ENERGI CELAH-PITA MATERIAL TiO2/KOMPLEKS LOGAM-KLOROFIL (M=Zn2+, Co2+) DARI DAUN SINGKONG (Manihot esculenta crant) (BANDGAP ENERGY OF MATERIAL OF TiO2/METAL-CHLOROPHYLL COMPLEX (M= Zn2+, Co2+) FROM CASSAVA LEAVES (Manihot esculenta crant))

Arif Sulaiman, I. Silalahi, A. Shofiyani, Ari Widiyantoro, Harlia Harlia
{"title":"ENERGI CELAH-PITA MATERIAL TiO2/KOMPLEKS LOGAM-KLOROFIL (M=Zn2+, Co2+) DARI DAUN SINGKONG (Manihot esculenta crant) (BANDGAP ENERGY OF MATERIAL OF TiO2/METAL-CHLOROPHYLL COMPLEX (M= Zn2+, Co2+) FROM CASSAVA LEAVES (Manihot esculenta crant))","authors":"Arif Sulaiman, I. Silalahi, A. Shofiyani, Ari Widiyantoro, Harlia Harlia","doi":"10.26418/indonesian.v5i1.49364","DOIUrl":null,"url":null,"abstract":"Synthesis and characterization of TiO2 films sensitized with chlorophyll and metal-chlorophyll complex (M=Zn2+, Co2+) were carried out. Chlorophyll isolated from cassava leaves shows absorption peaks on the UV-Vis spectra in the Soret band area (415 nm) and Q band area (665 nm). The metal-chlorophyll complex was prepared from the reaction of the isolated chlorophyll and ZnCl2 (for Zn2+-chlorophyll); CoCl2.6H2O (for Co2+-chlorophyll) under reflux condition at 65 ºC with a mole ratio of 1:1. The UV-Vis spectra of the isolated products showed a hypsochromic shift to 410 nm and 660 nm for Zn2+-chlorophyll whereas the spectrum of the Co2+-chlorophyll product demonstrated the shifts to 403 nm and 661 nm. These hypsochromic shifts are proposed to be a metal-to-ligand charge transfer (MLCT) transition as a result of chlorophyll metalation. The FTIR spectra of chlorophyll and metal-chlorophyll complexes have a similar pattern despite changes in the absorption of vibrational energy in several functional groups. The absorption of the C=N group shifted from 1372 cm-1 to 1368 cm-1 for both of the complexes, the C=C group of aromatic shifted from 1451 cm-1 to 1447 cm-1 (Zn2+-chlorophyll) and from 1451 cm-1 to 1445 cm-1 (Co2+-chlorophyll), and the C=O group of ketones shifted from 1627 cm-1 to 1645 cm-1 (Zn2+-chlorophyll) and from 1627 cm-1 to 1646 cm-1 (Co2+-chlorophyll). The shift pattern of the absorption peaks on the FTIR spectra indicates the coordination of metal ions towards the N atom in the pyrrole ring in the porphyrin structure of the chlorophyll. When the isolated chlorophyll as well as the chlorphyll complexes was sensitized on the surface of TiO2, variation of bandgap energy was observed. The calculation using the Tauc Plot method resulted in the bandgap energy of films of TiO2 at 3.20 eV, TiO2/chlorophyll at 2.97 eV, TiO2/Zn2+-chlorophyll at 2.87 eV, and TiO2/Co2+-chlorophyll at 2.90 eV","PeriodicalId":13554,"journal":{"name":"Indonesian Journal of Pure and Applied Chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-04-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indonesian Journal of Pure and Applied Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26418/indonesian.v5i1.49364","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Synthesis and characterization of TiO2 films sensitized with chlorophyll and metal-chlorophyll complex (M=Zn2+, Co2+) were carried out. Chlorophyll isolated from cassava leaves shows absorption peaks on the UV-Vis spectra in the Soret band area (415 nm) and Q band area (665 nm). The metal-chlorophyll complex was prepared from the reaction of the isolated chlorophyll and ZnCl2 (for Zn2+-chlorophyll); CoCl2.6H2O (for Co2+-chlorophyll) under reflux condition at 65 ºC with a mole ratio of 1:1. The UV-Vis spectra of the isolated products showed a hypsochromic shift to 410 nm and 660 nm for Zn2+-chlorophyll whereas the spectrum of the Co2+-chlorophyll product demonstrated the shifts to 403 nm and 661 nm. These hypsochromic shifts are proposed to be a metal-to-ligand charge transfer (MLCT) transition as a result of chlorophyll metalation. The FTIR spectra of chlorophyll and metal-chlorophyll complexes have a similar pattern despite changes in the absorption of vibrational energy in several functional groups. The absorption of the C=N group shifted from 1372 cm-1 to 1368 cm-1 for both of the complexes, the C=C group of aromatic shifted from 1451 cm-1 to 1447 cm-1 (Zn2+-chlorophyll) and from 1451 cm-1 to 1445 cm-1 (Co2+-chlorophyll), and the C=O group of ketones shifted from 1627 cm-1 to 1645 cm-1 (Zn2+-chlorophyll) and from 1627 cm-1 to 1646 cm-1 (Co2+-chlorophyll). The shift pattern of the absorption peaks on the FTIR spectra indicates the coordination of metal ions towards the N atom in the pyrrole ring in the porphyrin structure of the chlorophyll. When the isolated chlorophyll as well as the chlorphyll complexes was sensitized on the surface of TiO2, variation of bandgap energy was observed. The calculation using the Tauc Plot method resulted in the bandgap energy of films of TiO2 at 3.20 eV, TiO2/chlorophyll at 2.97 eV, TiO2/Zn2+-chlorophyll at 2.87 eV, and TiO2/Co2+-chlorophyll at 2.90 eV
研究了叶绿素和金属-叶绿素配合物(M=Zn2+, Co2+)敏化TiO2薄膜的合成与表征。从木薯叶片中分离出的叶绿素在紫外-可见光谱上的吸收峰位于Soret波段(415 nm)和Q波段(665 nm)。由分离的叶绿素与ZnCl2(对于Zn2+-叶绿素)反应制备金属-叶绿素配合物;CoCl2.6H2O(对于Co2+-叶绿素)在65℃回流条件下,摩尔比为1:1。Zn2+-叶绿素的紫外可见光谱在410 nm和660 nm处发生了次色移,而Co2+-叶绿素的紫外可见光谱在403 nm和661 nm处发生了次色移。这些亚色转移被认为是叶绿素金属化导致的金属到配体电荷转移(MLCT)转移。叶绿素和金属-叶绿素配合物的FTIR光谱具有相似的模式,尽管在几个官能团中振动能量的吸收发生了变化。两种配合物的C=N基团的吸收从1372 cm-1转移到1368 cm-1,芳香的C=C基团的吸收从1451 cm-1转移到1447 cm-1 (Zn2+-叶绿素)和从1451 cm-1转移到1445 cm-1 (Co2+-叶绿素),酮的C=O基团的吸收从1627 cm-1转移到1645 cm-1 (Zn2+-叶绿素)和从1627 cm-1转移到1646 cm-1 (Co2+-叶绿素)。红外光谱吸收峰的位移模式表明叶绿素卟啉结构中金属离子向吡咯环中的N原子配位。当分离出的叶绿素和叶绿素复合物在TiO2表面敏化时,观察到带隙能的变化。利用Tauc图法计算得到TiO2薄膜的带隙能为3.20 eV, TiO2/叶绿素为2.97 eV, TiO2/Zn2+-叶绿素为2.87 eV, TiO2/Co2+-叶绿素为2.90 eV
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信