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在VNi层状双氢氧化物中引入硫可实现苄胺在高电流密度下的高效电催化氧化。

Introducing Sulfur in VNi-Layered Double Hydroxide Enables Efficient Electrocatalytic Oxidation of Benzylamine with High Current Densities.

作者信息

Singh Baghendra, Kumar Rakesh, Verma Neetu, Draksharapu Apparao

机构信息

Southern Laboratories-208A, Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur 208016, India.

Department of Chemistry, Indian Institute of Technology (BHU), Varanasi 221005, India.

出版信息

ACS Appl Mater Interfaces. 2025 Jan 22;17(3):5008-5016. doi: 10.1021/acsami.4c20149. Epub 2025 Jan 8.

Abstract

The replacement of the thermodynamically unfavorable anodic oxygen evolution reaction (OER) with a more favorable organic oxidation reaction, such as the anodic oxidation of benzylamine, has garnered significant interest in hybrid water electrolyzer cells. This approach promises the production of value-added chemicals alongside hydrogen fuel generation, improving overall energy efficiency. However, achieving high current density for benzylamine oxidation without interference from OER remains a challenge, limiting the practical efficiency of the electrolyzer cell. In this study, we investigated a room temperature method for sulfur introduction in VNi-layered double hydroxide (LDH) catalyst and its application for electrocatalytic benzylamine oxidation. The S-introduction in VNi-LDH was found to modulate the electronic states of nickel and vanadium, increasing the number of active sites, electrochemical surface area, and charge transfer properties. The resulting S-VNi-LDH catalyst achieved a high current density of 400 mA cm at only 1.39 V vs RHE potential for benzylamine oxidation, avoiding interference from oxygen evolution. The catalyst demonstrated 100% selectivity (Faradaic Efficiency = 98.6%) for the conversion of benzylamine into benzonitrile within 2.5 h of the reaction. In a two-electrode electrolysis system, S-VNi-LDH achieved a current density of 400 mA cm at a cell voltage of 1.50 V when OER was substituted with benzylamine oxidation. The S-VNi-LDH showed energy consumption of 4.67 kWh/m H for OER and 1.31 kWh/m H during benzylamine oxidation, indicating a high energy efficiency with exceptional stability over five cycles, maintaining 98.6 ± 0.4% FE and consistent voltage. The S-VNi-LDH also oxidized various amines, including substituted benzylamines and secondary amines, achieving high conversion (95-97%) and faradaic efficiency (85.8-98%). This study presents an eco-friendly, room-temperature method for S-doping in VNi-LDH, which out performed the reported catalysts in the literature.

摘要

用更有利的有机氧化反应(如苄胺的阳极氧化)取代热力学上不利的阳极析氧反应(OER),已在混合水电解槽中引起了广泛关注。这种方法有望在产生氢燃料的同时生产增值化学品,提高整体能源效率。然而,在不受OER干扰的情况下实现苄胺氧化的高电流密度仍然是一个挑战,限制了电解槽的实际效率。在本研究中,我们研究了一种在VNi层状双氢氧化物(LDH)催化剂中引入硫的室温方法及其在电催化苄胺氧化中的应用。发现VNi-LDH中引入硫可调节镍和钒的电子态,增加活性位点数量、电化学表面积和电荷转移性能。所得的S-VNi-LDH催化剂在相对于可逆氢电极(RHE)仅1.39 V的电位下,对苄胺氧化实现了400 mA/cm²的高电流密度,避免了析氧干扰。该催化剂在反应2.5小时内将苄胺转化为苄腈的选择性为100%(法拉第效率=98.6%)。在两电极电解系统中,当用苄胺氧化取代OER时,S-VNi-LDH在1.50 V的电池电压下实现了400 mA/cm²的电流密度。S-VNi-LDH在OER时的能耗为4.67 kWh/m³H,在苄胺氧化时为1.31 kWh/m³H,表明其具有高能量效率,在五个循环中具有出色的稳定性,保持98.6±0.4%的法拉第效率和稳定的电压。S-VNi-LDH还能氧化各种胺,包括取代苄胺和仲胺,实现高转化率(95-97%)和法拉第效率(85.8-98%)。本研究提出了一种在VNi-LDH中进行硫掺杂的环保室温方法,该方法优于文献中报道的催化剂。

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