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20 Aug 02:45

[ASAP] Azobenzene Adsorption on the MoS2(0001) Surface: A Density Functional Investigation within van der Waals Corrections

by L. Cabral, Fernando P. Sabino, Matheus P. Lima, G. E. Marques, Victor Lopez-Richard, Juarez L. F. Da Silva

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The Journal of Physical Chemistry C
DOI: 10.1021/acs.jpcc.8b03068
10 Jul 02:16

[ASAP] ESIPT Fluorescent Chromism and Conformational Change of 3-(2-Benzothiazolyl)-4-hydroxy-benzenesulfonic acid by Amine Sorption

by Yuta Nakane, Takashi Takeda, Norihisa Hoshino, Ken-ichi Sakai, Tomoyuki Akutagawa

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The Journal of Physical Chemistry C
DOI: 10.1021/acs.jpcc.8b03248
09 Apr 14:15

Self‐Healing Biomaterials: From Molecular Concepts to Clinical Applications

by Mani Diba , Sergio Spaans , Ke Ning , Bastiaan D. Ippel , Fang Yang , Bas Loomans , Patricia Y. W. Dankers , Sander C. G. Leeuwenburgh
Advanced Materials Interfaces, Volume 5, Issue 17, September 7, 2018.
14 Mar 08:03

The photochromism, light harvesting and self-assembly activity of a multi-function Schiff-base compound based on the AIE effect

J. Mater. Chem. C, 2018, 6,4057-4064
DOI: 10.1039/C8TC00509E, Paper
Jie Chai, Yanbo Wu, Binsheng Yang, Bin Liu
Aggregation-induced emission (AIE) luminogens with photochromic properties show strong potential in molecular switches, photo-controllable materials, photo-patterning, etc.
The content of this RSS Feed (c) The Royal Society of Chemistry
15 Dec 14:21

The integrated adjustment of chlorine substitution and two-dimensional side chain of low band gap polymers in organic solar cells

Polym. Chem., 2018, 9,940-947
DOI: 10.1039/C7PY01792H, Paper
Zhen Yang, Hui Chen, Huan Wang, Daize Mo, Longzhu Liu, Pengjie Chao, Yulin Zhu, Chuanjun Liu, Wei Chen, Feng He
The chlorination and side-chain extension of benzothiadiazole derivatives can finely manipulate the open-circuit voltage in their solar cells.
The content of this RSS Feed (c) The Royal Society of Chemistry
15 Dec 14:20

Additive-Morphology Interplay and Loss Channels in “All-Small-Molecule” Bulk-heterojunction (BHJ) Solar Cells with the Nonfullerene Acceptor IDTTBM

by Ru-Ze Liang, Maxime Babics, Akmaral Seitkhan, Kai Wang, Paul Bythell Geraghty, Sergei Lopatin, Federico Cruciani, Yuliar Firdaus, Marco Caporuscio, David J. Jones, Pierre M. Beaujuge

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.

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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.

29 Nov 13:19

Impact of side chain placement on thermal stability of solar cells in thiophene-thiazolothiazole polymers

J. Mater. Chem. C, 2018, 6,3668-3674
DOI: 10.1039/C7TC04721E, Paper
Masahiko Saito, Itaru Osaka
We study the impact of side chain placement on the thermal stability of solar cells in thiophene-thiazolothiazole polymers.
The content of this RSS Feed (c) The Royal Society of Chemistry
25 Oct 14:22

Two-Photon Spectra of Chlorophylls and Carotenoid–Tetrapyrrole Dyads

by Daniel A. Gacek, Ana L. Moore, Thomas A. Moore and Peter Jomo Walla

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The Journal of Physical Chemistry B
DOI: 10.1021/acs.jpcb.7b08502