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Molybdenum carbide clusters for thermal conversion of CO2 to CO via reverse water-gas shift reaction 被引量:4
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作者 Ying Ma Zhanglong Guo +3 位作者 Qian Jiang kuang-hsu wu Huimin Gong Yuefeng Liu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2020年第11期37-43,共7页
Molybdenum carbides are highly active for CO2 conversion to CO via the reverse water-gas shift(RWGS)reaction, however the large grain size up to micrometers renders its relatively lower active sites utilization effici... Molybdenum carbides are highly active for CO2 conversion to CO via the reverse water-gas shift(RWGS)reaction, however the large grain size up to micrometers renders its relatively lower active sites utilization efficiency while generating CH4 as a by-product. In this work, a homogeneously dispersed molybdenum carbide hybrid catalyst with sub-nanosized cluster(the average size as small as 0.5 nm) is prepared via a facile carbothermal treatment for highly selective CO2-CO reduction. The partially disordered Mo2C clusters are characterized by synchrotron high-resolution XRD and atomic resolution HAADF-STEM analysis, for which the source cause of the disorder is pinpointed by XAFS analysis to be the nitrogen intercalants from the carbonaceous precursor. The partially disordered Mo2C clusters show a RWGS rate as high as 184.4 μmol gMo2C-1s-1 at 400 ℃ with a superior selectivity toward CO(> 99.5%). This work 2 highlights a facile strategy for fabricating highly dispersed and partially disordered Mo2C clusters at a sub-nano size with beneficial N-doping for delivering high catalytic activity and operational stability. 展开更多
关键词 Co2 conversion Reverse water-gas-shift reaction Molybdenum carbide cluster Sub-nanosize CO selectivity
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溶液相合成卤化石墨烯及其对氧化还原反应的电催化活性(英文) 被引量:1
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作者 kuang-hsu wu Da-Wei Wang +2 位作者 Qingcong Zeng Yang Li Ian R.Gentle 《催化学报》 SCIE CAS CSCD 北大核心 2014年第6期884-890,共7页
Metal-free carbon electrocatalyts for the oxygen reduction reaction (ORR) are attractive for their high activity and economic advantages. However, the origin of the activity has never been clearly elucidated in a syst... Metal-free carbon electrocatalyts for the oxygen reduction reaction (ORR) are attractive for their high activity and economic advantages. However, the origin of the activity has never been clearly elucidated in a systematic manner. Halogen group elements are good candidates for elucidating the effect, although it has been a difficult task due to safety issues. In this report, we demonstrate the synthesis of Cl-, Br- and I-doped reduced graphene oxide through two solution phase syntheses. We have evaluated the effectiveness of doping and performed electrochemical measurements of the ORR activity on these halogenated graphene materials. Our results suggest that the high electroneg-ativity of the dopant is not the key factor for high ORR activity; both Br- and I-doped graphene promoted ORR more efficiently than Cl-doped graphene. Furthermore, an unexpected sulfur-doping in acidic conditions suggests that a high level of sulfide can degrade the ORR activity of the graphene material. 展开更多
关键词 氧还原反应 液相合成 电催化活性 卤代 氧化石墨 还原活性 掺杂石墨 安全性问题
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