B,N共掺杂V2C纳米颗粒包埋FeP纳米片衬底作为碱性介质中水整体分解的独特双功能电催化剂

Dasari Sai Hemanth Kumar, Manzoor Ahmad Pandit, Vinay Kumar Kolakaluri and Krishnamurthi Muralidharan
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引用次数: 0

摘要

氢能作为满足能源需求的解决方案,强调了通过水电解制氢的高效和经济的电催化剂的需求。具有自支撑性质的异质界面材料由于其电子结构的调制、电化学表面积的提高和活性位点的增加而表现出了良好的电化学性能。在我们的研究中,我们成功地合成了由磷化铁(FeP)纳米片作为衬底的异质结构材料,通过水热法和热解法,包埋了硼(B)和氮(N)共掺杂的碳化钒(V2C)纳米颗粒。我们制备了FeP@B,N-V2C异质结构,以提高效率,使用不同重量比(5%,10%,15%和20%)的FeP底物,并相应地调整B,N-V2C纳米颗粒。评价了这些材料在碱性介质中催化电解水分解的适用性。与其他异质结构相比,10% FeP@B的N-V2C表现出最高的催化活性,在碱性介质中OER和HER的过电位分别为260 mV和235 mV,电流密度为10 mA cm−2。低Tafel值为56.85 mV dec - 1和118 mV dec - 1,在24小时内具有良好的稳定性,效率高达97.3%。电催化剂的有效性和稳定性通过其在1.57 V@10 mA cm−2的较低起始电位下进行整体水分解(OWS)的能力得到证实。在这些催化剂中观察到的低过电位和Tafel值归因于FeP纳米片与B,N共掺杂V2C纳米颗粒之间形成的异质结。由异质结引起的电化学活性的增强是由于更高的表面积,增加的孔隙率,降低的电化学电阻以及由于B,N共掺杂而引入的电活性中心。因此,该研究为开发用于能量转换应用的新型纳米材料提供了一个有希望的平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

B,N co-doped V2C nanoparticle embedded FeP nanoflake substrates as unique bifunctional electrocatalysts for overall water splitting in alkaline media†

B,N co-doped V2C nanoparticle embedded FeP nanoflake substrates as unique bifunctional electrocatalysts for overall water splitting in alkaline media†

Hydrogen energy as a solution to meet energy demands has highlighted the need for efficient and cost-effective electrocatalysts for hydrogen production through water electrolysis. Heterointerface materials with self-support have shown promising electrochemical performances due to their modulated electron structure, improved electrochemical surface area, and more active sites. In our study, we successfully synthesized a heterostructure material comprising iron phosphide (FeP) nanoflakes as a substrate, embedded with boron (B) and nitrogen (N) co-doped vanadium carbide (V2C) nanoparticles through a hydrothermal method followed by pyrolysis. We prepared FeP@B,N-V2C heterostructures to enhance efficiency using different weight ratios (5%, 10%, 15%, and 20%) of FeP substrates while adjusting B,N-V2C nanoparticles accordingly. The catalytic applicability of these materials was evaluated in electrochemical water splitting in an alkaline medium. Compared to other heterostructures, 10% FeP@B,N-V2C exhibited the highest catalytic activity, with overpotentials for the OER and HER in an alkaline medium of 260 mV and 235 mV, respectively, at a current density of 10 mA cm−2. The low Tafel values were determined as 56.85 mV dec−1 and 118 mV dec−1, with remarkable stability over 24 hours with a higher efficiency of 97.3%. The effectiveness and stability of electrocatalysts were corroborated by its ability in the overall water splitting (OWS), which occurred at a lower onset potential of 1.57 V@10 mA cm−2. The low overpotentials and Tafel values observed in these catalysts are attributed to the heterojunction formed between the FeP nanoflakes and B,N co-doped V2C nanoparticles. The enhancement in electrochemical activity resulting from the heterojunction is due to the higher surface area, increased porosity, decreased electrochemical resistance and the introduction in electroactive centres due to B,N co-doping. Consequently, this study provides a promising platform for developing novel nanomaterials for energy conversion applications.

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