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CeCu -BTC/CN S型异质结的构建及光催化将CO还原为CO和CH₄

Construction of CeCu -BTC/CN S-type heterojunctions and photocatalytic CO reduction to CO and CH.

作者信息

Zhang Hui, Sun Yi Hui, An Sheng Li, Guo Rui Hua, Wang Rui Fen, Ma Yu Wei

机构信息

College of Rare-Earth Industry, Inner Mongolia University of Science and Technology Baotou 014010 China

Inner Mongolia Key Laboratory of Advanced Ceramic Materials and Devices (Inner Mongolia University of Science and Technology) Baotou 014010 China.

出版信息

RSC Adv. 2025 Mar 19;15(11):8541-8552. doi: 10.1039/d4ra05721j. eCollection 2025 Mar 17.

Abstract

S-type heterojunction photocatalysts (CeCu -BTC/CN) of cerium-copper bimetallic organic framework (CeCu -BTC) and graphitic carbon nitride (g-CN) were constructed by a simple solvothermal method using cerium nitrate, copper nitrate, and urea as the raw materials, and 1,3,5-benzene-tricarboxylic acid as the ligand for the photocatalytic CO reduction to CO and CH. The results show that the built-in electric field constructed by Fermi energy level flattening transfers the electrons in an S-type manner, which not only preserves the strong reducing properties of the electrons in the material but also provides the maximum redox capacity and enables the composite samples to obtain higher visible-light trapping capacity and improve the separation efficiency of the carriers while refining the crystal particles. With the addition of only 1 mL of HO as the proton supply source, CeCu-BTC/CN exhibits the optimal photocatalytic performance. The CO and CH yields were 64.44 and 0.5575 μmol g, which were 7.56 and 2.42 times higher than those of g-CN, respectively, and the catalytic performances were basically stable after cycling tests.

摘要

采用硝酸铈、硝酸铜和尿素为原料,以1,3,5-苯三甲酸为光催化CO还原为CO和CH的配体,通过简单的溶剂热法构建了铈铜双金属有机框架(CeCu -BTC)与石墨相氮化碳(g-CN)的S型异质结光催化剂(CeCu -BTC/CN)。结果表明,由费米能级扁平化构建的内建电场以S型方式转移电子,这不仅保留了材料中电子的强还原性能,还提供了最大的氧化还原能力,使复合样品获得更高的可见光捕获能力,提高了载流子的分离效率,同时细化了晶体颗粒。仅添加1 mL HO作为质子供应源时,CeCu-BTC/CN表现出最佳的光催化性能。CO和CH的产率分别为64.44和0.5575 μmol g,分别比g-CN高7.56倍和2.42倍,循环测试后催化性能基本稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5911/11920967/c422377c2634/d4ra05721j-f1.jpg

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