催化作用
选择性
镍
无机化学
碳纤维
热解
纳米颗粒
覆盖层
材料科学
化学工程
甲烷
化学
有机化学
纳米技术
物理化学
冶金
复合数
工程类
复合材料
作者
Bruno Henrique Arpini,Adriano Henrique Braga,Laís Reis Borges,Pedro Vidinha,Renato V. Gonçalves,János Szanyi,Liane Marcia Rossi
标识
DOI:10.1021/acssuschemeng.1c05847
摘要
Controlling the selectivity of CO 2 hydrogenation is a challenge for the application of earth-abundant-based metal catalysts. Herein, we show that a high-temperature pyrolysis protocol can be applied to prepare a nickel catalyst embedded in N-doped carbon (Ni@NC), which provides an enhanced selectivity to CO in the nickel-catalyzed CO 2 hydrogenation reaction under atmospheric pressure. The nitrogen-containing carbon overlayer was obtained through controlled pyrolysis of the nickel–1,10-phenanthroline complex impregnated on SiO 2 . The Ni@NC/SiO 2 catalyst is more selective for CO, following the reverse water-gas shift reaction pathway, while an analogous “naked” Ni catalyst was more selective toward CH 4, following the CO 2 /CO complete hydrogenation pathway. Although the Ni@NC/SiO 2 catalyst has larger particle sizes than the naked Ni/SiO 2 catalyst, the binding strength of CO to the Ni@NC surface is significantly weaker. Consequently, the CO intermediate easily desorbs instead of being converted into methane. Hence, selectivity toward CO, which is an important intermediate to methanol and C 2+ products, or CH 4 can be modulated by a simple modification of the Ni surface through controlled carbon deposition.
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