蒸汽重整
甲醇
催化作用
接口(物质)
镉
相(物质)
Atom(片上系统)
材料科学
化学工程
化学
计算机科学
冶金
物理化学
制氢
有机化学
嵌入式系统
工程类
水溶液
吉布斯等温线
作者
Shunan Zhang,Haozhi Zhou,Zilong Shao,Baohuan Wei,Zhen Hu,Hao Liang,Ruonan Zhang,Xiaofang Liu,Hu Luo,Lin Xia,Yuhan Sun,Hui Wang
标识
DOI:10.1038/s41467-025-63060-7
摘要
Employing interface engineering to design innovative single-atom catalysts (SACs) for effective methanol steam reforming (MSR) presents an attractive yet formidable challenge. Here, we report phase-interface confined Cd/P25 SACs, where Cd atoms are stably anchored at the phase interface between anatase (101) and rutile (110) facets. The Cd-O-Ti phase interface sites formed exhibit asymmetric geometric and electronic properties that enable 100% methanol conversion, a low CO concentration (~0.1 mol%) in the effluent gas, and sustained stability exceeding 150 h. The H2 production rate at these interface sites is approximately 15-fold and 8-fold higher than that of anatase and rutile surface sites, respectively. Enhancing the phase interface density through atmosphere pretreatment can further increase the H2 production rate by an additional 11%. Furthermore, these powder SACs can be 3D printed into kilogram-scale monolithic catalysts, advancing practical in-situ hydrogen generation applications. Single-atom catalyst design for methanol steam reforming faces stability and activity hurdles. Here, Cd atoms anchored at anatase-rutile phase interfaces achieve exceptional catalytic efficiency, low CO production, and scalable hydrogen generation.
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