pp. 1-228 (April 2023)
pp. 1-200 (March 2023)
pp. 1-138 (February 2023)
pp. 1-144 (January 2023)
pp. 1-108 (December 2022)
pp. 1-106 (November 2022)
pp. 1-122 (October 2022)
pp. 1-124 (September 2022)
pp. 1-102 (August 2022)
pp. 1-112 (July 2022)
pp. 1-138 (June 2022)
pp. 1-186 (May 2022)
pp. 1-124 (April 2022)
pp. 1-104 (March 2022)
pp. 1-120 (February 2022)
pp. 1-124 (January 2022)
pp. 1-214 (June 2021)
pp. 1-90 (December 2021)
pp. 1-222 (April 2021)
pp. 1-324 (October 2021)
pp. 1-200 (February 2021)
pp. 1-222 (August 2021)
pp. 1-208 (December 2020)
pp. 1-112 (October 2020)
pp. 1-210 (August 2020)
pp. 1-204 (June 2020)
pp. 1-218 (April 2020)
pp. 1-182 (February 2020)
pp. 1-104 (December 2019)
pp. 1-116 (October 2019)
pp. 1-130 (August 2019)
pp. 1-224 (June 2019)
pp. 1-226 (April 2019)
pp. 1-216 (February 2019)
pp. 1-132 (December 2018)
pp. 1-182 (October 2018)
pp. 1-116 (August 2018)
pp. 1-228 (June 2018)
pp. 1-154 (April 2018)
pp. 1-198 (February 2018)
pp. 1-118 (December 2017)
pp. 1-162 (October 2017)
pp. 1-138 (August 2017)
pp. 1-190 (June 2017)
pp. 1-220 (April 2017)
pp. 1-164 (February 2017)
pp. 1-176 (December 2016)
pp. 1-138 (October 2016)
pp. 1-144 (August 2016)
pp. 1-122 (June 2016)
pp. 1-166 (April 2016)
pp. 1-222 (February 2016)
pp. 1-118 (December 2015)
pp. 1-194 (October 2015)
pp. 1-212 (August 2015)
pp. 1-150 (June 2015)
pp. 1-184 (April 2015)
pp. 1-200 (February 2015)
pp. 1-172 (December 2014)
pp. 1-230 (October 2014)
pp. 1-178 (August 2014)
pp. 1-138 (June 2014)
pp. 1-150 (April 2014)
pp. 1-122 (February 2014)
pp. 619-792 (December 2013)
pp. 475-618 (October 2013)
pp. 359-474 (August 2013)
pp. 249-358 (June 2013)
pp. 119-248 (April 2013)
pp. 1-118 (February 2013)
pp. 649-788 (December 2012)
pp. 523-647 (October 2012)
pp. 397-522 (August 2012)
pp. 255-396 (June 2012)
pp. 145-253 (April 2012)
pp. 1-143 (February 2012)
pp. 545-662 (December 2011)
pp. 451-544 (October 2011)
pp. 319-450 (August 2011)
pp. 193-317 (June 2011)
pp. 101-191 (April 2011)
pp. 1-99 (February 2011)
pp. 491-644 (December 2010)
pp. 399-489 (October 2010)
pp. 301-397 (August 2010)
pp. 187-299 (June 2010)
pp. 81-185 (April 2010)
pp. 1-80 (February 2010)
pp. 421-512 (December 2009)
pp. 337-419 (October 2009)
pp. 231-335 (August 2009)
pp. 161-229 (June 2009)
pp. 93-160 (April 2009)
pp. 1-91 (February 2009)
pp. 389-583 (December 2008)
pp. 289-388 (October 2008)
pp. 225-288 (August 2008)
pp. 131-222 (June 2008)
pp. 59-129 (April 2008)
pp. 1-58 (February 2008)
pp. 363-428 (December 2007)
pp. 305-361 (October 2007)
pp. 247-304 (August 2007)
pp. 193-246 (June 2007)
pp. 1-191 (April 2007)
pp. 259-361 (December 2006)
pp. 211-258 (October 2006)
pp. 103-210 (July 2006)
pp. 47-102 (April 2006)
pp. 1-46 (February 2006)
pp. 289-404 (December 2005)
pp. 243-288 (October 2005)
pp. 197-242 (August 2005)
pp. 151-196 (June 2005)
pp. 1-150 (April 2005)
pp. 235-280 (December 2004)
pp. 189-234 (October 2004)
pp. 139-188 (August 2004)
pp. 93-138 (June 2004)
pp. 47-92 (April 2004)
pp. 1-46 (February 2004)
pp. 231-276 (December 2003)
pp. 185-230 (October 2003)
pp. 139-183 (September 2003)
pp. 93-138 (July 2003)
pp. 47-92 (June 2003)
pp. 1-46 (April 2003)
Partic. vol. 15 pp. 45-50 (August 2014) doi: 10.1016/j.partic.2012.12.007
Effect of thermal treatment on structural change of anode electrocatalysts for direct methanol fuel cells
Mingjia Han, Jianhuang Zeng*, Jianwei Xia, Shijun Liao
Highlights
Abstract
Commercially available carbon-supported Pt, PtCo and PtRu catalysts from E-TEK are heat-treated in turn at 600 °C and 800 °C each for an hour. The as-received and as-heated catalysts are used as anode catalysts for direct methanol fuel cells. Structural and surface composition changes induced by heating are analyzed by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS), respectively. For the Pt catalyst, heating the catalysts caused only the mass activity decrease due to particle sintering, whereas the specific activity and CO tolerance remained unchanged. The performance of the PtCo and PtRu catalysts is affected differently by heating. Heating the PtRu catalyst adversely affects its catalytic activity and its CO tolerance due to Pt depletion at the surface. In contrast, although Pt depletion also takes place for the heated PtCo catalysts, these catalysts show an even higher specific activity and approximately the same CO tolerance. The observed difference is likely due to the optimum atomic ratio difference for Ru/Pt and Co/Pt; an increased atomic ratio on the surface for Co/Pt results in an activity enhancement, which is contrary to the effect of the increase of Ru/Pt atomic ratio.
Graphical abstract
Keywords
Structural changes; Methanol electrooxidation; CO tolerance; Pt depletion