TY - JOUR
T1 - Hetero-nanojunction armored with carbon layer for boosting water oxidation over RuO2 in acid
AU - Shang, Fanfan
AU - He, Huijie
AU - Lin, Yuan
AU - An, Bei
AU - Cai, Hairui
AU - Li, Xiaoqian
AU - Wang, Weitong
AU - Liang, Chao
AU - Yang, Shengchun
AU - Wang, Bin
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/7/9
Y1 - 2024/7/9
N2 - In this work, a high-performance electrocatalyst, (Co3O4|RuO2)@C, was developed for the oxygen evolution reaction (OER) in acid. Despite the low loading of Ru (0.66 wt%) and Co (0.35 wt%), the catalyst exhibited remarkable performance, achieving an overpotential of 202 mV at 10 mA cm−2. Notably, when employed as an anodic catalyst in a proton exchange membrane (PEM) electrolyzer, (Co3O4|RuO2)@C demonstrated exceptional stability, operating continuously for 300, 100, and 100 h at current densities of 10, 50, and 100 mA cm−2, respectively. Experiments and theoretical investigations revealed that the regulated electronic structure of RuO2 by the Co3O4|RuO2 nanojunction, coupled with the carbon coating layer, led to excellent OER performance of (Co3O4|RuO2)@C. The construction of the Co3O4|RuO2 nanojunction triggered the electron transfer from Co3O4 to RuO2, decreasing the energy barrier of *O → *OOH and mitigating the over-oxidation of Ru sites. Furthermore, the carbon layer surrounding the crystalline Co3O4|RuO2 facilitated mass/charge transfer across the electrolyte-catalyst interface and acted as a protective “chain mail” to enhance the durability of (Co3O4|RuO2)@C.
AB - In this work, a high-performance electrocatalyst, (Co3O4|RuO2)@C, was developed for the oxygen evolution reaction (OER) in acid. Despite the low loading of Ru (0.66 wt%) and Co (0.35 wt%), the catalyst exhibited remarkable performance, achieving an overpotential of 202 mV at 10 mA cm−2. Notably, when employed as an anodic catalyst in a proton exchange membrane (PEM) electrolyzer, (Co3O4|RuO2)@C demonstrated exceptional stability, operating continuously for 300, 100, and 100 h at current densities of 10, 50, and 100 mA cm−2, respectively. Experiments and theoretical investigations revealed that the regulated electronic structure of RuO2 by the Co3O4|RuO2 nanojunction, coupled with the carbon coating layer, led to excellent OER performance of (Co3O4|RuO2)@C. The construction of the Co3O4|RuO2 nanojunction triggered the electron transfer from Co3O4 to RuO2, decreasing the energy barrier of *O → *OOH and mitigating the over-oxidation of Ru sites. Furthermore, the carbon layer surrounding the crystalline Co3O4|RuO2 facilitated mass/charge transfer across the electrolyte-catalyst interface and acted as a protective “chain mail” to enhance the durability of (Co3O4|RuO2)@C.
UR - https://www.scopus.com/pages/publications/85198128222
U2 - 10.1039/d4qi00932k
DO - 10.1039/d4qi00932k
M3 - 文章
AN - SCOPUS:85198128222
SN - 2052-1553
VL - 11
SP - 5265
EP - 5272
JO - Inorganic Chemistry Frontiers
JF - Inorganic Chemistry Frontiers
IS - 16
ER -