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基于镁酞菁敏化的介孔碳氮化物光催化剂的光催化析氢反应。

Photocatalytic hydrogen evolution on dye-sensitized mesoporous carbon nitride photocatalyst with magnesium phthalocyanine.

机构信息

Department of Chemical System Engineering, The University of Tokyo, 7-3-1 Hongo Bunkyoku, Tokyo 113-8656, Japan.

出版信息

Phys Chem Chem Phys. 2010 Oct 28;12(40):13020-5. doi: 10.1039/c0cp00611d. Epub 2010 Aug 31.

Abstract

Spectral sensitization of a mesoporous graphite carbon nitride (mpg-C(3)N(4)) photocatalyst was investigated by depositing magnesium phthalocyanine (MgPc) to expand the absorption to wavelengths longer than those of the principal mpg-C(3)N(4). The obtained sample, MgPc/Pt/mpg-C(3)N(4) (Pt as a cocatalyst) showed stable photocatalytic evolution of hydrogen from aqueous solution in the presence of sacrificial reagents (triethanolamine), even under irradiation at wavelengths longer than 600 nm. Increasing the amount of MgPc led to ordered MgPc aggregation on the photocatalyst surfaces. The rate of photocatalytic hydrogen evolution was highest on a sample with an amount of MgPc corresponding to a monolayer on the Pt/mpg-C(3)N(4) photocatalyst surface. The obtained action spectra of hydrogen evolution and the observation that the amount of evolved hydrogen substantially surpassed the amount of MgPc, confirm that the introduced MgPc functioned as a photocatalytic sensitizer.

摘要

通过沉积镁酞菁(MgPc)来扩展吸收波长,使其长于主要的介孔石墨相氮化碳(mpg-C(3)N(4)),研究了介孔石墨相氮化碳(mpg-C(3)N(4))光催化剂的光谱敏化。所得的样品 MgPc/Pt/mpg-C(3)N(4)(Pt 作为共催化剂)在牺牲试剂(三乙醇胺)存在下,即使在波长大于 600nm 的光照射下,也能稳定地从水溶液中光催化析氢。增加 MgPc 的量会导致在光催化剂表面上有序的 MgPc 聚集。在 MgPc 量相当于 Pt/mpg-C(3)N(4)光催化剂表面单层的样品上,光催化析氢的速率最高。获得的析氢作用光谱以及观察到的实际析氢量大大超过 MgPc 的量,证实了引入的 MgPc 起到了光催化敏化剂的作用。

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