TY - JOUR
T1 - Morphological control of carbon-supported Pt-based nanoparticles via one-step synthesis
AU - Nakamoto, Tatsuichiro
AU - Seki, Ryohei
AU - Motomiya, Ken ichi
AU - Yokoyama, Shun
AU - Tohji, Kazuyuki
AU - Takahashi, Hideyuki
N1 - Funding Information:
This work was partially supported by JSPS KAKENHI Grant Number JP18H03416 .
Publisher Copyright:
© 2020
PY - 2020/4
Y1 - 2020/4
N2 - The morphology of Pt-based nanoparticles supported on carbon is controlled to enhance the oxygen reduction reaction (ORR) catalytic performance. Herein a simple one-step method without a polymer surfactant is demonstrated to synthesize Pt-Cu nanoclusters, Pt-Cu nanospheres, and Cu-doped Pt nanoplates. Metal precursors are reduced by sodium tetrahydroborate in a NaCl or NH4Cl aqueous solution containing carbon supports, and nanoparticles are directly deposited on carbon. Cl− ions generated from NaCl or NH4Cl delay the reduction of metal ions when O2 is dissolved in the synthesis solution, leading to larger particles. In addition, NH4 + ions guide the growth direction of Pt to form a plate-like morphology that exposes the {111} facets. However, stable amine complex lowers the Cu content in the nanoplates. Nanoclusters and nanospheres are obtained in the absence of Cl−/O2 and NH4 +, respectively. Half-cell measurements are performed in acidic media to evaluate the electrochemical properties. Cu-doped Pt nanoplates exhibit a 3.67-times higher ORR catalytic activity than the commercial Pt catalysts thanks to the synergistic effect with a small amount of Cu and selective exposure of the {111} facets. The result suggests that transition metals in Pt-based electrocatalysts may be unnecessary to form intermetallic alloyed crystals for the enhanced ORR performance.
AB - The morphology of Pt-based nanoparticles supported on carbon is controlled to enhance the oxygen reduction reaction (ORR) catalytic performance. Herein a simple one-step method without a polymer surfactant is demonstrated to synthesize Pt-Cu nanoclusters, Pt-Cu nanospheres, and Cu-doped Pt nanoplates. Metal precursors are reduced by sodium tetrahydroborate in a NaCl or NH4Cl aqueous solution containing carbon supports, and nanoparticles are directly deposited on carbon. Cl− ions generated from NaCl or NH4Cl delay the reduction of metal ions when O2 is dissolved in the synthesis solution, leading to larger particles. In addition, NH4 + ions guide the growth direction of Pt to form a plate-like morphology that exposes the {111} facets. However, stable amine complex lowers the Cu content in the nanoplates. Nanoclusters and nanospheres are obtained in the absence of Cl−/O2 and NH4 +, respectively. Half-cell measurements are performed in acidic media to evaluate the electrochemical properties. Cu-doped Pt nanoplates exhibit a 3.67-times higher ORR catalytic activity than the commercial Pt catalysts thanks to the synergistic effect with a small amount of Cu and selective exposure of the {111} facets. The result suggests that transition metals in Pt-based electrocatalysts may be unnecessary to form intermetallic alloyed crystals for the enhanced ORR performance.
KW - Carbon-supported nanoparticles
KW - Nanoplates
KW - One-step synthesis
KW - Oxygen reduction reaction
KW - Pt-based electrocatalysts
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U2 - 10.1016/j.nanoso.2020.100443
DO - 10.1016/j.nanoso.2020.100443
M3 - Article
AN - SCOPUS:85082047279
VL - 22
JO - Nano-Structures and Nano-Objects
JF - Nano-Structures and Nano-Objects
SN - 2352-507X
M1 - 100443
ER -