Fabrication of Hierarchically Porous Silicon Carbonitride/Nickel Nanocomposite Using Branch-Structured Polysilazane as a Hydrogen Evolution Reaction Catalyst

被引:0
|
作者
Huh, Tae-Hwan [1 ]
Jun, Jong Han [2 ]
Lee, Ji-Hoon [3 ]
Moon, Sunung [4 ]
Yoon, Yeosol [5 ]
Lim, Taeho [5 ]
Kim, Byung Hyo [1 ,4 ]
Kwark, Young-Je [1 ,4 ]
机构
[1] Soongsil Univ, Dept Mat Sci & Engn, Seoul 06978, South Korea
[2] Seoul Natl Univ, Dept Mat Sci & Engn, Seoul 08826, South Korea
[3] Univ Seoul, Dept Mat Sci & Engn, Seoul 02504, South Korea
[4] Soongsil Univ, Dept Green Chem & Mat Engn, Seoul 06978, South Korea
[5] Soongsil Univ, Dept Chem Engn, Seoul 06978, South Korea
来源
ACS APPLIED ENERGY MATERIALS | 2024年 / 7卷 / 22期
基金
新加坡国家研究基金会;
关键词
polysilazane; porous ceramic; nanocomposites; nickel; HER; electrocatalyst; IL-TEM; CERAMIC STRUCTURES; SICN CERAMICS; CARBON; NICKEL; ELECTROCATALYSTS; COMPOSITES; PYROLYSIS;
D O I
10.1021/acsaem.4c01884
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hierarchically porous silicon carbonitride/nickel (SiCN/Ni) nanocomposites for a catalyst of the hydrogen evolution reaction (HER) were fabricated using branch-structured polysilazane with phenyl substitution, phenylsilsesquiazane (PSSQZ), and nickelocene (NiCp2) as a precursor. The Ni nanoparticles are uniformly distributed in the SiCN matrix due to coordination between amine groups of PSSQZ and NiCp2. Hierarchical pore structure provided a path through which H2 outgas can diffuse as well as increase active sites where HER can occur due to its large surface area. As a result, the overpotential of 10 mA/cm2 of the hierarchically porous SiCN/Ni nanocomposite decreased from 540 to 390 mV. In addition, the multiwalled carbon nanotubes (MWCNTs) produced by the catalytic reaction of NiCp2 lowered the charge transfer resistance to 133 Omega. Furthermore, the fabricated hierarchically porous SiCN/Ni nanocomposite showed stable performance and long-term durability in acidic environments for 100 h because of the high corrosion resistance of the SiCN matrix.
引用
收藏
页码:10397 / 10406
页数:10
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