Yongwoo Kwon

Bio: Yongwoo Kwon is an academic researcher from KAIST. The author has contributed to research in topics: Photocatalytic water splitting & Oxide. The author has an hindex of 6, co-authored 7 publications receiving 342 citations. Previous affiliations of Yongwoo Kwon include Yonsei University.

Selective Activation of Methane on Single-Atom Catalyst of Rhodium Dispersed on Zirconia for Direct Conversion

Abstract: Direct methane conversion into value-added products has become increasingly important. Because of inertness of methane, cleaving the first C–H bond has been very difficult, requiring high reaction temperature on the heterogeneous catalysts. Once the first C–H bond becomes activated, the remaining C–H bonds are successively dissociated on the metal surface, hindering the direct methane conversion into chemicals. Here, a single-atom Rh catalyst dispersed on ZrO2 surface has been synthesized and used for selective activation of methane. The Rh single atomic nature was confirmed by extended X-ray fine structure analysis, electron microscopy images, and diffuse reflectance infrared Fourier transform spectroscopy. A model of the single-atom Rh/ZrO2 catalyst was constructed by density functional theory calculations, and it was shown that CH3 intermediates can be energetically stabilized on the single-atom catalyst. The direct conversion of methane was performed using H2O2 in the aqueous solution or using O2 in g...

Shape effects of cuprous oxide particles on stability in water and photocatalytic water splitting

Abstract: Cuprous oxide (Cu2O) has received much attention as a photocatalyst due to its direct band gap structure, small band gap energy, non-toxicity, and abundance. However, Cu2O usually suffers from poor stability because the oxidation state of copper is easily changed. In this work, Cu2O particles of three different shapes were prepared with distinct surface structures: cubes with (100) facets, octahedra with (111) facets, and rhombic dodecahedra with (110) facets. Their shape stability was estimated in deionized water with or without light irradiation. The Cu2O(100) facets were selectively deformed under dark conditions, as expected from density functional theory calculations. The rhombic dodecahedra showed the most violent degradation under light irradiation, with many large thorns appearing on the surface. When water splitting was attempted using the shaped Cu2O particles, the rhombic dodecahedra produced the most hydrogen, whereas the cubes produced none. Oxygen was not measured because the holes generated upon light absorption were used to oxidize the Cu2O surface to CuO. A conformal TiIrOx overlayer was successfully formed on the rhombic dodecahedral Cu2O particles, and the coated particles presented overall water splitting producing both hydrogen and oxygen. They also showed significantly improved stability over repeated water splitting reactions relative to bare Cu2O particles or TiOx-coated Cu2O particles.

'Click' preparation of CuPt nanorod-anchored graphene oxide as a catalyst in water.

Abstract: In this paper, a simple and powerful method of producing nanoparticle-anchored graphene oxide (GO) composites using a 'click' reaction is demonstrated. This method affords a facile means of anchoring of nanoparticles with various shapes and sizes on the GO. CuPt nanorods with controlled size, aspect ratio (from 1 to 11), and uniformity are synthesized. Transmission electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy measurements are made to monitor the formation and characterize the properties of the CuPt nanorod-grafted GO composites. Their catalytic properties in the water phase are investigated using an o-phenylenediamine oxidation reaction. The results of this study clearly demonstrate that nonpolar CuPt nanorods immobilized on GO can function as a catalyst in an aqueous solution and that GO can be used as a catalytic nanorod support.

Metal ion-assisted reshaping of Cu2O nanocrystals for catalytic applications

Abstract: Copper oxides have received much attention because of their potential in energy-related applications such as gas-phase reactions, photoreactions, and batteries. In this study, the surfaces of cube- and octahedron-shaped Cu2O nanocrystals are transformed into thorny CuO, which have larger surface areas and better stability in an oxidizing environment. When the shaped Cu2O crystals were treated in an aqueous solution at 100 °C with metal ions such as Pd, Pt, and Au, the crystals became hollow particles, retaining their original shape with CuO thorns on the surface. Addition of the metal ions initiated the transformation by galvanic replacement, and then the protons generated in the replacement catalyzed sequent dissolution of Cu2O and deposition of CuO. The resulting particles showed enhanced activity and stability for CO oxidation.

Electrocatalytic Oxygen Evolution Reaction in Acidic Environments – Reaction Mechanisms and Catalysts

Abstract: The low efficiency of the electrocatalytic oxidation of water to O2 (oxygen evolution reaction-OER) is considered as one of the major roadblocks for the storage of electricity from renewable sources in form of molecular fuels like H2 or hydrocarbons Especially in acidic environments, compatible with the powerful proton exchange membrane (PEM), an earth-abundant OER catalyst that combines high activity and high stability is still unknown Current PEM-compatible OER catalysts still rely mostly on Ir and/or Ru as active components, which are both very scarce elements of the platinum group Hence, the Ir and/or Ru amount in OER catalysts has to be strictly minimized Unfortunately, the OER mechanism, which is the most powerful tool for OER catalyst optimization, still remains unclear In this review, we first summarize the current state of our understanding of the OER mechanism on PEM-compatible heterogeneous electrocatalysts, before we compare and contrast that to the OER mechanism on homogenous catalysts Thereafter, an overview over monometallic OER catalysts is provided to obtain insights into structure-function relations followed by a review of current material optimization concepts and support materials Moreover, missing links required to complete the mechanistic picture as well as the most promising material optimization concepts are pointed out

Direct transformation of bulk copper into copper single sites via emitting and trapping of atoms

Abstract: Single-atom catalysts exhibit intriguing properties and receive widespread interest for their effectiveness in promoting a variety of catalytic reactions, making them highly desired motifs in materials science. However, common approaches to the synthesis of these materials often require tedious procedures and lack appropriate interactions between the metal atoms and supports. Here, we report a simple and practical strategy to access the large-scale synthesis of single-atom catalysts via direct atoms emitting from bulk metals, and the subsequent trapping on nitrogen-rich porous carbon with the assistance of ammonia. First, the ammonia coordinates with the copper atoms to form volatile Cu(NH3)x species based on the strong Lewis acid–base interaction. Then, following transportation under an ammonia atmosphere, the Cu(NH3)x species are trapped by the defects on the nitrogen-rich carbon support, forming the isolated copper sites. This strategy is readily scalable and has been confirmed as feasible for producing functional single-atom catalysts at industrial levels. Single-atom catalysts have proven successful in many catalytic applications. Now, Li, Wu and co-workers show that single-atom catalysts can be prepared directly from bulk metals using an ammonia atmosphere, owing to the formation of volatile metal–ammonia species that are trapped by the nitrogen-rich carbon support.

Chemical Synthesis of Single Atomic Site Catalysts.

Abstract: Manipulating metal atoms in a controllable way for the synthesis of materials with the desired structure and properties is the holy grail of chemical synthesis. The recent emergence of single atomic site catalysts (SASC) demonstrates that we are moving toward this goal. Owing to the maximum efficiency of atom-utilization and unique structures and properties, SASC have attracted extensive research attention and interest. The prerequisite for the scientific research and practical applications of SASC is to fabricate highly reactive and stable metal single atoms on appropriate supports. In this review, various synthetic strategies for the synthesis of SASC are summarized with concrete examples highlighting the key issues of the synthesis methods to stabilize single metal atoms on supports and to suppress their migration and agglomeration. Next, we discuss how synthesis conditions affect the structure and catalytic properties of SASC before ending this review by highlighting the prospects and challenges for the synthesis as well as further scientific researches and practical applications of SASC.

Robust noble metal-based electrocatalysts for oxygen evolution reaction

Abstract: The oxygen evolution reaction (OER) is a kinetically sluggish anodic reaction and requires a large overpotential to deliver appreciable current. Despite the fact that non-precious metal-based alkaline water electrocatalysts are receiving increased attention, noble metal-based electrocatalysts (NMEs) applied in proton exchange membrane water electrolyzers still have advantageous features of larger current and power densities with lower stack cost. Engineering NMEs for OER catalysis with high efficiency, durability and utilization rate is of vital importance in promoting the development of cost-effective renewable energy production and conversion devices. In this tutorial review, we covered the recent progress in the composition and structure optimization of NMEs for OER including Ir- and Ru-based oxides and alloys, and noble-metals beyond Ir and Ru with a variety of morphologies. To shed light on the fundamental science and mechanisms behind composition/structure–performance relationships and activity–stability relationships, integrated experimental and theoretical studies were pursued for illuminating the metal–support interaction, size effect, heteroatom doping effect, phase transformation, degradation processes and single-atom catalysis. Finally, the challenges and outlook are provided for guiding the rational engineering of OER electrocatalysts for applications in renewable energy-related devices.