Chong Lin, Shan Wang, Xuetong Zhang, Bin Xiao, Yepeng Zeng, Li Huang, Fei Luo, Kangye Liu, Jingyang Tian, Min Li, Minghui Cao, Yong Qian
{"title":"揭示对苯二甲酸酯官能团在镍-有机骨架纳米阵列电化学析氧反应中的作用","authors":"Chong Lin, Shan Wang, Xuetong Zhang, Bin Xiao, Yepeng Zeng, Li Huang, Fei Luo, Kangye Liu, Jingyang Tian, Min Li, Minghui Cao, Yong Qian","doi":"10.1021/acs.inorgchem.4c04958","DOIUrl":null,"url":null,"abstract":"The platelike nickel-terephthalate-type metal–organic framework nanoarrays (Ni-BDC NAs) on carbon cloth are obtained by employing agaric-like Ni(OH)<sub>2</sub> NAs as sacrificial templates. The microenvironment of Ni-BDC NAs is modulated by various neighboring functional groups (−NH<sub>2</sub>, −NO<sub>2</sub>, and −Br) on the carboxylate ligand, exerting minimal destructive effects on the structure and morphology of Ni-BDC NAs. The electrochemical oxygen evolution reaction (OER) of Ni-BDC–NH<sub>2</sub> NAs, Ni-BDC–NO<sub>2</sub> NAs, and Ni-BDC–Br NAs exhibited a significant enhancement compared to that of Ni-BDC NAs alone, as evidenced by both experimental and theoretical assessments. The presence of neighboring groups exerts a positive influence on the electronic coupling between Ni and O atoms, thereby facilitating the thermodynamically favorable formation of *O intermediates on Ni sites and accelerating the kinetics of the OER. The findings presented here provide valuable insights for the design and utilization of carboxylic acid molecules with functional group effects, enhancing the activity of the OER across diverse Ni centers.","PeriodicalId":40,"journal":{"name":"Inorganic Chemistry","volume":"28 1","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unraveling the Role of Functional Groups of Terephthalate in Enhancing the Electrochemical Oxygen Evolution Reaction of Nickel–Organic Framework Nanoarrays\",\"authors\":\"Chong Lin, Shan Wang, Xuetong Zhang, Bin Xiao, Yepeng Zeng, Li Huang, Fei Luo, Kangye Liu, Jingyang Tian, Min Li, Minghui Cao, Yong Qian\",\"doi\":\"10.1021/acs.inorgchem.4c04958\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The platelike nickel-terephthalate-type metal–organic framework nanoarrays (Ni-BDC NAs) on carbon cloth are obtained by employing agaric-like Ni(OH)<sub>2</sub> NAs as sacrificial templates. The microenvironment of Ni-BDC NAs is modulated by various neighboring functional groups (−NH<sub>2</sub>, −NO<sub>2</sub>, and −Br) on the carboxylate ligand, exerting minimal destructive effects on the structure and morphology of Ni-BDC NAs. The electrochemical oxygen evolution reaction (OER) of Ni-BDC–NH<sub>2</sub> NAs, Ni-BDC–NO<sub>2</sub> NAs, and Ni-BDC–Br NAs exhibited a significant enhancement compared to that of Ni-BDC NAs alone, as evidenced by both experimental and theoretical assessments. The presence of neighboring groups exerts a positive influence on the electronic coupling between Ni and O atoms, thereby facilitating the thermodynamically favorable formation of *O intermediates on Ni sites and accelerating the kinetics of the OER. The findings presented here provide valuable insights for the design and utilization of carboxylic acid molecules with functional group effects, enhancing the activity of the OER across diverse Ni centers.\",\"PeriodicalId\":40,\"journal\":{\"name\":\"Inorganic Chemistry\",\"volume\":\"28 1\",\"pages\":\"\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2025-01-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.inorgchem.4c04958\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.inorgchem.4c04958","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Unraveling the Role of Functional Groups of Terephthalate in Enhancing the Electrochemical Oxygen Evolution Reaction of Nickel–Organic Framework Nanoarrays
The platelike nickel-terephthalate-type metal–organic framework nanoarrays (Ni-BDC NAs) on carbon cloth are obtained by employing agaric-like Ni(OH)2 NAs as sacrificial templates. The microenvironment of Ni-BDC NAs is modulated by various neighboring functional groups (−NH2, −NO2, and −Br) on the carboxylate ligand, exerting minimal destructive effects on the structure and morphology of Ni-BDC NAs. The electrochemical oxygen evolution reaction (OER) of Ni-BDC–NH2 NAs, Ni-BDC–NO2 NAs, and Ni-BDC–Br NAs exhibited a significant enhancement compared to that of Ni-BDC NAs alone, as evidenced by both experimental and theoretical assessments. The presence of neighboring groups exerts a positive influence on the electronic coupling between Ni and O atoms, thereby facilitating the thermodynamically favorable formation of *O intermediates on Ni sites and accelerating the kinetics of the OER. The findings presented here provide valuable insights for the design and utilization of carboxylic acid molecules with functional group effects, enhancing the activity of the OER across diverse Ni centers.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.