2D graphdiyne materials: challenges and opportunities in energy field

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SCIENCE CHINA Chemistry, Volume 61, Issue 7: 765-786(2018) https://doi.org/10.1007/s11426-018-9270-y

2D graphdiyne materials: challenges and opportunities in energy field

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  • ReceivedMar 26, 2018
  • AcceptedApr 23, 2018
  • PublishedMay 31, 2018

Abstract

Graphdiyne (GDY), a novel two-dimensional (2D) carbon allotrope featuring one-atom-thick planar layers of sp and sp2 co-hybridized carbon network, is a rapidly rising star on the horizon of materials science. Because of its unparalleled structural, electronic, chemical and physical properties, it has been receiving unprecedented increases from fundamental studies to practical applications, particularly the field of energetic materials. In this review, we aim at providing an up-to-date comprehensive overview on the state-of-the-art research into GDY, from theoretical studies to the key achievements in the development of new GDY-based energetic materials for energy storage and conversion. By reviewing the state-of-the-art achievements, we aim to address the benefits and issues of GDY-based materials, as well as highlighting the existing key challenges and future opportunities in this exciting field.


Funded by

the Key Program of the Chinese Academy of Sciences(QYZDY-SSW-SLH015)

the National Natural Science Foundation of China(21790050)

the National Key Research and Development Project of China(2016YFA0200104)


Acknowledgment

This work was supported by the National Natural Science Foundation of China (21790050, 21790051), the National Key Research and Development Project of China (2016YFA0200104) and the Key Program of the Chinese Academy of Sciences (QYZDY-SSW-SLH015).


Interest statement

The authors declare that they have no conflict of interest.


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  • Figure 1

    A phase diagram showing materials consisting of carbon in a single hybridization state at the vertices, materials containing mixtures of two hybridization states along the edges, and materials with all three hybridization states within the triangle (color online).

  • Figure 2

    (a) Schematic of graphene to graphyne-linking aromatic groups by linear acetylene. Constructed full atomistic molecular models for grapheme (b), GY (c), GDY (d), GY-3 (e), and GY-4 (f) [21] (color online).

  • Figure 3

    (a) Structure of the interface between monolayer GDY and Cu(111) surface. (a) Top view and side view of the unit supercell, d is the interface distance. (b) Top views of top, hcp and fcc configurations, respectively. (c) is the relationship between binding energies and interface distance for different stacking configurations. The dashed line is the L-J fitting curve based on the fcc curve. (d) The change of bonding strength and gradient of charge density difference (CDD) during the interface peeling process. The curve in red is the difference between DFT-derived and fitted empirical curves. (e) The projected spin densities of states (PDOSs) of specific C and Cu atoms at different interface distances. (i) and (iii) are PDOSs for the sp2 C atom and the Cu atom below at interface distances of 3.2 and 1.91?? respectively; (ii) and (iv) are PDOSs for the sp C atom and the Cu atom below at interface distances of 3.2 and 1.91?? respectively. (f) PDOSs of graphdiyne and surface copper atoms at different interface distances. (i) is the PDOS of separated graphdiyne and surface copper atoms, (ii), (iii) and (iv) are PDOSs of the two components at interface distances of 3.2, 2.3 and 1.91??, respectively [36] (color online).

  • Figure 4

    (a) In-plane stiffness, (b) shear stiffness, and (c) Poisson’s ratio of graphyne-n as functions of the number of acetylenic linkages. (d) Dependence of the normalized in-plane stiffness, real bond density, and effective bond density on the number of acetylenic linkages [37] (color online).

  • Figure 5

    Optimized configurations of (a, b) bilayer and (c–e) trilayer GDY from top view. Band gap (by the left scale) and effective mass of carriers (me and mh, by the right scale) of AB(β1) (f) and AB(β2) (g) configuration of bilayer graphdiyne as a function of perpendicular electrical field strength. Filled squares and circles indicate the calculated m*e and m*h. (h) Band gaps of ABA(γ1), ABC(γ2), and ABC(γ3) trilayer configurations versus perpendicular electrical field strength [48] (color online).

  • Figure 6

    Synthesis and microscopic observations of multilayer GDY. (a) Schematic representation of the synthesis of GDY on Cu foil with hexaethynylbenzene as precursor. SEM images of large-area GDY films grown on the surface of copper foil (b, c), cracked film on the brim of copper foil (d), a turned up film (e). (f) AFM image of GDY film. (g) Tapping-mode 3D height AFM image. Schematic illustration (h) and a photograph (i) of the liquid/liquid interfacial synthetic procedure. (j) Optical microscope image on an HMDS/Si(100) substrate. (k) Atomic force microscope image on HMDS/Si(100) and cross-sectional analysis along the blue line. TEM image (l) and SAED pattern (m) on a holey elastic carbon matrix. Numerical values in panel f denote Miller indices. (n) GDY lattice of the ABC-stacking configuration (top view) determined by TEM/SAED. (o) High-resolution TEM micrograph (color online).

  • Figure 7

    The grooved template provided numerous regularly confined spacing at the microscale for the in situ synthesis of GDY, whereas the superlyophilicity of grooved templates is the key to allow a continuous mass transport of raw reactants and yield precisely patterned GDY stripes. (a) When a lyophilic template has been used to guide the growth of graphdiyne, air pockets usually existed in the middle part of the linear confined spacing, yielding just several graphdiyne dots in the two ends of the pillar gap regions. (b) When using a superlyophilic template, the hexaethynylbenzene-loading pyridine liquid can completely wet and pass through the linear confined spacing, allowing the generation of precisely patterned graphdiyne stripes. The contact angles of pyridine (γ=39.82?mN/m) droplet on the lyophilic (c) and superlyophilic (e) grooved templates. (d, f) The corresponding scanning electron microscopic (SEM) images of graphdiyne growth upon the copper foils. The dark areas are graphdiyne while the gray regions are copper foils. The scale bar is 500?μm. Adapted from Ref. [63] (color online).

  • Figure 8

    (a) Catalytic performance of N-doped GDY. From left to right: scheme of N-doped GDY; typical CV curves (scan rate 10?mV/s) of GDY and N-doped GDY on a GC RDE in an O2-saturated 0.1?M KOH solution; CV curves of N 550-GDY and Pt/C in Ar-saturated (black), O2-saturated (red), 3?M methanol and O2-saturated 0.1?M KOH (blue) solution. Adapted from Ref. [91]. (b) From left to right: LSV curves of GDY, NSGDY, NBGDY and NFGDY obtained from RDE measurements at 1600?rpm at a scan rate of 10?mV/s in O2-saturated 0.1?M KOH; LSV curves of NFGDY obtained from RDE measurements at different rotating rates from 400 to 1600?rpm; K–L plots of NFGDY calculated at different potentials on the basis of the RDE data; HO2-yields and electron transfer number of NFGD and 20% Pt/C at various disk electrode potentials obtained from the rotating ring-disk electrode tests (color online).

  • Figure 9

    (a) Schematic representation of the CoNC/GDY catalysts. (b) TEM and (c) STEM image and EDX elemental mapping of C, Co, and N for the CoNC/GDY catalyst. HER polarization curves of CoNC/GDY in (d) 1?M KOH initially and after 38000?CV scans (e) 0.5?M H2SO4 initially and after 38000?CV scans and (f) 1?M PBS initially and after 9000?CV scans. HER polarization curves of commercial Pt/C (10 wt.%) before and after 8000?CV scans in 1?M KOH (g), 0.5?M H2SO4 (h) and 1?M PBS (i). Adapted from Ref. [113] (color online).

  • Figure 10

    Low- and high-magnification SEM images of (a, b) NiCo-precursor NW/GDF and (c, d) NiCo2S4 NW/GDF. (e) Two electrode OER polarization curves (without iR compensation) of NiCo2S4 NW/GDF||NiCo2S4 NW/GDF, NiCo2S4 NW/CC||NiCo2S4 NW/CC, GDF||GDF, CC||CC, and RuO2||Pt/C. (f) Two-electrode cell stability of NiCo2S4 NW/GDF||NiCo2S4 NW/GDF electrode in 1.0?M KOH (color online).

  • Figure 11

    (a) Schematic diagram of the PEC cell, consisting of the assembled CdSe QDs/GDY photocathode, Pt wire as counter electrode, and corresponding interfacial migration process of the photogenerated excitons. (b) SEM images of the assembled CdSe QDs/GDY film. (c) The elemental mapping of carbon, selenium, sulfur and cadmium. (d) Open circuit potential response of the CdSe QDs/GDY photocathode under dark and illuminated conditions (300?W Xe lamp). (e) LSV scanning from 0.3 to ?0.4?V at 2?mV/s with light off (black trace) and on (red trace) [123] (color online).

  • Figure 12

    Lithium diffusion in GDY layers top view (a), side view (b). (c) CV curves at various scan rates. (d) Galvanostatic charge-discharge voltage profiles at various current densities. (e) Ragone plots of GDY/AC LICs compared with previously reported graphite and graphene LICs. (f) Cycling stability of GDY/AC LIC at a current density of 200?mA/g [143] (color online).

  • Figure 13

    (a) Schematic representation of an assembled GDY-based battery. (b) Cycle performance of the GDY-1, GDY-2, and GDY-3 electrodes at a current density of 500?mA/g between 5?mV and 3?V. Li-storage of GDY in a Li-ion cell: (c) Li-intercalated GDY. (d) Three different sites for occupation by Li atoms in GDY, absorption of Li atoms on (e, f) both sides and (g, h) one side of a GDY plane [146] (color online).

  • Figure 14

    (a) Schematic of a sodium ion battery based on GDY. (b) Cyclic voltammogram (CV) profiles of the GDY-based electrode at a scan rate of 0.2?mV/s. (c) Differential curves of charge/discharge profiles of the GDY-based electrode at a current density of 50?mA/g. (d) Galvanostatic charge-discharge profiles at a current density of 50?mA/g for the first three cycles. (e) Rate performance at varied current density ranging from 20 to 4000?mA/g. (f) Cycle performance at a current density of 100?mA/g [156] (color online).

  • Figure 15

    (a) Localized orbital locator (LOL) maps and Mayer bond order analysis for the Pt2-GDY fragment (off-center adsorption site). (b) ESP surfaces with an isovalue of 0.0004?e/au3 for Pt2-GDY (off-center adsorption site). (c) Cyclic voltammetry curves of different counter electrodes. (d) Photocurrent density-voltage (J-V) curves of DSSCs using different counter electrodes [163] (color online).

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