Xu Xiangfei
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[ASAP] Azobenzene Adsorption on the MoS2(0001) Surface: A Density Functional Investigation within van der Waals Corrections
[ASAP] ESIPT Fluorescent Chromism and Conformational Change of 3-(2-Benzothiazolyl)-4-hydroxy-benzenesulfonic acid by Amine Sorption
Self‐Healing Biomaterials: From Molecular Concepts to Clinical Applications
The photochromism, light harvesting and self-assembly activity of a multi-function Schiff-base compound based on the AIE effect
DOI: 10.1039/C8TC00509E, Paper
Aggregation-induced emission (AIE) luminogens with photochromic properties show strong potential in molecular switches, photo-controllable materials, photo-patterning, etc.
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The integrated adjustment of chlorine substitution and two-dimensional side chain of low band gap polymers in organic solar cells
DOI: 10.1039/C7PY01792H, Paper
The chlorination and side-chain extension of benzothiadiazole derivatives can finely manipulate the open-circuit voltage in their solar cells.
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Additive-Morphology Interplay and Loss Channels in “All-Small-Molecule” Bulk-heterojunction (BHJ) Solar Cells with the Nonfullerene Acceptor IDTTBM
Abstract
Achieving efficient bulk-heterojunction (BHJ) solar cells from blends of solution-processable small-molecule (SM) donors and acceptors is proved particularly challenging due to the complexity in obtaining a favorable donor–acceptor morphology. In this report, the BHJ device performance pattern of a set of analogous, well-defined SM donors—DR3TBDTT (DR3), SMPV1, and BTR—used in conjunction with the SM acceptor IDTTBM is examined. Examinations show that the nonfullerene “All-SM” BHJ solar cells made with DR3 and IDTTBM can achieve power conversion efficiencies (PCEs) of up to ≈4.5% (avg. 4.0%) when the solution-processing additive 1,8-diiodooctane (DIO, 0.8% v/v) is used in the blend solutions. The figures of merit of optimized DR3:IDTTBM solar cells contrast with those of “as-cast” BHJ devices from which only modest PCEs <1% can be achieved. Combining electron energy loss spectrum analyses in scanning transmission electron microscopy mode, carrier transport measurements via “metal-insulator-semiconductor carrier extraction” methods, and systematic recombination examinations by light-dependence and transient photocurrent analyses, it is shown that DIO plays a determining role—establishing a favorable lengthscale for the phase-separated SM donor–acceptor network and, in turn, improving the balance in hole/electron mobilities and the carrier collection efficiencies overall.
A set of structurally analogous small-molecule (SM) donors with distinct side-chain manifolds shows significant differences in their performance patterns in bulk-heterojunction (BHJ) devices with the nonfullerene SM acceptor IDTTBM. Reducing the lengthscale of the phase-separated network between donor and acceptor effectively suppresses nongeminate recombination in the BHJ active layers and improves the carrier mobility balance.
Impact of side chain placement on thermal stability of solar cells in thiophene-thiazolothiazole polymers
DOI: 10.1039/C7TC04721E, Paper
We study the impact of side chain placement on the thermal stability of solar cells in thiophene-thiazolothiazole polymers.
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