties with high specific discharge capacities, excellent cycling durability (241 mA h g(-1) at 100 cycles), and improved high-rate performance (155 mA h g(-1) at 1000 mA g(-1)), which is the highest performance in comparison with previously reported V2O5-based cathode materials. The improved electrochemical feature is due to the attractive properties of the carbon-encapsulated hollow porous structure: (I) excellent cycling durability with high specific capacity relative to the adoption of carbon encapsulation as a physical buffer layer and the effective accommodation of volume changes due to the hollow porous structure, (II) improved high-rate performance because of a shorter Li-ion diffusion pathway resulting from interior void spaces and well-defined pores at the surface. This unique electrode structure can potentially provide new cathode materials for high-performance lithium-ion batteries.

A Titanium-Doped SiOx Passivation Layer for Greatly Enhanced Performance of a Hematite-Based Photoelectrochemical System.

This study introduces an in situ fabrication of nanoporous hematite with a Ti-doped SiOx passivation layer for a high-performance water-splitting system. The nanoporous hematite with a Ti-doped SiOx layer (Ti-(SiOx /np-Fe2 O3 )) has a photocurrent density of 2.44 mA cm(-2) at 1.23 VRHE and 3.70 mA cm(-2) at 1.50 VRHE . When a cobalt phosphate co-catalyst was applied to Ti-(SiOx /np-Fe2 O3 ), the photocurrent density reached 3.19 mA cm(-2) at 1.23 VRHE with stability, which shows great potential of the use of the Ti-doped SiOx layer with a synergistic effect of decreased charge recombination, the increased number of active sites, and the reduced hole-diffusion pathway from the hematite to the electrolyte.

Synergistic Effects of a Multifunctional Graphene Based Interlayer on Electrochemical Behavior and Structural Stability.

The ability to rationally design and manipulate the interfacial structure in lithium ion batteries (LIBs) is of utmost technological importance for achieving desired performance requirements as it provides synergistic effects to the electrochemical properties and cycling stability of electrode materials. However, despite considerable efforts and progress made in recent years through the interface engineering based on active electrode materials, relatively little attention has been devoted to address the physical aspects of the interface and interfacial layer between the anode materials layer and the current collector. Here, we propose and successfully grow unique graphene directly on a Cu current collector as an ideal interfacial layer using the modified chemical vapor deposition (CVD). The anode with an engineered graphene interlayer exhibits remarkably improved electrochemical performances, such as large reversible specific capacity (921.4 mAh g(-1) at current density of 200 mA g(-1)), excellent Coulombic efficiency (close to approximately 96%), and superior cycling capacity retention and rate properties compared to the bare Cu. These excellent electrochemical features are discussed in terms of multiple beneficial effects of graphene on interfacial stability and adhesion between the anode and the collector, oxidation or corrosion resistance of the graphene grown Cu current collector, and electrical contact conductance during the charge/discharge process.

Ruthenium and ruthenium oxide nanofiber supports for enhanced activity of platinum electrocatalysts in the methanol oxidation reaction.

Novel supports for the dispersion of Pt electrocatalysts in fuel cells are constantly being developed in order to improve the electrochemical performance and reduce the cost. The electrocatalytic activity and stability in fuel cells largely depend on the surface morphology and structure of the support. In this study, Ru and RuO2 nanofibers prepared by electrospinning and post-calcination have been considered as Pt-catalyst supports. The composite material loaded with 20 wt% Pt catalyst exhibited a high anodic current density of 641.7 mA mgPt(-1), a high IF/IB ratio of 1.9, and excellent electrocatalytic stability compared to commercial Pt/C. The improved anodic current density of the composite is attributed to the high dispersion of the Pt catalyst over the large surface area of the nanosized support grains, while its low onset potential, high IF/IB ratio, and excellent electrocatalytic stability are ascribed to a bifunctional effect resulting from the existence of Ru atoms on the support surface. Finally, the efficient electron transfer and a rapid diffusion rate of the electrolyte are due to the unique network structure of the supports. Thus, the Ru and RuO2 nanofiber composites act as promising Pt-catalyst supports for the methanol oxidation reaction.

Activated mesoporous carbon nanofibers fabricated using water etching-assisted templating for high-performance electrochemical capacitors.

Activated mesoporous carbon nanofibers (AMCNFs) are synthesized by a sequential process of electrospinning, water etching-assisted templating, and acid treatment. Their morphologies, crystal structures, melting behavior, chemical bonding states, surface properties, and electrochemical performance are investigated for three different polyacrylonitrile (PAN) to polyvinylpyrrolidone (PVP) weight ratios - PAN : PVP = 8 : 2, 7 : 3, and 6 : 4. Compared to other samples, the AMCNFs with an optimum weight ratio of 6 : 4 show the highest specific surface area of 692 m(2) g(-1), a high volume percentage of mesopores of 43.9%, and an increased amount of carboxyl groups (10.5%). This results in a high specific capacitance of 207 F g(-1), a high-rate capability with a capacitance retention of 93%, a high energy density of 24.8-23.1 W h kg(-1), and an excellent cycling durability of up to 3000 cycles. The electrochemical performance improvement can be explained by the combined effect of the high surface area relative to the increased electrical double-layers, the high volume fraction of mesopores relative to shorter diffusion routes and low resistance pathways for ions, and the increased amount of carboxyl groups on the CNF surface relative to enhanced wettability.

Comparison of Electrodes for High-Performance Electrochemical Capacitors: Multi-Layer MnO2/Pt and Composite MnO2/Pt on Carbon Nanofibres.

Four different types of electrodes for high-performance electrochemical capacitors were prepared using electrospinning method and/or impregnation methods: (1) conventional carbon nanofibres (CNF) supports, and CNFs decorated with (2) MnO2 nanophases, (3) multi-layer MnO2/Pt nanophases, and (4) composite MnO2 and Pt nanophases. Their morphological, structural, chemical, and electrochemical properties were characterized using field-emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and galvanostatic charge/discharge measurements. Composite MnO2 and Pt nanophases decorated on the CNFs exhibited superior capacitance (-252.3 F/g at 10 mV/s), excellent capacitance retention (-93.5% after 300 cycles), and high energy densities (13.53-18.06 Wh/kg). The enhanced electrochemical performances can be explained by the composite structure, presenting well-dispersed MnO2 nanophases leading to high capacitance, and well-dispersed Pt nanophases leading to improved electrical conductivity.