物理化学学报 >> 2020, Vol. 36 >> Issue (9): 1912005.doi: 10.3866/PKU.WHXB201912005
所属专题: 精准纳米合成
收稿日期:2019-12-02
录用日期:2019-12-30
发布日期:2020-02-14
通讯作者:
赵宇飞,宋宇飞
E-mail:songyf@mail.buct.edu.cn;zhaoyufei@mail.buct.edu.cn
作者简介:赵宇飞,出生于1985年。于2007年获得山西大学双学士学位。2011–2012年,于牛津大学Dermot O’Hare教授实验室交流学习。2013年于北京化工大学获得博士学位。现为北京化工大学化工资源有效利用国家重点实验室教授。主要研究方向为二维插层材料的可控合成及精细结构表征,LDHs基纳米材料的拓扑结构转变,面向高值精细化学品的光/电催化合成基金资助:
Tian Li, Xiaojie Hao, Sha Bai, Yufei Zhao(
), Yu-Fei Song(
)
Received:2019-12-02
Accepted:2019-12-30
Published:2020-02-14
Contact:
Yufei Zhao,Yu-Fei Song
E-mail:songyf@mail.buct.edu.cn;zhaoyufei@mail.buct.edu.cn
About author:Emails: zhaoyufei@mail.buct.edu.cn, +86-10-64431832 (Y.S.)Supported by:摘要:
水滑石(LDHs)是一种阴离子黏土材料,由于其主体层板厚度的可调性,使其在光/电催化、电池、超级电容器、传感器以及生物医药等领域都具有广泛应用。降低层厚至单层可使材料的物理化学性质发生根本改变,从而优化催化性能。近期研究表明,利用自上而下,自下而上的方法,可以实现单层LDHs类材料的合成,但是受限于产量(g级)以及成本设备等问题,目前规模化制备高质量单层LDHs类材料还没有工业案例。成核晶化隔离法是目前唯一规模化合成纳米LDHs的工业化方法,具有成本低,产量可吨级放大等优点。本综述从合成方法、表征手段、应用三个角度讨论了单层及超薄LDHs的精准调控,详细论述了近期关于单层及超薄LDHs合成突破以及LDHs的规模化生产进展,并对其性能进行了总结,为后续设计高性能单层LDHs提供思路。
李天, 郝晓杰, 白莎, 赵宇飞, 宋宇飞. 单层类水滑石纳米片的可控合成及规模生产展望[J]. 物理化学学报, 2020, 36(9), 1912005. doi: 10.3866/PKU.WHXB201912005
Tian Li, Xiaojie Hao, Sha Bai, Yufei Zhao, Yu-Fei Song. Controllable Synthesis and Scale-up Production Prospect of Monolayer Layered Double Hydroxide Nanosheets[J]. Acta Phys. -Chim. Sin. 2020, 36(9), 1912005. doi: 10.3866/PKU.WHXB201912005
表1
单层及超薄LDH合成方法"
| Number | Method | Thickness | Solvent | Remarks | Ref. |
| 1 | Organic solvent exfoliation | DDS, butanol | Organic LDH compounds are delaminated in vacuum drying at room temperature | 6 | |
| 2 | Formamide exfoliation | Amino acids, formamide | The characteristic peak of LDH in XRD disappears, The strong hydrogen bond between the anion and the polar solvent in the intercalation leads to the penetration of a large number of solvents in the intercalation, thus promoting exfoliation | 36 | |
| 3 | Formamide exfoliation | 0.8 nm | Formamide | No prior modification of amino acids or surfactants is required, requiring approximately 2.5 d and excess formamide | 37 |
| 4 | Formamide exfoliation | 0.7–1.4 nm | Formamide | The samples were dispersed in formamide and treated with ultrasonic water bath at continuous intervals of 30 min | 41 |
| 5 | Liquid exfoliation at low temperature | 0.6 nm | Sodium hydroxide/ urea solution | At low temperature, the exfoliation degree was larger, the thickness was reduced to 0.6 nm at -10 ℃ | 42 |
| 6 | Temperature shock method | ~0.18 nm | H2O | The LDH solution was frozen in liquid nitrogen and then melted in 80 water bath with a delamination rate of 61% | 44 |
| 7 | Ostwald ripening driven exfoliation | 4–9 nm | H2O, DMF | While, the as-exfoliated nanosheets are still vertically aligned on the electrode and possess a good structural integrity, which exhibits good electrical contact and effectively avoids the restacking of the exfoliated nanosheets | 43 |
| 8 | Aqueous miscible organic solvent treatment method | H2O, acetone | LDH wet samples were re-dispersed in acetone and stirred for 1 h, then washed with acetone. Dry samples were kept in monolayer | 45 | |
| 9 | Amino acid reconstruction method | ~0.8–1.5 nm | Amino acids | LDH was calcination in air and then reconstruct in aqueous solution of amino acid | 46 |
| 10 | Water-Plasma-Enabled Exfoliation | 1.54 nm | H2O | The as-obtained pristine CoFe LDHs were subjected to water-plasma treatment in a dielectric barrier discharge (DBD) plasma reactor for 5 min to obtain ultrathin CoFe LDHs nanosheets | 47 |
| 11 | Dry Exfoliation | 0.6 nm | Ar dry exfoliation is a clean, time-saving, non-toxic method and avoids the adsorption of solvent molecules | 48 | |
| 12 | Reverse microemulsion method | 1.5 nm | H2O, iso-octane, DDS, 1-butanol | Particle size in diameter and thickness can be effectively controlled by the ratio of water to surfactant, but surfactant residues are unavoidable | 49 |
| 13 | One step synthesis by formamide | 0.8 nm | H2O, formamide | The monolayer LDH was synthesized by adding formamide directly during the reaction | 52 |
| 14 | One-step synthesis by ethylene glycol | 0.85 nm | Ethylene glycol | It remains stable when dispersed in water or dried into powder | 56 |
| 15 | One step synthesis by H2O2 | 1.44 nm | H2O, H2O2 | LDHs catalyzes the rapid decomposition of H2O2 and releases a large amount of O2, which causes the layers to move violently, resulting in the separation of LDHs layers | 57 |
| 16 | One step synthesis by NH3·H2O | 0.8 nm | H2O | The gel was synthesized by co-precipitation, washed and re-dispersed by ultrasound in water, and the sample remained stable for 20 d at -4 ℃ | 58 |
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