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Träfflista för sökning "WFRF:(Liu Haiguang) srt2:(2021)"

Sökning: WFRF:(Liu Haiguang) > (2021)

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1.
  • Zhao, Haiguang, et al. (författare)
  • Gram-scale synthesis of carbon quantum dots with a large Stokes shift for the fabrication of eco-friendly and high-efficiency luminescent solar concentrators
  • 2021
  • Ingår i: Energy & Environmental Science. - : Royal Society of Chemistry. - 1754-5692 .- 1754-5706. ; 14:1, s. 396-406
  • Tidskriftsartikel (refereegranskat)abstract
    • Luminescent solar concentrators (LSCs) are large-area sunlight collectors coupled to small area solar cells, for efficient solar-to-electricity conversion. The three key points for the successful market penetration of LSCs are: (i) removal of light losses due to reabsorption during light collection; (ii) high light-to-electrical power conversion efficiency of the final device; (iii) long-term stability of the LSC structure related to the stability of both the matrix and the luminophores. Among various types of fluorophores, carbon quantum dots (C-dots) offer a wide absorption spectrum, high quantum yield, non-toxicity, environmental friendliness, low-cost, and eco-friendly synthetic methods. However, they are characterized by a relatively small Stokes shift, compared to inorganic quantum dots, which limits the highest external optical efficiency that can be obtained for a large-area single-layer LSC (>100 cm2) based on C-dots below 2%. Herein, we report highly efficient large-area LSCs (100–225 cm2) based on colloidal C-dots synthesized via a space-confined vacuum-heating approach. This one batch reaction could produce Gram-scale C-dots with a high quantum yield (QY) (∼65%) using eco-friendly citric acid and urea as precursors. Thanks to their very narrow size distribution, the C-dots produced via the space-confined vacuum-heating approach had a large Stokes shift of 0.53 eV, 50% larger than C-dots synthesized via a standard solvothermal reaction using the same precursors with a similar absorption range. The large-area LSC (15 × 15 × 0.5 cm3) prepared by using polyvinyl pyrrolidone (PVP) polymer as a matrix exhibited an external optical efficiency of 2.2% (under natural sun irradiation, 60 mW cm−2, uncharacterized spectrum). After coupling to silicon solar cells, the LSC exhibited a power conversion efficiency (PCE) of 1.13% under natural sunlight illumination (20 mW cm−2, uncharacterized spectrum). These unprecedented results were obtained by completely suppressing the reabsorption losses during light collection, as proved by optical spectroscopy. These findings demonstrate the possibility of obtaining eco-friendly, high-efficiency, large-area LSCs through scalable production techniques, paving the way to the lab-to-fab transition of this kind of devices.
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2.
  • Han, Yi, et al. (författare)
  • Highly efficient ratiometric nanothermometers based on colloidal carbon quantum dots
  • 2021
  • Ingår i: Journal of materials chemistry. B. - : Royal Society of Chemistry. - 2050-750X .- 2050-7518. ; 9:20, s. 4111-4119
  • Tidskriftsartikel (refereegranskat)abstract
    • Optical nanothermometers have attracted much attention due to their non-contact and precise measurement with high spatial resolution at the micro- and nanoscales. They can be applied in various fields such as micro-opto-electronics, photonics, and biomedical thermal and pH sensing, while most thermal sensors reported so far contain heavy metals or have low sensitivity. Herein, we demonstrate a highly sensitive ratiometric thermal sensor based on colloidal C-dots. C-dots exhibit dual emission originating from the band gap emission and surface-dominant emission, which show a different temperature-dependent photoluminescence (PL) response. Among different surface-functionalized C-dots, C-dots@OH exhibit an absolute thermal sensitivity of -0.082 degrees C-1, which is the highest among various types of ratiometric thermosensors, making it a very promising candidate for high-sensitivity, self-calibrated nanoscale thermometry. As a proof-of-concept, C-dots@OH were employed to monitor the intracellular temperature (32-42 degrees C), showing a clear trend for temperature variation in a single cell, indicating that C-dots could offer a powerful tool for a potential precise measurement of the intracellular temperature. They could also be used as thermal sensors for nano-electronic and optoelectronic devices.
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3.
  • Wang, Xiaohan, et al. (författare)
  • Colloidal carbon quantum dots as light absorber for efficient and stable ecofriendly photoelectrochemical hydrogen generation
  • 2021
  • Ingår i: Nano Energy. - : Elsevier. - 2211-2855 .- 2211-3282. ; 86
  • Tidskriftsartikel (refereegranskat)abstract
    • Solar-driven hydrogen production is one of the most promising strategies for solar-to-hydrogen energy conversion. Compared to inorganic quantum dots (QDs), carbon quantum dots (C-dots) have attracted a lot of attention for optoelectronic devices due to their structure-dependent optical properties and green composition. However, the solar-to-hydrogen conversion efficiency of most of the photoelectrochemical (PEC) devices based on colloidal QDs is still low. Here we demonstrated a highly efficient and stable ecofriendly PEC device using C-dots sensitized TiO2 photoanode, Pt loaded on carbon nanofibers as counter electrode, and glucose aqueous solution as electrolyte. The red-color C-dots were prepared using a solvothermal reaction, with an absorption spectrum ranging from 300 to 600 nm and a quantum yield (QY) of 50%. The C-dots have excitation independent photoluminescence peak positions and highly crystalline structure. The hydroxyl group on the C-dots can strongly interact with the TiO2, forming a very stable complex. Benefiting from these features, the PEC devices based on C-dots exhibit a saturated photocurrent density as high as ~4 mA/cm2 at 0.6 V vs. RHE and the device is very stable (keeping 95% of its initial value after 10-hour illumination upon 100 mW/cm2). This work indicates the promising properties of the C-dots/TiO2 system, which holds huge potential for applications in the fields of optoelectronic and catalytic devices.
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  • Resultat 1-3 av 3

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