Electrocatalytic and Selective Oxidation of Glycerol to Formate on 2D 3d-Metal Phosphate Nanosheets and Carbon-Negative Hydrogen Generation

IF 5.7 Q2 CHEMISTRY, PHYSICAL
Inderjeet Chauhan, Pothoppurathu M. Vijay, Ravi Ranjan, Kshirodra Kumar Patra and Chinnakonda S. Gopinath*, 
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引用次数: 0

Abstract

In the landscape of green hydrogen production, alkaline water electrolysis is a well-established, yet not-so-cost-effective, technique due to the high overpotential requirement for the oxygen evolution reaction (OER). A low-voltage approach is proposed to overcome not only the OER challenge by favorably oxidizing abundant feedstock molecules with an earth-abundant catalyst but also to reduce the energy input required for hydrogen production. This alternative process not only generates carbon-negative green H2 but also yields concurrent value-added products (VAPs), thereby maximizing economic advantages and transforming waste into valuable resources. The essence of this study lies in a novel electrocatalyst material. In the present study, unique and two-dimensional (2D) ultrathin nanosheet phosphates featuring first-row transition metals are synthesized by a one-step solvothermal method, and evaluated for the electrocatalytic glycerol oxidation reaction (GLYOR) in an alkaline medium and simultaneous H2 production. Co3(PO4)2 (CoP), Cu3(PO4)2 (CuP), and Ni3(PO4)2 (NiP) exhibit 2D sheet morphologies, while FePO4 (FeP) displays an entirely different snowflake-like morphology. The 2D nanosheet morphology provides a large surface area and a high density of active sites. As a GLYOR catalyst, CoP ultrathin (∼5 nm) nanosheets exhibit remarkably low onset potential at 1.12 V (vs RHE), outperforming that of NiP, FeP, and CuP around 1.25 V (vs RHE). CoP displays 82% selective formate production, indicating a superior capacity for C–C cleavage and concurrent oxidation; this property could be utilized to valorize larger molecules. CoP also exhibits highly sustainable electrochemical stability for a continuous 200 h GLYOR operation, yielding 6.5 L of H2 production with a 4 cm2 electrode and 98 ± 0.5% Faradaic efficiency. The present study advances our understanding of efficient GLYOR catalysts and underscores the potential of sustainable and economically viable green hydrogen production methodologies.

Abstract Image

二维 3d 磷酸盐金属纳米片上甘油到甲酸盐的电催化和选择性氧化及负碳制氢
在绿色制氢领域,碱性水电解是一种成熟但成本效益不高的技术,原因是氧进化反应(OER)需要较高的过电位。我们提出了一种低电压方法,不仅可以通过使用富土催化剂有利地氧化丰富的原料分子来克服氧进化反应的挑战,还可以减少制氢所需的能量输入。这种替代工艺不仅能产生负碳绿色氢气,还能同时产生增值产品 (VAP),从而最大限度地发挥经济优势,变废为宝。这项研究的精髓在于一种新型电催化剂材料。本研究采用一步溶热法合成了独特的二维(2D)超薄纳米片磷酸盐,其中含有第一排过渡金属,并对其在碱性介质中的甘油氧化反应(GLYOR)以及同时产生 H2 的电催化性能进行了评估。Co3(PO4)2 (CoP)、Cu3(PO4)2 (CuP) 和 Ni3(PO4)2 (NiP) 呈现出二维片状形态,而 FePO4 (FeP) 则呈现出完全不同的雪花状形态。二维纳米片形态提供了较大的表面积和高密度的活性位点。作为一种 GLYOR 催化剂,CoP 超薄(∼5 nm)纳米片的起始电位非常低,仅为 1.12 V(相对于 RHE),超过了 NiP、FeP 和 CuP 在 1.25 V 左右的起始电位(相对于 RHE)。CoP 显示出 82% 的甲酸选择性生成,表明其具有卓越的 C-C 裂解和同步氧化能力;这一特性可用于较大分子的估值。CoP 还在连续 200 小时的 GLYOR 操作中表现出高度可持续的电化学稳定性,4 平方厘米的电极可产生 6.5 升 H2,法拉第效率为 98 ± 0.5%。本研究加深了我们对高效 GLYOR 催化剂的了解,并强调了可持续且经济可行的绿色制氢方法的潜力。
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来源期刊
ACS Materials Au
ACS Materials Au 材料科学-
CiteScore
5.00
自引率
0.00%
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0
期刊介绍: ACS Materials Au is an open access journal publishing letters articles reviews and perspectives describing high-quality research at the forefront of fundamental and applied research and at the interface between materials and other disciplines such as chemistry engineering and biology. Papers that showcase multidisciplinary and innovative materials research addressing global challenges are especially welcome. Areas of interest include but are not limited to:Design synthesis characterization and evaluation of forefront and emerging materialsUnderstanding structure property performance relationships and their underlying mechanismsDevelopment of materials for energy environmental biomedical electronic and catalytic applications
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