报告题目：Photocatalytic Reduction of CO₂ into CO from the Aqueous Solution over Photocatalysts

报告时间：2021年10月04日上午10:00-11:30

报告地点：腾讯会议

会议ID: 784 8908 5732

报 告 人：Prof. Tsunehiro Tanaka（教授、日本京都大学）

报告主持人：Prof. Masakazu Ampo（教授、beat365正版唯一官网&大阪府立大学）

报告摘要:

Photocatalytic conversion of CO₂ to reduction products, such as CO, HCOOH, HCHO, CH₃OH, and CH₄, is one of the most attractive propositions for producing green energy by artificial photosynthesis.

Herein, we found that Ga₂O₃ photocatalysts exhibit high conversion of CO₂. Doping of Zn species into Ga₂O₃ suppresses the H₂ evolution derived from overall water splitting and, consequently, Zn-doped, Ag-modified Ga₂O₃ exhibits higher selectivity toward CO evolution than bare, Ag-modified Ga₂O₃. We observed stoichiometric amounts of evolved O₂ and CO like CO₂ splitting. Mass spectrometry clarified that the carbon source of the evolved CO is not the residual

carbon species on the photocatalyst surface, but the CO₂ introduced in the gas phase. Doping of the photocatalyst with Zn is expected to prevent H2 formation preserving the active site for CO synthesis.

High CO yield could be achieved but simultaneous evolution of oxygen is not preferable for practical use. In order to cut off the evolution of oxygen by oxidation of water molecules, we adopt ammonia NH₃ as a sacrificial oxidizing reagent instead of water H₂O. In this case, not only cutting off the oxygen evolution but also the formation of N₂ and controllable H₂ formation could be achieved.Thus, syn-gas formation from CO₂, water, and NH3 was realized.

Further, the most active another catalytic system will be introduced.

References:

K. Teramura, Z. Wang, T. Tanaka, et al., Chemistry-A European Journal, 2014, 20, 9906.

Z. Wang, K. Teramura, T. Tanaka, et al., J. Mater. Chem. A, 2015, 3, 11313; ibid, Catal. Sci. Technol.,

2016, 6, 1025.

K. Teramura, K. Hori, T. Tanaka, et al., J. Phys. Chem. C, 2017, 121, 8711.

Z. Huang, K. Teramura, T. Tanaka et al., Chem. Sci., 2017, 8, 5797.

P. Rui, K. Teramura, T. Tanaka, et al. ACS Sustainable Chem. Eng., 2019, 7, 2083.

报告人简介:

Tsunehiro Tanaka教授，现任日本京都大学工程学院分子工程系教授，1987年于日本京都大学化学专业获得博士学位，1987-1990年在美国北海道大学化学系(Department of Chemistry, Faculty of Science, Hokkaido University)做助理教授，1990年进入日本京都大学工程学院工作。1996年在中国兰州物理化学研究所担任客座教授。1996年在意大利都灵大学物理无机材料化学系担任客座学者。目前担任日本京都大学催化剂与电池元素战略计划主任，英国皇家学会《Catalysis Science & Technology》副主编。曾获得“日本催化协会青年科学家奖”。目前主要从事多相光催化研究；机动车催化剂元素战略研发；催化反应表征研究等。