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作为锌空气电池阴极用于将O电催化转化为H₂O的碳纳米片上的Ni-LDH芯片二维杂化物

2 D Hybrid of Ni-LDH Chips on Carbon Nanosheets as Cathode of Zinc-Air Battery for Electrocatalytic Conversion of O into H O.

作者信息

Huang Junheng, Chen Junxiang, Fu Changle, Cai Pingwei, Li Yan, Cao Linlin, Liu Wei, Yu Peng, Wei Shiqiang, Wen Zhenhai, Li Jinghong

机构信息

CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Provincial Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, 350002, P.R. China.

National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, 230029, P.R. China.

出版信息

ChemSusChem. 2020 Mar 20;13(6):1496-1503. doi: 10.1002/cssc.201902429. Epub 2019 Nov 4.

Abstract

It remains great challenge to develop precious-metal-free electrocatalysts to implement high-activity electrochemical conversion of O into value-added hydroperoxide species (HO ), which are vulnerable when exposed to various transition-metal-based catalysts. A strategy based on steric hindrance and layered nickel-based layered double hydroxide (Ni-LDH) induction has been developed for one-pot inlaying high-density ultrathin 2 D Ni-LDH chips on in situ-grown carbon nanosheets (Ni-LDH C/CNSs). The resulting material exhibits high electrocatalytic selectivity with a faradaic efficiency up to 95 % for oxygen reduction into peroxide and attains a fairly high mass activity of approximately 22.2 A g , outperforming most metal-based catalysts reported previously. Systematic studies demonstrate that the greatly increased defect concentration at Ni edge sites of Ni-LDH chips results in more active sites, which contributes a favorable thermodynamically neutral adsorption of OOH* and adsorbed H O molecules relatively weakly. Additionally, the modified CNSs effectively suppress H O decomposition and avoid O-O bond cleavage to produce H O by steric effects. The synergistic effect of CNSs and Ni-LDH chips therefore leads to high activity and high selectivity in a two-electron pathway. A proof-of-concept zinc-air fuel cell is proposed and set up to demonstrate the feasibility of green synthesis of peroxide, generating an impressive H O production rate of 5239.67 mmol h  g .

摘要

开发无贵金属电催化剂以实现将O高效电化学转化为增值氢过氧化物物种(HO )仍然是一个巨大的挑战,这些物种在暴露于各种过渡金属基催化剂时很容易受到影响。已开发出一种基于空间位阻和层状镍基层状双氢氧化物(Ni-LDH)诱导的策略,用于在原位生长的碳纳米片(Ni-LDH C/CNSs)上一锅镶嵌高密度超薄二维Ni-LDH芯片。所得材料表现出高电催化选择性,将氧还原为过氧化物的法拉第效率高达95%,并获得约22.2 A g 的相当高的质量活性,优于先前报道的大多数金属基催化剂。系统研究表明,Ni-LDH芯片的Ni边缘位点处缺陷浓度的大幅增加导致更多活性位点,这有利于OOH*的热力学中性吸附,而吸附的H O分子相对较弱。此外,改性的CNSs通过空间效应有效抑制H O分解并避免O-O键断裂以产生H O。因此,CNSs和Ni-LDH芯片的协同效应导致在双电子途径中具有高活性和高选择性。提出并建立了一个概念验证锌空气燃料电池,以证明过氧化物绿色合成的可行性,产生了令人印象深刻的5239.67 mmol h g 的H O生成速率。

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