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Reversible solid oxide cells (rSOCs) have significant potential as efficient energy conversion and storage systems. Nevertheless, the practical application of their conventional air electrodes, such as La0.8Sr0.2MnO3-δ (LSM), Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF), and PrBa0.8Ca0.2Co2O5+δ (PBCC), remains unsatisfactory due to interface delamination during prolonged electrochemical operation. Using micro-focusing X-ray absorption spectroscopy (µ-XAS), a decrease (increase) in the co-valence state from the electrode surface to the electrode/electrolyte interface is observed, leading to the above delamination. Utilizing the one-pot method to incorporate an oxygen-vacancy-enriched CeO2 electrode into these air electrodes, the uniform distribution of the Co valence state is observed, alleviating the structural delamination. PBCC-CeO2 electrodes exhibited a degradation rate of 0.095 mV h-1 at 650 °C during a nearly 500-h test as compared with 0.907 mV h-1 observed during the 135-h test for PBCC. Additionally, a remarkable increase in electrolysis current density from 636 to 934 mA cm-2 under 1.3 V and a maximum power density from 912 to 989 mW cm-2 upon incorporating CeO2 into PBCC is also observed. BSCF-CeO2 and LSM-CeO2 also show enhanced electrochemical performance and prolonged stability as compared to BSCF and LSM. This work offers a strategy to mitigate the structural delamination of conventional electrodes to boost the performance of rSOCs.
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Protonic ceramic fuel cells with high efficiency and low emissions exhibit high potential as next-generation sustainable energy systems. However, the practical proton conductivity of protonic ceramic electrolytes is still not satisfied due to poor membrane sintering. Here, we show that the dynamic displacement of Y3+ adversely affects the high-temperature membrane sintering of the benchmark protonic electrolyte BaZr0.1Ce0.7Y0.1Yb0.1O3-δ, reducing its conductivity and stability. By introducing a molten salt approach, pre-doping of Y3+ into A-site is realized at reduced synthesis temperature, thus suppressing its further displacement during high-temperature sintering, consequently enhancing the membrane densification and improving the conductivity and stability. The anode-supported single cell exhibits a power density of 663 mW cm-2 at 600 °C and long-term stability for over 2000 h with negligible performance degradation. This study sheds light on protonic membrane sintering while offering an alternative strategy for protonic ceramic fuel cells development.
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With the rapid development of novel energy conversion and storage technologies, there is a growing demand for enhanced performance in a wide range of electrocatalysts. Perovskite oxides (ABO3 ) have caused widespread concerns due to their excellent electrocatalytic properties, low cost, stable and reliable performance. In recent years, the research on anion O-site doping of perovskite oxides has been a cynosure, which is considered as a promising route for enhancing performance. However, a systematic review summarizing the research progress of anion-doped perovskite oxides is still lacking. Therefore, this review mainly introduces the elements and strategies of various common anions doped at O-site of perovskite oxides, analyzes their influence on the physical and chemical properties of perovskites, and separately concludes their applications in electrocatalysis. This review will provide ideas and prospects for the development of subsequent anion doping strategies for high performance perovskite oxides.
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MXene-supported noble metal alloy catalysts exhibit remarkable electrocatalytic activity in various applications. However, there is no facile one-step method for synthesizing these catalysts, because the synthesis of MXenes requires a strongly oxidizing environment and the preparation of platinum nanoalloys requires a strongly reducing environment and high temperatures. Hence, achieving coupling in one step is extremely challenging. In this paper, a straightforward one-step molten salt method for preparing MXene-supported platinum nanoalloy catalysts is proposed. The molten salt acts as the reaction medium to dissolve the transition metals and platinum ions at high temperatures. Transition metal ions oxidize the A-site element from its MAX precursor at high temperatures, and the resulting transition metals further reduce platinum ions to form alloys. By coupling Al oxidation and platinum ion reduction using a molten salt solvent, this method directly converts Ti3 AlC2 to a Pt-M@Ti3 C2 Tx catalyst (where M denotes the transition metal). It further offers the possibility of extending the Pt-M phase to binary, ternary, or quaternary platinum-containing nanoalloys and converting the Al-containing MAX phase to Ti2 AlC and Ti3 AlCN. Due to the strong interfacial interaction, the as-prepared Pt-Co@Ti3 C2 Tx is superior to commercial Pt/C (20 wt.%) in the hydrogen evolution reaction.
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Electrosynthesis of hydrogen peroxide via selective two-electron transfer oxygen reduction or water oxidation reactions offers a cleaner, cost-effective alternative to anthraquinone processes. However, it remains a challenge to achieve high Faradaic efficiencies at elevated current densities. Herein, we report that oxygen-deficient Pr1.0Sr1.0Fe0.75Zn0.25O4-δ perovskite oxides rich of oxygen vacancies can favorably bind the reaction intermediates to facilitate selective and efficient two-electron transfer pathways. These oxides exhibited superior Faradic efficiencies (~99%) for oxygen reduction over a wide potential range (0.05 to 0.45 V versus reversible hydrogen electrode) and current densities surpassing 50 mA cm-2 under high ionic strengths. We further found that the oxides perform a high selectivity (~80%) for two-electron transfer water oxidation reaction at a low overpotential (0.39 V). Lastly, we devised a membrane-free electrolyser employing bifunctional electrocatalysts, achieving a record-high Faradaic efficiency of 163.0% at 2.10 V and 50 mA cm-2. This marks the first report of the concurrent oxygen reduction and water oxidation catalysed by efficient bifunctional oxides in a novel membrane-free electrolyser for scalable hydrogen peroxide electrosynthesis.
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Importance: Although it has been postulated that chronic inflammation caused by rheumatoid arthritis (RA) contributes to the development of Parkinson disease (PD), the association between these 2 conditions has yet to be determined. Objective: To evaluate the association between RA and subsequent PD risk. Design, Setting, and Participants: This retrospective cohort study used the Korean National Health Insurance Service database to collect population-based, nationally representative data on patients with RA enrolled from 2010 to 2017 and followed up until 2019 (median follow-up, 4.3 [IQR, 2.6-6.4] years after a 1-year lag). A total of 119â¯788 patients who were first diagnosed with RA (83â¯064 with seropositive RA [SPRA], 36â¯724 with seronegative RA [SNRA]) were identified during the study period and included those who underwent a national health checkup within 2 years before the RA diagnosis date (64â¯457 patients). After applying exclusion criteria (eg, age <40 years, other rheumatic diseases, previous PD), 54â¯680 patients (39â¯010 with SPRA, 15â¯670 with SNRA) were included. A 1:5 age- and sex-matched control group of patients without RA was also included for a total control population of 273â¯400. Exposures: Rheumatoid arthritis as defined using International Classification of Diseases, Tenth Revision codes M05 for SPRA and M06 (except M06.1 and M06.4) for SNRA; prescription of any disease-modifying antirheumatic drug; and enrollment in the Korean Rare and Intractable Diseases program. Main Outcomes and Measures: The main outcome was newly diagnosed PD. Data were analyzed from May 10 through August 1, 2022, using Cox proportional hazards regression analyses. Results: From the 328â¯080 individuals analyzed (mean [SD] age, 58.6 [10.1] years; 74.9% female and 25.1% male), 1093 developed PD (803 controls and 290 with RA). Participants with RA had a 1.74-fold higher risk of PD vs controls (95% CI, 1.52-1.99). An increased risk of PD was found in patients with SPRA (adjusted hazard ratio [aHR], 1.95; 95% CI, 1.68-2.26) but not in patients with SNRA (aHR, 1.20; 95% CI, 0.91-1.57). Compared with the SNRA group, those with SPRA had a higher risk of PD (aHR, 1.61; 95% CI, 1.20-2.16). There was no significant interaction between covariates on risk of PD. Conclusions and Relevance: In this study, RA was associated with an increased risk of PD, and seropositivity of RA conferred an augmented risk of PD. The findings suggest that physicians should be aware of the elevated risk of PD in patients with RA and promptly refer patients to a neurologist at onset of early motor symptoms of PD without synovitis.
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Antirreumáticos , Artritis Reumatoide , Enfermedad de Parkinson , Humanos , Masculino , Femenino , Persona de Mediana Edad , Adulto , Estudios Retrospectivos , Enfermedad de Parkinson/tratamiento farmacológico , Artritis Reumatoide/diagnóstico , Artritis Reumatoide/tratamiento farmacológico , Artritis Reumatoide/epidemiología , Antirreumáticos/uso terapéutico , República de Corea/epidemiología , Factores de RiesgoRESUMEN
Dry reforming of methane (DRM) has been emerging as a viable solution to achieving carbon neutrality enhanced by the Paris Agreement as it converts the greenhouse gases of CO2 and CH4 into industrially useful syngas. However, there have been limited studies on the DRM catalyst under mild operating conditions with a high dilution gas ratio due to their deactivation from carbon coking and metal sintering. Herein, we apply the triple-phase boundary (TPB) concept to DRM catalyst via exsolution phenomenon that can secure elongated TPB by controlling the Fe-doping ratio in perovskite oxide. Remarkably, the exsolved catalyst with prolongated TPB shows exceptional CO2 and CH4 conversion rates of 95.9 % and 91.6 %, respectively, stable for 1000â hours under a dilution-free system. DFT calculations confirm that the Lewis acid of support and Lewis base of metal at the TPB promote the adsorption of reactants, resulting in lowering the overall CO2 dissociation and CH4 dehydrogenation energy.
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Understanding proton transport in Ruddlesden-Popper (RP) oxides, as attractive electrode materials for protonic ceramic fuel cells, is challenging because of the complexity of intrinsic oxygen defects in first-series RP oxides (A2BO4). We investigated the processes of intrinsic oxygen defects in proton transportation, such as formation of defects, incorporation of dissociative water into the defective lattice, transfer of a proton along the oxygen sites, and electronic properties of the transition state (TS) in A2BO4. The coexistence of oxygen vacancies (VO) and interstitial oxygen (Oi), VO+Oi defect pair, presents advantageous hydration energies and lattice distortions efficiently accelerating proton transport in the lattice. Moreover, the inherent driving force for proton transport is related to the O 2p band level by O-H···O bond interactions in the TS. Our findings elucidate the fundamental mechanism of proton conduction affected by intrinsic oxygen defects, which will motivate the community to focus more on defect engineering to enhance performance.
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To significantly increase the amount of exsolved particles, the complete phase reconstruction from simple perovskite to Ruddlesden-Popper (R-P) perovskite is greatly desirable. However, a comprehensive understanding of key parameters affecting the phase reconstruction to R-P perovskite is still unexplored. Herein, we propose the Gibbs free energy for oxygen vacancy formation in Pr0.5(Ba/Sr)0.5TO3-δ (T = Mn, Fe, Co, and Ni) as the important factor in determining the type of phase reconstruction. Furthermore, using in-situ temperature & environment-controlled X-ray diffraction measurements, we report the phase diagram and optimum 'x' range required for the complete phase reconstruction to R-P perovskite in Pr0.5Ba0.5-xSrxFeO3-δ system. Among the Pr0.5Ba0.5-xSrxFeO3-δ, (Pr0.5Ba0.2Sr0.3)2FeO4+δ - Fe metal demonstrates the smallest size of exsolved Fe metal particles when the phase reconstruction occurs under reducing condition. The exsolved nano-Fe metal particles exhibit high particle density and are well-distributed on the perovskite surface, showing great catalytic activity in fuel cell and syngas production.
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Recently, triple (H+ /O2- /e- ) conducting oxides (TCOs) have shown tremendous potential to improve the performance of various types of energy conversion and storage applications. The systematic understanding of the TCO is limited by the difficulty of properly identifying the proton movement in the TCO. Herein, the isotope exchange diffusion profile (IEDP) method is employed via time-of-flight secondary ion mass spectrometry to evaluate kinetic properties of proton in the layered perovskite-type TCOs, PrBa0.5 Sr0.5 Co1.5 Fe0.5 O5+ δ (PBSCF).Within the strategy, the PBSCF shows two orders of magnitude higher proton tracer diffusion coefficient (D* H , 1.04 × 10-6 cm2 s-1 at 550 °C) than its oxygen tracer diffusion coefficient at even higher temperature range (D* O, 1.9 × 10-8 cm2 s-1 at 590 °C). Also, the surface exchange coefficient of a proton (k*H ) is successfully obtained in the value of 2.60 × 10-7 cm s-1 at 550 °C. In this research, an innovative way is provided to quantify the proton kinetic properties (D* H and k*H ) of TCOs being a crucial indicator for characterizing the electrochemical behavior of proton and the mechanism of electrode reactions.
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Dry reforming of methane (DRM) is a feasible solution to address the reduction of greenhouse gases stipulated by the Paris Climate Agreement, given that it adds value by converting trivial gases, CO2 and CH4 , simultaneously into useful syngas. However, the conventional Ni catalyst undergoes deactivation due to carbon coking and particle agglomeration. Here we demonstrate a highly efficient and durable DRM catalyst: exsolved Co-Ni-Fe ternary alloy nanoparticles on the layered perovskite PrBaMn1.7 Co0.1 Ni0.2 O5+δ produced by topotactic exsolution. This method readily allows the generation of a larger number of exsolved nanoparticles with enhanced catalytic activity above that of Ni monometallic and Co-Ni bimetallic particles. The enhancement is achieved by the upshift of the d-band center of Co-Ni-Fe relative to those of Co-Ni and Ni, meaning easier charge donation to the adsorbate. Furthermore, the exsolved catalyst shows exceptional stability, with continuous DRM operation for about 350â hours.
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For rechargeable metal-air batteries, which are a promising energy storage device for renewable and sustainable energy technologies, the development of cost-effective electrocatalysts with effective bifunctional activity for both oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) has been a challenging task. To realize highly effective ORR and OER electrocatalysts, we present a hybrid catalyst, Co3O4-infiltrated La0.5Sr0.5MnO3-δ (LSM@Co3O4), synthesized using an electrospray and infiltration technique. This study expands the scope of the infiltration technique by depositing ~18 nm nanoparticles on unprecedented ~70 nm nano-scaffolds. The hybrid LSM@Co3O4 catalyst exhibits high catalytic activities for both ORR and OER (~7 times, ~1.5 times, and ~1.6 times higher than LSM, Co3O4, and IrO2, respectively) in terms of onset potential and limiting current density. Moreover, with the LSM@Co3O4, the number of electrons transferred reaches four, indicating that the catalyst is effective in the reduction reaction of O2 via a direct four-electron pathway. The study demonstrates that hybrid catalysts are a promising approach for oxygen electrocatalysts for renewable and sustainable energy devices.
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Suministros de Energía Eléctrica , Técnicas Electroquímicas , Metales/química , Oxígeno/química , CatálisisRESUMEN
Visualizing the oxygen vacancy distributions is highly desirable for understanding the atomistic oxygen diffusion mechanisms in perovskites. In particular, the direct observation of the one-dimensional oxygen vacancy channels has not yet been achieved in perovskites with dual ion (i.e., cation and anion) ordering. Here, we perform atomic-resolution imaging of the one-dimensional oxygen vacancy channels and their structural dynamics in a NdBaCo2O5.5 double perovskite oxide. An in situ heating transmission electron microscopy investigation reveals the disordering of oxygen vacancy channels by local rearrangement of oxygen vacancies at the specific temperature. A density functional theory calculation suggests that the possible pathway of oxygen vacancy migration is a multistep route via Co-O and Nd-Ov (oxygen vacancy) sites. These findings could provide robust guidance for understanding the static and dynamic behaviors of oxygen vacancies in perovskite oxides.
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With the need for more stable and active metal catalysts for dry reforming of methane, in situ grown nanoparticles using exsolution are a promising approach. However, in conventional exsolution, most nanoparticles remain underneath the surface because of the sluggish diffusion rate of cations. Here, we report the atomic layer deposition (ALD)-combined topotactic exsolution on La0.6Sr0.2Ti0.85Ni0.15O3-δ toward developing active and durable catalysts. The uniform and quantitatively controlled layer of Fe via ALD facilitates the topotactic exsolution, increasing finely dispersed nanoparticles. The introduction of Fe2O3 yields the formation of Ni-Fe alloy owing to the spontaneous alloy formation energy of -0.43 eV, leading to an enhancement of the catalytic activity for dry methane reforming with a prolonged stability of 410 hours. Overall, the abundant alloy nanocatalysts via ALD mark an important step forward in the evolution of exsolution and its application to the field of energy utilization.
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The crystalline phase of layered transition metal dichalcogenides (TMDs) directly determines their material property. The most thermodynamically stable phase structures in TMDs are the semiconducting 2H and metastable metallic 1T phases. To overcome the low phase purity and instability of 1T-TMDs, which limits the utilization of their intrinsic properties, various synthesis strategies for 1T-TMDs have been proposed in phase-engineering studies. Herein, a facile and scalable synthesis of 1T-phase molybdenum disulfide (MoS2 ) via the molten-metal-assisted intercalation (MMI) approach is introduced, which exploits the capillary action of molten potassium and the difference between the electron affinity of MoS2 and the ionization potential of potassium. Highly reactive molten potassium metal can readily intercalate into the MoS2 interlayers, inducing an efficient phase transition from the 2H to 1T crystal structure. The ionic bonding between the intercalated potassium and sulfur lowers the energy barrier of the 1T-phase transition, enhancing the phase stability of the 1T crystals. Owing to the high purity and stability of the 1T phase, the electrocatalytic performance for the hydrogen evolution reaction is significantly higher in 1T-MoS2 (MMI) than in 2H-MoS2 and even in 1T-MoS2 synthesized using n-butyllithium.
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Atmospheric carbon dioxide (CO2 ) has increased from 278 to 408 parts per million (ppm) over the industrial period and has critically impacted climate change. In response to this crisis, carbon capture, utilization, and storage/sequestration technologies have been studied. So far, however, the economic feasibility of the existing conversion technologies is still inadequate owing to sluggish CO2 conversion. Herein, we report an aqueous zinc- and aluminum-CO2 system that utilizes acidity from spontaneous dissolution of CO2 in aqueous solution to generate electrical energy and hydrogen (H2 ). The system has a positively shifted onset potential of hydrogen evolution reaction (HER) by 0.4â V compared to a typical HER under alkaline conditions and facile HER kinetics with low Tafel slope of 34â mV dec-1 . The Al-CO2 system has a maximum power density of 125â mW cm-2 which is the highest value among CO2 utilization electrochemical system.
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Developing cost-effective, efficient bifunctional electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is the heart of metal-air batteries as a renewable-energy technology. Herein, well-distributed nanopolyhedron (NP) Co3O4 grown on iron (Fe) encapsulated in graphitic layers on a nitrogenated, porous two-dimensional (2D) structure, namely, a C2N matrix, (NP Co3O4/Fe@C2N), presents an outstanding bifunctional catalytic activity with a comparable overpotential and Tafel slope to those of benchmark Pt/C and IrO2. The rationally designed atomic configuration of Co3O4 on the C2N matrix has a well-controlled NP morphology with a (111) plane, leading to bifunctional activities for the ORR and OER. Interestingly, the specific interaction between the NP Co3O4 nanoparticles and the C2N matrix introduces synergistic coupling and changes the electronic configuration of Co atoms and the C2N framework. Benefiting from the synergistic coupling of Co3O4 with the C2N matrix, the NP Co3O4/Fe@C2N electrocatalyst exhibits exceptionally high stability and an even lower charge-discharge overpotential gap of 0.85 V at 15 mA cm-2 than that of the Pt/C+IrO2 catalyst (1.01 V) in Zn-air batteries. This work provides insights into the rational design of a metal oxide on a C2N matrix for bifunctional, low-cost electrochemical catalysts.
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Developing efficient bifunctional catalysts for overall water splitting that are earth-abundant, cost-effective, and durable is of considerable importance from the practical perspective to mitigate the issues associated with precious metal-based catalysts. Herein, we introduce a heterostructure comprising perovskite oxides (La0.5Sr0.5CoO3-δ) and molybdenum diselenide (MoSe2) as an electrochemical catalyst for overall water electrolysis. Interestingly, formation of the heterostructure of La0.5Sr0.5CoO3-δ and MoSe2 induces a local phase transition in MoSe2, 2 H to 1 T phase, and more electrophilic La0.5Sr0.5CoO3-δ with partial oxidation of the Co cation owing to electron transfer from Co to Mo. Together with these synergistic effects, the electrochemical activities are significantly improved for both hydrogen and oxygen evolution reactions. In the overall water splitting operation, the heterostructure showed excellent stability at the high current density of 100 mA cm-2 over 1,000 h, which is exceptionally better than the stability of the state-of-the-art platinum and iridium oxide couple.
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Exsolution has been intensively studied in the fields of energy conversion and storage as a method for the preparation of catalytically active and durable metal nanoparticles. Under typical conditions, however, only a limited number of nanoparticles can be exsolved from the host oxides. Herein, we report the preparation of catalytic nanoparticles by selective exsolution through topotactic ion exchange, where deposited Fe guest cations can be exchanged with Co host cations in PrBaMn1.7Co0.3O5+δ. Interestingly, this phenomenon spontaneously yields the host PrBaMn1.7Fe0.3O5+δ, liberating all the Co cations from the host owing to the favorable incorporation energy of Fe into the lattice of the parent host (ΔEincorporation = -0.41 eV) and the cation exchange energy (ΔEexchange = -0.34 eV). Remarkably, the increase in the number of exsolved nanoparticles leads to their improved catalytic activity as a solid oxide fuel cell electrode and in the dry reforming of methane.
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Carbon capture, utilization, and sequestration technologies have been extensively studied to utilize carbon dioxide (CO2), a greenhouse gas, as a resource. So far, however, effective technologies have not been proposed owing to the low efficiency conversion rate and high energy requirements. Here, we present a hybrid Na-CO2 cell that can continuously produce electrical energy and hydrogen through efficient CO2 conversion with stable operation for over 1,000 hr from spontaneous CO2 dissolution in aqueous solution. In addition, this system has the advantage of not regenerating CO2 during charging process, unlike aprotic metal-CO2 cells. This system could serve as a novel CO2 utilization technology and high-value-added electrical energy and hydrogen production device.