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  • 1
    Online Resource
    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-01, No. 42 ( 2019-05-01), p. 2048-2048
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-01, No. 42 ( 2019-05-01), p. 2048-2048
    Abstract: Urea is an end-product of the metabolism of nitrogenous compounds, which can be detected in the blood as well as urine [1]. Ammonia catabolized by protein metabolism is converted into urea by liver and kidneys [2] . Consequently, the concentration of urea in the urine or blood is a suitable biomarker that monitors liver and kidney function. If a sensor platform can immediately determine the level of urea in the biological fluid, it will be valuable for many patients when estimating the concentration of urea in the blood. Investigation on urea biosensors has been mainly guided out the advancement of enzyme-based catalysts [3]. However, the limitations such as denaturation of enzyme and mobilization to the catalysts lead to the lack of stability. Consequently, the improvement of non-enzyme-based catalysts can work the constraints mentioned above, thereby allowing the progression of urea biosensors. Many non-enzymatic catalysts have been investigated to catch urea molecules, including noble metals, transition metals, and metal hydroxide [4] -[6]. With them, the Ni-based catalysts are the most encouraging suggestion, because it gives excellent electrocatalytic efficiency, biocompatibility, nontoxicity, and high electron transfer. [7] . Although nickel-based catalysts are admitted being an excellent facilitator for the urea electrooxidation, published investigations are few in the nickel-based catalysts for biosensor applications. The inadequacy of research in the biosensor area is related to the mechanism of nickel-based catalysts in alkaline medium. Ni(OH) 2 (Ni 2+ ) is electrochemically oxidized to NiOOH (Ni 3+ ) before electrocatalytic urea oxidation. However, since the pH of human blood is neutral (7.35-7.45), it is necessary to develop catalysts as a biomarker for urea electrooxidation which does not depend on pH. Therefore, the nickel-based catalysts intrinsically involving Ni 3+ ion will more efficiently improve the electrooxidation performance of the urea. In this study, A composite catalyst based on silver-nickel oxide hydroxide nanorods (Ag-NiOOH) was synthesized for non-enzymatic urea detection. The Ag-NiOOH was characterized by energy dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and X-ray diffraction techniques. The morphology and the structure of the Ag-NiOOH were investigated using scanning electron microscopy. The Ag-NiOOH coated carbon paper was employed to fabricate a new electrochemical sensor for urea detection. The Ag-NiOOH/carbon paper electrode showed a very high sensitivity of 177 μAmM −1 cm −2 , a low detection limit of 5 μM and a response time of 1.5 s. Detailed discussion on the performance of Ag-NiOOH and the role of inherent Ni 3+ ions as a catalyst in urea biosensor will be given. References Coll, Elisabeth, et al. "Serum cystatin C as a new marker for noninvasive estimation of glomerular filtration rate and as a marker for early renal impairment." American journal of kidney diseases 36.1 (2000): 29-34. Jakhar, Seema, et al. "Preparation, characterization and application of urease nanoparticles for construction of an improved potentiometric urea biosensor." Biosensors and Bioelectronics 100 (2018): 242-250. Liu, Baohong, et al. "Studies on a potentiometric urea biosensor based on an ammonia electrode and urease, immobilized on a γ-aluminum oxide matrix." Analytica chimica acta 341.2-3 (1997): 161-169. Boggs, Bryan et al. "Urea electrolysis: direct hydrogen production from urine." Chemical Communications 32 (2009): 4859-4861. Chen, Sheng, et al. "Size Fractionation of Two‐Dimensional Sub‐Nanometer Thin Manganese Dioxide Crystals towards Superior Urea Electrocatalytic Conversion." Angewandte Chemie International Edition 55.11 (2016): 3804-3808. Wu, Mao-Sung, et al. "Hydrothermal growth of vertically-aligned ordered mesoporous nickel oxide nanosheets on three-dimensional nickel framework for electrocatalytic oxidation of urea in alkaline medium." Journal of power sources 272 (2014): 711-718. Li, Chengchao, et al. "A novel amperometric biosensor based on NiO hollow nanospheres for biosensing glucose." Talanta 77.1 (2008): 455-459. Acknowledgement This work was supported by Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD) and the Ocean University of China-Auburn University (OUC-AU) Grants program.
    Type of Medium: Online Resource
    ISSN: 2151-2043
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    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 2
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    Online Resource
    The Electrochemical Society ; 2017
    In:  ECS Meeting Abstracts Vol. MA2017-02, No. 21 ( 2017-09-01), p. 1019-1019
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2017-02, No. 21 ( 2017-09-01), p. 1019-1019
    Abstract: The polymer electrolyte membrane fuel cell(PEMFC) is being considered as a clean source of power for the application of future energy owing to its high-power density, lower operating temperature than other fuel cells, and environment-friendliness [1]. For commercialization, the cost of bipolar plates (BPs) is a crucial factor among cell components, which comprises a high percentage of the total volume, weight, and the cost [2] . Graphite BPs is widely used due to high chemical stability and low surface contact resistance, but brittleness and machining cost are the critical concerns [3]. Stainless steel is commonly utilized an alternative material due to their high strength and chemical stability, low gas permeability. However, stainless steel suffers corrosion during PEMFC operation. Such corrosion deteriorates cell performance by dissolution of the metal ion into gas diffusion layer and increased interfacial contact resistance(ICR) of the formation of the passivation film [4] . Titanium nitride(TiN) can be one of the promising protective coating material in PEMFC due to the excellent durability, chemical stability, as well as good electrical conductivity. Various methods such as CVD [5], PVD [6] , and sputtering [7] have been investigated to fabricate TiN films. In this study, we explore electrophoretic deposition (EPD) of TiN layers. It is known that EPD provides simple, versatile, easy adjustment of coating thickness and cost-effective method to fabricate homogeneous coatings onto complex shape as well as a porous substrate [8].  TiN powders were coated successfully onto a 316 stainless steel by EPD. The different particle size of TiN including 20nm, 80nm and 800nm TiN powders was used to investigate morphology of coating layers, EPD kinetics and mechanism. In addition, two kinds of additives, PDADMAC and PEI were used to obtain a uniform suspension and EPD mechanism. Although both additives cationic polymers, different polymeric structure and molecular weight would influence condition of suspensions and potentially properties of coating layers. The morphologies and structure of TiN coated surface were analyzed by SEM and XRD. The potentiodynamic and potentiostatic electrochemical tests were conducted to measure the corrosion resistance for the applicability of EPD of TiN as a protective layer of bipolar plate in PEMFC. References [1] Schäfer, Andreas, John B. Heywood, and Malcolm A. Weiss. "Future fuel cell and internal combustion engine automobile technologies: A 25-year life cycle and fleet impact assessment."  Energy  31.12 (2006): 2064-2087. [2] Wang, Heli, Mary Ann Sweikart, and John A. Turner. "Stainless steel as bipolar plate material for polymer electrolyte membrane fuel cells."  Journal of Power Sources  115.2 (2003): 243-251. [3] Beaudin, Marc, et al. "Energy storage for mitigating the variability of renewable electricity sources: An updated review."  Energy for Sustainable Development  14.4 (2010): 302-314. [4] Makkus, Robert C., et al. "Use of stainless steel for cost competitive bipolar plates in the SPFC."  Journal of power sources  86.1 (2000): 274-282. [5] Mahieu, Stijn, Diederik Depla, and Roger De Gryse. "Characterization of the hardness and the substrate fluxes during reactive magnetron sputtering of TiN."  Surface and Coatings Technology  202.11 (2008): 2314-2318. [6] Altun, Hikmet, and Hakan Sinici. "Corrosion behaviour of magnesium alloys coated with TiN by cathodic arc deposition in NaCl and Na 2 SO 4 solutions."  Materials Characterization  59.3 (2008): 266-270. [7] Zhang, Dongming, et al. "Corrosion behavior of TiN-coated stainless steel as bipolar plate for proton exchange membrane fuel cell."  International Journal of Hydrogen Energy  35.8 (2010): 3721-3726. [8] Kanamura, Kiyoshi, and Jun-ichi Hamagami. "Innovation of novel functional material processing technique by using electrophoretic deposition process."  Solid State Ionics  172.1 (2004): 303-308.   Acknowledgement This work was partially supported by Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD), the Ocean University of China-Auburn University (OUC-AU) Grants program, and the International Collaborative Energy Technology R & D Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP), granted financial resource from the Ministry of Trade, Industry & Energy, Republic of Korea (20158520000210).
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2017
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  • 3
    Online Resource
    Online Resource
    The Electrochemical Society ; 2017
    In:  ECS Meeting Abstracts Vol. MA2017-02, No. 49 ( 2017-09-01), p. 2107-2107
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2017-02, No. 49 ( 2017-09-01), p. 2107-2107
    Abstract: The level of biological molecules, such as urea, glucose, dopamine, and creatinine has been measured by various sensing platform for biomedical applications. For example, the urea level deviated from the reference values which causes several diseases such as renal and hepatic issues, is closely related to our life. Monitoring of urea is also important for fertilizer production as well as development of indirect hydrogen storage materials. Various types of urea sensors, including enzymatic sensors, have been researched to measure abovementioned molecules, courtesy of high selectivity and sensitivity. However, enzymatic sensors have the stability problems caused by denaturation of enzyme. A various metals or metal oxides, such as Pt, Cu/CuO, Ni/NiO, Zn/ZnO, have been widely investigated for the detection of different molecules. Among them, Ni based catalyst presents better performance in the electro-catalytic oxidation of molecules such as urea and glucose. Although Ni based catalyst has shown a good performance, problems such as degradation and expansion of the Ni based catalyst structure during the oxidation still exist. Moreover, the level of pH to operate the electrode for detecting the bio molecules indicates the alkaline the solution which is inability to perform in the physiological condition of approximately pH 7. In other words, the concentration of OH - anions is a dominant factor in Ni based catalyst. In this study, silver catalyst deposited on a synthesized ZnO rods/ carbon substrate was prepared at low-temperature process for the enzyme-free urea sensor. The morphologies and structural properties of Ag catalyst deposited ZnO rods were analyzed by SEM and XRD, and the quantity of the silver catalyst was measured by EDS. Thereafter electrochemical properties of the electrode were performed. The catalytic effect of Ag/ZnO rods electrode for urea sensing was investigated in terms of sensitivity and selectivity. Detailed discussion on the mechanism of Ag/ZnO rods catalytic effect will be given.  References R. Lan, J.T.S. Irvine, S. Tao. “Ammonia and related chemicals as potential indirect hydrogen storage materials.” Int. J. Hydrogen Energy , 37 (2012), pp. 1482–1494 D. Aronson, M.A. Mittleman, A.J. Burger. “Elevated blood urea nitrogen level as a predictor of mortality in patients admitted for decompensated heart failure.” Am. J. Med. , 116 (2004), pp. 466–473 G. Dhawan, G. Sumana, B.D. “Malhotra Recent developments in urea biosensors.” J. Biochem. Eng. , 44 (2009), pp. 42–45 Y. Wang, H. Xu, J. Zhang, J.G. Li. “Electrochemical sensors for clinic analysis.” Sensors , 8 (2008), pp. 2043–2081 M. Singh, N. Verma, A.K. Garg, N. Redhu. “Urea biosensors.” Sens. Actuators B , 134 (2008), pp. 345–351 V. Vedharathinam, G.G. Botte. “Understanding the electro-catalytic oxidation mechanism of urea on nickel electrodes in alkaline medium.” Electrochim. Acta , 81 (2012), pp. 292–300 Q.F. Yi, W. Huang, W.Q. Yu, L. Li, X.P. Liu. “Hydrothermal synthesis of titanium-supported nickel nanoflakes for electrochemical oxidation of glucose.” Electroanalysis , 20 (2008), pp. 2016–2022 Acknowledgement This work was supported by Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD).
    Type of Medium: Online Resource
    ISSN: 2151-2043
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    Publisher: The Electrochemical Society
    Publication Date: 2017
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  • 4
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    Online Resource
    The Electrochemical Society ; 2018
    In:  ECS Meeting Abstracts Vol. MA2018-02, No. 57 ( 2018-07-23), p. 2041-2041
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2018-02, No. 57 ( 2018-07-23), p. 2041-2041
    Abstract: Wearable electronics have evolved from life-supporting devices for solders to fashion accessories such as smart watches. Wearable devices are not limited to on-body devices because they can be further transformed by integrating with other surfaces such building and vehicles. Accordingly, the market demand for wearables has greatly increased, and the research of gas sensor has attempted to adapt wearables with the power of nanotechnology. On the wearable platform, miniature gas sensors will provide real-time information of the atmosphere to protect each personnel from possible hazardous chemical attacks. In addition, wearable gas sensor can be facilitated to monitor human’s breath as medical applications. [1] The main keys for wearable gas sensors are to decrease working temperature and increase sensing performance. Recently, two-dimensional (2D) nanostructured materials have been highlighted as new sensing materials due to their working ability at low temperature. Unlike conventional metal oxides, 2D materials such as graphene are able to work at room temperature with comparable gas response to NO 2 gas. However, insufficient sensing performance, such as sluggish recovery and low gas response, need to be developed. [2] As one attempt to enhance performance, 2D material was hybridized with metal oxide. By incorporating two nanostructured materials, synergistic effect, which comes from benefits of each materials, can improve sensing performance. [3] Another novel innovation is the introduction of newly discovered 2D materials. 2D transition metal carbides and/or carbonitrides (called MXenes) are a new family of 2D materials, and much interest is being paid to them due to their attractive properties for many different applications, particularly in energy storage. Ti 3 C 2 is the first discovered and most researched MXene. Considering the surface functional groups on Ti 3 C 2 , this MXene has the potential to be suitable material for wearable gas sensing applications working at low temperature. [4] In this study, 2D nanostructured materials and their hybrids were investigated for wearable gas sensing applications. Graphene oxide (GO) was incorporated with TiO2 nanoparticles, and the composite was photo-reduced under UV irradiation. Room temperature gas sensing was carried out against various VOC gases, and sensing performance was evaluated by comparing with pure GO. With the tailored hetero-junction at the interfaces of GO and TiO 2 , the composite can identify ethanol, methanol, and acetone, and its gas response was enhanced. After photo-reduction, the gas sensing behavior was converted from n-type to p-type due to reduction of GO. Color change of the composites was also observed. In addition, we introduced new 2D nanostructured materials, MXenes, for gas sensing. Ti 3 C 2 (MXene) was synthesized by selectively eliminating Al from Ti 3 AlC 2 (MAX) using LiF salt and HCl acid. Ti 3 C 2 was deposited as sensing material on a flexible polymer film using facile drop casting. The structural and morphological study of the prepared Ti 3 C 2 was conducted by XRD, SEM, and EDS, and the surface bonding was probed by FTIR. The sensing properties of the Ti 3 C 2 sensor were investigated with various reducing gases at RT, and the predicted sensing mechanism was proposed. [5] References [1] Patel, S., Park, H., Bonato, P., Chan, L., & Rodgers, M. (2012). A review of wearable sensors and systems with application in rehabilitation. Journal of neuroengineering and rehabilitation, 9(1), 21. [2] Choi, S. J., & Kim, I. D. (2018). Recent Developments in 2D Nanomaterials for Chemiresistive-Type Gas Sensors. Electronic Materials Letters, 1-40. [3] Meng, F. L., Guo, Z., & Huang, X. J. (2015). Graphene-based hybrids for chemiresistive gas sensors. TrAC Trends in Analytical Chemistry, 68, 37-47. [4] Yu, X. F., Li, Y. C., Cheng, J. B., Liu, Z. B., Li, Q. Z., Li, W. Z., ... & Xiao, B. (2015). Monolayer Ti2CO2: a promising candidate for NH3 sensor or capturer with high sensitivity and selectivity. ACS applied materials & interfaces, 7(24), 13707-13713. [5] Lee, E., VahidMohammadi, A., Prorok, B. C., Yoon, Y. S., Beidaghi, M., & Kim, D. J. (2017). Room Temperature Gas Sensing of Two-Dimensional Titanium Carbide (MXene). ACS applied materials & interfaces, 9(42), 37184-37190. This research was partially supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP), grant funded by the Korea Government Ministry of Trade, Industry and Energy (20158520000210), and Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD).
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2018
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 2020
    In:  ECS Meeting Abstracts Vol. MA2020-01, No. 27 ( 2020-05-01), p. 1947-1947
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-01, No. 27 ( 2020-05-01), p. 1947-1947
    Abstract: The level of urea in urine can be a crucial biomarker to detect kidney failure, dehydration, renal function, and hepatic failure. [1] Thus, rapid and accurate sensing of urea is essential in a diagnostic clinic, especially for point-of-care testing devices (POCT). Paper-based analytical devices have been demonstrated as POCT due to its disposability, portability, low cost, and environmental-friendly quality. [2] In order to measure urea, electrochemical biosensors based on the enzyme were explored, but the application of enzyme has its limitations due to low shelf-life, complicated immobilization procedure, high cost, and complicate operating condition which is not fit to POCT application. [3] To overcome the limitations of enzyme, non-enzymatic urea sensor have attracted from researchers due to advantages such as good stability, re-usability, high sensitivity, redox flexibility, simplicity, and low cost. [4] As a non-enzymatic catalyst, nano metal oxides such as NiO, SnO 2 , and Fe 2 O 3 , exhibited catalytic activity on urea by the formation of the redox couple on the sensor surface.[5] [6] [7] To utilize non-enzymatic catalysts with comparable properties of enzyme, the development to increase reaction surface area has been emphasized by using nanomaterial, hierarchical structure, and support matrix.[8] [9] However, those processes involve complicate fabrication steps and often need additional post-process to remove the template leading to poisoning of the catalyst. As a potential approach for template-free process, paper can be used for an electrochemical sensor substrate. Paper has a complex fiber matrix that can provide pore pathways for the electrolyte to infiltrate inside, and by distributing catalyst uniformly within the paper, which formsmore reaction sites. Therefore, e nhancement of performance and simplification of the fabrication can be achieved with the use of paper. In this study, the simple, disposable paper-based device was developed for urea electro-oxidation by using paper matrix as support. The paper-based electrode was fabricated by a screen printing method with filter paper, and different combinations of nano-metal oxides, NiO, SnO 2 , and Fe 2 O 3 . The metal oxide catalysts were loaded on the working electrode area and compared the performance. Structure and morphology of paper-based electrode were characterized by XRD and SEM. Investigation of selectivity and LOD was conducted by potentiostat. A detailed description of the fabrication of paper-based electrode and sensing performances will be presented. References [1] Boggs, Bryan K., Rebecca L. King, and Gerardine G. Botte. "Urea electrolysis: direct hydrogen production from urine." Chemical Communications 32 (2009): 4859-4861. [2] Martinez, Andres W., et al. "Patterned paper as a platform for inexpensive, low‐volume, portable bioassays." Angewandte Chemie International Edition 46.8 (2007): 1318-1320. [3] Riklin, Azalla, et al. "Improving enzyme–electrode contacts by redox modification of cofactors." Nature 376.6542 (1995): 672. [4] Nie, Huagui, et al. "Nonenzymatic electrochemical detection of glucose using well-distributed nickel nanoparticles on straight multi-walled carbon nanotubes." Biosensors and Bioelectronics 30.1 (2011): 28-34. [5] Arain, Munazza, et al. "Simpler and highly sensitive enzyme-free sensing of urea via NiO nanostructures modified electrode." RSC Advances 6.45 (2016): 39001-39006. [6] Ansari, S. G., et al. "Electrochemical enzyme-less urea sensor based on nano-tin oxide synthesized by hydrothermal technique." Chemico-biological interactions 242 (2015): 45-49. [7] Das, Gautam, et al. "NiO-Fe2O3 based graphene aerogel as urea electrooxidation catalyst." Electrochimica Acta 237 (2017): 171-176. [8] Wu, Mao-Sung, Ren-Yu Ji, and Yo-Ru Zheng. “Nickel Hydroxide Electrode with a Monolayer of Nanocup Arrays as an Effective Electrocatalyst for Enhanced Electrolysis of Urea.” Electrochimica Acta 144 (October 2014): 194–99. [9] Liang, Yanhui, et al. "Enhanced electrooxidation of urea using NiMoO4· xH2O nanosheet arrays on Ni foam as anode." Electrochimica Acta 153 (2015): 456-460. Acknowledgement This work was partially supported by Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD), and the Ocean University of China-Auburn University (OUC-AU) Grants program.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
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  • 6
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    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-02, No. 51 ( 2019-09-01), p. 2225-2225
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-02, No. 51 ( 2019-09-01), p. 2225-2225
    Abstract: Recently emerging materials for advancing gas sensor technology have potentialized versatile applications of a sensor in the society of safety, health, environmental protection and much more [1]. In accordance with significant progress of chemical and physical approaches, gas sensing materials are not limited to metal oxide but include various 2D nanostructures such as graphene and metal dichalcogenides, etc. [2, 3] . Of these, the rise of interest on newly discovered 2D transition metal carbides and/or carbonitrides (called MXenes) have recently shown their potential as sensing materials with their intriguing surface chemistry [4]. The first MXene material introducing in chemiresistive sensor is titanium carbide (Ti 3 C 2 T x ). Gas sensing capabilities of Ti 3 C 2 T x MXene to detect various gases were demonstrated with their sensing mechanism [5], and now, further enhancement of its sensing performance is actively studied in many academic domains. Beginning with Ti 3 C 2 T x , vast diversity in a combination of constituent elements and ordered structure in MXenes offers future possibilities to find out a new generation of sensing materials with their superior performance. In this study, 2D V 2 CT x gas sensors were firstly demonstrated in chemiresistive sensing. The sensor device was fabricated with single/few-layer 2D V 2 CT x on polyimide film after the selective etching process. This device measured both polar and non-polar chemical species such as hydrogen and methane at room temperature (23 °C) with an ultra-low limit of detection of 2 ppm and 25 ppm, respectively. 2D V 2 CT x gas sensors showed excellent gas sensing performance in terms of high response toward non-polar gases, which is originated from the surface oxygen functional groups on the surface of V 2 CT x nanoflakes. Compared to the sensing properties of Ti 3 C 2 T x MXene [5], 2D V 2 CT x sensor showed higher selectivity and long-term stability. This comparative result suggests that the modification of ordered structure and constituent elements of MXenes play a pivot role in the interaction between analyte and MXenes leading to an extensive change in performance. References [1] Barzegar, Maryam, and Bharati Tudu. "Two-dimensional materials for gas sensors: from first discovery to future possibilities." Surface Innovations 6.4–5 (2018): 205-230. [2] Yang, Shengxue, Chengbao Jiang, and Su-huai Wei. "Gas sensing in 2D materials." Applied Physics Reviews 4.2 (2017): 021304. [3] Lee, Eunji, et al. "Enhanced Gas-Sensing Performance of GO/TiO2 Composite by Photocatalysis." Sensors 18.10 (2018): 3334. [4] Xiao, Bo, et al. "MXenes: Reusable materials for NH3 sensor or capturer by controlling the charge injection." Sensors and Actuators B: Chemical 235 (2016): 103-109. [5] Lee, Eunji, et al. "Room temperature gas sensing of two-dimensional titanium carbide (MXene)." ACS applied materials & interfaces 9.42 (2017): 37184-37190. Acknowledgement This research was partially supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP), grant funded by the Korea Government Ministry of Trade, Industry and Energy (20158520000210), and Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD).
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 7
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    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-01, No. 44 ( 2019-05-01), p. 2075-2075
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-01, No. 44 ( 2019-05-01), p. 2075-2075
    Abstract: By virtue of the technology in ubiquitous computing and smart textile, gas sensor with wearability has been developed to play an imperative role in improving future healthcare. [1] The sensor revolution can significantly impact on outpatient care and management of chronical diseases by offering real-time condition monitoring. The combination of many technology is on the verge of producing this dramatic advance, and the significance placed on the development of sensor performance. [2] Recently, two-dimensional (2D) nanostructured materials have been regarded as instrumental sensing materials due to their working ability at low temperature. One attractive approach to enhance performance of 2D materials-based sensor is to hybridize with metal oxide. By grafting two nanostructured materials, sensing performance can be highly advanced by hybridization effects. [3] Another innovative strategy is to adapt newly discovered 2D materials. 2D transition metal carbides and/or carbonitrides (called MXenes) have recently shown excellent properties particularly in energy storage, and water purification applications. [4] Boundless combination of constituent elements and ordered structure in MXenes provides many opportunities to tailor its properties for different applications. In this study, 2D nanostructured nanomaterials and their hybrids were explored to develop wearable chemical sensor for precise health monitoring systems. Graphene oxide (GO) and molybdenum disulfide (MoS 2 ) were studied to understand the effect of surface dangling bonds on gas sensing properties. To enhance sensing performance, 2D nanomaterials was combined with metal oxides. The gas sensing performance of the GO/TiO 2 hybrid was improved by decorating titanium dioxide (TiO 2 ). [5] After photo-reduction, the gas sensing behavior was converted from n-type to p-type with extended long-term stability. Moreover, 2D MXene was introduced as a promising room-temperature sensing material with their intriguing surface chemistry. The capability of titanium carbide (Ti 3 C 2 T x ) to sense an array of VOC gases was demonstrated, and its possible sensing mechanism was proposed in terms of the interaction between sensing species and the oxygen terminated surface of MXene. Another MXene material, vanadium carbide (V 2 CT x ), was also investigated. 2D V 2 CT x gas sensors showed outstanding gas sensing performance including high sensitivity toward non-polar gases such as hydrogen and methane. Transformation of ordered structure and constituent elements of MXenes largely influenced on interaction between analyte and MXenes showing outstanding selectivity and limit of detection to non-polar gases. References Gravina, Raffaele, et al. "Multi-sensor fusion in body sensor networks: State-of-the-art and research challenges." Information Fusion 35 (2017): 68-80. Yao, Shanshan, Puchakayala Swetha, and Yong Zhu. "Nanomaterial‐Enabled Wearable Sensors for Healthcare." Advanced healthcare materials 7.1 (2018): 1700889. Chatterjee, Shyamasree Gupta, et al. "Graphene–metal oxide nanohybrids for toxic gas sensor: a review." Sensors and Actuators B: Chemical 221 (2015): 1170-1181. Anasori, Babak, Maria R. Lukatskaya, and Yury Gogotsi. "2D metal carbides and nitrides (MXenes) for energy storage." Nature Reviews Materials 2 (2017): 16098. Lee, Eunji, et al. "Enhanced Gas-Sensing Performance of GO/TiO2 Composite by Photocatalysis." Sensors 18.10 (2018): 3334. Acknowledgement This research was partially supported by the Korea Institute of Energy Technology Evaluation and Planning (KETEP), grant funded by the Korea Government Ministry of Trade, Industry and Energy (20158520000210), and Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD).
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 8
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    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-02, No. 51 ( 2019-09-01), p. 2227-2227
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-02, No. 51 ( 2019-09-01), p. 2227-2227
    Abstract: Urea in the urine, protein metabolism, is present in the final product of human. The level of urea is a crucial biomarker that can assess the metabolic activity of humans such as the liver and renal function. [1] A high level of urea in the urine can result in kidney failure, dehydration, and gastrointestinal bleeding, while a low level can lead to nephritic syndrome, hepatic failure, etc. [2] Therefore, accurate and rapid sensing of urea is essential in a diagnostic clinic. Recently, paper-based analytical devices (PAD) are gaining its popularity as a manageable device for point-of-care equipment due to its inexpensive, portable, disposable, and environmentally-friendly qualities.[3] The majority of electrochemical biosensors rely on enzymes, such as urease; yet, utilization of enzyme is limited due to its high cost, poor reproducibility, and most of all, thermal and chemical instability which can influence the duration of sensor that depends on storage conditions such as temperature, pH, and humidity.[4] In addition, non-enzymatic biosensors has been attracted with the advantage of simplicity, redox flexibility, stability, and low cost. As a non-enzymatic metal-based material, Ni-based nanomaterials exhibited excellent catalytic activity over urea originated from catalytic effect for the formation of the redox couple of Ni(II) and Ni(III) on the surface. [5] When compared to enzymatic-based sensors, non-enzymatic catalysts tend to present lower sensitivity and higher limit of detection corresponding to lower performances of urea biosensor. To address this limit, there have been efforts to modify nanostructures with various shapes such as nanofiber, nanoparticle, and nanoflake arrays. Here we investigated a hollow sphere structure with nanosheet building block by using a hydrothermal method. The hollow sphere structure can increase the selectivity and sensitivity for urea biosensor by providing facile transport channels through electrolyte that exploits its inner and outer surfaces as the active site with maintaining the structural stability of the catalyst. Integration of non-enzymatic hierarchical catalyst on disposable PAD will lead to a high potential for the development of point-of-care testing devices. In this study, a non-enzymatic electrochemical paper-based sensor using hollow structure NiO was developed and demonstrated for the determination of urea. PADs were fabricated by sputtering on cotton paper, and hollow NiO was synthesized by hydrothermal method. Structure and morphologies of hierarchical NiO on PAD were characterized by XRD and SEM. Electrochemical properties such as selectivity and LOD were conducted by using a potentiostat with urea solution. A detailed description of the fabrication process and discussion of structure formation and sensing performances of hollow nickel oxide catalyst will be presented. References [1] Boggs, Bryan K., Rebecca L. King, and Gerardine G. Botte. "Urea electrolysis: direct hydrogen production from urine." Chemical Communications 32 (2009): 4859-4861. [2] Srivastava, Saurabh, et al. "A self assembled monolayer based microfluidic sensor for urea detection." Nanoscale 3.7 (2011): 2971-2977. [3] Martinez, Andres W., et al. "Patterned paper as a platform for inexpensive, low‐volume, portable bioassays." Angewandte Chemie International Edition 46.8 (2007): 1318-1320. [4] Riklin, Azalla, et al. "Improving enzyme–electrode contacts by redox modification of cofactors." Nature 376.6542 (1995): 672. [5] Nie, Huagui, et al. "Nonenzymatic electrochemical detection of glucose using well-distributed nickel nanoparticles on straight multi-walled carbon nanotubes." Biosensors and Bioelectronics 30.1 (2011): 28-34. Acknowledgement This work was partially supported by Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD), and the Ocean University of China-Auburn University (OUC-AU) Grants program.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
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  • 9
    In: ECS Transactions, The Electrochemical Society, Vol. 77, No. 11 ( 2017-07-07), p. 1711-1717
    Type of Medium: Online Resource
    ISSN: 1938-6737 , 1938-5862
    Language: English
    Publisher: The Electrochemical Society
    Publication Date: 2017
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  • 10
    Online Resource
    Online Resource
    The Electrochemical Society ; 2019
    In:  ECS Meeting Abstracts Vol. MA2019-01, No. 42 ( 2019-05-01), p. 2047-2047
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2019-01, No. 42 ( 2019-05-01), p. 2047-2047
    Abstract: The utilization of urea has attracted more attention due to its various applications such as fuel cell, hydrogen production, wastewater remediation, and electrochemical sensors. [1] Especially, urea is a crucial biomarker to detect various human metabolic disorders such as renal function and liver disease. Therefore, the measurement of the urea level plays an important role in monitoring metabolic activity of human. Electrochemical sensing method is considered one of the most promising technique for urea detection due to its simplicity and reliable sensing. [2] The enzyme-based catalyst is widely used for urea oxidation. However, the enzyme has the stability issue due to the denaturing of the enzyme. Hence, non-enzymatic biosensors by metal-based catalysts have been studied. Compared with noble metal catalysts, nickel-based catalysts are inexpensive and abundant. Furthermore, bimetallic nickel-based oxides (nickel cobalt oxide [3], nickel molybdenum oxide [4] , and nickel manganese oxide [5]) have been developed for efficient urea oxidation reaction in alkaline medium. Despite many efforts to achieve higher catalytic effect with bimetallic oxides, the improvement of catalytic property of urea oxidation is still challenging due to the low exposure of active sites and low electrical conductivity The hollow structured catalyst can improve the performance of urea detection by providing structural stability of catalyst and facile transport channels for electrolyte with exploiting its inner and outer surface as active sites. With introducing the template-free hydrothermal method with SDBS, Ni-Mn-based oxide is synthesized. Due to the synergetic catalytic effect between NiO and MnO and morphological effect of hollow structure, higher oxidation current and lower onset potential could be achieved. In this study, nickel manganese oxide catalyst with the variation of Ni:Mn atomic ratios were synthesized by one-pot template-free hydrothermal method. Structure and morphologies of synthesized nickel and manganese oxide hollow structure were characterized by XRD and SEM. And the atomic ratio of nickel manganese oxide was confirmed by EDS. CV measurement was conducted in a three-compartment cell with a potentiostat 1M KOH with 0.33M urea. CA measurement was also performed to measure the selectivity and limit of detection. Detailed mechanism and discussion of the formation of structure and sensing properties of nickel manganese oxide catalyst will be presented. References [1] Boggs, Bryan K., Rebecca L. King, and Gerardine G. Botte. "Urea electrolysis: direct hydrogen production from urine." Chem. Commun 32 (2009): 4859-4861. [2] Das, Gautam, and Hyon Hee Yoon. "Polyaniline/carbon nanofiber and organic charge transfer complex based composite electrode for electroanalytical urea detection." Jpn. J. Appl. Phys 54.6S1 (2015): 06FK01. [3] Guo, Fen, et al. "Preparation of nickel-cobalt nanowire arrays anode electro-catalyst and its application in direct urea/hydrogen peroxide fuel cell." Electrochimica Acta 199 (2016): 290-296. [4] Liang, Yanhui, et al. "Enhanced electrooxidation of urea using NiMoO4· xH2O nanosheet arrays on Ni foam as anode." Electrochimica Acta 153 (2015): 456-460. [5] Periyasamy, Sivakumar, et al. "Exceptionally active and stable spinel nickel manganese oxide electrocatalysts for urea oxidation reaction." ACS applied materials & interfaces 8.19 (2016): 12176-12185. Acknowledgement This work was partially supported by Agency for Defense Development (ADD) as global cooperative research for high performance and light weight bio-urine based fuel cell (UD160050BD), and the Ocean University of China-Auburn University (OUC-AU) Grants program.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2019
    detail.hit.zdb_id: 2438749-6
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