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Regulating crystal phase of TiO_(2) to enhance catalytic activity of Ni/TiO_(2) for solar-driven dry reforming of methane
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作者 HE Zhanjun GONG Kun +3 位作者 DAI Yuanyuan NIU Qiang LIN Tiejun ZHONG Liangshu 《燃料化学学报(中英文)》 EI CAS CSCD 北大核心 2024年第9期1203-1213,共11页
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... 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 TiOx 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 CH4,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. 展开更多
关键词 dry reforming of methane photothermal catalysis crystal phase TiO_(2) metal-support interaction
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光热催化甲烷干重整研究进展 被引量:7
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作者 黄敏 +1 位作者 林铁 钟良枢 《物理化学学报》 SCIE CAS CSCD 北大核心 2023年第9期22-34,共13页
随着工业化的推进,化石能源的消耗产生大量温室气体,其中CH_(4)和CO_(2)占据温室气体排放的98%以上。将CH_(4)和CO_(2)转化为高附加值化学品具有重要的意义,一直受到工业界和学术界广泛关注。传统的热催化甲烷干重整(DRM)可实现将CH_(4)... 随着工业化的推进,化石能源的消耗产生大量温室气体,其中CH_(4)和CO_(2)占据温室气体排放的98%以上。将CH_(4)和CO_(2)转化为高附加值化学品具有重要的意义,一直受到工业界和学术界广泛关注。传统的热催化甲烷干重整(DRM)可实现将CH_(4)和CO_(2)转化为合成气,但该反应过程受热力学限制,需要很高的能量输入,并且由于反应温度较高,催化剂易发生积碳而失活。绿色环保的光催化技术可以使甲烷干重整反应在温和条件下进行,但是存在太阳光利用率和反应转化率较低等问题。最近光热协同催化受到学术界广泛关注。许多研究结果表明,在相对温和的条件下,光热催化DRM可以获得良好的催化效果,可有效实现太阳能转化为化学能。本文简要介绍近期光热催化甲烷干重整反应的研究进展,总结不同金属催化剂在光热催化甲烷干重整中的应用,同时提出了光热催化甲烷干重整存在的一些挑战及展望。 展开更多
关键词 甲烷干重整 光热催化 LSPR 金属基催化剂
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