掺杂杂原子的 MoO3 作为高效电催化剂在酸性和碱性介质中进行氢进化反应

IF 4.1 3区 化学 Q1 CHEMISTRY, ANALYTICAL Journal of Electroanalytical Chemistry Pub Date : 2024-11-26 DOI:10.1016/j.jelechem.2024.118827
Arti Maurya, Nidhi Pradhan, Mahendra Yadav
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引用次数: 0

摘要

一般来说,缓慢的动力学和成本问题阻碍了水分离电催化剂的开发。在实际应用中,设计和开发一种在酸性和碱性介质中都能有效进行氢进化反应(HER)的廉价催化剂至关重要。在这里,钌(Ru)和氧化钼(MoO3)本身在碱性介质中不能有效地进行氢进化反应,但通过简单的两步合成工艺制备的掺杂镍和钌的氧化钼(MoO3)纳米球状材料(Ni-Ru-MoO3)在酸性和碱性介质中均可作为高效的氢进化反应电催化剂。所制备的催化剂成本低廉,活性可与昂贵的贵金属催化剂媲美,这是该研究的新颖之处。由于 MoO3 上掺杂的 Ni 和 Ru 的协同效应以及 Ni-Ru-MoO3 孔隙率的提高,使其成为一种高效催化剂。它只需要 59 和 151 mV 的过电位就能达到 10 mA/cm2 的电流密度,并且在 1 M KOH 和 0.5 M H2SO4 溶液中对 HER 的 Tafel 斜坡值分别为 64 和 68 mV/dec,与基准昂贵催化剂 Pt/C 的相应值相当。此外,这种催化剂即使在 50 mA/cm2 的高电流密度和 24 小时的时间内也表现出显著的稳定性、低电荷转移电阻值和高电化学活性表面积值,这表明它具有很强的电子导电性和很高的电催化活性。这项研究提出了一种良好的策略,即通过简单地掺杂杂质元素来调整 MoO3 的电子结构,使其成为一种高效的 HER 催化剂。
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Heteroatom doped MoO3 as efficient electrocatalyst towards hydrogen evolution reaction in acidic as well as alkaline medium
In general, slow kinetics and cost concern impede the development of electrocatalyst for water splitting. For practical application, the design and development of an inexpensive catalyst efficient towards hydrogen evolution reaction (HER) in acidic as well as alkaline medium is crucial. Here, Ruthenium (Ru) and MoO3 alone are not efficient for HER in the alkaline medium but, Ni and Ru doped MoO3 nanosphere shaped material (Ni-Ru-MoO3) prepared by the facile two-step synthesis process, acts as efficient electrocatalyst towards HER in acidic as well as alkaline medium. The low cost of the prepared catalyst and comparable activity with costly noble metal catalyst is novelty of this work. Due to the synergistic effect of Ni and Ru doping on the MoO3 and enhanced porosity Ni-Ru-MoO3 acts as efficient catalyst. It merely requires 59 and 151 mV overpotential to reach 10 mA/cm2 of current density and exhibits small Tafel slope values as 64 and 68 mV/dec for HER in 1 M KOH and 0.5 M H2SO4 solution, respectively, which are comparable to the respective values obtained for benchmark costly catalyst Pt/C. In addition, this catalyst shows remarkable stability even at high current density of 50 mA/cm2 and time 24 h, low value of charge transfer resistance and high value of electrochemically active surface area, suggesting its substantial electronic conductivity and high electrocatalytic activity. This work presents a good strategy for tuning the electronic structure of MoO3 to make it an efficient catalyst for HER by simply doping it with hetero elements.
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来源期刊
CiteScore
7.80
自引率
6.70%
发文量
912
审稿时长
2.4 months
期刊介绍: The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied. Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.
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Heteroatom doped MoO3 as efficient electrocatalyst towards hydrogen evolution reaction in acidic as well as alkaline medium Tailoring Pd-Co/PPD/NS composite electrode for efficient electrocatalytic dechlorination of 4-chlorophenol Editorial Board Developing efficient anodic electrocatalyst: Three-dimensional interconnected network of bimetallic Pd–Ni aerogel for advanced electrocatalysis of ethanol Enhancing catalytic efficiency: InSe quantum dots’ role in hydrogen evolution reaction
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