Seokhoon Choi

Wafer-scale transferable molybdenum disulfide thin-film catalysts for photoelectrochemical hydrogen production

We demonstrate that wafer-scale, transferable, and transparent thin-film catalysts based on MoS2, which consists of cheap and earth abundant elements, can provide a low onset potential of 1 mA cm−2 at 0.17 V versus a reversible hydrogen electrode and the high photocurrent density of 24.6 mA cm−2 at 0 V for a p-type Si photocathode. c-Domains with vertically stacked (100) planes in the transferable 2H-MoS2 thin films, which are grown via a thermolysis method, act as active sites for the hydrogen evolution reaction, and photogenerated electrons are efficiently transported through the n-MoS2/p-Si heterojunction.

A wafer-scale antireflective protection layer of solution-processed TiO2 nanorods for high performance silicon-based water splitting photocathodes

Sustainable and efficient conversion of solar energy to transportable green energy and storable fuels, hydrogen, represents a solution to the energy crisis and reduces the consumption of fossil fuels, which are mainly responsible for the rise in global temperature. Solar water splitting using semiconductors, such as silicon, is promising to satisfy the global energy demand by producing hydrogen molecules. However, the solar to hydrogen conversion efficiency of a silicon photoelectrode is suppressed by overpotential, high reflectance and/or instability in liquid electrolytes. Herein, we report the synthesis of multifunctional solution-processed TiO2 nanorods on a 4-inch p-silicon wafer with controllable heights and diameters for highly efficient water splitting photocathodes. The solution-processed passivation layer of TiO2 nanorods reduces the overpotential of the silicon photocathode due to its catalytic properties. The TiO2 NRs also dramatically improves the light absorption of silicon due to the antireflective ability of the nanorods. The reflectance of silicon is decreased from 37.5% to 1.4% and enhances the saturated photocurrent density. The Pt-decorated (1–2.5 nm diameter) TiO2 nanorods/p-Si photocathodes show a short circuit current density of up to 40 mA cm−2, an open circuit voltage ∼440 mV and incident photon to current conversion efficiency of >90% using 0.5 M H2SO4 electrolyte with simulated 1 sun irradiation. The heterostructure photocathodes are stable for more than 52 h without noticeable degradation and an ideal regenerative cell efficiency of 2.5% is achieved.

Drastically enhanced hydrogen evolution activity by 2D to 3D structural transition in anion-engineered molybdenum disulfide thin films for efficient Si-based water splitting photocathodes

We synthesized transferrable and transparent anion-engineered molybdenum disulfide thin-film catalysts through a simple thermolysis method by using [(NH4)2MoS4] solution and powder precursors with different sulphur/phosphorus weight ratios. The synthesized sulphur-doped molybdenum phosphide (S:MoP) thin film changed from a two-dimensional van der Waals structure to a three-dimensional hexagonal structure by introduction of phosphorus atoms in the MoS2 thin film. The S:MoP thin film catalyst, which is composed of cheap and earth abundant elements, could provide the lowest onset potential and the highest photocurrent density for planar p-type Si photocathodes. The density functional theory calculations indicate that the surface of S:MoP thin films absorb hydrogen better than that of MoS2 thin films. The structurally engineered thin film catalyst facilitates the easy transfer of photogenerated electrons from the p-Si light absorber to the electrolyte. Anion-engineering of the MoS2 thin film catalyst would be an efficient way to enhance the catalytic activity for photoelectrochemical water splitting.

Toward High-Performance Hematite Nanotube Photoanodes: Charge-Transfer Engineering at Heterointerfaces

Vertically ordered hematite nanotubes are considered to be promising photoactive materials for high-performance water-splitting photoanodes. However, the synthesis of hematite nanotubes directly on conducting substrates such as fluorine-doped tin oxide (FTO)/glass is difficult to be achieved because of the poor adhesion between hematite nanotubes and FTO/glass. Here, we report the synthesis of hematite nanotubes directly on FTO/glass substrate and high-performance photoelectrochemical properties of the nanotubes with NiFe cocatalysts. The hematite nanotubes are synthesized by a simple electrochemical anodization method. The adhesion of the hematite nanotubes to the FTO/glass substrate is drastically improved by dipping them in nonpolar cyclohexane prior to postannealing. Bare hematite nanotubes show a photocurrent density of 1.3 mA/cm(2) at 1.23 V vs a reversible hydrogen electrode, while hematite nanotubes with electrodeposited NiFe cocatalysts exhibit 2.1 mA/cm(2) at 1.23 V which is the highest photocurrent density reported for hematite nanotubes-based photoanodes for solar water splitting. Our work provides an efficient platform to obtain high-performance water-splitting photoanodes utilizing earth-abundant hematite and noble-metal-free cocatalysts.

Microscopic Evidence for Strong Interaction between Pd and Graphene Oxide that Results in Metal‐Decoration‐Induced Reduction of Graphene Oxide

Graphene oxide (GO) is reduced spontaneously when palladium nanoparticles are decorated on the surface. The oxygen functional groups at the GO surface near the nanoparticles are absorbed to the palladium to produce a palladium oxide interlayer. Palladium therefore grows on the GO with preferred orientations, resulting in unique microstructural and electrical properties.

Dual anode LIGBT on SOI substrates

The device characteristics of a new SOI LIGBT, called the Dual Anode LIGBT, were investigated by 2-dimensional numerical simulation. It was shown that the negative differential resistance regime was completely eliminated without an additional process step and mask. The forward voltage drop of the DA-LIGBT at a current density of 100 A/cm/sup 2/, was 30% lower than that of the conventional SSA-LIGBT. This is attributed to the path of the electron carriers under the cathode region. The turn-off speed of the DA-LIGT is about one order faster than that of the LIGBT. The proposed DA-LIGBT may be an attractive device for power integrated circuits.

Substantially enhanced front illumination photocurrent in porous SnO2 nanorods/networked BiVO4 heterojunction photoanodes

BiVO4 is a promising photoanode for photoelectrochemical applications owing to its suitable band edge position for oxygen evolving reactions. High photocurrent under front illumination is very much essential to design tandem structures with a wireless configuration. However, the performance of BiVO4 under front illumination is limited due to poor charge transport properties. Here, we show that network-like BiVO4 coupled with porous SnO2 nanorods (NRs) is a promising model to enhance the front illumination performance. A very high photocurrent density of 5.6 mA cm−2 and 5.5 mA cm−2 has been obtained from the front and back illumination at 1.23 V vs. the reversible hydrogen electrode, respectively. We demonstrate that the appropriate nanostructuring of SnO2 NRs/BiVO4 is the underlying technology to tune the performance under directional illumination. The SnO2 NRs/BiVO4 exhibits a maximum incident photon to current efficiency of ∼80% under front and back illumination. A systematic study reveals that the optimized network like BiVO4 coated on porous SnO2 NRs synergistically boosts both the charge separation and transfer efficiencies of the photoanode resulting in a significantly high photocurrent for illumination on either side. This work provides a direction to achieve enhanced photocurrent during front and back side illumination in order to realize a wireless tandem configuration.

Synthesis of Numerous Edge Sites in MoS2 via SiO2 Nanorods Platform for Highly Sensitive Gas Sensor

The utilization of edge sites in two-dimensional materials including transition-metal dichalcogenides (TMDs) is an effective strategy to realize high-performance gas sensors because of their high catalytic activity. Herein, we demonstrate a facile strategy to synthesize the numerous edge sites of vertically aligned MoS2 and larger surface area via SiO2 nanorod (NRs) platforms for highly sensitive NO2 gas sensor. The SiO2 NRs encapsulated by MoS2 film with numerous edge sites and partially vertical-aligned regions synthesized using simple thermolysis process of [(NH4)2MoS4]. Especially, the vertically aligned MoS2 prepared on 500 nm thick SiO2 NRs (500MoS2) shows approximately 90 times higher gas-sensing response to 50 ppm NO2 at room temperature than the MoS2 film prepared on flat SiO2, and the theoretical detection limit is as low as ∼2.3 ppb. Additionally, it shows reliable operation with reversible response to NO2 gas without degradation at an operating temperature of 100 °C. The use of the proposed facile approach to synthesize vertically aligned TMDs using nanostructured platform can be extended for various TMD-based devices including sensors, water splitting catalysts, and batteries.