化学学报 ›› 2025, Vol. 83 ›› Issue (4): 326-331.DOI: 10.6023/A25010025 上一篇    下一篇

研究通讯

NiTe纳米催化剂用于高效电化学合成H2O2

侯赟鑫a,b, 胡芬a,b, 林声键b, 陈青松b,*(), 温珍海b,*()   

  1. a 福州大学化学学院 福州 350108
    b 中国科学院福建物质结构研究所结构化学国家重点实验室、福建省氢能材料与技术重点实验室 福州 350002
  • 投稿日期:2025-01-17 发布日期:2025-02-21
  • 基金资助:
    国家重点研发计划项目(2022YFE0115900); 国家自然科学基金项目(22225902); 国家自然科学基金项目(U22A20436); 福州市科技计划项目(2023-P-009)

NiTe Nanocatalyst for Efficient Electrochemical Synthesis of H2O2

Yunxin Houa,b, Fen Hua,b, Shengjian Linb, Qingsong Chenb(), Zhenhai Wenb()   

  1. a College of Chemistry, Fuzhou University, Fuzhou 350108, China
    b State Key Laboratory of Structural Chemistry, and Fujian Provincial Key Laboratory of Materials and Techniques toward Hydrogen Energy, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China
  • Received:2025-01-17 Published:2025-02-21
  • Contact: E-mail: chenqs@fjirsm.ac.cn;wen@fjirsm.ac.cn; Tel.: 0086-0591-6317353
  • Supported by:
    National Key Research & Development Program of China(2022YFE0115900); National Natural Science Foundation of China(22225902); National Natural Science Foundation of China(U22A20436); Science and Technology Program of Fuzhou(2023-P-009)

过氧化氢在工业、医疗和污水处理等多领域具有重要的应用价值. 本研究采用水相合成法成功制备了NiTe纳米材料. 研究结果表明, 以氧气和纯水为原料, 采用多孔阳离子交换树脂作为介导的固态电解质器件中, 在电位为0.31 V (vs. RHE)时, H2O2法拉第效率高达85%, 在200 mV电位窗口内保持法拉第效率超过80%. 此外, 在0.11 V (vs. RHE)时, H2O2产率可达4334.39 mmol•h-1•g-1. NiTe催化剂中Te的电子结构调控效应, 结合富含的晶界和缺陷位点, 以及小尺寸和多孔的复合结构, 为其提供了理想的活性中心和优异的结构基础. 固态电解质器件的应用不仅显著降低成本和操作风险, 还能直接生产纯净的过氧化氢溶液, 提高生产效率. 该研究为氧气高效电还原产过氧化氢提供了新思路.

关键词: 纳米材料, NiTe, 固态电解质, 氧还原, 过氧化氢

Hydrogen peroxide has significant applications across various sectors, including industry, healthcare, and wastewater treatment. NiTe nanomaterial has been synthesized using a facile aqueous-phase method in this work. Specifically, 5 mmol of nickel acetate tetrahydrate (Ni(CH3COO)2•4H2O) was dissolved in deionized water and reacted with 10 mmol of tartaric acid to form solution A. Simultaneously, 5 mmol of tellurium dioxide powder was heated in 10 mmol of ammoniated tartaric acid to prepare solution B. Both solution A and B were adjusted to a pH value of 10. Solution B was gradually introduced into solution A under continuous agitation to ensure homogeneous mixing. Subsequently, 7.5 mmol of sodium borohydride (NaBH4) was added to the mixture under vigorous mechanical stirring, resulting in the formation of a black NiTe precipitate. The research results indicate that, using oxygen and pure water as raw materials, and employing porous cation exchange resins as solid-state electrolyte in the electrolyzer, the Faradaic efficiency of H2O2 reaches 85% at a potential of 0.31 V (vs. RHE) and maintains a Faradaic efficiency of over 80% within a potential window of 200 mV. Additionally, at 0.11 V (vs. RHE), the H2O2 production rate can reach 4334.39 mmol•h-1•g-1. In stability assessments, the NiTe catalyst exhibited continuous and stable H2O2 production for over 6 h. The electronic structure modulation effect of Te in the NiTe catalyst, combined with abundant grain boundaries and defect sites, as well as the small particle size and hybrid porous structure, provides ideal active centers and excellent structural foundation, which endows NiTe with excellent catalytic performance. The application of solid-state electrolyte devices not only significantly reduces costs and operational risks but also enables the direct production of pure hydrogen peroxide solution, thereby improving production efficiency. This research offers a new approach for the efficient electrochemical production of hydrogen peroxide from oxygen.

Key words: nanomaterial, NiTe, solid electrolyte, oxygen reduction, hydrogen peroxide