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  • Haider, Mohammad Ali  (7)
  • 1
    Online Resource
    Online Resource
    The Electrochemical Society ; 2023
    In:  ECS Meeting Abstracts Vol. MA2023-01, No. 54 ( 2023-08-28), p. 357-357
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2023-01, No. 54 ( 2023-08-28), p. 357-357
    Abstract: Boosting the lower oxygen reduction reaction (ORR) activity of perovskite cathode material is essential for the development and widespread use of IT-SOFC. Oxygen ion migration at the cathode-electrolyte interface can enhance by introducing structural modifications consisting of high grain boundary density and heterointerfaces [1]. Herein, we fabricated Sr 2 CoNbO 6- δ @Sm 0.2 Ce 0.8 O 1.9 (SCNO@SDC) nanofiber composite using an electrospinning technique and examined the electrochemical impedance for the symmetric cell in air atmosphere. The distinct phases of SCNO and SDC were observed from XRD and FESEM-EDAX analysis. The ionic conductivity was analysed to monitor the electrochemical activity of synthesised material, and the results illustrated that the activation energy for the nanofiber was 0.51 eV lower than conventional composites’ 0.73 eV. The thermal expansion coefficient showed improvement as the value of 14.3 Х 10 -6 K -1 for nanofiber composite than the 17.6 Х 10 -6 K -1 of SCNO-SDC [2]. The symmetric SCNO|SDC|SCNO cell electrodes from nanofiber were fabricated, and electrochemical performance was compared with 20% SDC-SCNO composite in an air atmosphere with varying temperatures from 500 o C to 700 o C. Figure 1. compares polarisation resistance with increased temperature for nanofiber and conventional electrodes. The polarization resistance significantly decreased from 2.76 Ω cm 2 to 0.69 Ω cm 2 for the nanofiber composite than the conventional electrode 5.2 Ω cm 2 to 2.1 Ω cm 2 [3]. The sluggish ORR activity improved due to unique microstructure, high porosity, and specific surface area, which provides extensive triple phase boundaries and a continuous path for charge transfer [4] . Therefore, SCNO@SDC nanofiber composite offers an alternative approach for attaining efficient performance of IT-SOFC. References Choi, Y., Cho, H. J., Kim, J., Kang, J. Y., Seo, J., Kim, J. H., & Jung, W. (2022). Nanofiber Composites as Highly Active and Robust Anodes for Direct-Hydrocarbon Solid Oxide Fuel Cells. ACS nano , 16 (9), 14517-14526. Li, Z., Peng, M., Zhao, Y., Li, J., & Sun, Y. (2021). Minimized thermal expansion mismatch of cobalt-based perovskite air electrodes for solid oxide cells. Nanoscale , 13 (47), 20299-20308. Kumari, N., Tiwari, P. K., Haider, M. A., & Basu, S. (2017). Electrochemical performance of infiltrated Cu-GDC and Cu-PDC cathode for CO2 electrolysis in a solid oxide cell. ECS Transactions , 78 (1), 3329. Zhao, B., Zhang, L., Zhen, D., Yoo, S., Ding, Y., Chen, D., & Liu, M. (2017). A tailored double perovskite nanofiber catalyst enables ultrafast oxygen evolution. Nature communications , 8 (1), 1-9. Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2023
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  • 2
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2023-01, No. 54 ( 2023-08-28), p. 386-386
    Abstract: Proton conducting solid oxide cell (H-SOC) is a highly efficient energy conversion device converting electrical energy into hydrogen by splitting water using solid oxide proton conductor at intermediate temperature range (500-700 0 C) [ 1 ]. To enhance electrochemical performances in terms of efficient hydrogen generation, robust and durable air electrode materials are required to facilitate faster water oxidation and oxygen reduction reaction, which are the key steps for both electrolyser and fuel cell at a lower temperature [ 2-3 ]. In the present study, we have developed ‘La’ and ‘Nd’ A-site co-doped strontium cobaltite and cobalt ferrite: La 0.35 Nd 0.35 Sr 0.3 Co 0.8 Fe 0.2 O 3-δ (LNSCF) a perovskite type cathode material exhibiting higher electrical and electrochemical performances. The electrical and O 2- ion conductivity of the material shows metallic nature, and the highest conductivity values are 973 S cm -1 and 0.318 S cm -1 respectively at 400 o C. The higher value of electrical and ionic conductivity is attributed to highly efficient Co 2+ to Co 3+ and Fe 3+ to Fe 4+ transition. Electrochemical impedance spectroscopy analysis of the symmetrical cell (LNSCF/Zirconium and Yttrium doped Barium Cerate (BZCY)/LNSCF) revealed the value of Area Specific Resistance (ASR) to be 0.14, 0.47 and 3.06 Ω cm 2 at 800,700 and 600 o C respectively. When operated in H-SOFC mode with humidified hydrogen as fuel and Air (3%H 2 O) as oxidant, the LNSCF based single cell: Ni-BZCY/BZCY (385m)/ LNSCF+BZCY achieves a maximum current density of 522, 383, and 231mA/cm 2 at 800, 700, and 600 o C, respectively at 0.002 V. Whereas, in H-SOEC mode a maximum current density of -1380, -862 and -517 mA/cm 2 are obtained at 800, 700, and 600 o C, respectively at 2.5 V. The contribution of different ions (O 2- and H 2+ ) and electrons (e - ) in the electrochemical performances are evaluated using ion-blocking cells. The figure (1) below represents the Current Density versus Voltage (i-V) characteristic attributes for both H-SOFC and H-SOEC. References: Bi L., Boulfrad S., and Traversa E. 2014 Steam electrolysis by solid oxide electrolysis cell (SOEC) with proton-conducting oxides. Chem. Soc. Review 43 8255 Duan C., Kee R., Zhu H., Sullivan N., Zhu L., Bian L., Jennings, D., and O’ Hayre R. Highly efficient protonic ceramic electrochemical cell for fuel generation and power production. Nature Energy 4 230 -240 Choi S., Davenport TC., Haile SM. 2019 Protonic Ceramic electrochemical cells for hydrogen production and electricity generation: Exceptional reversibility, Stability and demonstrated faradaic efficiency. Energy and Environmental Sciences 12 206 Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2023
    detail.hit.zdb_id: 2438749-6
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  • 3
    Online Resource
    Online Resource
    The Electrochemical Society ; 2023
    In:  ECS Transactions Vol. 111, No. 6 ( 2023-05-19), p. 2271-2276
    In: ECS Transactions, The Electrochemical Society, Vol. 111, No. 6 ( 2023-05-19), p. 2271-2276
    Abstract: Improved oxygen reduction reaction (ORR) performance of perovskite cathode material is crucial for the widespread utilization and advancement of the intermediate temperature solid oxide fuel cell (IT-SOFC). A composite of Sr 2 CoNbO 6-δ @Sm 0.2 Ce 0.8 O 2- δ (SCNO@SDC) nanofibers is fabricated using electrospinning, followed by high-temperature sintering process, and its electrochemical activity towards ORR is analyzed. The XRD and STEM confirmed the phase and morphology of the nanofiber composites. Conductivity studies revealed that the activation energy of the nanofiber composite was 0.51 eV lower than that of the conventional composite, which is 0.73 eV. Moreover, the polarization resistance of the nanofiber decreased from 1.38 to 0.345 Ω cm 2 , whereas that of the conventional electrode decreased from 2.6 to 1.05 Ω cm 2 in the air atmosphere between 500°C to 700°C.
    Type of Medium: Online Resource
    ISSN: 1938-5862 , 1938-6737
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2023
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  • 4
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2022-01, No. 37 ( 2022-07-07), p. 1633-1633
    Abstract: Oxygen reduction reaction (ORR) in a double perovskite material is considered to be the most sluggish reaction in the intermediate temperature operation of a solid oxide fuel cell (SOFC). ORR is often inhibited by poor oxygen surface exchange rates or bulk diffusion in the material. In order to understand the rate-limiting process of the material, we have fabricated a dense thin-film double perovskite of composition Sr 2 CoNbO 6- δ . The pulse laser deposition (PLD) method is employed to fabricate geometrically well-defined symmetric electrodes of SCN on an electrolyte substrate for accurate assessment of electrode impedance. Electrode thickness is varied from 40 nm to 80 nm by changing the deposition parameters in PLD. On increasing the thickness, the electrode impedance is observed to increase, suggesting bulk diffusion of oxygen anions limiting the electrochemical performance in the electrode material.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2022
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  • 5
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2022-01, No. 4 ( 2022-07-07), p. 557-557
    Abstract: Global progression towards e-mobility to reduce the carbon footprint has led to the demand for smart grid energy storage systems. Amongst the available electrical energy storage technologies, rechargeable batteries serve as a pragmatic option to cater to the intermittent character of renewable energy supplies owing to their high energy efficiency and flexible power characteristics. In contrast to the existing lithium-ion batteries (LIBs), Na-ion batteries appear as a sustainable substitute due to their dependence on widely distributed, and abundant sodium reserves. However, the commercialization of Na-ion batteries has been hampered primarily by the inefficient performance of electrode materials particularly cathode. Among the prevailing cathode materials, the class of layered transition metal oxide with O3 and P2 structural configuration imparts decent specific capacity and has been studied extensively over the past few years. Though the presence of comparatively larger Na ions induces better initial capacity but suffer the drawback of undergoing complex phase transformation during charge-discharge cycling. Moreover, P2-phase exhibits lower diffusion energy barrier due to the direct passage of sodium ions from one prismatic site to another. Therefore, materials with the aforementioned P2 orientation have been synthesized deploying earth-abundant elements like Mn, and Fe for sodium-ion battery applications. To comprehend the diffusional behavior of Na-ions, we have carried out molecular dynamics simulation of P2-Na 2/3 Mn 1-x Fe x O 2 (x=0, 1/3, 1/2) material. The preliminary computational calculations reveal enhanced Na-ion self-diffusivity with increased Fe dopant onto P2-Na 2/3 MnO 2 material, while the diffusivity showcased a decreasing trend with further increase in Fe substitution that might be ascribed to the phase stabilization aspect of Mn element and charge compensation attribute of Fe 3+ /Fe 4+ and Mn 3+ /Mn 4+ redox couples.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2022
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  • 6
    Online Resource
    Online Resource
    The Electrochemical Society ; 2021
    In:  ECS Meeting Abstracts Vol. MA2021-01, No. 46 ( 2021-05-30), p. 1842-1842
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2021-01, No. 46 ( 2021-05-30), p. 1842-1842
    Abstract: Simple perovskite structured electrode materials of the series (La x Sr 1-x CoO 3- δ ) are commonly utilised for high-temperature solid-state electrochemical cells and Li-air batteries with some limitations observed on prolong operations due to the structural instability associated with the segregation of strontium ions. In order to overcome this structural incompatibility, doping of heterovalent dopant at the B-site is proposed which could possibly improve upon the stability by controlling the segregation of surface cations. In addition, the doped structure is likely to provide faster oxygen anion transport through the vacancies in the structure, thereby improving its electrochemical performance. Herein, oxygen anion diffusion in pure La 0.7 Sr 0.3 CoO 3-- δ (LSC) and Nb-doped La 0.7 Sr 0.3 Co 0.95 Nb 0.05 O 3- δ (LCSN) perovskite structure is calculated using molecular dynamics (MD) simulations. Self diffusion coefficient of oxygen ions in the LSCN structure is observed to increase by an order of magnitude (1.356×10 -8 cm 2 /s) on Nb doping as compared to the undoped LSC structure (6.499×10 -9 cm 2 /s) at 1073 K. On varying the Nb concentration from 0.05 to 0.15 and optimum Nb concentration is estimated to be 0.05 corresponding to a maximum oxygen anion diffusivity in the structure (1.356×10 -8 cm 2 /s) at 1073 K.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2021
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  • 7
    Online Resource
    Online Resource
    The Electrochemical Society ; 2021
    In:  ECS Meeting Abstracts Vol. MA2021-03, No. 1 ( 2021-07-23), p. 141-141
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2021-03, No. 1 ( 2021-07-23), p. 141-141
    Abstract: For solid oxide fuel cells (SOFCs), the electrode fabrication with the electrolyte showing a good thermal expansion coefficient (TEC) match at high temperatures is considered a key element in deciding upon the potential of a candidate electrode material. Here, in this work a Nb doped perovskite La 0.7 Sr 0.3 Co 0.95 Nb 0.05 O 3- δ (LCSN) material is tested for the desired properties of a SOFC cathode. The results are showing improved (TEC) by about 28% for the temperature range of 200 - 2100 K and an increase in ionic conductivity by 19% at 873 K as compared to the base material, La 0.7 Sr 0.3 CoO 3-- δ (LSC). The material is further fabricated in the form of a nanostructured thin-film electrode using a pulse laser disposition system with thickness varying from 50 nm to 100 nm on a GDC electrolyte. The impedance of the electrode in a symmetric cell is observed to vary with the thickness, suggesting oxygen anion transport, limiting the electrode performance.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2021
    detail.hit.zdb_id: 2438749-6
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