Chao Jiang, Jilin Bai, Qingyang Shen, Xin Ku, Wei Liao and Dehua Xiong
{"title":"制备具有更多氧缺陷的 S 掺杂 CuCoO2 纳米片,实现高效氧进化反应†。","authors":"Chao Jiang, Jilin Bai, Qingyang Shen, Xin Ku, Wei Liao and Dehua Xiong","doi":"10.1039/D4NJ03425B","DOIUrl":null,"url":null,"abstract":"<p >Noble metal catalysts are excellent oxygen evolution reaction (OER) catalysts, but the expensive price and scarce reserves constrain the development of water splitting. CuCoO<small><sub>2</sub></small> is known as a promising catalytic material due to its abundant raw materials and unique structure. However, its OER performance requires further enhancement. In this research, S-doped CuCoO<small><sub>2</sub></small> nanocrystals were synthesized through a one-step solvothermal method. The electrochemical test results revealed that 0.33 mmol S doped CuCoO<small><sub>2</sub></small> (CCOS-3) exhibits superior catalytic activity (<em>η</em><small><sub>10</sub></small> = 375.5 mV, Tafel slope = 83.4 mV dec<small><sup>−1</sup></small>) in 1.0 M KOH electrolyte. Furthermore, after an 18 hours OER stability test, the CCOS-3 exhibited a minimal overpotential degradation of 27 mV. Brunauer–Emmett–Teller (BET) tests showed that the surface area of CCOS-3 is 12.51 m<small><sup>2</sup></small> g<small><sup>−1</sup></small>. X-ray photoelectron spectroscopy (XPS) and ultraviolet-visible-near infrared (UV-Vis-NIR) absorption spectra results revealed that S doping boosts the quantity of oxygen defect sites and narrows the band gap of CuCoO<small><sub>2</sub></small>. Therefore, the charge transfer within the material is accelerated and the catalytic activity is optimized. This work may offer a novel insight into enhancing the OER performance of CuCoO<small><sub>2</sub></small> catalysts through nonmetallic doping.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 38","pages":" 16692-16698"},"PeriodicalIF":2.5000,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation of S-doped CuCoO2 nanosheets with more oxygen defects for efficient oxygen evolution reaction†\",\"authors\":\"Chao Jiang, Jilin Bai, Qingyang Shen, Xin Ku, Wei Liao and Dehua Xiong\",\"doi\":\"10.1039/D4NJ03425B\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Noble metal catalysts are excellent oxygen evolution reaction (OER) catalysts, but the expensive price and scarce reserves constrain the development of water splitting. CuCoO<small><sub>2</sub></small> is known as a promising catalytic material due to its abundant raw materials and unique structure. However, its OER performance requires further enhancement. In this research, S-doped CuCoO<small><sub>2</sub></small> nanocrystals were synthesized through a one-step solvothermal method. The electrochemical test results revealed that 0.33 mmol S doped CuCoO<small><sub>2</sub></small> (CCOS-3) exhibits superior catalytic activity (<em>η</em><small><sub>10</sub></small> = 375.5 mV, Tafel slope = 83.4 mV dec<small><sup>−1</sup></small>) in 1.0 M KOH electrolyte. Furthermore, after an 18 hours OER stability test, the CCOS-3 exhibited a minimal overpotential degradation of 27 mV. Brunauer–Emmett–Teller (BET) tests showed that the surface area of CCOS-3 is 12.51 m<small><sup>2</sup></small> g<small><sup>−1</sup></small>. X-ray photoelectron spectroscopy (XPS) and ultraviolet-visible-near infrared (UV-Vis-NIR) absorption spectra results revealed that S doping boosts the quantity of oxygen defect sites and narrows the band gap of CuCoO<small><sub>2</sub></small>. Therefore, the charge transfer within the material is accelerated and the catalytic activity is optimized. 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引用次数: 0
摘要
贵金属催化剂是优良的氧进化反应(OER)催化剂,但其昂贵的价格和稀缺的储量限制了水分离技术的发展。众所周知,CuCoO2 因其丰富的原材料和独特的结构而成为一种前景广阔的催化材料。然而,其 OER 性能需要进一步提高。本研究采用一步溶热法合成了掺杂 S 的 CuCoO2 纳米晶体。电化学测试结果表明,在 1.0 M KOH 电解液中,0.33 mmol 掺杂 S 的 CuCoO2(CCOS-3)表现出卓越的催化活性(η10 = 375.5 mV,Tafel 斜坡 = 83.4 mV dec-1)。此外,经过 18 小时的 OER 稳定性测试后,CCOS-3 的过电位衰减最小,仅为 27 mV。布鲁纳-艾美特-泰勒(BET)测试表明,CCOS-3 的表面积为 12.51 m2 g-1。X 射线光电子能谱(XPS)和紫外-可见-近红外(UV-Vis-NIR)吸收光谱结果表明,S 掺杂增加了氧缺陷位点的数量,缩小了 CuCoO2 的带隙。因此,加速了材料内部的电荷转移,优化了催化活性。这项研究为通过非金属掺杂提高 CuCoO2 催化剂的 OER 性能提供了新的见解。
Preparation of S-doped CuCoO2 nanosheets with more oxygen defects for efficient oxygen evolution reaction†
Noble metal catalysts are excellent oxygen evolution reaction (OER) catalysts, but the expensive price and scarce reserves constrain the development of water splitting. CuCoO2 is known as a promising catalytic material due to its abundant raw materials and unique structure. However, its OER performance requires further enhancement. In this research, S-doped CuCoO2 nanocrystals were synthesized through a one-step solvothermal method. The electrochemical test results revealed that 0.33 mmol S doped CuCoO2 (CCOS-3) exhibits superior catalytic activity (η10 = 375.5 mV, Tafel slope = 83.4 mV dec−1) in 1.0 M KOH electrolyte. Furthermore, after an 18 hours OER stability test, the CCOS-3 exhibited a minimal overpotential degradation of 27 mV. Brunauer–Emmett–Teller (BET) tests showed that the surface area of CCOS-3 is 12.51 m2 g−1. X-ray photoelectron spectroscopy (XPS) and ultraviolet-visible-near infrared (UV-Vis-NIR) absorption spectra results revealed that S doping boosts the quantity of oxygen defect sites and narrows the band gap of CuCoO2. Therefore, the charge transfer within the material is accelerated and the catalytic activity is optimized. This work may offer a novel insight into enhancing the OER performance of CuCoO2 catalysts through nonmetallic doping.