TY - JOUR
T1 - Multi-Scale Engineered 2D Carbon Polyhedron Array with Enhanced Electrocatalytic Performance
AU - Song, Xiaokai
AU - Song, Yujie
AU - Li, Xiaopeng
AU - Wu, Xiaotong
AU - Wang, Zequn
AU - Sun, Xuhui
AU - An, Meng
AU - Wei, Xiaoqian
AU - Zhao, Yingji
AU - Wei, Jiamin
AU - Bi, Chenglu
AU - Sun, Jianhua
AU - Nara, Hiroki
AU - You, Jungmok
AU - Yamauchi, Yusuke
N1 - Publisher Copyright:
© 2023 The Authors. Small published by Wiley-VCH GmbH.
PY - 2024/3/15
Y1 - 2024/3/15
N2 - Electrocatalyst engineering from the atomic to macroscopic level of electrocatalysts is one of the most powerful routes to boost the performance of electrochemical devices. However, multi-scale structure engineering mainly focuses on the range of atomic-to-particle scale such as hierarchical porosity engineering, while catalyst engineering at the macroscopic level, such as the arrangement configuration of nanoparticles, is often overlooked. Here, a 2D carbon polyhedron array with a multi-scale engineered structure via facile chemical etching, ice-templating induced self-assembly, and high-temperature pyrolysis processes is reported. Controlled phytic acid etching of the carbon precursor introduces homogeneous atomic phosphorous and nitrogen doping, as well as a well-defined mesoporous structure. Subsequent ice-templated self-assembly triggers the formation of a 2D particle array superstructure. The atomic-level doping gives rise to high intrinsic activity, while the well-engineered porous structure and particle arrangement addresses the mass transport limitations at the microscopic particle level and macroscopic electrode level. As a result, the as-prepared electrocatalyst delivers outstanding performance toward oxygen reduction reaction in both acidic and alkaline media, which is better than recently reported state-of-the-art metal-free electrocatalysts. Molecular dynamics simulation together with extensive characterizations indicate that the performance enhancement originates from multi-scale structural synergy.
AB - Electrocatalyst engineering from the atomic to macroscopic level of electrocatalysts is one of the most powerful routes to boost the performance of electrochemical devices. However, multi-scale structure engineering mainly focuses on the range of atomic-to-particle scale such as hierarchical porosity engineering, while catalyst engineering at the macroscopic level, such as the arrangement configuration of nanoparticles, is often overlooked. Here, a 2D carbon polyhedron array with a multi-scale engineered structure via facile chemical etching, ice-templating induced self-assembly, and high-temperature pyrolysis processes is reported. Controlled phytic acid etching of the carbon precursor introduces homogeneous atomic phosphorous and nitrogen doping, as well as a well-defined mesoporous structure. Subsequent ice-templated self-assembly triggers the formation of a 2D particle array superstructure. The atomic-level doping gives rise to high intrinsic activity, while the well-engineered porous structure and particle arrangement addresses the mass transport limitations at the microscopic particle level and macroscopic electrode level. As a result, the as-prepared electrocatalyst delivers outstanding performance toward oxygen reduction reaction in both acidic and alkaline media, which is better than recently reported state-of-the-art metal-free electrocatalysts. Molecular dynamics simulation together with extensive characterizations indicate that the performance enhancement originates from multi-scale structural synergy.
KW - carbon polyhedron array
KW - catalyst engineering
KW - intrinsic activity
KW - mass transfer
KW - oxygen reduction reaction
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U2 - 10.1002/smll.202305459
DO - 10.1002/smll.202305459
M3 - Article
C2 - 37922532
AN - SCOPUS:85175526888
SN - 1613-6810
VL - 20
JO - Small
JF - Small
IS - 11
M1 - 2305459
ER -