Regulating crystal phase of TiO2 to enhance catalytic activity of Ni/TiO2 for solar-driven dry reforming of methane
Ni/TiO 2 catalyst is widely employed for photo-driven DRM reaction while the influence of crystal structure of TiO 2 remains unclear. In this work, the rutile/anatase ratio in supports was successfully controlled by varying the calcination temperature of anatase-TiO 2 . Structural characterizations revealed that a distinct TiO x coating on the Ni nanoparticles (NPs) was evident for Ni/TiO 2 -700 catalyst due to strong metal-support interaction. It is observed that the TiO x overlayer gradually disappeared as the ratio of rutile/anatase increased, thereby enhancing the exposure of Ni active sites. The exposed Ni sites enhanced visible light absorption and boosted the dissociation capability of CH 4 , which led to the much elevated catalytic activity for Ni/ TiO 2 -950 in which rutile dominated. Therefore, the catalytic activity of solar-driven DRM reaction was significantly influenced by the rutile/anatase ratio. Ni/TiO 2 -950, characterized by a predominant rutile phase, exhibited the highest DRM reactivity, with remarkable H 2 and CO production rates reaching as high as 87.4 and 220.2 mmol/(g·h), respectively. These rates were approximately 257 and 130 times higher, respectively, compared to those obtained on Ni/TiO 2 -700 with anatase. This study suggests that the optimization of crystal structure of TiO 2 support can effectively enhance the performance of photothermal DRM reaction.
Authors
- Liangshu Zhong (ORCID: https://orcid.org/0000-0002-4167-8630)
- Zhanjun He
- Yuanyuan Dai (ORCID: https://orcid.org/0000-0003-1180-7881)
- Tiejun Lin (ORCID: https://orcid.org/0000-0002-9177-070X)
- Qiang Niu (ORCID: https://orcid.org/0000-0002-6880-6874)
- Kun Gong
Institutions
- Chinese Academy of Sciences (CN)
- Inner Mongolia Electric Power (China) (CN)
- Shanghai Advanced Research Institute (CN)
- University of Chinese Academy of Sciences (CN)
Publication Details
- Journal
- Journal of Fuel Chemistry and Technology
- Published
- 2024-09-01
- DOI
- https://doi.org/10.1016/s1872-5813(24)60452-4
- Citations
- 10
- Primary Topic
- Catalysts for Methane Reforming
- Type
- article
- Field-Weighted Citation Impact
- 1.07