Shuang Xia, Xiao Fu, Bin Wang, Yi Wang, Zhongqing Liu
Using cobalt sulfate and nickel sulfate as main electrolytes, ammonium sulfate as an auxiliary electrolyte and buffer agent, and cheap iron pieces (FP) as the substrates, nickel and/or cobalt phosphide/metal heterogeneous catalytic electrode (M2P/M/FP) was grown on the substrate in situ by electrodeposition followed by low temperature phosphating. M2P/M/FP functioned as a good bifunctional electrode for HER and OER in 1 mol/L KOH, where Co2P/Co/FP needed an overpotential of 52 and 288 mV, and (NC)2P/(NC)/FP required that of 75 mV and 293 mV to afford 10 mA/cm2. Previous similar studies often ignored the role of metal and only considered the water electrolysis catalysis of metal phosphide. In this research, it was clarified that for water electrolysis, the essence of high catalysis activity of the M2P/M/FP electrode was the electronic interaction between metal and metal phosphide.
{"title":"Enhanced water electrolysis by construction and control of nickel (cobalt) phosphide/metal interface","authors":"Shuang Xia, Xiao Fu, Bin Wang, Yi Wang, Zhongqing Liu","doi":"10.1002/jccs.202400064","DOIUrl":"10.1002/jccs.202400064","url":null,"abstract":"<p>Using cobalt sulfate and nickel sulfate as main electrolytes, ammonium sulfate as an auxiliary electrolyte and buffer agent, and cheap iron pieces (FP) as the substrates, nickel and/or cobalt phosphide/metal heterogeneous catalytic electrode (M<sub>2</sub>P/M/FP) was grown on the substrate in situ by electrodeposition followed by low temperature phosphating. M<sub>2</sub>P/M/FP functioned as a good bifunctional electrode for HER and OER in 1 mol/L KOH, where Co<sub>2</sub>P/Co/FP needed an overpotential of 52 and 288 mV, and (NC)<sub>2</sub>P/(NC)/FP required that of 75 mV and 293 mV to afford 10 mA/cm<sup>2</sup>. Previous similar studies often ignored the role of metal and only considered the water electrolysis catalysis of metal phosphide. In this research, it was clarified that for water electrolysis, the essence of high catalysis activity of the M<sub>2</sub>P/M/FP electrode was the electronic interaction between metal and metal phosphide.</p>","PeriodicalId":17262,"journal":{"name":"Journal of The Chinese Chemical Society","volume":"71 7","pages":"651-661"},"PeriodicalIF":1.6,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141106183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Reasonable design is of great significance for improving the performance of electrochemiluminescence (ECL) co-reactant accelerators. The different d-band structure of metal single atoms will produce different oxidation states, which may change the adsorption of reaction intermediates to the catalyst and affect its catalytic activity. In this study, we have demonstrated that the ECL performances of graphite carbon nitride (CN) can be promoted by modulating the metal oxidation states of co-reaction accelerator for the first time. The oxidation states of Au were modulated by the different electronic metal–support interaction (EMSI) between the co-reaction accelerator (Au single atoms, Au nanoparticles [Au NPs]) and CN, and the effects of Au oxidation states on the ECL performances of CN were investigated. Comparison to pristine CN and CN nanosheets supported Au nanoparticles (Au NPs/CN), stronger and more stable ECL intensity of CN nanosheets supported Au single-atoms (AuS/CN) was obtained. The ECL signal of AuS/CN was about 32.2 times that of the original CN, and 2.8 times that of Au NPs/CN in the same Au loading content (0.8%). Detailed mechanism revealed that AuS/CN with higher Au oxidation state has better conductivity and stronger catalytic activity, which promotes the electric reduction of CN and S2O82−, increases the lifetime of the excited state CN*, and significantly improves the ECL performance of CN. In addition, this work provides a detailed understanding of the essence of EMSI for the ECL intensity amplification and established a feasible method for the improvement of ECL capacities of co-reactant accelerators.
{"title":"Improvement on electrochemiluminescence properties of graphite carbon nitride by metal oxidation state regulation","authors":"Rui Zou, Rui Guo, Jinkui Cheng","doi":"10.1002/jccs.202400094","DOIUrl":"10.1002/jccs.202400094","url":null,"abstract":"<p>Reasonable design is of great significance for improving the performance of electrochemiluminescence (ECL) co-reactant accelerators. The different d-band structure of metal single atoms will produce different oxidation states, which may change the adsorption of reaction intermediates to the catalyst and affect its catalytic activity. In this study, we have demonstrated that the ECL performances of graphite carbon nitride (CN) can be promoted by modulating the metal oxidation states of co-reaction accelerator for the first time. The oxidation states of Au were modulated by the different electronic metal–support interaction (EMSI) between the co-reaction accelerator (Au single atoms, Au nanoparticles [Au NPs]) and CN, and the effects of Au oxidation states on the ECL performances of CN were investigated. Comparison to pristine CN and CN nanosheets supported Au nanoparticles (Au NPs/CN), stronger and more stable ECL intensity of CN nanosheets supported Au single-atoms (Au<sup>S</sup>/CN) was obtained. The ECL signal of Au<sup>S</sup>/CN was about 32.2 times that of the original CN, and 2.8 times that of Au NPs/CN in the same Au loading content (0.8%). Detailed mechanism revealed that Au<sup>S</sup>/CN with higher Au oxidation state has better conductivity and stronger catalytic activity, which promotes the electric reduction of CN and S<sub>2</sub>O<sub>8</sub><sup>2−</sup>, increases the lifetime of the excited state CN*, and significantly improves the ECL performance of CN. In addition, this work provides a detailed understanding of the essence of EMSI for the ECL intensity amplification and established a feasible method for the improvement of ECL capacities of co-reactant accelerators.</p>","PeriodicalId":17262,"journal":{"name":"Journal of The Chinese Chemical Society","volume":"71 8","pages":"811-819"},"PeriodicalIF":1.6,"publicationDate":"2024-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140967479","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In this paper, the design concept aims to convey the overall background of the published literature, emphasizing the concept of food safety. It utilizes a magnifying glass to symbolize the analysis of various parts of preserved eggs described in the text. Additionally, the spectrogram concept in the bottom right corner highlights the detection methods. More details about this figure will be discussed by Dr. Tsung-Ting Shih and his co-workers on page 474–481 in this issue.