TY - JOUR
T1 - Active site localization of methane oxidation on Pt nanocrystals
AU - Kim, Dongjin
AU - Chung, Myungwoo
AU - Carnis, Jerome
AU - Kim, Sungwon
AU - Yun, Kyuseok
AU - Kang, Jinback
AU - Cha, Wonsuk
AU - Cherukara, Mathew J.
AU - Maxey, Evan
AU - Harder, Ross
AU - Sasikumar, Kiran
AU - K. R. S. Sankaranarayanan, Subramanian
AU - Zozulya, Alexey
AU - Sprung, Michael
AU - Riu, Dohhyung
AU - Kim, Hyunjung
N1 - Publisher Copyright:
© 2018, The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - High catalytic efficiency in metal nanocatalysts is attributed to large surface area to volume ratios and an abundance of under-coordinated atoms that can decrease kinetic barriers. Although overall shape or size changes of nanocatalysts have been observed as a result of catalytic processes, structural changes at low-coordination sites such as edges, remain poorly understood. Here, we report high-lattice distortion at edges of Pt nanocrystals during heterogeneous catalytic methane oxidation based on in situ 3D Bragg coherent X-ray diffraction imaging. We directly observe contraction at edges owing to adsorption of oxygen. This strain increases during methane oxidation and it returns to the original state after completing the reaction process. The results are in good agreement with finite element models that incorporate forces, as determined by reactive molecular dynamics simulations. Reaction mechanisms obtained from in situ strain imaging thus provide important insights for improving catalysts and designing future nanostructured catalytic materials.
AB - High catalytic efficiency in metal nanocatalysts is attributed to large surface area to volume ratios and an abundance of under-coordinated atoms that can decrease kinetic barriers. Although overall shape or size changes of nanocatalysts have been observed as a result of catalytic processes, structural changes at low-coordination sites such as edges, remain poorly understood. Here, we report high-lattice distortion at edges of Pt nanocrystals during heterogeneous catalytic methane oxidation based on in situ 3D Bragg coherent X-ray diffraction imaging. We directly observe contraction at edges owing to adsorption of oxygen. This strain increases during methane oxidation and it returns to the original state after completing the reaction process. The results are in good agreement with finite element models that incorporate forces, as determined by reactive molecular dynamics simulations. Reaction mechanisms obtained from in situ strain imaging thus provide important insights for improving catalysts and designing future nanostructured catalytic materials.
UR - http://www.scopus.com/inward/record.url?scp=85052213805&partnerID=8YFLogxK
U2 - 10.1038/s41467-018-05464-2
DO - 10.1038/s41467-018-05464-2
M3 - Article
C2 - 30143615
AN - SCOPUS:85052213805
SN - 2041-1723
VL - 9
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 3422
ER -