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通过直接聚合尿素合成的多孔石墨相氮化碳用于高效的太阳光驱动光催化制氢。

Porous graphitic carbon nitride synthesized via direct polymerization of urea for efficient sunlight-driven photocatalytic hydrogen production.

机构信息

i-Lab, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, 398 Ruoshui Road, Suzhou 215123, P. R. China.

出版信息

Nanoscale. 2012 Sep 7;4(17):5300-3. doi: 10.1039/c2nr30948c. Epub 2012 Jul 10.

DOI:10.1039/c2nr30948c
PMID:22776858
Abstract

Energy captured directly from sunlight provides an attractive approach towards fulfilling the need for green energy resources on the terawatt scale with minimal environmental impact. Collecting and storing solar energy into fuel through photocatalyzed water splitting to generate hydrogen in a cost-effective way is desirable. To achieve this goal, low cost and environmentally benign urea was used to synthesize the metal-free photocatalyst graphitic carbon nitride (g-C₃N₄). A porous structure is achieved via one-step polymerization of the single precursor. The porous structure with increased BET surface area and pore volume shows a much higher hydrogen production rate under simulated sunlight irradiation than thiourea-derived and dicyanamide-derived g-C₃N₄. The presence of an oxygen atom is presumed to play a key role in adjusting the textural properties. Further improvement of the photocatalytic function can be expected with after-treatment due to its rich chemistry in functionalization.

摘要

直接从太阳光中捕获能量,为满足兆瓦级绿色能源资源的需求提供了一种有吸引力的方法,同时对环境的影响最小。通过光催化水分解将太阳能收集和储存到燃料中,以经济有效的方式产生氢气是理想的。为了实现这一目标,使用低成本且环境友好的尿素来合成无金属光催化剂石墨相氮化碳(g-C₃N₄)。通过单一前体的一步聚合实现了多孔结构。与硫脲衍生和双氰胺衍生的 g-C₃N₄相比,具有增加的 BET 表面积和孔体积的多孔结构在模拟太阳光照射下显示出更高的产氢率。假定氧原子的存在在调节结构性能方面起着关键作用。由于其在功能化方面的丰富化学性质,通过后处理可以进一步提高光催化性能。

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