Pd Atomic Engineering of Nanoporous Ni/NiO for Efficient Nitrophenol Hydrogenation Reaction

被引:16
作者
Wei, Fanghui [1 ]
Luo, Min [2 ]
Lan, Jiao [1 ]
Xie, Feng [1 ]
Cai, Lebin [1 ]
Chan, Ting-Shan [3 ]
Peng, Ming [1 ,4 ]
Tan, Yongwen [1 ]
机构
[1] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China
[2] Shanghai Tech Inst Elect & Informat, Shanghai 201411, Peoples R China
[3] Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
[4] 12568 Hunan Univ, Greater Bay Area Inst Innovat, Guangzhou 511300, Guangdong, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
nanoporous Ni; NiO; Pd; atomic engineering; nitrophenol hydrogenation reaction; energy conversion; SINGLE-ATOM; REDUCTION; 4-NITROPHENOL; BOOST;
D O I
10.1021/acsami.3c03491
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The catalytic hydrogenation of nitrophenols is widelyutilizedfor both industrial synthesis and environmental protection, thus efficientand cost-effective catalysts are in urgent need. Still, the cost andscarcity of the materials still inhibit their application and theactive sites are not well specified, especially in the complex catalysts.Herein, we developed an atomic Pd-doped nanoporous Ni/NiO (Pd-1@np-Ni/NiO) catalyst via facial dealloying for efficient nitrophenolhydrogenation reaction under mild conditions. Pd-1@np-Ni/NiOachieves an excellent specific activity (1301 min(-1) mg(Pd) (-1), 35.2 times that of commercialPd/C), nearly 100% selectivity, and continuous reproducibility. Thecatalytic performance is highly relevant to the Ni sites on the catalystsregarding the exposure sites and the intrinsic property. The metal/metaloxide interfacial structure could cooperatively accelerate the catalyticreaction kinetics. The atomic dopants could effectively modulate theelectronic structure, facilitate the absorption of molecules, andreduce the energy barrier of catalytic hydrogenation reaction. Basedon the efficient catalyst, the protype nitrophenol//NaBH4 battery is designed for efficient material conversion and poweroutput, which is very attractive for green energy systems.
引用
收藏
页码:26746 / 26754
页数:9
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