纳米材料基催化剂
催化作用
烧结
氨
材料科学
纳米颗粒
化学工程
开裂
分解
多孔性
氢
制氢
氨生产
无机化学
纳米技术
化学
复合材料
有机化学
工程类
作者
Seok‐Jin Kim,Thien S. Nguyen,Javeed Mahmood,Cafer T. Yavuz
标识
DOI:10.1016/j.cej.2023.142474
摘要
Catalytic ammonia decomposition enables ammonia to be a hydrogen gas carrier for a carbon-free fuel economy. The challenge is to obtain high conversion yields and rates at low temperatures for a prolonged time. A promising approach is to engineer a catalyst support to minimize deleterious effects like sintering. Here, we compared a conventional 2D planar porous framework support with a vertically standing 2D structure to ascertain the effects of support geometry on the catalytic performance. The catalysts were made by loading ruthenium (Ru) nanoparticles onto the structures, and the catalytic activities were monitored by varying the ammonia (NH3) feeding rate and reaction temperature. Unlike the planar version, the vertically standing 2D support prevented nanoparticle aggregation, retained the original nanoparticle size, and showed an excellent hydrogen production rate (95.17 mmol gRu−1 min−1) at a high flow rate of 32,000 mL gcat−1 h−1 at a temperature of 450 °C.
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