C15-Phase Platinum-Lanthanide Intermetallics for Efficient Hydrogen Evolution: Identifying Lanthanide's Enhanced Mechanism.

Platinum-Lanthanide (Pt-Ln) intermetallic compounds (IMCs) are a promising new class of electrocatalytic materials, yet their synthesis remains a significant challenge, and the role of ordered Ln sites in enhancing catalytic performance is not fully understood. Herein, an effective and rapid avenue for synthesizing carbon-supported C15-phase PtLn IMCs (Ln: Sm, Eu, Gd, and Tb) through Joule heating technology is proposed. The JH-PtLn/C IMCs exhibit excellent electrocatalytic performance toward alkaline hydrogen evolution reaction (HER), in which JH-PtTb/C presents the lowest overpotential of 17 mV at 10 mA cm.

Asymmetric Rh-O-Co bridge sites enable superior bifunctional catalysis for hydrazine-assisted hydrogen production.

Hydrazine-assisted water splitting is a promising strategy for energy-efficient hydrogen production, yet challenges remain in developing effective catalysts that can concurrently catalyze both the hydrogen evolution reaction (HER) and hydrazine oxidation reaction (HzOR) in acidic media. Herein, we report an effective bifunctional catalyst consisting of Rh clusters anchored on CoO branched nanosheets (Rh-CoO BNSs) synthesized an innovative arginine-induced strategy. The Rh-CoO BNSs exhibit unique Rh-O-Co interfacial sites that facilitate charge redistribution between Rh clusters and the CoO substrate, thereby optimizing their valence electronic structures.

Identifying Highly Active and Selective Cobalt X-Ides for Electrocatalytic Hydrogenation of Quinoline.

Earth-abundant Co X-ides are emerging as promising catalysts for the electrocatalytic hydrogenation of quinoline (ECHQ), yet challenging due to the limited fundamental understanding of ECHQ mechanism on Co X-ides. This work identifies the catalytic performance differences of Co X-ides in ECHQ and provides significant insights into the catalytic mechanism of ECHQ. Among selected Co X-ides, the CoO presents the best ECHQ performance with a high conversion of 98.

Lattice Strain Engineering on Metal-Organic Frameworks by Ligand Doping to Boost the Electrocatalytic Biomass Valorization.

As an efficient and environmental-friendly strategy, electrocatalytic oxidation can realize biomass lignin valorization by cleaving its aryl ether bonds to produce value-added chemicals. However, the complex and polymerized structure of lignin presents challenges in terms of reactant adsorption on the catalyst surface, which hinders further refinement. Herein, NiCo-based metal-organic frameworks (MOFs) are employed as the electrocatalyst to enhance the adsorption of reactant molecules through π-π interaction.

Cyanogel-Induced Facile Synthesis of Palladium Hydride for Electrocatalytic Oxygen Reduction.

Palladium hydride (PdH) is one of the well-known electrocatalytic materials, yet its synthesis is still a challenge through an energy-efficient and straightforward method. Herein, we propose a new and facile cyanogel-assisted synthesis strategy for the preparation of PdH at a mild environment with NaBH as the hydrogen source. Unlike traditional inorganic Pd precursors, the unique Pd-CN-Pd bridge in Pd[Pd(CN)] ⋅ aHO cyanogel offers more favourable spatial sites for insertion of H atoms.

Molecular architectures of iron complexes for oxygen reduction catalysis-Activity enhancement by hydroxide ions coupling.

Developing cost-effective and high-performance electrocatalysts for oxygen reduction reaction (ORR) is critical for clean energy generation. Here, we propose an approach to the synthesis of iron phthalocyanine nanotubes (FePc NTs) as a highly active and selective electrocatalyst for ORR. The performance is significantly superior to FePc in randomly aggregated and molecularly dispersed states, as well as the commercial Pt/C catalyst.

Importing Antibonding-Orbital Occupancy through Pd-O-Gd Bridge Promotes Electrocatalytic Oxygen Reduction.

The active-site density, intrinsic activity, and durability of Pd-based materials for oxygen reduction reaction (ORR) are critical to their application in industrial energy devices. This work constructs a series of carbon-based rare-earth (RE) oxides (Gd O , Sm O , Eu O , and CeO ) by using RE metal-organic frameworks to tune the ORR performance of the Pd sites through the Pd-RE O interface interaction. Taking Pd-Gd O /C as a representative, it is identified that the strong coupling between Pd and Gd O induces the formation of the Pd-O-Gd bridge, which triggers charge redistribution of Pd and Gd O .

Rare-Earth-Modified Metal-Organic Frameworks and Derivatives for Photo/Electrocatalysis.

Metal-organic frameworks (MOFs) and their derivatives have attracted much attention in the field of photo/electrocatalysis owing to their ultrahigh porosity, tunable properties, and superior coordination ability. Regulating the valence electronic structure and coordination environment of MOFs is an effective way to enhance their intrinsic catalytic performance. Rare earth (RE) elements with 4f orbital occupancy provide an opportunity to evoke electron rearrangement, accelerate charged carrier transport, and synergize the surface adsorption of catalysts.

Reinforcing CoO Covalency via Ce(4f)─O(2p)─Co(3d) Gradient Orbital Coupling for High-Efficiency Oxygen Evolution.

Rare-earth (RE)-based transition metal oxides (TMO) are emerging as a frontier toward the oxygen evolution reaction (OER), yet the knowledge regarding their electrocatalytic mechanism and active sites is very limited. In this work, atomically dispersed Ce on CoO is successfully designed and synthesized by an effective plasma (P)-assisted strategy as a model (P-Ce SAs@CoO) to investigate the origin of OER performance in RE-TMO systems. The P-Ce SAs@CoO exhibits favorable performance with an overpotential of only 261 mV at 10 mA cm and robust electrochemical stability, superior to individual CoO.

Spin-Selective Coupling in Mott-Schottky Er O -Co Boosts Electrocatalytic Oxygen Reduction.

Alkaline oxygen reduction reaction (ORR) is critical to electrochemical energy conversion technology, yet the rational breaking of thermodynamic inhibition for ORR through spin regulation remains a challenge. Herein, a Mott-Schottky catalyst consisting of Er O -Co particles uniformly implanted into carbon nanofibers (Er O -Co/CNF) is designed for enhancing ORR via spin-selective coupling. The optimized Er O -Co/CNF affords a high half-wave potential (0.

Improving the Oxygen Evolution Activity of Layered Double-Hydroxide via Erbium-Induced Electronic Engineering.

Layered double-hydroxide (LDH) has been considered an important class of electrocatalysts for the oxygen evolution reaction (OER), but the adsorption-desorption behaviors of oxygen intermediates on its surface still remain unsatisfactory. Apart from transition-metal doping to solve this electrocatalytic problem of LDH, rare-earth (RE) species have sprung up as emerging dopants owing to their unique 4f valence-electronic configurations. Herein, the Er is chosen as a RE model to improve OER activity of LDH via constructing nickel foam supported Er-doped NiFe-LDH catalyst (Er-NiFe-LDH@NF).

Engineering 3d-2p-4f Gradient Orbital Coupling to Enhance Electrocatalytic Oxygen Reduction.

The development of highly efficient and economical materials for the oxygen reduction reaction (ORR) plays a key role in practical energy conversion technologies. However, the intrinsic scaling relations exert thermodynamic inhibition on realizing highly active ORR electrocatalysts. Herein, a novel and feasible gradient orbital coupling strategy for tuning the ORR performance through the construction of Co 3d-O 2p-Eu 4f unit sites on the Eu O -Co model is proposed.

Ethanol-Induced Hydrogen Insertion in Ultrafine IrPdH Boosts pH-Universal Hydrogen Evolution.

Engineering Pt-free catalysts for hydrogen evolution reaction (HER) with high activity and stability is of great significance in electrochemical hydrogen production. Herein, in situ chemical H intercalation into ultrafine Pd to activate this otherwise HER-inferior material to form the ultrafine IrPdH hydride as an efficient and stable HER electrocatalyst is proposed. The formation of PdIrH depends on a new hydrogenation strategy via using ethanol as the hydrogen resource.

Rare-Earth Single-Atom Catalysts: A New Frontier in Photo/Electrocatalysis.

Single-atom catalysts (SACs) provide well-defined active sites with 100% atom utilization, and can be prepared using a wide range of support materials. Therefore, they are attracting global attention, especially in the fields of energy conversion and storage. To date, research has focused on transition-metal and precious-metal-based SACs.

Boosting Electrocatalytic Oxygen Evolution over Ce-Co S Core-Shell Nanoneedle Arrays by Electronic and Architectural Dual Engineering.

An dual electronic and architectural engineering strategy is a good way to rationally design earth-abundant and highly efficient electrocatalysts of the oxygen evolution reaction (OER) for sustainable hydrogen-based energy devices. Here, a Ce-doped Co S core-shell nanoneedle array (Ce-Co S @CC) supported on a carbon cloth has been designed and developed to accelerate the sluggish kinetics of the OER. Profiting from valance alternative Ce doping, a fine core-shell structure and vertically aligned nanoneedle arrayed architecture, Ce-Co S @CC integrates modulated electronic structure, highly exposed active sites, and multidimensional mass diffusion channels; together, these afford a favorable catalyzed OER.

Hydrogen-Intercalation-Induced Lattice Expansion of Pd@Pt Core-Shell Nanoparticles for Highly Efficient Electrocatalytic Alcohol Oxidation.

Lattice engineering on specific facets of metal catalysts is critically important not only for the enhancement of their catalytic performance but also for deeply understanding the effect of facet-based lattice engineering on catalytic reactions. Here, we develop a facile two-step method for the lattice expansion on specific facets, i.e.

Recent Advances in Electrocatalysts for Alkaline Hydrogen Oxidation Reaction.

With the rapid development of anion-exchange membrane technology and adequate supply of high-performance non-noble metal oxygen reduction reaction (ORR) catalysts in alkaline media, the commercialization of anion exchange membrane fuel cells (AEMFCs) become possible. However, the kinetics of the anodic hydrogen oxidation reaction (HOR) in AEMFCs is significantly decreased compared to the HOR in proton exchange membrane fuel cells (PEMFCs). Therefore, it is urgent to develop HOR catalysts with low price, high activity, and robust stability.

Recent Advances in Amino-Based Molecules Assisted Control of Noble-Metal Electrocatalysts.

Morphology-control synthesis is an effective means to tailor surface structure of noble-metal nanocrystals, which offers a sensitive knob for tuning their electrocatalytic properties. The functional molecules are often indispensable in the morphology-control synthesis through preferential adsorption on specific crystal facets, or controlling certain crystal growth directions. In this review, the recent progress in morphology-control synthesis of noble-metal nanocrystals assisted by amino-based functional molecules for electrocatalytic applications are focused on.

The use of amino-based functional molecules for the controllable synthesis of noble-metal nanocrystals: a minireview.

Controlling the morphologies and structures of noble-metal nanocrystals has always been a frontier field in electrocatalysis. Functional molecules such as capping agents, surfactants and additives are indispensable in shape-control synthesis. Amino-based functional molecules have strong coordination abilities with metal ions, and they are widely used in the morphology control of nanocrystals.

Dual Single-Atomic Ni-N and Fe-N Sites Constructing Janus Hollow Graphene for Selective Oxygen Electrocatalysis.

Nitrogen-coordinated metal single atoms in carbon have aroused extensive interest recently and have been growing as an active research frontier in a wide range of key renewable energy reactions and devices. Herein, a step-by-step self-assembly strategy is developed to allocate nickel (Ni) and iron (Fe) single atoms respectively on the inner and outer walls of graphene hollow nanospheres (GHSs), realizing separate-sided different single-atom functionalization of hollow graphene. The Ni or Fe single atom is demonstrated to be coordinated with four N atoms via the formation of a Ni-N or Fe-N planar configuration.

General Strategy for Synthesis of Ordered Pt M Intermetallics with Ultrasmall Particle Size.

Controllable synthesis of atomically ordered intermetallic nanoparticles (NPs) is crucial to obtain superior electrocatalytic performance for fuel cell reactions, but still remains arduous. Herein, we demonstrate a novel and general hydrogel-freeze drying strategy for the synthesis of reduced graphene oxide (rGO) supported Pt M (M=Mn, Cr, Fe, Co, etc.) intermetallic NPs (Pt M/rGO-HF) with ultrasmall particle size (about 3 nm) and dramatic monodispersity.

Oxygen Vacancy-Rich In-Doped CoO/CoP Heterostructure as an Effective Air Cathode for Rechargeable Zn-Air Batteries.

An efficient and low-cost electrocatalyst for reversible oxygen electrocatalysis is crucial for improving the performance of rechargeable metal-air batteries. Herein, a novel oxygen vacancy-rich 2D porous In-doped CoO/CoP heterostructure (In-CoO/CoP FNS) is designed and developed by a facile free radicals-induced strategy as an effective bifunctional electrocatalyst for rechargeable Zn-air batteries. The electron spin resonance and X-ray absorption near edge spectroscopy provide clear evidence that abundant oxygen vacancies are formed in the interface of In-CoO/CoP FNS.