Snapback-Free Reverse-Conducting SOI LIGBT with an Integrated Self-Biased MOSFET

A novel snapback-free RC-LIGBT with integrated self-biased N-MOSFET is proposed and investigated by simulation. The device features an integrated self-biased N-MOSFET(ISM) on the anode active region. One side of the ISM is shorted to the P+ anode electrode of RC-LIGBT and the other side is connected to the N+ anode via a floating ohmic contact. The adaptively turn-on/off of the ISM contributes to improve the static and dynamic performance of the ISM RC-LIGBT. In the forward-state, due to the off-state of the ISM, the snapback could be effectively suppressed without requiring extra device area compared with the SSA (separated shorted anode) and STA (segmented trenches in the anode) LIGBTs. In the reverse conduction, the ISM is turned on and the parasitic NPN in the ISM is punched through, which provides a current path for the reverse current. Meanwhile, during the turn-off and reverse recovery states, the ISM turns on, providing a rapid electron extraction path. Thus, a superior tradeoff between the on-state voltage drop (Von) and turnoff loss (Eoff) as well as an improved reverse recovery characteristic can be obtained. Compared with the STA device, the proposed ISM RC-LIGBT reduces Eoff by 21.5% without snapback. Its reverse recovery charge is reduced by 53.7%/58.6% compared to that of the SSA LIGBT with Lb=40/60μm at the same Von. Due to the prominent static and dynamic characteristic, the power loss of ISM RC-LIGBT in a completed switching cycle is reduced.

Fabrication and Characterization of Thin-Film SOFC Supported by Microchannel-Structured Zirconia Substrate for Direct Methane Operation

Ni-cermet anode demonstrates excellent catalytic activity and electrical conductivity but suffers from carbon deposition issue. To utilize Ni-cermet anode while preventing carbon deposition, a synergic strategy is employed to design anode electrode. In particular, Zr is incorporated into Ce0.8Sm0.2O2-δ lattice to tailor oxygen storage and catalytic properties of Ni-Ce0.8-xSm0.2ZrxO2-δ anode for improving electrochemical oxidizations of various fuel species. An inert thick YSZ microtubular substrate with radially well-aligned microchannels open at the inner surface is used to support multi thin functional layers of solid oxide cell, i.e., Ni current collector, Ni-Ce0.8-xSm0.2ZrxO2-δ anode, YSZ/SDC electrolyte, and LSCF cathode. The thick YSZ substrate is able to inhibit the ratio of fuel to product gases in the thin anode functional layer, which favors the prevention of carbon buildup in the thin anode layer when synergistically combined with Ni-Ce0.8-xSm0.2ZrxO2-δ anode material. The microchannels embedded in the YSZ substrate can also avoid too much dilutions of the fuel in the anode functional layer. The cell is fabricated and tested with both hydrogen and methane as the fuel. A short-term test is conducted with methane as fuel and good stability is obtained. The fundamental mechanisms for the prevention of carbon buildup in anode functional layer are also discussed.

Covalently Bonded Ir(IV) on Conducted Blue TiO2 for Efficient Electrocatalytic Oxygen Evolution Reaction in Acid Media

The stability of anode electrode has been a primary obstacle for the oxygen evolution reaction (OER) in acid media. We design Ir-oxygen of hydroxyl-rich blue TiO2 through covalent bonds (Ir–O2–2Ti) and investigate the outcome of favored exposure of different amounts of covalent Ir–oxygen linked to the conductive blue TiO2 in the acidic OER. The Ir-oxygen-blue TiO2 nanoclusters show a strong synergy in terms of improved conductivity and tiny amount usage of Ir by using blue TiO2 supporter, and enhanced stability using covalent Ir-oxygen-linking (i.e., Ir oxide) in acid media, leading to high acidic OER performance with a current density of 10 mA cm−2 at an overpotential of 342 mV, which is much higher than that of IrO2 at 438 mV in 0.1 M HClO4 electrolyte. Notably, the Ir–O2–2Ti has a great mass activity of 1.38 A/mgIr at an overpotential 350 mV, which is almost 27 times higher than the mass activity of IrO2 at the same overpotential. Therefore, our work provides some insight into non-costly, highly enhanced, and stable electrocatalysts for the OER in acid media.

Using BCN nanostructure as anode electrode for photoelectrocatalytic degradation of organics: a statistical approach

In this study, boron carbon nitride (BCN) nanostructures were used as photocatalyst which was synthesized in a chemical vapor deposition reactor. Photoelectrocatalysis was used for degradation organic pollutants from produced water. BCN nanostructures were coated on a coil-type copper wire to be as anode electrode in the photoelectrocatalytic process. The effect of different parameters on chemical oxygen demand (COD) removal efficiency from produced water was investigated by a central composite design (CCD) to maximize photoelectrocatalysis influence as one of the most used methods of wastewater treatment. A 12 run Plackett–Burman design was used for screening of the parameters (initial COD, electrical conductivity, applied cell voltage, UV lamp wavelength, H2O2 concentration, residence time, and initial pH) which led to the selection of residence time and initial pH as effective parameters. Since the core goal of this study was to maximize the COD removal efficiency, the steepest ascent method was used to propel these two parameters to the optimum region. Finally, CCD showed that applying photoelectrocatalysis could lead to 88.79% of the COD removal efficiency which would be an optimum value at a residence time of 15.85 min and a pH value of 3.3. Ultimately, this result was confirmed by experimentation at those conditions.

The Electrochemical Stability of Starch Carbon as an Important Property in the Construction of a Lithium-Ion Cell

This paper shows use of starch-based carbon (CSC) and graphene as the anode electrode for lithium-ion cell. To describe electrochemical stability of the half-cell system and kinetic parameters of charging process in different temperatures, electrochemical impedance spectroscopy (EIS) measurement was adopted. It has been shown that smaller resistances are observed for CSC. Additionally, Bode plots show high electrochemical stability at higher temperatures. The activation energy for the SEI (solid–electrolyte interface) layer, charge transfer, and electrolyte were in the ranges of 24.06–25.33, 68.18–118.55, and 13.84–15.22 kJ mol−1, respectively. Moreover, the activation energy of most processes is smaller for CSC, which means that this electrode could serve as an eco-friendly biodegradable lithium-ion cell element.