Poly(styrene sulfonic acid)-Grafted Carbon Black Synthesized by Surface-Initiated Atom Transfer Radical Polymerization.

Owing to their excellent electrical conductivity and robust mechanical properties, carbon-based nanocomposites are being used in a wide range of applications and devices, such as electromagnetic wave interference shielding, electronic devices, and fuel cells. While several approaches have been developed for synthesizing carbon nanotubes and carbon-black-based polymer nanocomposites, most studies have focused on the simple blending of the carbon material with a polymer matrix. However, this results in uncontrolled interactions between the carbon filler and the polymer chains, leading to the agglomeration of the carbon filler. Herein, we report a new strategy for synthesizing sulfonated polystyrene (PSS)-grafted carbon black nanoparticles (NPs) via surface-initiated atom-transfer radical polymerization. Treatments with O2 plasma and H2O2 result in the effective attachment of the appropriate initiator to the carbon black NPs, thus allowing for the controlled formation of the PSS brushes. The high polymeric processability and desirable mechanical properties of the PSS-grafted carbon black NPs enable them suitable for use in nonfluorinated-hydrocarbon-based polymer electrolyte membranes for fuel cells, which must exhibit high proton conductivity without interrupting the network of channels consisting of ionic clusters (i.e., sulfonic acid moieties).

Rational Design of Ultrathin Gas Barrier Layer via Reconstruction of Hexagonal Boron Nitride Nanoflakes to Enhance the Chemical Stability of Proton Exchange Membrane Fuel Cells.

Hexagonal boron nitride (hBN) has great potential as a promising gas barrier layer in proton exchange membrane fuel cells (PEMFCs) as it shows high proton conductivity as well as excellent gas-blocking capability. However, structural defects and mechanical damage during the transfer of the hBN layer and membrane swelling have limited the application of hBN sheets to PEMFCs. Here, an ultrathin gas barrier layer is successfully fabricated on a proton exchange membrane via reconstruction of mechanically exfoliated hBN nanoflakes using a direct spin-coating process. The hBN-coated layer effectively suppresses the gas crossover and inhibits the formation of reactive oxygen radicals in the electrodes without reducing the proton conductivity of the membrane. It is also demonstrated that the structural advantages of hBN-coated gas barrier layers promise high performance of a unit cell even after a open-circuit voltage (OCV) hold test for 100 h. Furthermore, through in-depth postmortem analyses, a time-dependent degradation mechanism of membrane electrode assembly under the OCV condition is rationally proposed.

Effect of Heat Treatment on Structure of Carbon Shell-Encapsulated Pt Nanoparticles for Fuel Cells.

Polymer electrolyte membrane fuel cells (PEMFCs) have attracted much attention as highly efficient, eco-friendly energy conversion devices. However, carbon-supported Pt (Pt/C) catalysts for PEMFCs still have several problems, such as low long-term stability, to be widely commercialized in fuel cell applications. To address the stability issues of Pt/C such as the dissolution, detachment, and agglomeration of Pt nanoparticles under harsh operating conditions, we design an interesting fabrication process to produce a highly active and durable Pt catalyst by introducing a robust carbon shell on the Pt surface. Furthermore, this approach provides insights into how to regulate the carbon shell layer for fuel cell applications. Through the application of an appropriate amount of H2 gas during heat treatment, the carbon shell pores, which are integral to the structure, can be systematically modulated to facilitate oxygen adsorption for the oxygen reduction reaction. Simultaneously, the carbon shell functions as a protective barrier, preventing catalyst degradation. In this regard, we investigate an in-depth analysis of the effects of critical parameters including H2 content and the flow rate of H2/N2 mixed gas during heat treatment to prepare better catalysts.

Redesign of Anode Catalyst for Sustainable Survival of Fuel Cells.

Polymer electrolyte membrane fuel cells (PEMFCs) suffer from severe performance degradation when operating under harsh conditions such as fuel starvation, shut-down/start-up, and open circuit voltage. A fundamental solution to these technical issues requires an integrated approach rather than condition-specific solutions. In this study, an anode catalyst based on Pt nanoparticles encapsulated in a multifunctional carbon layer (MCL), acting as a molecular sieve layer and protective layer is designed. The MCL enabled selective hydrogen oxidation reaction on the surface of the Pt nanoparticles while preventing their dissolution and agglomeration. Thus, the structural deterioration of a membrane electrode assembly can be effectively suppressed under various harsh operating conditions. The results demonstrated that redesigning the anode catalyst structure can serve as a promising strategy to maximize the service life of the current PEMFC system.

Correlation between platinum nanoparticle surface rearrangement induced by heat treatment and activity for an oxygen reduction reaction.

Heat treatment of nanoparticles could induce the surface rearrangement for more stable facet exposure induced by thermodynamics. By changing the heat treatment environment, we confirmed the correlation between the oxygen reduction activity and the effect of surface oxide and the degree of surface rearrangement of Pt nanoparticles. Native surface oxide was not a critical factor for oxygen reduction activity. However, the degree of surface rearrangement could affect the activity, which was confirmed by the surface sensitive techniques such as CO(ad) oxidation and potential of zero total charge. Analysis indicated that the driving force for nanoparticle surface rearrangement was affected by the heat treatment environment such as gas, in our case.

Chemical tuning of electrochemical properties of Pt-skin surfaces for highly active oxygen reduction reactions.

Pt-skin surfaces were successfully fabricated by the chemical deposition of additional Pt on corrugated Pt-Ni nanoparticles with Pt-skeleton surfaces. Compared to the Pt-skin formed by heat annealing, the chemically-tuned Pt-skin had a higher Pt coordination number and surface crystallinity, which resulted in superior ORR activity and durability.

Engineering Rich-Cation Vacancies in CuCo2O4 Hollow Spheres with a Large Surface Area Derived from a Template-Free Approach for Ultrahigh Capacity and High-Energy Density Supercapacitors.

Intriguing cationic defects with hollow nano-/microstructures are a critical challenge but a potential strategy to discover electrochemical energy conversion and storage devices with improved electrochemical performances. Herein, we successfully produced a highly porous, and large surface area of self-templated CuCo2O4 hollow spheres (CCOHSs) with cationic defects via a solvothermal route. We hypothesized that the inside-out Ostwald ripening mechanism of the template-free strategy was the framework for forming the CCOHSs. Cationic defects (Cu) within the CCOHSs were identified by employing various analytical techniques, including energy-dispersive X-ray spectroscopy analysis of both scanning and transmission electron microscopy, X-ray photon spectroscopy, and inductively coupled plasma-atomic emission spectroscopy. The resulting CCOHSs had significant properties, such as a high specific surface area of 98.32 m2 g-1, rich porosity, and battery-type electrode behavior in supercapacitor applications. Notably, the CCOHSs demonstrated an outstanding specific capacity of 1003.7 C g-1 at 1 A g-1, with excellent structural integrity and cycle stability. Moreover, the fabricated asymmetric CCOHS//activated carbon device exhibited a high energy density of 65.2 Wh kg-1 at a power density of 777.8 W kg-1.

Fine-tuning of ultrathin carbon shells coated on metal nanoparticles: carbon etching and defect healing effects.

Carbon-incorporated metal nanoparticles are heat-treated in various gas atmospheres to create carbon shells with different porosity. A highly porous carbon shell is formed due to the carbon etching effect by H2, and the defect healing effect by CO is discovered through additional CO gas treatment of the H2/N2 gas-treated sample.

Origin and Formation Mechanism of Carbon Shell-Encapsulated Metal Nanoparticles for Powerful Fuel Cell Durability.

Proton exchange membrane fuel cells (PEMFCs) face technical issues of performance degradation due to catalyst dissolution and agglomeration in real-world operations. To address these challenges, intensive research has been recently conducted to introduce additional structural units on the catalyst surface. Among various concepts for surface modification, carbon shell encapsulation is known to be a promising strategy since the carbon shell can act as a protective layer for metal nanoparticles. As an interesting approach to form carbon shells on catalyst surfaces, the precursor ligand-induced formation is preferred due to its facile synthesis and tunable control over the carbon shell porosity. However, the origin of the carbon source and the carbon shell formation mechanism have not been studied in depth yet. Herein, this study aims to investigate carbon sources through the use of different precursors and the introduction of new methodologies related to the ligand exchange phenomenon. Subsequently, we provide new insights into the carbon shell formation mechanism using X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Finally, the thermal stability and electrochemical durability of carbon shells are thoroughly investigated through in situ transmission electron microscopy (in situ TEM) and accelerated durability tests.

Activity Quantification of Fuel Cell Catalysts via Sequential Poisoning by Multiple Reaction Inhibitors.

The development of non-Pt or carbon-based catalysts for anion exchange membrane fuel cells (AEMFCs) requires identification of the active sites of the catalyst. Since not only metals but also carbon materials exhibit oxygen reduction reaction (ORR) activity in alkaline conditions, the contribution of carbon-based materials to ORR performance should also be thoroughly analyzed. However, the conventional CN- poisoning experiments, which are mainly used to explain the main active site of M-N-C catalysts, are limited to only qualitative discussions, having the potential to make fundamental errors. Here, we report a modified electrochemical analysis to quantitatively investigate the contribution of the metal and carbon active sites to ORR currents at a fixed potential by sequentially performing chronoamperometry with two reaction inhibitors, CN- and benzyl trimethylammonium (BTMA+). As a result, we discover how to quantify the individual contributions of two active sites (Pt nanoparticles and carbon support) of carbon-supported Pt (Pt/C) nanoparticles as a model catalyst. This study is expected to provide important clues for the active site analysis of carbon-supported non-Pt catalysts, such as M-N-C catalysts composed of heterogeneous elements.

Interspersing CeOx Clusters to the Pt-TiO2 Interfaces for Catalytic Promotion of TiO2-Supported Pt Nanoparticles.

We propose an interface-engineered oxide-supported Pt nanoparticle-based catalyst with improved low-temperature activity toward CO oxidation. By wet-impregnating 1 wt % Ce on TiO2, we synthesized hybrid oxide support of CeOx-TiO2, in which dense CeOx clusters formed on the surface of TiO2. Then, the Pt/CeOx-TiO2 catalyst was synthesized by impregnating 2 wt % Pt on the CeOx-TiO2 supporting oxide. Pt-CeOx-TiO2 triphase interfaces were eventually formed upon impregnation of Pt on CeOx-TiO2. The Pt-CeOx-TiO2 interfaces open up the interface-mediated Mars-van Krevelen CO oxidation pathway, thus providing additional interfacial reaction sites for CO oxidation. Consequently, the specific reaction rate of Pt/CeOx-TiO2 for CO oxidation was increased by 3.2 times compared with that of Pt/TiO2 at 140 °C. Our results demonstrate a widely applicable and straightforward method of catalytic activation of the interfaces between metal nanoparticles and supporting oxides, which enabled fine-tuning of the catalytic performance of oxide-supported metal nanoparticle classes of heterogeneous catalysts.

High performance langasite based SAW NO2 gas sensor using 2D g-C3N4@TiO2 hybrid nanocomposite.

Nitrogen dioxide (NO2) gas has emerged as a severe air pollutant that causes damages to the environment, human life and global ecosystems etc. However, the currently available NO2 gas sensors suffers from insufficient selectivity, sensitivity and long response times that impeding their practical applicability for room temperature (RT) gas sensing. Herein, we report a high performance langasite (LGS) based surface acoustic wave (SAW) RT NO2 gas sensor using 2-dimensional (2D) g-C3N4@TiO2 nanoplates (NP) with {001} facets hybrid nanocomposite as a chemical interface. The g-C3N4@TiO2 NP/LGS SAW device showed a significant negative frequency shift (∆f) of ~19.8 kHz which is 2.4 fold higher than that of the pristine TiO2 NP/LGS SAW sensor toward 100 ppm of NO2 at RT. In addition, the hybrid SAW device fascinatingly exhibited a fast response/recovery time with a low detection limit, high selectivity, and an effective long term stability toward NO2 gas. It also exhibited an enhanced and robust negative frequency shifts under various relative humidity conditions ranging from 20% to 80% for 100 ppm of NO2 gas. The high performance of the g-C3N4 @TiO2 NP/LGS SAW gas sensor can be attributed to the enhanced mass loading effect which was assisted by the large surface area, oxygen vacancies, OH and amine functional groups of the n-n hybrid heterojunction of g-C3N4@TiO2 NP that provide abundant active sites for the adsorption and diffusion of NO2 gas molecules. These results emphasize the significance of the integration of 2D materials with metal oxides for SAW based RT gas sensing technology holds great promise in environmental protection.

Emerging carbon shell-encapsulated metal nanocatalysts for fuel cells and water electrolysis.

The development of low-cost, high-efficiency electrocatalysts is of primary importance for hydrogen energy technology. Noble metal-based catalysts have been extensively studied for decades; however, activity and durability issues still remain a challenge. In recent years, carbon shell-encapsulated metal (M@C) catalysts have drawn great attention as novel materials for water electrolysis and fuel cell applications. These electrochemical reactions are governed mainly by interfacial charge transfer between the core metal and the outer carbon shell, which alters the electronic structure of the catalyst surface. Furthermore, the rationally designed and fine-tuned carbon shell plays a very interesting role as a protective layer or molecular sieve layer to improve the performance and durability of energy conversion systems. Herein, we review recent advances in the use of M@C type nanocatalysts for extensive applications in fuel cells and water electrolysis with a focus on the structural design and electronic structure modulation of carbon shell-encapsulated metal/alloys. Finally, we highlight the current challenges and future perspectives of these catalytic materials and related technologies in this field.

Enhancement of Catalytic Activity and Durability of Pt Nanoparticle through Strong Chemical Interaction with Electrically Conductive Support of Magnéli Phase Titanium Oxide.

In this study, we address the catalytic performance of variously sized Pt nanoparticles (NPs) (from 1.7 to 2.9 nm) supported on magnéli phase titanium oxide (MPTO, Ti4O7) along with commercial solid type carbon (VXC-72R) for oxygen reduction reaction (ORR). Key idea is to utilize a robust and electrically conductive MPTO as a support material so that we employed it to improve the catalytic activity and durability through the strong metal-support interaction (SMSI). Furthermore, we increase the specific surface area of MPTO up to 61.6 m2 g-1 to enhance the SMSI effect between Pt NP and MPTO. After the deposition of a range of Pt NPs on the support materials, we investigate the ORR activity and durability using a rotating disk electrode (RDE) technique in acid media. As a result of accelerated stress test (AST) for 30k cycles, regardless of the Pt particle size, we confirmed that Pt/MPTO samples show a lower electrochemical surface area (ECSA) loss (<20%) than that of Pt/C (~40%). That is explained by the increased dissolution potential and binding energy of Pt on MPTO against to carbon, which is supported by the density functional theory (DFT) calculations. Based on these results, we found that conductive metal oxides could be an alternative as a support material for the long-term fuel cell operation.

Facile Strategy for Mass Production of Pt Catalysts for Polymer Electrolyte Membrane Fuel Cells Using Low-Energy Electron Beam.

There are so many variables affecting the large-scale chemical synthesis of nanoparticles that mass production remains a challenge. Here, using a high-efficiency compact electron beam generator irradiating a low-energy electron beam, we fabricate carbon-supported Pt nanoparticles (Pt/C) in an open chamber to present the applicability of an electron beam to the mass production of metal nanocatalysts for polymer electrolyte membrane fuel cells (PEMFCs). The amount of dispersants (glycerol) and radical scavengers (isopropyl alcohol, IPA), the most important factors in the electron beam-induced fabrication process, is systematically controlled to find the conditions for the synthesis of the particle structure suitable for PEMFC applications. Furthermore, the effects of the structural changes on the electrochemical properties of the catalysts are thoroughly investigated. Through in-depth studies, it is clearly revealed that while dispersants control the nucleation step of monomers affecting the degree of dispersion of nanoparticles, radical scavengers with strong oxidizing power have an effect on the particle growth rate. Therefore, this study is expected to present the applicability of low-energy electron beam to the mass production of metal nanocatalysts for PEMFCs, and to provide insights into the fabrication of nanoparticles using low-energy electron beams.

Quaternary Ammonium-Bearing Perfluorinated Polymers for Anion Exchange Membrane Applications.

Perfluorinated polymers are widely used in polymer electrolyte membranes because of their excellent ion conductivity, which are attributed to the well-defined morphologies resulting from their extremely hydrophobic main-chains and flexible hydrophilic side-chains. Perfluorinated polymers containing quaternary ammonium groups were prepared from Nafion- and Aquivion-based sulfonyl fluoride precursors by the Menshutkin reaction to give anion exchange membranes. Perfluorinated polymers tend to exhibit poor solubility in organic solvents; however, clear polymer dispersions and transparent membranes were successfully prepared using N-methyl-2-pyrrolidone at high temperatures and pressures. Both perfluorinated polymer-based membranes exhibited distinct hydrophilic-hydrophobic phase-separated morphologies, resulting in high ion conductivity despite their low ion exchange capacities and limited water uptake properties. Moreover, it was found that the capacitive deionization performances and stabilities of the perfluorinated polymer membranes were superior to those of the commercial Fumatech membrane.

Electrochemical Analysis for Demonstrating CO Tolerance of Catalysts in Polymer Electrolyte Membrane Fuel Cells.

Since trace amounts of CO in H2 gas produced by steam reforming of methane causes severe poisoning of Pt-based catalysts in polymer electrolyte membrane fuel cells (PEMFCs), research has been mainly devoted to exploring CO-tolerant catalysts. To test the electrochemical property of CO-tolerant catalysts, chronoamperometry is widely used under a CO/H2 mixture gas atmosphere as an essential method. However, in most cases of catalysts with high CO tolerance, the conventional chronoamperometry has difficulty in showing the apparent performance difference. In this study, we propose a facile and precise test protocol to evaluate the CO tolerance via a combination of short-term chronoamperometry and a hydrogen oxidation reaction (HOR) test. The degree of CO poisoning is systematically controlled by changing the CO adsorption time. The HOR polarization curve is then measured and compared with that measured without CO adsorption. When the electrochemical properties of PtRu alloy catalysts with different atomic ratios of Pt to Ru are investigated, contrary to conventional chronoamperometry, these catalysts exhibit significant differences in their CO tolerance at certain CO adsorption times. The present work will facilitate the development of catalysts with extremely high CO tolerance and provide insights into the improvement of electrochemical methods.

Modulating Catalytic Activity and Durability of PtFe Alloy Catalysts for Oxygen Reduction Reaction Through Controlled Carbon Shell Formation.

Demand on synthetic approaches to high performance electrocatalyst with enhanced durability is increasing for fuel cell applications. In this work, we present a facile synthesis of carbon shell-coated PtFe nanoparticles by using acetylacetonates in metal precursors as carbon sources without an additional polymer coating process for the carbon shell formation. The carbon shell structure is systematically controlled by changing the annealing conditions such as the temperature and gas atmosphere. PtFe catalysts annealed at 700 °C under H2-mixed N2 gas show much higher oxygen reduction reaction (ORR) activity and superior durability compared to a Pt catalyst due to the ultrathin and porous carbon shells. In addition, when increasing the annealing temperature, the carbon shells encapsulating the PtFe nanoparticles improves the durability of the catalysts due to the enhanced crystallinity of the carbon shells. Therefore, it is demonstrated that the developed hybrid catalyst structure with the carbon shells not only allows the access of reactant molecules to the active sites for oxygen reduction reaction but also prevents the agglomeration of metal nanoparticles on carbon supports, even under harsh operating conditions. The proposed synthetic approach and catalyst structure are expected to provide more insights into the development of highly active and durable catalysts for practical fuel cell applications.

Boosting the oxygen reduction activity of a nano-graphene catalyst by charge redistribution at the graphene-metal interface.

N-Doped carbon materials have been intensively studied to replace Pt catalysts for the oxygen reduction reaction (ORR) in anion exchange membrane fuel cells (AEMFCs). However, the low doping level in these catalysts results in a limited number of ORR active sites, so high catalyst loading is still required. Hence, the electrode thickness becomes extra thick, causing large mass transfer resistance in AEMFCs. In this study, we propose a unique hybrid catalyst concept utilizing charge redistribution at the graphene-transition metal interface to modify the electronic structure of graphene and simultaneously create multiple carbon active sites. The hybrid catalyst consists of n-type nano-graphene shells (NGS) three-dimensionally coated on the surface of transition metal nanoparticles highly dispersed on carbon supports. The n-type NGS catalysts efficiently facilitate oxygen adsorption owing to facile charge transfer from the metal nanoparticles underneath and provide abundant active carbon sites owing to their structural benefits. As a result, despite the same catalyst loading, the NGS catalyst shows high ORR activity and greater durability than a carbon-supported Pt (Pt/C) catalyst.

Boosting Fuel Cell Durability under Shut-Down/Start-Up Conditions Using a Hydrogen Oxidation-Selective Metal-Carbon Hybrid Core-Shell Catalyst.

Performance degradation generated by reverse current flow during fuel cell shut-down/start-up is a big challenge for commercialization of polymer electrolyte membrane fuel cells in automobile applications. Under transient operating conditions, the formation of H2/O2 boundaries on Pt surfaces and the occurrence of undesired oxygen reduction reaction (ORR) in an anode cause severe degradation of carbon supports and Pt catalysts in a cathode because of an increase of the cathode potential up to ∼1.5 V. Herein, to directly prevent the formation of H2/O2 boundaries in the anode, we propose a unique metal-carbon hybrid core-shell anode catalyst having Pt nanoparticles encapsulated in nanoporous carbon shells for selective H2 permeation. This hybrid catalyst exhibits high hydrogen oxidation reaction (HOR) selectivity along with fully subdued ORR activity during long-term operation because of the excellent stability of the carbon molecular sieves. Furthermore, the HOR-selective catalyst effectively suppresses the reverse current flow in a single cell under shut-down/start-up conditions.