Junfeng Zeng’s research while affiliated with Hunan University and other places

What is this page?


This page lists works of an author who doesn't have a ResearchGate profile or hasn't added the works to their profile yet. It is automatically generated from public (personal) data to further our legitimate goal of comprehensive and accurate scientific recordkeeping. If you are this author and want this page removed, please let us know.

Publications (6)


Micropore Effect for Boosting Carbon Dioxide Electroreduction over Nitrogen-Doped Carbon
  • Article

April 2025

·

2 Reads

ACS Applied Energy Materials

Minyang Dai

·

Junfeng Zeng

·

Ke Luo

·

[...]

·

Wenpeng Ni


(a) N2 adsorption–desorption isotherms of H-[R1R2Im]BPh4-FDA (R1 = M and Bn; R2 = E, HE, and DHP). (b) N2 adsorption–desorption isotherms of H-[BnR2Im]Br/BPh4-FDA. (c) Pore size distributions of H-[BnR2Im]Br/BPh4-FDA. (d) FT-IR spectra of H-[BnR2Im]Br/BPh4-FDA and [BnDHPIm]BPh4. (e) Solid-state CP/MAS ¹³C NMR spectrum of H-[BnDHPIm]Br/BPh4-FDA and ¹³C NMR spectrum (in DMSO-d6) of [BnDHPIm]BPh4. (f) XPS spectra of H-[BnR2Im]Br/BPh4-FDA. (g) XPS spectra of C 1s, N 1s, B 1s, and Br 3d of H-[BnDHPIm]Br/BPh4-FDA. (h) IL content and OH content of H-[BnR2Im]Br/BPh4-FDA. (i) Comparison of H-[BnR2Im]Br/BPh4-FDA and reported HCPIP samples in terms of specific surface areas and IL contents (the original data are shown in Table S4†)
(a and b) SEM images of H-[BnDHPIm]Br/BPh4-FDA. (c and d) TEM images of H-[BnDHPIm]Br/BPh4-FDA. (e) Elemental (O, B, and Br) mapping images of H-[BnDHPIm]Br/BPh4-FDA. (f) TGA curves of [BnDHPIm]Br, [BnDHPIm]BPh4, and H-[BnDHPIm]Br/BPh4-FDA
(a) CO2 adsorption isotherms of H-[BnR2Im]Br/BPh4-FDA (R2 = E, HE, and DHP) at 273 and 298 K. (b) The relationship between the CO2 uptake (at 273 K and 1 bar) of H-[BnR2Im]Br/BPh4-FDA and its OH content and specific surface area. (c) N2 adsorption isotherms of H-[BnR2Im]Br/BPh4-FDA at 273 K. (d) IAST CO2/N2 selectivity of H-[BnR2Im]Br/BPh4-FDA at 273 K. [Calculated by using the IAST model for the CO2/N2 (15% CO2 + 85% N2) mixture] (e) Henry's law CO2/N2 selectivity of H-[BnR2Im]Br/BPh4-FDA at 273 K. [Calculated by using the Henry's law constants in the linear low-pressure range (<0.11 bar)] (f) Qst of H-[BnR2Im]Br/BPh4-FDA for CO2 adsorption
(a) Catalytic activities of H-[BnDHPIm]Br/BPh4-FDA + TBABr, [BnDHPIm]BPh4 + TBABr, and TBABr alone in the cycloaddition reaction of CO2 and SO at different reaction times. (b) The relationship between the catalytic activity of H-[BnR2Im]Br/BPh4-FDA (R2 = E, HE, and DHP) in the cycloaddition reaction of CO2 and SO and its OH content and CO2 uptake. (c) Cycling performance of H-[BnDHPIm]Br/BPh4-FDA. (d) The cycloaddition reactions of CO2 with various epoxides catalyzed by H-[BnDHPIm]Br/BPh4-FDA + TBABr under ambient conditions. Reaction conditions: 12.5 mmol epoxide, 1 bar (balloon) CO2, (a) H-[BnDHPIm]Br/BPh4-FDA (4 wt%) + TBABr (2 mol%), [BnDHPIm]BPh4 (4 wt%) + TBABr (2 mol%), TBABr (2 mol%), 80 °C; (b) H-[BnR2Im]Br/BPh4-FDA (4 wt%) + TBABr (2 mol%), 80 °C, 15 h; (c) H-[BnDHPIm]Br/BPh4-FDA (4 wt%) + TBABr (2 mol%), 80 °C, 15 h; (d) H-[BnDHPIm]Br/BPh4-FDA (4 wt%) + TBABr (2 mol%)
(a) DFT-optimized geometries of [BnDHPIm]⁺ and the complex of [BnDHPIm]⁺ and CO2. Bond lengths are reported in Å. (b) In situ FT-IR spectra of CO2 adsorbed on H-[BnDHPIm]Br/BPh4-FDA with Ar purging for 15 min at room temperature, and the FT-IR spectrum of the background. (c) Partial ¹H NMR titration spectra of [BnDHPIm]BPh4 in DMSO-d6 with different amounts of SO (the complete spectra are shown in Fig. S28†). The values (0–10.0 eq.) in the spectra represent the molar ratios of SO/[BnDHPIm]BPh4. (d) FT-IR spectra of H-[BnDHPIm]Br/BPh4-FDA, SO, and H-[BnDHPIm]Br/BPh4-FDA with SO adsorbed. (e) In situ FT-IR spectra of H-[BnDHPIm]Br/BPh4-FDA with SO adsorbed at 80 °C for 60 min. (f) In situ FT-IR spectra of H-[BnDHPIm]Br/BPh4-FDA + TBABr catalyzing the cycloaddition reaction of SO and CO2 at ambient pressure and 80 °C for 15 min

+2

Non-cationic hyper-crosslinked ionic polymers with hierarchically ordered porous structures: facile synthesis and applications for highly efficient CO2 capture and conversion
  • Article
  • Full-text available

August 2024

·

41 Reads

Hyper-crosslinked porous ionic polymers (HCPIPs) have garnered significant attention due to their unique ionic properties and high specific surface areas. However, the limited variety of monomers, low ionic density, and difficulty in functionalization restrict their development. Herein, a series of functionalized non-cationic HCPIPs with high ionic density are designed and directly synthesized via an innovative and straightforward approach – anion (and cation) hyper-crosslinking of tetraphenylborate-based ionic liquids (ILs). These HCPIPs offer controllable hydroxyl group content (0–2.40 mmol g⁻¹), high IL content (1.20–1.78 mmol g⁻¹), and large specific surface area (636–729 m² g⁻¹) with hierarchically ordered porous structures. These HCPIPs demonstrate exceptional CO2 adsorption capacities and CO2/N2 adsorption selectivities, reaching up to 2.68–3.01 mmol g⁻¹ and 166–237, respectively, at 273 K and 1 bar. Furthermore, these ionic porous materials serve as highly efficient heterogeneous catalysts for CO2 cycloaddition to epoxides under mild conditions (1 bar CO2, 60–80 °C, 12–24 h). Notably, the CO2 adsorption performances and catalytic activities of these HCPIPs are regulated by the hydroxyl groups within their structures, with enhancements observed as the number of hydroxyl groups increases. This work presents a facile and widely applicable method for constructing high-performance and task-specific HCPIPs.

Download



Citations (1)


... A precise identification of the local structures of nonmetallic species beyond the first coordination shell (n ≥ 2) of metal centers in a heteroatom doping SAC system is still challenging by current characterizing techniques. 49 (Figure 4a). Their most stable configuration and corresponding relative formation energy were explored (Figure 4a and Figure S16). ...

Reference:

Fe-NC Single-Atom Catalyst with Hierarchical Porous Structure and P–O Bond Coordination for Oxygen Reduction
Regulating Nonmetallic Species Beyond the First Coordination Shell of Single-Atom Catalysts for High-Performance Electrocatalysis
  • Citing Article
  • January 2023

Energy & Environmental Science