GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Royal Society of Chemistry (RSC)  (3)
  • Zhao, Junsong  (3)
Material
Publisher
  • Royal Society of Chemistry (RSC)  (3)
Language
Years
  • 1
    In: Energy & Environmental Science, Royal Society of Chemistry (RSC), Vol. 14, No. 10 ( 2021), p. 5406-5415
    Abstract: Metal halide perovskites have attracted great attention and are rapidly developing mainly due to their excellent optoelectronic properties. Currently, the efficiency of inverted (p–i–n) PSCs is around 23%, which is catching up with that of the regular structured devices. Short-term and low-efficiency operational stability are the main obstacles to the commercialization of PSCs. Although many modified materials have been proven to effectively enhance device performance, they do not satisfy operational stability at high efficiency. Here, we propose a multidentate-cross-linking strategy, which uses multi-branched and adequate chemical anchor sites in three-dimensional star-polymer to directly chelate perovskite materials in multiple directions, thereby regulating the morphology of perovskite, passivating defects at surface/GBs, inhibiting the non-radiative recombination, and improving the stability of the device. As a result, the modified PSC achieves a 22.74% efficiency, which is one of the highest values reported for the inverted PSCs. Meanwhile, the encapsulated modified device exhibits significant advancement of operational stability with 93% of the initial efficiency (∼22.00%) under maximum power point tracking at 45 °C for 1000 h, and an estimated T80 (time to retain 80% of the initial efficiency) lasted nearly 4000 h. The three-dimensional star-polymer multidentate-cross-linking strategy has proved to be a new direction for realizing commercial applications of PSCs with excellent operational stability for high-efficiency devices.
    Type of Medium: Online Resource
    ISSN: 1754-5692 , 1754-5706
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2021
    detail.hit.zdb_id: 2439879-2
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    In: Energy & Environmental Science, Royal Society of Chemistry (RSC), Vol. 15, No. 10 ( 2022), p. 4414-4424
    Abstract: Additive engineering is an effective strategy for defect passivation and performance improvement of perovskite solar cells (PSCs). However, few additives have achieved outstanding stability with high efficiency by simultaneously passivating deep and shallow defects. Herein, we design a novel ionic silicone polymer (PECL) with multi-active sites as an additive to modify inverted PSCs. The C–O groups in the PECL polymer can chelate with undercoordinated Pb 2+ and Pb clusters to passivate deep defects; and the ionic groups in the PECL polymer can generate electrostatic interaction with both positively and negatively charged vacancies, which help to repair shallow defects. Moreover, we quantitatively reveal the effect of deep and shallow defects on the efficiency and stability of PSCs separately, by establishing the correlation between additives with different functional groups and the performance of devices. Consequently, the power conversion efficiency of the PECL-modified inverted PSC increases from 20.02% to 23.11%. More importantly, the encapsulated PSCs maintain 95% of their initial steady-state power output after 1500 hours under AM 1.5 illumination at the maximum power point at 45 °C. Therefore, we provide a universal guideline of polymer structure design for defect healing in stabilizing PSCs with high efficiency.
    Type of Medium: Online Resource
    ISSN: 1754-5692 , 1754-5706
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2439879-2
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Organic Chemistry Frontiers Vol. 9, No. 23 ( 2022), p. 6556-6565
    In: Organic Chemistry Frontiers, Royal Society of Chemistry (RSC), Vol. 9, No. 23 ( 2022), p. 6556-6565
    Abstract: Herein, we report a nickel-catalyzed remote arylalkylation of unactivated γ,δ- and δ,ε-alkenes in alkenyl carbonyl compounds with arylboronic acids and alkyl halides. Kinetically and thermodynamically disfavored 6- and 7-membered nickelacycles were stabilized by the 8-aminoquinoline directing group and subsequent intercepted by the alkyl halides to achieve remote arylalkylation. The practical protocol was compatible with α- or β-substituted terminal alkenes and internal alkenes, providing rapid access to branched molecules bearing two skipped and vicinal stereocenters with high diastereoselectivity (most 〉 20 : 1 dr). Moreover, the radical-based Ni I –Ni III –Ni I catalytic cycle was suggested by combined experimental and density functional theory (DFT) computational studies to understand the mechanism and diastereoselectivity.
    Type of Medium: Online Resource
    ISSN: 2052-4129
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...