Functionalized and Platinum-Decorated Multi-Layer Oxidized Graphene as a Proton, and Electron Conducting Separator in Solid Acid Fuel Cells

In the present article, electrodes containing a composite of platinum on top of a plasma-oxidized multi-layer graphene film are investigated as model electrodes that combine an exceptional high platinum utilization with high electrode stability. Graphene is thereby acting as a separator between the phosphate-based electrolyte and the platinum catalyst. Electrochemical impedance measurements in humidified hydrogen at 240 °C show area-normalized electrode resistance of 0.06 Ω·cm−2 for a platinum loading of ∼60 µgPt·cm−2, resulting in an outstanding mass normalized activity of almost 280 S·mgPt−1, exceeding even state-of-the-art electrodes. The presented platinum decorated graphene electrodes enable stable operation over 60 h with a non-optimized degradation rate of 0.15% h−1, whereas electrodes with a similar design but without the graphene as separator are prone to a very fast degradation. The presented results propose an efficient way to stabilize solid acid fuel cell electrodes and provide valuable insights about the degradation processes which are essential for further electrode optimization.

Suitable binder for Li-ion battery anode produced from rice husk

Rice husk (RH) is a globally abundant and sustainable bioresource composed of lignocellulose and inorganic components, the majority of which consist of silicon oxides (approximately 20% w/w in dried RH). In this work, a RH-derived C/SiOx composite (RHC) was prepared by carbonization at 1000 °C for use in Li-ion battery anodes. To find a suitable binder for RHC, the RHC-based electrodes were fabricated using two different contemporary aqueous binders: polyacrylic acid (PAA) and a combination of carboxymethyl cellulose and styrene butadiene rubber (CMC/SBR). The rate and cycling performances of the RHC electrodes with respect to the insertion/extraction of Li ions were evaluated in a half-cell configuration. The cell was shorted for 24 h to completely lithiate the RHC. Impedance analysis was conducted to identify the source of the increase in the resistance of the RHC electrodes. The RHC electrode fabricated using PAA exhibited higher specific capacity for Li-ion extraction during the cycling test. The PAA binder strengthened the electrode and alleviated the increase in electrode resistance caused by the formation of the interphase film. The high affinity of PAA for SiOx in RHC was responsible for the stabilization of the anodic performance of Li-ion batteries.

Application of Octanohydroxamic Acid for Salting out Liquid–Liquid Extraction of Materials for Energy Storage in Supercapacitors

The ability to achieve high areal capacitance for oxide-based supercapacitor electrodes with high active mass loadings is critical for practical applications. This paper reports the feasibility of the fabrication of Mn3O4-multiwalled carbon nanotube (MWCNT) composites by the new salting-out method, which allows direct particle transfer from an aqueous synthesis medium to a 2-propanol suspension for the fabrication of advanced Mn3O4-MWCNT electrodes for supercapacitors. The electrodes show enhanced capacitive performance at high active mass loading due to reduced particle agglomeration and enhanced mixing of the Mn3O4 particles and conductive MWCNT additives. The strategy is based on the multifunctional properties of octanohydroxamic acid, which is used as a capping and dispersing agent for Mn3O4 synthesis and an extractor for particle transfer to the electrode processing medium. Electrochemical studies show that high areal capacitance is achieved at low electrode resistance. The electrodes with an active mass of 40.1 mg cm−2 show a capacitance of 4.3 F cm−2 at a scan rate of 2 mV s−1. Electron microscopy studies reveal changes in electrode microstructure during charge-discharge cycling, which can explain the increase in capacitance. The salting-out method is promising for the development of advanced nanocomposites for energy storage in supercapacitors.

Lightweight Polymer-Carbon Composite Current Collector for Lithium-Ion Batteries

A hermetic dense polymer-carbon composite-based current collector foil (PCCF) for lithium-ion battery applications was developed and evaluated in comparison to state-of-the-art aluminum (Al) foil collector. Water-processed LiNi0.5Mn1.5O4 (LMNO) cathode and Li4Ti5O12 (LTO) anode coatings with the integration of a thin carbon primer at the interface to the collector were prepared. Despite the fact that the laboratory manufactured PCCF shows a much higher film thickness of 55 µm compared to Al foil of 19 µm, the electrode resistance was measured to be by a factor of 5 lower compared to the Al collector, which was attributed to the low contact resistance between PCCF, carbon primer and electrode microstructure. The PCCF-C-primer collector shows a sufficient voltage stability up to 5 V vs. Li/Li+ and a negligible Li-intercalation loss into the carbon primer. Electrochemical cell tests demonstrate the applicability of the developed PCCF for LMNO and LTO electrodes, with no disadvantage compared to state-of-the-art Al collector. Due to a 50% lower material density, the lightweight and hermetic dense PCCF polymer collector offers the possibility to significantly decrease the mass loading of the collector in battery cells, which can be of special interest for bipolar battery architectures.

Nano Carbon-based as Supercapacitor Electrode from Cocoa Skin

Most cocoa shells contain carbon which can be used as an electrode. Through nano carbon, cocoa skin has the potential to be an electrode material in supercapacitors. Nano carbon is a form of carbon that has a large surface area and pore volume. Material characteristics through FT-IR test showed that the intensity of wave absorption in the graphite group (C-C) decreased which indicates an increase in carbon. The XRD results show that carbon nano has a peak of purity close to graphite at 2θ: 24.75º on the lattice values (002). So that the nano carbon based supercapacitor electrode has an electrode resistance value of 0.0307 S/m with a specific capacitance value of 5.19 F/g.

Study of Partially Transient Organic Epidermal Sensors

In this study, an all-organic, partially transient epidermal sensor with functional poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) conjugated polymer printed onto a water-soluble polyethylene oxide (PEO) substrate is studied and presented. The sensor’s electronic properties were studied under static stress, dynamic load, and transient status. Electrode resistance remained approximately unchanged for up to 2% strain, and increased gradually within 6.5% strain under static stress. The electronic properties’ dependence on dynamic load showed a fast response time in the range of 0.05–3 Hz, and a reversible stretching threshold of 3% strain. A transiency study showed that the PEO substrate dissolved completely in water, while the PEDOT:PSS conjugated polymer electrode remained intact. The substrate-less, intrinsically soft PEDOT:PSS electrode formed perfect contact on human skin and stayed attached by Van der Waals force, and was demonstrated as a tattoolike epidermal sensor.