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石墨炔是由2种不同杂化形式的碳原子拓扑有序构成的二维碳同素异形体。石墨炔中共存的sp和sp2杂化碳原子使得表面电子局域不均匀分布,从而为设计化学反应、位点选择掺杂、可控的原子担载提供了可能。本文从石墨炔独特的富炔结构出发,总结了石墨炔的精准修饰技术:1)石墨炔与纳米颗粒复合,利用金属-石墨炔的成键,提升材料间的电荷转移;2)利用炔键所赋予的化学反应位点,实现异质原子定点可控掺杂;3)利用石墨炔炔键电子与金属空轨道作用,调控离子或原子的传输与锚定。石墨炔的炔键结构为发展新合成方法,拓展材料在能源、催化等领域的应用提供了新的思路。
Abstract:Graphyne is a two-dimensional carbon allotropy that consists of different hybrid forms of carbon atoms in topological order. In different kinds of graphyne, carbon atoms undergo a rich bonding process through sp and sp2 hybridization, i.e., aromatic bonds, single bonds, and triple bonds, forming electron covalent frameworks and pores. Different bond lengths provide a higher structural flexibility and make coordination environmental regulation easier. For instance, the coexistence of sp and sp2 hybrid carbon atoms in graphdiyne(i.e., a typical and only artificially synthesized graphyne) makes the surface local electrons distributed unevenly, which makes it possible to design chemical reactions, site selective doping, and controllable atomic loading. The effective synthesis of graphdiyne(GDY) has thus brought a vitality to the research and development of carbon materials, providing a platform for carbon materials in various fields such as energy conversion and storage, optics, electronics, and magnetism, and having opportunities for the development of transformative materials. This unique alkyne bond rich structure provides almost infinite possibilities for the precise GDY tailoring towards different specific application scenarios. This review thus represented recent development on the GDY modifications and the corresponding functionalities of alkyne bonds. The precise modifications of graphdiyne(GDY) with the unique acetylene rich structure can be summarized as follows: 1) Compounding graphdiyne with nanoparticles(NPs), or the formation of metal graphdiyne bonding to enhance the charge transfer between materials. The structure rich in sp carbon can hybridize with other active components(such as molecules and NPs) to form a larger electron cloud density overlap, resulting in intense interactions. The composition with NPs can accelerate electron transfer and enhance the activity and stability for catalysis. GDY is easy to obtain and lose electrons, which is referred as an “electron sponge” property. A portion of GDY electrons can transfer with the hybrid across the interface. The electron cloud at a polarized region generates unique electron transfer enhancement characteristics. 2) Utilizing acetylene bonds as the chemical reaction sites to achieve controlled doping of heteroatoms at desired sites. The sp and sp2 hybrid carbon atoms have a higher chemical activity, providing greater possibilities for the targeted introduction of heteroatoms. Especially, the triple bonds can create a form of nitrogen doping(i.e. sp-N) through pericyclic reaction and click reaction. Some work reveal a clear upward trend with the concentration of sp-N for ORR, OER and CO2RR reaction. Meanwhile, the doping of sp-N atoms with clear chemical sites paves a way for the development of high-performance carbon based catalytic materials via precise site modifications. Furthermore, optimized doping configuration and suitable spatial distance can enhance a catalytic activity when doping multiple elements. These findings clearly demonstrate that GDY can control the doping at desired sites for synergistic effects and catalytic performance optimization. 3) The regulation of ions or atoms transportation or anchoring metal atoms. The two-dimensional plane topology of GDY is orderly distributed with molecular pores of specific sizes. The molecular pore and the surrounding acetylene rich structure endow it with a unique localized electron distribution. Therefore, regulating the size of stacking pores and the surrounding environment will affect the mass transfer process, thus applying graphene into more fields like seawater desalination and photothermal steaming evaporation. More importantly, the electrons from alkyne bond can interact with the metal empty orbits. The unique properties of GDY make it a suitable carrier for anchoring single metal atoms. The anchored metal atoms on the surface of GDY tends to be in zero valence, which in turn brings unique catalytic properties. Summary and prospects Graphene is a novel two-dimensional carbon material composed of sp and sp2 hybrid carbon atom topologies. This material has attracted widespread attention in various fields such as materials, chemistry, physics, information, biology, and the environment due to its high conjugation, abundant acetylene bonds, regular ordered pores, and adjustable electronic structure, which still has many challenges and opportunities in the future.1) Developing large-scale, high-quality, and low-cost synthesis technology can provide a solid material foundation for theoretical research and practical applications. The preparation methods for other types of graphene(such as GY, GY-3, and GY-4) are still in the exploratory stage. Obtaining novel graphene materials will expand the application field and clarify the structure-activity relationship. 2) The alkyne bonds of graphene provide more designability. Designing chemical reactions based on alkyne bonds is of great significance for improving the performance of non-metallic catalytic materials. Synthesizing graphene and its derivatives with precise structures, controlling the degree of reaction and functionalization of alkyne bonds can effectively expand the scope and depth of “alkyne chemistry”. 3) A more precise manipulation of the pore structure of graphene is needed. The precise regulation from molecular pores to nanopores will deepen the understanding of the atoms/ions transport and anchoring in GDY, and fully leverage its structural advantages. Accurately controlling the anchoring points, atomic numbers, and atomic types of metal elements is crucial for developing atomic catalytic materials, enhancing catalytic activity, selectivity and stability. The unique rich alkyne bond and pore structure of graphene provide infinite possibilities for the precise synthesis and controllable preparation. This review can provide a reference to understand the development of graphene materials for various applications.
[1] INAGAKI M, KANG F, TOYODA M, et al. Advanced materials science and engineering of carbon[J]. MRS Bull, 2013, 39:1018.
[2] WANG Y Z, YANG P J, ZHENG L X, et al. Carbon nanomaterials with sp2 or/and sp hybridization in energy conversion and storage applications:A review[J]. Energy Storage Mater, 2020, 26:349–370.
[3] BAUGHMAN R H, ECKHARDT H, KERTESZ M. Structure-property predictions for new planar forms of carbon:Layered phases containing sp2 and sp atoms[J]. J Chem Phys, 1987, 87(11):6687–6699.
[4] LI G X, LI Y L, LIU H B, et al. Architecture of graphdiyne nanoscale films[J]. Chem Commun, 2010, 46(19):3256–3258.
[5] LI J, ZHU L, TUNG C H, et al. Engineering graphdiyne for solar photocatalysis[J]. Angew Chem Int Ed, 2023, 62(22):e202301384.
[6] ZHOU X, FU B H, LI L J, et al. Hydrogen-substituted graphdiyne encapsulated cuprous oxide photocathode for efficient and stable photoelectrochemical water reduction[J]. Nat Commun, 2022, 13:5770.
[7] SHANG H, ZUO Z C, YU L, et al. Low-temperature growth of all-carbon graphdiyne on a silicon anode for high-performance lithium-ion batteries[J]. Adv Mater, 2018, 30(27):1801459.
[8] HUANG H H, LI K N, FAN X F, et al. Storage of Na in layered graphdiyne as high capacity anode materials for sodium ion batteries[J].J Mater Chem A, 2019, 7(44):25609–25618.
[9] KRISHNAMOORTHY K, THANGAVEL S, CHELORA VEETIL J, et al. Graphdiyne nanostructures as a new electrode material for electrochemical supercapacitors[J]. Int J Hydrog Energy, 2016, 41(3):1672–1678.
[10] PARVIN N, JIN Q, WEI Y Z, et al. Few-layer graphdiyne nanosheets applied for multiplexed real-time DNA detection[J]. Adv Mater, 2017,29(18):1606755.
[11] LIU J M, CHEN C Y, ZHAO Y L. Progress and prospects of graphdiyne-based materials in biomedical applications[J]. Adv Mater,2019, 31(42):1804386.
[12] JIN J, GUO M Y, LIU J M, et al. Graphdiyne nanosheet-based drug delivery platform for photothermal/chemotherapy combination treatment of cancer[J]. ACS Appl Mater Interfaces, 2018, 10(10):8436–8442.
[13] GAO X, ZHOU J Y, DU R, et al. Robust superhydrophobic foam:A graphdiyne-based hierarchical architecture for oil/water separation[J].Adv Mater, 2016, 28(1):168–173.
[14] LIU Q, LI J Q, HADJICHRISTIDIS N. Graphdiyne aerogel architecture via a modified Hiyama coupling reaction for gas adsorption[J]. Chem Commun, 2023, 59(15):2165–2168.
[15] LI B S, LAI C, ZHANG M M, et al. Graphdiyne:A rising star of electrocatalyst support for energy conversion[J]. Adv Energy Mater,2020, 10(16):2000177.
[16]詹舒辉,赵亚松,杨乃亮,等.石墨炔孔结构:设计、合成和应用[J].高等学校化学学报, 2021, 42(2):333–348.ZHAN Shuhui, ZHAO Yasong, YANG Nailiang, et al. Chem J Chin Univ, 2021, 42(2):333–348.
[17]赵亚松,张丽娟,齐健,等.石墨二炔及其电子转移增强特性[J].物理化学学报, 2018, 34(9):1048–1060.ZHAO Yasong, ZHANG Lijuan, QI Jian, et al. Acta Phys Chim Sin,2018, 34(9):1048–1060.
[18] GAO X, LIU H B, WANG D, et al. Graphdiyne:Synthesis, properties,and applications[J]. Chem Soc Rev, 2019, 48(3):908–936.
[19]黄长水,李玉良.二维碳石墨炔的结构及其在能源领域的应用[J].物理化学学报, 2016, 32(6):1314–1329.HUANG Changshui, LI Yuliang. Acta Phys Chim Sin, 2016, 32(6):1314–1329.
[20] ZHANG C, XUE Y R, ZHENG X C, et al. Loaded Cu-Er metal iso-atoms on graphdiyne for artificial photosynthesis[J]. Mater Today,2023, 66:72–83.
[21] BAI L, ZHENG Z Q, WANG Z Q, et al. Acetylenic bond-driven efficient hydrogen production of a graphdiyne based catalyst[J]. Mater Chem Front, 2021, 5(5):2247–2254.
[22] YANG Z, SONG Y W, REN X, et al. A universal way to prepare graphyne derivatives with variable band gap and lithium storage properties[J]. Carbon, 2021, 182:413–421.
[23] REN H, SHAO H, ZHANG L J, et al. A new graphdiyne nanosheet/Pt nanoparticle-based counter electrode material with enhanced catalytic activity for dye-sensitized solar cells[J]. Adv Energy Mater, 2015,5(12):1500296.
[24] WANG S, YI L X, HALPERT J E, et al. A novel and highly efficient photocatalyst based on P25–graphdiyne nanocomposite[J]. Small, 2012,8(2):265–271.
[25] YANG N L, LIU Y Y, WEN H, et al. Photocatalytic properties of graphdiyne and graphene modified TiO2:From theory to experiment[J].ACS Nano, 2013, 7(2):1504–1512.
[26] LIU R J, LIU H B, LI Y L, et al. Nitrogen-doped graphdiyne as a metal-free catalyst for high-performance oxygen reduction reactions[J].Nanoscale, 2014, 6(19):11336–11343.
[27] LV Q, SI W Y, YANG Z, et al. Nitrogen-doped porous graphdiyne:A highly efficient metal-free electrocatalyst for oxygen reduction reaction[J]. ACS Appl Mater Interfaces, 2017, 9(35):29744–29752.
[28] LI J, YI Y, ZUO X, et al. Graphdiyne/graphene/graphdiyne sandwiched carbonaceous anode for potassium-ion batteries[J]. ACS Nano, 2022,16(2):3163–3172.
[29] WANG N, HE J J, TU Z Y, et al. Synthesis of chlorine-substituted graphdiyne and applications for lithium-ion storage[J]. Angew Chem Int Ed, 2017, 56(36):10740–10745.
[30] ZOU H Y, ARACHCHIGE L J, RONG W F, et al. Low-valence metal single atoms on graphdiyne promotes electrochemical nitrogen reduction via M-to-N2π-backdonation[J]. Adv Funct Mater, 2022,32(24):2200333.
[31] WANG N, LI X D, TU Z Y, et al. Synthesis and electronic structure of boron-graphdiyne with an sp-hybridized carbon skeleton and its application in sodium storage[J]. Angew Chem Int Ed, 2018, 57(15):3968–3973.
[32] SHEN X Y, LI X D, ZHAO F H, et al. Preparation and structure study of phosphorus-doped porous graphdiyne and its efficient lithium storage application[J]. 2D Mater, 2019, 6(3):035020.
[33] AUTRETO P A S, DE SOUSA J M, GALVAO D S. Site-dependent hydrogenation on graphdiyne[J]. Carbon, 2014, 77:829–834.
[34] YANG Z, CUI W W, WANG K, et al. Chemical modification of the sp-hybridized carbon atoms of graphdiyne by using organic sulfur[J].Chem A Eur J, 2019, 25(22):5643–5647.
[35] ZHAO Y S, YANG N L, YAO H Y, et al. Stereodefined codoping of sp-N and S atoms in few-layer graphdiyne for oxygen evolution reaction[J]. J Am Chem Soc, 2019, 141(18):7240–7244.
[36] ZHAO Y S, WAN J W, YAO H Y, et al. Few-layer graphdiyne doped with sp-hybridized nitrogen atoms at acetylenic sites for oxygen reduction electrocatalysis[J]. Nat Chem, 2018, 10(9):924–931.
[37] LIU B K, ZHAN S H, DU J, et al. Revealing the mechanism of sp-N doping in graphdiyne for developing site-defined metal-free catalysts[J]. Adv Mater, 2022:2206450.
[38] ZHAO Y S, WAN J W, YANG N L, et al. Sp-Hybridized nitrogen doped graphdiyne for high-performance Zn–air batteries[J]. Mater Chem Front, 2021, 5:7987–7992.
[39] BU H X, ZHAO M W, ZHANG H Y, et al. Isoelectronic doping of graphdiyne with boron and nitrogen:Stable configurations and band gap modification[J]. J Phys Chem A, 2012, 116(15):3934–3939.
[40] ZHAO Y S, YANG N L, WANG C D, et al. Boosting hydrogen evolution reaction on few-layer graphdiyne by sp-N and B co-doping[J]. APL Mater, 2021, 9(7):071102.
[41] HE J J, WANG N, YANG Z, et al. Fluoride graphdiyne as a free-standing electrode displaying ultra-stable and extraordinary high Li storage performance[J]. Energy Environ Sci, 2018, 11(10):2893–2903.
[42] AN J, ZHANG H Y, QI L, et al. Self-expanding ion-transport channels on anodes for fast-charging lithium-ion batteries[J]. Angew Chem Int Ed, 2022, 61(7):e202113313.
[43] WANG K, WANG N, HE J J, et al. Preparation of 3D architecture graphdiyne nanosheets for high-performance sodium-ion batteries and capacitors[J]. ACS Appl Mater Interfaces, 2017, 9(46):40604–40613.
[44] CRANFORD S W, BUEHLER M J. Selective hydrogen purification through graphdiyne under ambient temperature and pressure[J].Nanoscale, 2012, 4(15):4587–4593.
[45] ZHOU Z H, TAN Y T, YANG Q, et al. Gas permeation through graphdiyne-based nanoporous membranes[J]. Nat Commun, 2022,13(1):1–6.
[46] MA H, YANG B B, WANG Z, et al. A three dimensional graphdiyne-like porous triptycene network for gas adsorption and separation[J]. RSC Adv, 2022, 12(44):28299–28305.
[47] XUE M M, QIU H, GUO W L. Exceptionally fast water desalination at complete salt rejection by pristine graphyne monolayers[J].Nanotechnology, 2013, 24(50):505720.
[48] ZHAN S H, CHEN X B, XU B, et al. Hollow multishelled structured graphdiyne realized radioactive water safe-discharging[J]. Nanotoday,2022, 47:101626.
[49] FU X L, ZHAO X, LU T B, et al. Graphdiyne-based single-atom catalysts with different coordination environments[J]. Angew Chem Int Ed, 2023, 62(16):e202219242.
[50] XUE Y R, HUANG B L, YI Y P, et al. Anchoring zero valence single atoms of nickel and iron on graphdiyne for hydrogen evolution[J]. Nat Commun, 2018, 9(1):1–10.
[51] HUI L, XUE Y R, YU H D, et al. Highly efficient and selective generation of ammonia and hydrogen on a graphdiyne-based catalyst[J].J Am Chem Soc, 2019, 141(27):10677–10683.
[52] YU H D, XUE Y R, HUI L, et al. Graphdiyne-based metal atomic catalysts for synthesizing ammonia[J]. Natl Sci Rev, 2021, 8(8):nwaa213.
[53] ZHENG Z Q, WANG Z Q, XUE Y R, et al. Selective conversion of CO2 into cyclic carbonate on atom level catalysts[J]. ACS Mater Au,2021, 1(2):107–115.
[54] SHI G D, XIE Y L, DU L L, et al. Constructing Cu-C bonds in a graphdiyne-regulated Cu single-atom electrocatalyst for CO2 reduction to CH4[J]. Angew Chem Int Ed, 2022, 61(23):e202203569.
[55] HUI L, XUE Y R, XING C Y, et al. Highly loaded independent Pt0atoms on graphdiyne for pH-general methanol oxidation reaction[J].Adv Sci, 2022, 9(16):2104991.
[56] HE T W, ZHANG L, KOUR G, et al. Electrochemical reduction of carbon dioxide on precise number of Fe atoms anchored graphdiyne[J].J CO2 Util, 2020, 37:272–277.
基本信息:
DOI:10.14062/j.issn.0454-5648.20230445
中图分类号:O613.71
引用信息:
[1]王祖民,杨乃亮,于然波,等.炔键赋予的石墨炔位点选择性修饰[J].硅酸盐学报,2024,52(02):390-404.DOI:10.14062/j.issn.0454-5648.20230445.
基金信息:
国家自然科学基金重点项目(51932001)
2023-06-28
2023
2024-01-09
2024-01-02
2024
1
2023-12-04
2023-12-04
2023-12-04