The investigation of non-noble metal doped mesoporous cobalt oxide catalysts for the water-gas shift reaction

Hyun Suk Na, Chang Il Ahn, Ajay Jha, Kyung Soo Park, Won Jun Jang, Jae Oh Shim, Dae Woon Jeong, Hyun Seog Roh, Jong Wook Bae

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

In this study, we report an investigation of the low temperature water-gas shift (LT-WGS) reaction over a series of non-noble metal doped (Me = Mn, Fe, Co, and Ni) mesoporous Co3O4 catalysts. The effect of metal dopants on the structure and reducibility of the mesoporous Co3O4 oxide was examined using X-ray diffraction (XRD), N2-adsorption/desorption isotherm measurements, and H2-temperature programmed reduction (TPR) measurements. Experimental results revealed that among the Me-doped Co3O4 catalysts, Ni/Co3O4 demonstrated the highest catalytic performance (XCO = 93% with 47% H2 yield at 280 °C). The higher activity of the Ni-doped Co3O4 catalyst was mainly due to its smaller crystallite size (8.6 nm) and strong interaction between Co and Ni, which lead to the higher reducibility of Co3O4 compared to the other metal-doped Co3O4. To further optimize the loading of Ni- over the mesoporous Co3O4, a series of Ni(x%)/Co3O4 catalysts were prepared by varying the Ni-loading in the range of 3 to 15 wt%. Among these catalysts, 5 wt% Ni- was found to be the optimum loading, whereas higher Ni-loaded samples (10 and 15 wt%) showed a decrease in catalytic performance and hydrogen yield during the WGS reaction.

Original languageEnglish
Pages (from-to)52754-52760
Number of pages7
JournalRSC Advances
Volume6
Issue number58
DOIs
Publication statusPublished - 2016 Jan 1

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Water gas shift
Cobalt
Metals
Catalysts
Oxides
Crystallite size
Isotherms
Hydrogen
Desorption
Doping (additives)
cobalt oxide
Adsorption
X ray diffraction
Temperature

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Chemical Engineering(all)

Cite this

Na, H. S., Ahn, C. I., Jha, A., Park, K. S., Jang, W. J., Shim, J. O., ... Bae, J. W. (2016). The investigation of non-noble metal doped mesoporous cobalt oxide catalysts for the water-gas shift reaction. RSC Advances, 6(58), 52754-52760. https://doi.org/10.1039/c6ra11410e
Na, Hyun Suk ; Ahn, Chang Il ; Jha, Ajay ; Park, Kyung Soo ; Jang, Won Jun ; Shim, Jae Oh ; Jeong, Dae Woon ; Roh, Hyun Seog ; Bae, Jong Wook. / The investigation of non-noble metal doped mesoporous cobalt oxide catalysts for the water-gas shift reaction. In: RSC Advances. 2016 ; Vol. 6, No. 58. pp. 52754-52760.
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abstract = "In this study, we report an investigation of the low temperature water-gas shift (LT-WGS) reaction over a series of non-noble metal doped (Me = Mn, Fe, Co, and Ni) mesoporous Co3O4 catalysts. The effect of metal dopants on the structure and reducibility of the mesoporous Co3O4 oxide was examined using X-ray diffraction (XRD), N2-adsorption/desorption isotherm measurements, and H2-temperature programmed reduction (TPR) measurements. Experimental results revealed that among the Me-doped Co3O4 catalysts, Ni/Co3O4 demonstrated the highest catalytic performance (XCO = 93{\%} with 47{\%} H2 yield at 280 °C). The higher activity of the Ni-doped Co3O4 catalyst was mainly due to its smaller crystallite size (8.6 nm) and strong interaction between Co and Ni, which lead to the higher reducibility of Co3O4 compared to the other metal-doped Co3O4. To further optimize the loading of Ni- over the mesoporous Co3O4, a series of Ni(x{\%})/Co3O4 catalysts were prepared by varying the Ni-loading in the range of 3 to 15 wt{\%}. Among these catalysts, 5 wt{\%} Ni- was found to be the optimum loading, whereas higher Ni-loaded samples (10 and 15 wt{\%}) showed a decrease in catalytic performance and hydrogen yield during the WGS reaction.",
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Na, HS, Ahn, CI, Jha, A, Park, KS, Jang, WJ, Shim, JO, Jeong, DW, Roh, HS & Bae, JW 2016, 'The investigation of non-noble metal doped mesoporous cobalt oxide catalysts for the water-gas shift reaction', RSC Advances, vol. 6, no. 58, pp. 52754-52760. https://doi.org/10.1039/c6ra11410e

The investigation of non-noble metal doped mesoporous cobalt oxide catalysts for the water-gas shift reaction. / Na, Hyun Suk; Ahn, Chang Il; Jha, Ajay; Park, Kyung Soo; Jang, Won Jun; Shim, Jae Oh; Jeong, Dae Woon; Roh, Hyun Seog; Bae, Jong Wook.

In: RSC Advances, Vol. 6, No. 58, 01.01.2016, p. 52754-52760.

Research output: Contribution to journalArticle

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T1 - The investigation of non-noble metal doped mesoporous cobalt oxide catalysts for the water-gas shift reaction

AU - Na, Hyun Suk

AU - Ahn, Chang Il

AU - Jha, Ajay

AU - Park, Kyung Soo

AU - Jang, Won Jun

AU - Shim, Jae Oh

AU - Jeong, Dae Woon

AU - Roh, Hyun Seog

AU - Bae, Jong Wook

PY - 2016/1/1

Y1 - 2016/1/1

N2 - In this study, we report an investigation of the low temperature water-gas shift (LT-WGS) reaction over a series of non-noble metal doped (Me = Mn, Fe, Co, and Ni) mesoporous Co3O4 catalysts. The effect of metal dopants on the structure and reducibility of the mesoporous Co3O4 oxide was examined using X-ray diffraction (XRD), N2-adsorption/desorption isotherm measurements, and H2-temperature programmed reduction (TPR) measurements. Experimental results revealed that among the Me-doped Co3O4 catalysts, Ni/Co3O4 demonstrated the highest catalytic performance (XCO = 93% with 47% H2 yield at 280 °C). The higher activity of the Ni-doped Co3O4 catalyst was mainly due to its smaller crystallite size (8.6 nm) and strong interaction between Co and Ni, which lead to the higher reducibility of Co3O4 compared to the other metal-doped Co3O4. To further optimize the loading of Ni- over the mesoporous Co3O4, a series of Ni(x%)/Co3O4 catalysts were prepared by varying the Ni-loading in the range of 3 to 15 wt%. Among these catalysts, 5 wt% Ni- was found to be the optimum loading, whereas higher Ni-loaded samples (10 and 15 wt%) showed a decrease in catalytic performance and hydrogen yield during the WGS reaction.

AB - In this study, we report an investigation of the low temperature water-gas shift (LT-WGS) reaction over a series of non-noble metal doped (Me = Mn, Fe, Co, and Ni) mesoporous Co3O4 catalysts. The effect of metal dopants on the structure and reducibility of the mesoporous Co3O4 oxide was examined using X-ray diffraction (XRD), N2-adsorption/desorption isotherm measurements, and H2-temperature programmed reduction (TPR) measurements. Experimental results revealed that among the Me-doped Co3O4 catalysts, Ni/Co3O4 demonstrated the highest catalytic performance (XCO = 93% with 47% H2 yield at 280 °C). The higher activity of the Ni-doped Co3O4 catalyst was mainly due to its smaller crystallite size (8.6 nm) and strong interaction between Co and Ni, which lead to the higher reducibility of Co3O4 compared to the other metal-doped Co3O4. To further optimize the loading of Ni- over the mesoporous Co3O4, a series of Ni(x%)/Co3O4 catalysts were prepared by varying the Ni-loading in the range of 3 to 15 wt%. Among these catalysts, 5 wt% Ni- was found to be the optimum loading, whereas higher Ni-loaded samples (10 and 15 wt%) showed a decrease in catalytic performance and hydrogen yield during the WGS reaction.

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