| 1. |
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- 2019
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Tidskriftsartikel (refereegranskat)
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| 2. |
- Chen, Cheng, et al.
(författare)
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Molecular Engineering of Triphenylamine-Based Non-Fullerene Electron-Transport Materials for Efficient Rigid and Flexible Perovskite Solar Cells
- 2018
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Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 10:45, s. 38970-38977
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Tidskriftsartikel (refereegranskat)abstract
- There has been a growing interest in the design and synthesis of non-fullerene electron transport materials (ETMs) for perovskite solar cells (PSCs), which may overcome the drawbacks of traditional fullerene derivatives. In this work, a novel donor-acceptor (D-A) structured ETM termed TPA-3CN is presented by molecular engineering of triphenylamine (TPA) as the donor group and (3-cyano-4,5,5-trimethyl-2(5H)-furanylidene) malononitrile as the acceptor group. To further improve the electron mobility and conductivity and achieve excellent photovoltaic performance, a solution processable n-type dopant is introduced during the ETM spin-coating step. After device optimization, PSCs based on the doped TPA-3CN exhibit an impressive power conversion efficiency (PCE) of 19.2% with a negligible hysteresis. Benefitting from the low temperature and good solution processability of ETM TPA-3CN, it was further applied in flexible inverted PSCs and an impressive PCE of 13.2% was achieved, which is among the highest values reported for inverted flexible fullerene-free PSCs.
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| 3. |
- Zhu, Xingwang, et al.
(författare)
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Mo-O-Bi Bonds as interfacial electron transport bridges to fuel CO2 photoreduction via in-situ reconstruction of black Bi2MoO6/ BiO2-x heterojunction
- 2022
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Ingår i: Chemical Engineering Journal. - : ELSEVIER SCIENCE SA. - 1385-8947 .- 1873-3212. ; 429
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Tidskriftsartikel (refereegranskat)abstract
- High photogenerated carrier separation efficiency plays a crucial role in determining the rate of photocatalytic CO2 reduction, but the directional transfer of carrier remains challenging. Here, improved CO2 photoreduction rate and enhanced stability were realized by in-situ construction of BiO2-x nanoparticles on Bi2MoO6 nanoflowers using H2/Ar low temperature plasma. As evidenced by DFT calculations and photocurrent measurements, the Mo-O-Bi bonds between the Bi2MoO6 and BiO2-x interfaces act as a charge transport bridge, facilitating the directional transport of electrons and thus enhancing the rate of photocatalytic reduction reactions involving multiple electrons. Compared with pristine Bi2MoO6, Bi2MoO6/BiO2-x heterojunction has excellent photostability (12 h) and efficient photocatalytic activity (approximate to 3.0 times). This indicates that the charge transfer bridge can effectively inhibit the charge recombination and deactivation of pristine Bi2MoO6. This interatomic charge transfer bridges mode can not only solve the stability problem of bismuth-based materials, but also help to design more photocatalytic systems for efficient reduction of CO2.
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| 4. |
- Liu, Gaopeng, et al.
(författare)
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Edge-Site-Rich Ordered Macroporous BiOCl Triggers C(sic)O Activation for Efficient CO2 Photoreduction
- 2022
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Ingår i: Small. - : WILEY-V C H VERLAG GMBH. - 1613-6810 .- 1613-6829. ; 18:6
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Tidskriftsartikel (refereegranskat)abstract
- Endowing a semiconductor with tunable edge active sites will effectively enhance catalytic performance. Herein, an edge-site-rich ordered macroporous BiOCl (BiOCl-P) with abundant dangling bonds is constructed via the colloidal crystal template method. The edge-site-rich ordered macroporous structure provides abundant adsorption sites for CO2 molecules, as well as forms numerous localized electron enrichment areas, accelerating charge transfer. DFT calculations reveal that the dangling bonds-rich configuration can effectively reduce the CO2 activation energy barrier, boost the C(sic)O double bond dissociation, and facilitate the proton electron coupling reaction. As a result, the BiOCl-P achieves a higher CO and CH4 generation rate of 78.07 and 3.03 mu mol g(-1) under 4 h Xe lamp irradiation in a solid-gas system. Finally, the CO2 molecules conversion process is further investigated by in situ Fourier-transform infrared spectroscopy. This work realizes a new avenue toward the design of vibrant semiconductors on the nanoscale to boost inert CO2 photoreduction.
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| 5. |
- Wang, Junbo, et al.
(författare)
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Influence of Molecular Configurations on the Desulfonylation Reactions on Metal Surfaces
- 2022
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Ingår i: Journal of the American Chemical Society. - : AMER CHEMICAL SOC. - 0002-7863 .- 1520-5126. ; 144:47, s. 21596-21605
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Tidskriftsartikel (refereegranskat)abstract
- On-surface synthesis is a powerful methodology for the fabrication of low-dimensional functional materials. The precursor molecules usually anchor on different metal surfaces via similar configurations. The activation energies are therefore solely determined by the chemical activity of the respective metal surfaces. Here, we studied the influence of the detailed adsorption configuration on the activation energy on different metal surfaces. We systematically studied the desulfonylation homocoupling for a molecular precursor on Au(111) and Ag(111) and found that the activation energy is lower on inert Au(111) than on Ag(111). Combining scanning tunneling microscopy observations, synchrotron radiation photoemission spectroscopy measurements, and density functional theory calculations, we elucidate that the phenomenon arises from different molecule-substrate interactions. The molecular precursors anchor on Au(111) via Au-S interactions, which lead to weakening of the phenyl-S bonds. On the other hand, the molecular precursors anchor on Ag(111) via Ag-O interactions, resulting in the lifting of the S atoms. As a consequence, the activation barrier of the desulfonylation reactions is higher on Ag(111), although silver is generally more chemically active than gold. Our study not only reports a new type of on-surface chemical reaction but also clarifies the influence of detailed adsorption configurations on specific on-surface chemical reactions.
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| 6. |
- Zhu, Xingwang, et al.
(författare)
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Accelerated Photoreduction of CO2 to CO over a Stable Heterostructure with a Seamless Interface
- 2021
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Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 13:33, s. 39523-39532
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Tidskriftsartikel (refereegranskat)abstract
- Photocatalytic CO2 reduction is a means of alleviating energy crisis and environmental deterioration. In this work, a rising two-dimensional (2D) material rarely reported in the field of photocatalytic CO2 reduction, black phosphorus (BP) nanosheets, is synthesized, on which Co2P is in situ grown by solvothermal treatment using BP itself as a P source. Co2P on the BP nanosheets (BPs) surface can prevent the destruction of BPs in ambient air and, in the meantime, favor charge separation and CO2 adsorption and activation during the catalytic process. Upon light irradiation, Co2P can extract the photogenerated electrons effectively across the intimate interface and lower the CO2 activation energy barrier, supported by both experimental characterizations and theoretical calculations. Benefitting from integrated advantages of BPs and Co2P, the optimal Co2P/BPs exhibit photocatalytic reduction of CO2 to CO at a rate of 25.5 mu mol g(-1) h(-1) with a selectivity of 91.4%, both of which are higher than those of pristine BPs. This work presents ideas for stabilizing BPs and improving their CO2 reduction performance simultaneously.
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| 7. |
- Zhu, Xingwang, et al.
(författare)
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Nanostructure and functional group engineering of black phosphorus via plasma treatment for CO2 photoreduction
- 2021
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Ingår i: Journal of CO2 Utilization. - : ELSEVIER SCI LTD. - 2212-9820 .- 2212-9839. ; 54
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Tidskriftsartikel (refereegranskat)abstract
- As an emerging two-dimensional (2D) semiconductor, black phosphorus (BP) has attracted great interest in photocatalytic CO2 reduction, but the performance is restricted by the low surface reactivity and poor stability. Exfoliating BP into the 2D structure is an effective method to increase the exposure of active sites. However, the intrinsic surface reactivity and stability cannot be improved, and, the widely used liquid-phase exfoliation method is time-consuming and laborious. In this work, we successfully exfoliates the bulk BP into ultrathin BP nanosheets with dense surface amino-functional groups (BP-NH2) using NH3 plasma treatment. The 2D structure can shorten the photo-excited charges migration distance and improve the exposure of surface-active sites. Furthermore, the amino-functional groups on ultrathin BP nanosheets can prevent the destruction of BP nanosheets in ambient air, favoring the charge separation, CO2 adsorption and activation during the catalytic process. Benefiting from integrated advantages of amino functional groups, the optimal BP-NH2 exhibits a photocatalytic CO2 reduction rate to CO of 27.6 mu mol g(-1) h(-1) with a selectivity of 87.0 %, both of which are higher than those of pristine bulk BP. This work presents ideas for stabilizing BP and improving the CO2 reduction performance simultaneously.
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