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Quantum chemical design of near‐infrared sensitive fused ring electron acceptors containing selenophene as π‐bridge for high‐performance organic solar cells

Journal of physical organic chemistry, 2021-08, Vol.34 (8), p.n/a

2021

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A Synergistic Strategy of Manipulating the Number of Selenophene Units and Dissymmetric Central Core of Small Molecular Acceptors Enables Polymer Solar Cells with 17.5 % Efficiency

Angewandte Chemie International Edition, 2021-08, Vol.60 (35), p.19241-19252

International ed. in English, 2021

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Green synthesis of halogenated thiophenes, selenophenes and benzo[b]selenophenes using sodium halides as a source of electrophilic halogens

Tetrahedron letters, 2017-02, Vol.58 (7), p.638-641

2017

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The selenium substitution of solvent additive enables efficient polymer solar cells with efficiency of 19.4

Nano energy, 2024-10, Vol.129, p.110067, Article 110067

2024

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High-Mobility Naphthalene Diimide and Selenophene-Vinylene-Selenophene-Based Conjugated Polymer: n-Channel Organic Field-Effect Transistors and Structure-Property Relationship

Advanced functional materials, 2016-07, Vol.26 (27), p.4984-4997

2016

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Double Asymmetric Core Optimizes Crystal Packing to Enable Selenophene‐based Acceptor with Over 18 % Efficiency in Binary Organic Solar Cells

Angewandte Chemie International Edition, 2023-03, Vol.62 (10), p.e202216340-n/a

International ed. in English, 2023

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A selenophene-containing near-infrared unfused acceptor for efficient organic solar cells

Chemical engineering journal (Lausanne, Switzerland : 1996), 2022-02, Vol.429, p.132298, Article 132298

2022

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Multi‐Selenophene Strategy Enables Dimeric Acceptors‐Based Organic Solar Cells with over 18.5% Efficiency

Advanced energy materials, 2024-08, Vol.14 (30), p.n/a

2024

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Multi‐Selenophene‐Containing Narrow Bandgap Polymer Acceptors for All‐Polymer Solar Cells with over 15 % Efficiency and High Reproducibility

Angewandte Chemie International Edition, 2021-07, Vol.60 (29), p.15935-15943

International ed. in English, 2021

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Recent advances in the chemistry of selenium-containing heterocycles: Five-membered ring systems

Coordination chemistry reviews, 2016-04, Vol.312, p.149-177

2016

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Additive-Free Bulk-Heterojuction Solar Cells with Enhanced Power Conversion Efficiency, Comprising a Newly Designed Selenophene-Thienopyrrolodione Copolymer

Advanced functional materials, 2013-03, Vol.23 (10), p.1297-1304

2013

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Iron(III) chloride and dialkyl diselenides promoted intramolecular cascade cyclization leading to synthesis of selenophene-fused quinoline based heterocycles

Tetrahedron letters, 2022-07, Vol.101, p.153907, Article 153907

2022

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On the Conformation of Dimeric Acceptors and Their Polymer Solar Cells with Efficiency over 18

Angewandte Chemie International Edition, 2023-11, Vol.62 (45), p.e202302888-e202302888

International ed. in English, 2023

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An approach to the construction of 3-aryl- and 3-hydroxy-substituted benzo[b]selenopheno[2,3-d]thiophenes

Tetrahedron letters, 2022-11, Vol.110, p.154166, Article 154166

2022

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Near-infrared absorbing polymer acceptors enabled by selenophene-fused core and halogenated end-group for binary all-polymer solar cells with efficiency over 16

Nano energy, 2022-02, Vol.92, p.106718, Article 106718

2022

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A follow-up investigation: Organic solar cells based on chalcogenophene-Thieno[3,4-c]pyrrole-4,6-dione-chalcogenophene containing random conjugated polymers

Journal of electroanalytical chemistry (Lausanne, Switzerland), 2023-03, Vol.932, p.117213, Article 117213

2023

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A Selenophene-Based Low-Bandgap Donor-Acceptor Polymer Leading to Fast Ambipolar Logic

Advanced materials (Weinheim), 2012-03, Vol.24 (12), p.1558-1565

2012

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Improved efficiency by selenophene-substitution for cyclometalated tris-Ir(III) complex based organic solar cells

Journal of organometallic chemistry, 2024-03, Vol.1008, p.123050, Article 123050

2024

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Multi‐Selenophene Incorporated Thiazole Imide‐Based n‐Type Polymers for High‐Performance Organic Thermoelectrics

Angewandte Chemie International Edition, 2024-01, Vol.63 (3), p.e202316214-n/a

International ed. in English, 2024

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Improved All-Polymer Solar Cell Performance by Using Matched Polymer Acceptor

Advanced functional materials, 2016-08, Vol.26 (31), p.5669-5678

2016

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Pyrene‐Based Dopant‐Free Hole‐Transport Polymers with Fluorine‐Induced Favorable Molecular Stacking Enable Efficient Perovskite Solar Cells

Angewandte Chemie (International ed.), 2022-06, Vol.61 (24), p.e202201847-n/a

International ed. in English, 2022

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A study on the cellular and cytotoxic effects of S and Se heterocycles on the myeloid leukemia cell line PLB-985

Phosphorus, sulfur, and silicon and the related elements, 2022, Vol.197 (8), p.876-884

2022

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Effect of Selenophene in a DPP Copolymer Incorporating a Vinyl Group for High-Performance Organic Field-Effect Transistors

Advanced materials (Weinheim), 2013-01, Vol.25 (4), p.524-528

2013

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Side Group Engineering of Small Molecular Acceptors for High‐Performance Fullerene‐Free Polymer Solar Cells: Thiophene Being Superior to Selenophene

Advanced functional materials, 2017-09, Vol.27 (34), p.n/a

2017

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High Aspect Ratio Conjugated Polymer Nanowires for High Performance Field-Effect Transistors and Phototransistors

ACS nano, 2015-05, Vol.9 (5), p.5264-5274

2015

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Quantum chemical design of near‐infrared sensitive fused ring electron acceptors containing selenophene as π‐bridge for high‐performance organic solar cells

A Synergistic Strategy of Manipulating the Number of Selenophene Units and Dissymmetric Central Core of Small Molecular Acceptors Enables Polymer Solar Cells with 17.5 % Efficiency

Green synthesis of halogenated thiophenes, selenophenes and benzo[b]selenophenes using sodium halides as a source of electrophilic halogens

The selenium substitution of solvent additive enables efficient polymer solar cells with efficiency of 19.4

High-Mobility Naphthalene Diimide and Selenophene-Vinylene-Selenophene-Based Conjugated Polymer: n-Channel Organic Field-Effect Transistors and Structure-Property Relationship

Double Asymmetric Core Optimizes Crystal Packing to Enable Selenophene‐based Acceptor with Over 18 % Efficiency in Binary Organic Solar Cells

A selenophene-containing near-infrared unfused acceptor for efficient organic solar cells

Multi‐Selenophene Strategy Enables Dimeric Acceptors‐Based Organic Solar Cells with over 18.5% Efficiency

Multi‐Selenophene‐Containing Narrow Bandgap Polymer Acceptors for All‐Polymer Solar Cells with over 15 % Efficiency and High Reproducibility

Recent advances in the chemistry of selenium-containing heterocycles: Five-membered ring systems

Additive-Free Bulk-Heterojuction Solar Cells with Enhanced Power Conversion Efficiency, Comprising a Newly Designed Selenophene-Thienopyrrolodione Copolymer

Iron(III) chloride and dialkyl diselenides promoted intramolecular cascade cyclization leading to synthesis of selenophene-fused quinoline based heterocycles

On the Conformation of Dimeric Acceptors and Their Polymer Solar Cells with Efficiency over 18

An approach to the construction of 3-aryl- and 3-hydroxy-substituted benzo[b]selenopheno[2,3-d]thiophenes

Near-infrared absorbing polymer acceptors enabled by selenophene-fused core and halogenated end-group for binary all-polymer solar cells with efficiency over 16

A follow-up investigation: Organic solar cells based on chalcogenophene-Thieno[3,4-c]pyrrole-4,6-dione-chalcogenophene containing random conjugated polymers

A Selenophene-Based Low-Bandgap Donor-Acceptor Polymer Leading to Fast Ambipolar Logic

Improved efficiency by selenophene-substitution for cyclometalated tris-Ir(III) complex based organic solar cells

Multi‐Selenophene Incorporated Thiazole Imide‐Based n‐Type Polymers for High‐Performance Organic Thermoelectrics

Improved All-Polymer Solar Cell Performance by Using Matched Polymer Acceptor

Pyrene‐Based Dopant‐Free Hole‐Transport Polymers with Fluorine‐Induced Favorable Molecular Stacking Enable Efficient Perovskite Solar Cells

A study on the cellular and cytotoxic effects of S and Se heterocycles on the myeloid leukemia cell line PLB-985

Effect of Selenophene in a DPP Copolymer Incorporating a Vinyl Group for High-Performance Organic Field-Effect Transistors

Side Group Engineering of Small Molecular Acceptors for High‐Performance Fullerene‐Free Polymer Solar Cells: Thiophene Being Superior to Selenophene

High Aspect Ratio Conjugated Polymer Nanowires for High Performance Field-Effect Transistors and Phototransistors

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