TY - JOUR
T1 - Charge partitioning by intertwined metal-oxide nano-architectural networks for the photocatalytic dry reforming of methane
AU - Shoji, Shusaku
AU - Bin Mohd Najib, Abdillah Sani
AU - Yu, Min Wen
AU - Yamamoto, Tomokazu
AU - Yasuhara, Sou
AU - Yamaguchi, Akira
AU - Peng, Xiaobo
AU - Matsumura, Syo
AU - Ishii, Satoshi
AU - Cho, Yohei
AU - Fujita, Takeshi
AU - Ueda, Shigenori
AU - Chen, Kuo Ping
AU - Abe, Hideki
AU - Miyauchi, Masahiro
N1 - Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2022/2/17
Y1 - 2022/2/17
N2 - The photocatalytic dry reforming of methane (photoDRM: CH4 + CO2 = 2CO + 2H2) converts greenhouse gases into valuable synthesis gas with photon energy. However, previous photoDRM catalysts comprising supported metal nanoparticles hardly avoid the recombination of photoexcited charges. Herein, we report that significant photoDRM performance can be achieved by a metal-oxide nanocomposite consisting of nanometer-thick, intertwined networks of fibrous rhodium metal and cerium dioxide, i.e., Rh#CeO2. The Rh#CeO2 nanocomposite exhibits the world-highest conversion and yield in photoDRM under UV light irradiation, being accompanied with no other side reactions such as reverse water gas shift reaction. Theoretical simulations and Kelvin probe force microscopy demonstrate that the photoexcited electrons and holes in Rh#CeO2 are efficiently partitioned into the Rh- and CeO2 nanophases, respectively. The efficient charge partitioning in Rh#CeO2 accounts for the selective photoDRM reaction.
AB - The photocatalytic dry reforming of methane (photoDRM: CH4 + CO2 = 2CO + 2H2) converts greenhouse gases into valuable synthesis gas with photon energy. However, previous photoDRM catalysts comprising supported metal nanoparticles hardly avoid the recombination of photoexcited charges. Herein, we report that significant photoDRM performance can be achieved by a metal-oxide nanocomposite consisting of nanometer-thick, intertwined networks of fibrous rhodium metal and cerium dioxide, i.e., Rh#CeO2. The Rh#CeO2 nanocomposite exhibits the world-highest conversion and yield in photoDRM under UV light irradiation, being accompanied with no other side reactions such as reverse water gas shift reaction. Theoretical simulations and Kelvin probe force microscopy demonstrate that the photoexcited electrons and holes in Rh#CeO2 are efficiently partitioned into the Rh- and CeO2 nanophases, respectively. The efficient charge partitioning in Rh#CeO2 accounts for the selective photoDRM reaction.
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U2 - 10.1016/j.checat.2021.11.015
DO - 10.1016/j.checat.2021.11.015
M3 - Article
AN - SCOPUS:85126077889
SN - 2667-1107
VL - 2
SP - 321
EP - 329
JO - Chem Catalysis
JF - Chem Catalysis
IS - 2
ER -