Heteroatom-Coordinated Palladium Molecular Catalysts for Sustainable Electrochemical Production of Hydrogen Peroxide.

Currently, hydrogen peroxide (H2O2) manufacturing involves an energy-intensive anthraquinone technique that demands expensive solvent extraction and a multistep process with substantial energy consumption. In this work, we synthesized Pd-N4-CO, Pd-S4-NCO, and Pd-N2O2-C single-atom catalysts via an in situ synthesis approach involving heteroatom-rich ligands and activated carbon under mild reaction conditions. It reveals that palladium atoms interact strongly with heteroatom-rich ligands, which provide well-defined and uniform active sites for oxygen (O2) electrochemically reduced to hydrogen peroxide. Interestingly, the Pd-N4-CO electrocatalyst shows excellent performance for the electrocatalytic reduction of O2 to H2O2 via a two-electron transfer process in a base electrolyte, exhibiting a negligible amount of onset overpotential and >95% selectivity within a wide range of applied potentials. The electrocatalysts based on the activity and selectivity toward 2e- ORR follow the order Pd-N4-CO > Pd-N2O2-C > Pd-S4-NCO in agreement with the pull-push mechanism, which is the Pd center strongly coordinated with high electronegativity donor atoms (N and O atoms) and weakly coordinated with the intermediate *OOH to excellent selectivity and sustainable production of H2O2. According to density functional theory, Pd-N4 is the active site for selectivity toward H2O2 generation. This work provides an emerging technique for designing high-performance H2O2 electrosynthesis catalysts and the rational integration of several active sites for green and sustainable chemical synthesis via electrochemical processes.

Description of Photodegradation Mechanisms and Structural Characteristics in Carbon@Titania Yolk-Shell Nanostructures by XAS.

Carbon@titania yolk-shell nanostructures are successfully synthesized at different calcination conditions. These unique structure nanomaterials can be used as a photocatalyst to degrade the emerging water pollutant, acetaminophen (paracetamol). The photodegradation analysis studies have shown that the samples with residual carbon nanospheres have improved the photocatalytic efficiency. The local electronic and atomic structure of the nanostructures are analyzed by X-ray absorption spectroscopy (XAS) measurements. The spectra confirm that the hollow shell has an anatase phase structure, slight lattice distortion, and variation in Ti 3d orbital orientation. In situ XAS measurements reveal that the existence of amorphous carbon nanospheres inside the nano spherical shell inhibit the recombination of electron-hole pairs; more mobile holes are formed in the p-d hybridized bands near the Fermi surface and enables the acceleration of the carries that significantly enhance the photodegradation of paracetamol under UV-visible irradiation. The observed charge transfer process from TiO2  hybridized orbital to the carbon nanospheres reduces the recombination rate of electrons and holes, thus increasing the photocatalytic efficiency.

Generating Multi-Carbon Products by Electrochemical CO2 Reduction via Catalytically Harmonious Ni/Cu Dual Active Sites.

Despite the unique advantages of single-atom catalysts, molecular dual-active sites facilitate the C-C coupling reaction for C2 products toward the CO2 reduction reaction (CO2 RR). The Ni/Cu proximal dual-active site catalyst (Ni/Cu-PASC) is developed, which is a harmonic catalyst with dual-active sites, by simply mixing commercial Ni-phthalocyanine (Ni-Pc) and Cu-phthalocyanine (Cu-Pc) molecules physically. According to scanning transmission electron microscopy (STEM) and transmission electron microscopy (TEM) energy dispersive spectroscopy (EDS) data, Ni and Cu atoms are separated, creating dual-active sites for the CO2 RR. The Ni/Cu-PASC generates ethanol with an FE of 55%. Conversely, Ni-Pc and Cu-Pc have only detected single-carbon products like CO and HCOO- . In situ X-ray absorption spectroscopy (XAS) indicates that CO generation is caused by the stable Ni active site's balanced electronic state. The CO production from Ni-Pc consistently increased the CO concentration over Cu sites attributed to subsequent reduction reaction through a C-C coupling on nearby Cu. The CO bound (HCOO- ) peak, which can be found on Cu-Pc, vanishes on Ni/Cu-PASC, as shown by in situ fourier transformation infrared (FTIR). The characteristic intermediate of *CHO instead of HCOO- proves to be the prerequisite for multi-carbon products by electrochemical CO2 RR. The work demonstrates that the harmonic dual-active sites in Ni/Cu-PASC can be readily available by the cascading proximal active Ni- and Cu-Pc sites.

Efficient H2 Evolution Coupled with Anodic Oxidation of Iodide over Defective Carbon-Supported Single-Atom Mo-N4 Electrocatalyst.

We successfully prepared nitrogen-doped defective carbon spheres (Mo-N4/d-C) with a high loading of 0.996 wt % via a designed vapor-deposition process for IOR-based hydrogen generation. The synthesized Mo-N4/d-C catalyst provides a record current density of 10 mA cm-2 at 0.77 V. Further, the Mo-N4/d-C catalyst shows a Tafel slope of 25.58 mV dec-1, exceptional stability over time in acidic media, a higher hydrogen generation rate of 0.1063 mL gcat-1 min-1, a high Faradaic efficiency of 99.8%, and a reduction of the energy consumption up to ∼50% for hydrogen evolution by anodic oxidation reaction of iodide (IOR) compared with the conventional OER-based electrolysis. Computational calculations demonstrate that the Mo-N4/d-C structure plays a vital effect on the activity of iodide oxidation, which is competitive with the Pt catalyst.

A Powerful Protocol Based on Anode-Free Cells Combined with Various Analytical Techniques.

Lithium (Li) metal is the ultimate negative electrode due to its high theoretical specific capacity and low negative electrochemical potential. However, the handling of lithium metal imposes safety concerns in transportation and production due to its reactive nature. Recently, anode-free lithium metal batteries (AFLMBs) have drawn much attention because of several of their advantages, including higher energy density, lower cost, and fewer safety concerns during cell production compared to LMBs. Pushing the reversible Coulombic efficiency (CE) of AFLMBs up to 99.98% is key to achieving their 80% capacity retention over more than 1000 cycles. However, interfacial irreversible phenomena such as electrolyte decomposition reactions on both electrodes, dead Li formation, and Li dendrite formation result in poor capacity retention and short circuits in LMBs and AFLMBs. Therefore, it is of great importance and scientific interest to explore those interfacial irreversible phenomena to improve the cell's cycle life. Although significant contributions toward mitigating electrolyte decomposition, dead lithium, and dendritic lithium formation have been reported at the lithium anode, real irreversible phenomena are usually hidden or difficult to discover due to excess lithium employed in LMBs and simultaneous events taking place in both electrodes or at the interfaces.An integrated protocol is suggested to include Li||Cu, cathode||Li, and cathode||Cu configurations to provide overall quantification and determination of various sources of irreversible Coulombic efficiency (irr-CE) in AFLMBs and LMBs. Combining Li||Cu, cathode||Li, and cathode||Cu configurations is essential for separating the root sources of the capacity loss and irr-CE in LMBs and AFLMBs. Remarkably, integrating an anode-free cell with various analytical techniques can serve as a powerful protocol to decouple and quantify those interfacial irreversible phenomena according to our recent reports.In this Account, we focus on the protocol based on an anode-free cell combined with various analytical methods to investigate interfacial irreversible phenomena. Complementary advanced tools such as transmission X-ray microscopy (visualizing Li plating/stripping mechanism), nuclear magnetic resonance spectroscopy (quantifying dead lithium), and gas chromatography-mass spectroscopy (decoupling interfacial reactions) were employed to extract the intrinsic reasons and sources of individual irreversible reactions in LMBs and AFLMBs. Quantitative evaluation of nucleation and growth of Li metal deposition are addressed, along with solid electrolyte interphase (SEI) fracture, visualization of lithium dendrite growth, decoupling of oxidative and reductive electrolyte decomposition mechanisms, and irreversible efficiency (i.e., dead Li and SEI formation) to reveal the intrinsic causes of individual irr-CE in AFLMBs. Meanwhile, an anode-free protocol can also be utilized as a powerful and multifunctional tool to develop electrolyte formulations or artificial layers for LMBs and AFLMBs. Therefore, we also suggest that the anode-free configurations with significant irreversible phenomena can effectively screen and develop new electrolytes. Finally, the concepts of the protocol with an anode-free cell combined with various advanced analytical tools can be extended to provide an in-depth understanding of other metal batteries and solid-state anode-free metal batteries.

Nucleation and Growth Mechanism of Lithium Metal Electroplating.

Understanding the mechanism of Li nucleation and growth is essential for providing long cycle life and safe lithium ion batteries or lithium metal batteries. However, no quantitative report on Li metal deposition is available, to the best of our knowledge. We propose a model for quantitatively understanding the Li nucleation and growth mechanism associated with the solid-electrolyte interphase (SEI) formation, which we name the Li-SEI model. The current transients at various overpotentials initiate the nucleation and growth of Li metal on bare Cu foil. The Li-SEI model considering a three-dimensional diffusion-controlled instantaneous process (J3D-DC) with the simultaneous reduction of electrolyte decomposition (JSEI) due to the SEI fracture is employed for investigating the Li nucleation and growth mechanism. The individual contributions of experimental and theoretical transient states, i.e., the fundamental kinetic values of diffusion coefficient (D), rate of nucleation (N0), and rate constant of electrolyte decomposition (kSEI), can be determined from the Li-SEI model. Interestingly, JSEI increases with time, indicating that the current contributing from the electrolyte decomposition increases with time due to the SEI fracture upon Li deposition. Meanwhile, the kSEI increases with overpotential, indicating the SEI fracture is more serious at higher overpotential or higher growth rate. The kSEI is smaller in the electrolyte with fluoroethylene carbonate (FEC) additive, indicating that FEC additive can significantly suppress the SEI fracture during Li metal deposition. This proposed model opens a new way to quantitatively understand the Li nucleation and growth mechanism and electrolyte decomposition on various substrates or in different electrolytes.

In situ analytical techniques for battery interface analysis.

Lithium-ion batteries, simply known as lithium batteries, are distinct among high energy density charge-storage devices. The power delivery of batteries depends upon the electrochemical performances and the stability of the electrode, electrolytes and their interface. Interfacial phenomena of the electrode/electrolyte involve lithium dendrite formation, electrolyte degradation and gas evolution, and a semi-solid protective layer formation at the electrode-electrolyte interface, also known as the solid-electrolyte interface (SEI). The SEI protects electrodes from further exfoliation or corrosion and suppresses lithium dendrite formation, which are crucial needs for enhancing the cell performance. This review covers the compositional, structural and morphological aspects of SEI, both artificially and naturally formed, and metallic dendrites using in situ/in operando cells and various in situ analytical tools. Critical challenges and the historical legacy in the development of in situ/in operando electrochemical cells with some reports on state-of-the-art progress are particularly highlighted. The present compilation pinpoints the emerging research opportunities in advancing this field and concludes on the future directions and strategies for in situ/in operando analysis.

Sequentially surface modified hematite enables lower applied bias photoelectrochemical water splitting.

Hematite (α-Fe2O3) is a suitable candidate for photoelectrochemical water splitting due to its well-suited band structure, stability, and availability. However, water splitting using a low external potential is the major challenge that limits the practical application of hematite. Here, we achieve a very low onset potential using a sequential surface treatment approach to overcome two fundamental limiting factors, sluggish hole transfer, and interfacial recombination, independently. First, a heavily doped Fe2-xSnxO3 surface passivation layer was created by Sn4+ surface treatment which can robustly inhibit interfacial recombination. Then, an NiOOH catalyst layer was deposited that greatly enhances the charge transfer process across the passivated electrode/electrolyte interface. By exploiting this approach, the optimized sequentially treated photoanode (Fe2O3/Fe2-xSnxO3/NiOOH) exhibits a low photocurrent onset potential of 0.49 V vs. RHE and a saturated photocurrent density of 2.4 mA cm-2 V at 1.5 V vs. RHE. Transient photocurrent and impedance spectroscopy measurements further reveal that the combined Fe2-xSnxO3/NiOOH layers reduce interfacial recombination and enhance charge transfer across the electrode/electrolyte interface. The results provide convincing evidence that it is possible to address the problems of surface trap recombination and sluggish catalysis independently by employing surface passivation layers first and catalysts later sequentially.

Improved Raman and photoluminescence sensitivity achieved using bifunctional Ag@SiO2 nanocubes.

SiO2 coated silver nanocubes Ag@SiO2 with enhanced surface-enhanced Raman scattering (SERS) and metal enhanced photoluminescence (MEPL) sensitivity were synthesized and characterized. The silver nanocubes (NCs) were synthesized by the polyol method and modified, first with different coupling agents, such as 3-mercaptopropyltrimethoxysilane (MPTMS) and 3-aminopropyltrimethoxysilane (APS), and secondly with tetraethylorthosilicate (TEOS) to improve their SERS and photoluminescence (PL) performances. The SERS and PL intensity of rhodamine 6G (R6G) can be manipulated by tuning the Ag nanocube's SiO2 shell thickness. Modified Ag NCs (with a 2 nm silica layer) were prepared using 1 mM APS and 1 mM TEOS and found to have a SERS intensity 3 fold higher than bare Ag NCs. Additionally, it was found that APS modified Ag@SiO2 NCs possessed both enhanced SERS and PL intensities.

Direct in situ observation of Li2O evolution on Li-rich high-capacity cathode material, Li[Ni(x)Li((1-2x)/3)Mn((2-x)/3)]O2 (0 ≤ x ≤ 0.5).

High-capacity layered, lithium-rich oxide cathodes show great promise for use as positive electrode materials for rechargeable lithium ion batteries. Understanding the effects of oxygen activating reactions on the cathode's surface during electrochemical cycling can lead to improvements in stability and performance. We used in situ surfaced-enhanced Raman spectroscopy (SERS) to observe the oxygen-related surface reactions that occur during electrochemical cycling on lithium-rich cathodes. Here, we demonstrate the direct observation of Li2O formation during the extended plateau and discuss the consequences of its formation on the cathode and anode. The formation of Li2O on the cathode leads to the formation of species related to the generation of H2O together with LiOH and to changes within the electrolyte, which eventually result in diminished performance. Protection from, or mitigation of, such devastating surface reactions on both electrodes will be necessary to help realize the potential of high-capacity cathode materials (270 mAhg(-1) versus 140 mAhg(-1) for LiCoO2) for practical applications.

Boosting the Interfacial Stability of the Li6PS5Cl Electrolyte with a Li Anode via In Situ Formation of a LiF-Rich SEI Layer and a Ductile Sulfide Composite Solid Electrolyte.

Due to its good mechanical properties and high ionic conductivity, the sulfide-type solid electrolyte (SE) can potentially realize all-solid-state batteries (ASSBs). Nevertheless, challenges, including limited electrochemical stability, insufficient solid-solid contact with the electrode, and reactivity with lithium, must be addressed. These challenges contribute to dendrite growth and electrolyte reduction. Herein, a straightforward and solvent-free method was devised to generate a robust artificial interphase between lithium metal and a SE. It is achieved through the incorporation of a composite electrolyte composed of Li6PS5Cl (LPSC), polyethylene glycol (PEG), and lithium bis(fluorosulfonyl)imide (LiFSI), resulting in the in situ creation of a LiF-rich interfacial layer. This interphase effectively mitigates electrolyte reduction and promotes lithium-ion diffusion. Interestingly, including PEG as an additive increases mechanical strength by enhancing adhesion between sulfide particles and improves the physical contact between the LPSC SE and the lithium anode by enhancing the ductility of the LPSC SE. Moreover, it acts as a protective barrier, preventing direct contact between the SE and the Li anode, thereby inhibiting electrolyte decomposition and reducing the electronic conductivity of the composite SE, thus mitigating the dendrite growth. The Li|Li symmetric cells demonstrated remarkable cycling stability, maintaining consistent performance for over 3000 h at a current density of 0.1 mA cm-2, and the critical current density of the composite solid electrolyte (CSE) reaches 4.75 mA cm-2. Moreover, the all-solid-state lithium metal battery (ASSLMB) cell with the CSEs exhibits remarkable cycling stability and rate performance. This study highlights the synergistic combination of the in-situ-generated artificial SE interphase layer and CSEs, enabling high-performance ASSLMBs.

Mechanistic Study on Artificial Stabilization of Lithium Metal Anode via Thermal Pyrolysis of Ammonium Fluoride in Lithium Metal Batteries.

The use of the "Holy Grail" lithium metal anode is pivotal to achieve superior energy density. However, the practice of a lithium metal anode faces practical challenges due to the thermodynamic instability of lithium metal and dendrite growth. Herein, an artificial stabilization of lithium metal was carried out via the thermal pyrolysis of the NH4F salt, which generates HF(g) and NH3(g). An exposure of lithium metal to the generated gas induces a spontaneous reaction that forms multiple solid electrolyte interface (SEI) components, such as LiF, Li3N, Li2NH, LiNH2, and LiH, from a single salt. The artificially multilayered protection on lithium metal (AF-Li) sustains stable lithium stripping/plating. It suppresses the Li dendrite under the Li||Li symmetric cell. The half-cell Li||Cu and Li||MCMB systems depicted the attributions of the protective layer. We demonstrate that the desirable protective layer in AF-Li exhibited remarkable capacity retention (CR) results. LiFePO4 (LFP) showed a CR of 90.6% at 0.5 mA cm-2 after 280 cycles, and LiNi0.5Mn0.3Co0.2O2 (NCM523) showed 58.7% at 3 mA cm-2 after 410 cycles. Formulating the multilayered protection, with the simultaneous formation of multiple SEI components in a facile and cost-effective approach from NH4F as a single salt, made the system competent.

In-Depth Insight into a Passive Film through Hydrogen-Bonding Network in an Aqueous Zinc Battery.

Electrochemical stability and interfacial reactions are crucial for rechargeable aqueous zinc batteries. Electrolyte engineering with low-cost aqueous electrolytes is highly required to stabilize their interfacial reactions. Herein, we propose a design strategy using glutamic additive and its derivatives with modification of hydrogen-bonding network to enable Zn aqueous battery at a low concentration (2 m ZnSO4 + 1 m Li2SO4). Computational, in situ/ex situ spectroscopic, and electrochemical studies suggest that additives with moderate interactions, such as 0.1 mol % glutamic additive (G1), preferentially absorb on the Zn surface to homogenize Zn2+ plating and favorably interact with Zn2+ in bulk to weaken the interaction between H2O and Zn2+. As a result, uniform deposition and stable electrochemical performance are realized. The Zn||Cu half-cell lasts for more than 200 cycles with an average Coulombic efficiency (CE) of >99.32% and the Zn||Zn symmetrical cells for 1400 h with a low and stable overpotential under a current density of 0.5 mA cm-2, which is better than the reported results. Moreover, adding 0.1 mol % G1 to the Zn||LFP full cell improves its electrochemical performance with stable cycling and achieves a remarkable capacity of 147.25 mAh g-1 with a CE of 99.79% after 200 cycles.

The Entanglement of Li Capping and Deposition: An Operando Optical Microscopy Study.

Dendrite growth and low Coulombic efficiency impede the practical application of Li-metal batteries. As such, monitoring Li deposition and stripping in real-time is crucial to understanding the fundamental lithium growth kinetics. This work presents an operando optical microscopic technique that enables precise current density control and quantification of Li layer properties (i.e., thickness and porosity) to study Li growth in various electrolytes. We discover the robustness and porosity of the remaining capping layer after the Li stripping process as the critical features governing the subsequent dendrite propagation behavior, resulting in distinct capping and stacking phenomena that affect Li growth upon cycling. While dendrite propagation quickly occurs through the fracture of the fragile Li capping layer, uniform Li plating/stripping can be facilitated by the compact and robust capping layer even at high current densities. This technique can be extended to evaluate dendrite suppression treatments in various metal batteries, providing in-depth information on metal growth mechanisms.

Lewis Acid Probe for Basicity of Sulfide Electrolytes Investigated by 11B Solid-State NMR.

Sulfide-based solid-state lithium-ion batteries (SSLIB) have attracted a lot of interest globally in the past few years for their high safety and high energy density over the traditional lithium-ion batteries. However, sulfide electrolytes (SEs) are moisture-sensitive which pose significant challenges in the material preparation and cell manufacturing. To the best of our knowledge, there is no tool available to probe the types and the strength of the basic sites in sulfide electrolytes, which is crucial for understanding the moisture stability of sulfide electrolytes. Herein, we propose a new spectral probe with the Lewis base indicator BBr3 to probe the strength of Lewis basic sites on various sulfide electrolytes by 11B solid-state NMR spectroscopy (11B-NMR). The active sulfur sites and the corresponding strength of the sulfide electrolytes are successfully evaluated by the proposed Lewis base probe. The probed strength of the active sulfur sites of a sulfide electrolyte is consistent with the results of DFT (density functional theory) calculation and correlated with the H2S generation rate when the electrolyte was exposed in moisture atmosphere. This work paves a new way to investigate the basicity and moisture stability of the sulfide electrolytes.

Double shelled hollow CoS2@MoS2@NiS2 polyhedron as advanced trifunctional electrocatalyst for zinc-air battery and self-powered overall water splitting.

Electrocatalysts play important role in various energy conversion and storage devices. The catalytic performance of electrocatalysts can be enhanced through the increasement of intrinsic catalytic activity by optimizing electronic structure and the improvement of exposed active sites by designing proper nanostructures. In this work, CoS2@MoS2@NiS2 nano polyhedron with double-shelled structure was prepared using metal organic framework as a precursor. Due to the rational integration of multifunctional active center, the strong electronic interaction of the various component, the high electrochemical surface area and shortened mass transport induced by the special structure, CoS2@MoS2@NiS2 exhibits high catalytic activity for hydrogen evolution reaction (HER), oxygen evolution reaction (OER) and oxygen reduction reaction (ORR). Specifically, low overpotentials of 156 and 200 mV was achieved to deliver a current density of 10 mA cm-2 for HER and OER, and a high half-wave potential of 0.80 V was observed for ORR. More importantly, the Zn-air battery assembled by CoS2@MoS2@NiS2 exhibits a high-power density of 80.28 mW cm-2 and could effectively drive overall water splitting. This work provides a new platform for designing multifunctional catalysts with high activity for energy conversion and storage.

Highly Concentrated Salt Electrolyte for a Highly Stable Aqueous Dual-Ion Zinc Battery.

A zinc metal anode for zinc-ion batteries is a promising alternative to solve safety and cost issues in lithium-ion batteries. The Zn metal is characterized by its high theoretical capacity (820 mAh g-1), low redox potential (0.762 V vs SHE), low toxicity, high abundance on Earth, and high stability in water. Taking advantage of the stability of Zn in water, an aqueous Zn ion battery with low cost, high safety, and easy-to-handle features can be developed. To minimize water-related parasitic reactions, this work utilizes a highly concentrated salt electrolyte (HCE) with dual salts─1 m Zn(OTf)2 + 20 m LiTFSI. MD simulations prove that Zn2+ is preferentially coordinated with O in the TFSI- anion from HCE instead of O in H2O. HCE has a broadened electrochemical stability window due to suppressed H2 and O2 evolution. Some advanced ex situ and in situ/in operando analysis techniques have been applied to evaluate the morphological structure and the composition of the in situ formed passivation layer. A dual-ion full Zn||LiMn2O4 cell employing HCE has an excellent capacity retention of 92% after 300 cycles with an average Coulombic efficiency of 99.62%. Meanwhile, the low concentration electrolyte (LCE) cell degrades rapidly and is short-circuited after 66 cycles with an average Coulombic efficiency of 96.91%. The battery's excellent cycling performance with HCE is attributed to the formation of a stable anion-derived solid-electrolyte interphase (SEI) layer. On the contrary, the high free water activity in LCE leads to a water-derived interfacial layer with unavoidable dendrite growth during cycling.

Lithium Oxalate as a Lifespan Extender for Anode-Free Lithium Metal Batteries.

Anode-free lithium metal batteries (AFLMBs) have been extensively studied due to their intrinsic high energy and safety without a metallic Li anode in cell design. Yet, the dendrite and dead-Li buildup continuously consumes the active Li upon cycling, leading to the poor lifespan of AFLMBs. Here, we introduce lithium oxalate into the cathode as an electrode additive providing a Li reservoir to extend the lifespan of AFLMBs. The AFLMB using 20% lithium oxalate and a LiNi0.3Co0.3Mn0.3O2 composite cathode exhibits >80 and 40% capacity retention after 50 and 100 cycles, respectively, outperforming the poor cycle life of fewer than 20 cycles obtained from the cell using a pure LiNi0.3Co0.3Mn0.3O2 cathode. Surprisingly, the average Coulombic efficiency of AFLMBs is found to improve as the amount of lithium oxalate increases in the composite cathode. This abnormal phenomenon could be attributed to the as-formed carbon dioxide after the first activation cycle forming a Li2CO3-rich solid-electrolyte interphase and improving the Li deposition and stripping efficiency. The findings in this work provide a new strategy to delay the capacity roll-over of AFLMBs from an electrode engineering perspective, which can be coupled with other approaches such as functional electrolytes synergistically to further improve the cycle life of AFLMBs for practical application.

Nanostructured Ti(0.7)Mo(0.3)O2 support enhances electron transfer to Pt: high-performance catalyst for oxygen reduction reaction.

The slow rate of the oxygen reduction reaction (ORR) and the instability of Pt-based catalysts are two of the most important issues that must be solved in order to make proton exchange membrane fuel cells (PEMFCs) a reality. Additionally, the serious carbon corrosion on the cathode side is a critical problem with respect to the durability of catalyst that limits its wide application. Here, we present a new approach by exploring robust noncarbon Ti(0.7)Mo(0.3)O(2) used as a novel functionalized cocatalytic support for Pt. This approach is based on the novel nanostructure Ti(0.7)Mo(0.3)O(2) support with "electronic transfer mechanism" from Ti(0.7)Mo(0.3)O(2) to Pt that can modify the surface electronic structure of Pt, owing to a shift in the d-band center of the surface Pt atoms. Furthermore, another benefit of Ti(0.7)Mo(0.3)O(2) is the extremely high stability of Pt/Ti(0.7)Mo(0.3)O(2) during potential cycling, which is attributable to the strong metal/support interaction (SMSI) between Pt and Ti(0.7)Mo(0.3)O(2). This also enhances the inherent structural and chemical stability and the corrosion resistance of the TiO(2)-based oxide in acidic and oxidative environments. We also demonstrate that the ORR current densities generated using cocatalytic Pt/Ti(0.7)Mo(0.3)O(2) are respectively ~7- and 2.6-fold higher than those of commercial Pt/C and PtCo/C catalysts with the same Pt loading. This new approach opens a reliable path to the discovery advanced concept in designing new catalysts that can replace the traditional catalytic structure and motivate further research in the field.