scholarly journals Correction to “Tracking Charge Transfer to Residual Metal Clusters in Conjugated Polymers for Photocatalytic Hydrogen Evolution”

2020 ◽  
Author(s):  
Michael Sachs ◽  
Hyojung Cha ◽  
Jan Kosco ◽  
Catherine M. Aitchison ◽  
Laia Francàs ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Conjugated Polymers ◽  
Hydrogen Evolution ◽  
Metal Clusters ◽  
Photocatalytic Hydrogen Evolution

scholarly journals Tracking Charge Transfer to Residual Metal Clusters in Conjugated Polymers for Photocatalytic Hydrogen Evolution

2020 ◽  
Vol 142 (34) ◽  
pp. 14574-14587 ◽  
Author(s):  
Michael Sachs ◽  
Hyojung Cha ◽  
Jan Kosco ◽  
Catherine M. Aitchison ◽  
Laia Francàs ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Conjugated Polymers ◽  
Hydrogen Evolution ◽  
Metal Clusters ◽  
Photocatalytic Hydrogen Evolution

scholarly journals Conjugated Polymer Donor-Molecular Acceptor Nanohybrids for Photocatalytic Hydrogen Evolution

2019 ◽  
Author(s):  
Haofan Yang ◽  
Xiaobo Li ◽  
Reiner Sebastian Sprick ◽  
Andrew I. Cooper
Keyword(s):  
Photocatalytic Activity ◽  
Charge Transfer ◽  
Conjugated Polymers ◽  
Hydrogen Evolution ◽  
Conjugated Polymer ◽  
Apparent Quantum Yield ◽  
High Hydrogen ◽  
Photocatalytic Hydrogen Evolution ◽  
Efficient Charge ◽  
Donor Acceptor

A library of 237 organic binary/ternary nanohybrids consisting of conjugated polymers donors and both fullerene and non-fullerene molecular acceptors was prepared and screened for sacrificial photocatalytic hydrogen evolution. These donor-acceptor nanohybrids (DANHs) showed significantly enhanced hydrogen evolution rates compared with the parent donor or acceptor compounds. DANHs of <a></a><a>a polycarbazole</a>-based donor combined with a methanofullerene acceptor (PCDTBT/PC<sub>60</sub>BM) showed a high hydrogen evolution rate of 105.2 mmol g<sup>-1</sup> h<sup>-1</sup> under visible light (λ > 420 nm). This DANH photocatalyst produced 5.9 times more hydrogen than a sulfone-containing polymer (P10) under the same conditions, which is one of the most efficient organic photocatalysts reported so far. An apparent quantum yield of hydrogen evolution of 3.0 % at 595 nm was measured for this DANH. The photocatalytic activity of the DANHs, which in optimized cases reached 179.0 mmol g<sup>-1</sup> h<sup>-1</sup>, is attributed to efficient charge transfer at the polymer donor/molecular acceptor interface. We also show that ternary donor<sub>A</sub>-donor<sub>B</sub>-acceptor nanohybrids can give higher activities than binary donor-acceptor hybrids in some cases.

scholarly journals Conjugated Polymer Donor-Molecular Acceptor Nanohybrids for Photocatalytic Hydrogen Evolution

2019 ◽  
Author(s):  
Haofan Yang ◽  
Xiaobo Li ◽  
Reiner Sebastian Sprick ◽  
Andrew I. Cooper
Keyword(s):  
Photocatalytic Activity ◽  
Charge Transfer ◽  
Conjugated Polymers ◽  
Hydrogen Evolution ◽  
Conjugated Polymer ◽  
Apparent Quantum Yield ◽  
High Hydrogen ◽  
Photocatalytic Hydrogen Evolution ◽  
Efficient Charge ◽  
Donor Acceptor

A library of 237 organic binary/ternary nanohybrids consisting of conjugated polymers donors and both fullerene and non-fullerene molecular acceptors was prepared and screened for sacrificial photocatalytic hydrogen evolution. These donor-acceptor nanohybrids (DANHs) showed significantly enhanced hydrogen evolution rates compared with the parent donor or acceptor compounds. DANHs of <a></a><a>a polycarbazole</a>-based donor combined with a methanofullerene acceptor (PCDTBT/PC<sub>60</sub>BM) showed a high hydrogen evolution rate of 105.2 mmol g<sup>-1</sup> h<sup>-1</sup> under visible light (λ > 420 nm). This DANH photocatalyst produced 5.9 times more hydrogen than a sulfone-containing polymer (P10) under the same conditions, which is one of the most efficient organic photocatalysts reported so far. An apparent quantum yield of hydrogen evolution of 3.0 % at 595 nm was measured for this DANH. The photocatalytic activity of the DANHs, which in optimized cases reached 179.0 mmol g<sup>-1</sup> h<sup>-1</sup>, is attributed to efficient charge transfer at the polymer donor/molecular acceptor interface. We also show that ternary donor<sub>A</sub>-donor<sub>B</sub>-acceptor nanohybrids can give higher activities than binary donor-acceptor hybrids in some cases.

scholarly journals Conjugated Polymer Donor-Molecular Acceptor Nanohybrids for Photocatalytic Hydrogen Evolution

2019 ◽  
Author(s):  
Haofan Yang ◽  
Xiaobo Li ◽  
Reiner Sebastian Sprick ◽  
Andrew I. Cooper
Keyword(s):  
Photocatalytic Activity ◽  
Charge Transfer ◽  
Conjugated Polymers ◽  
Hydrogen Evolution ◽  
Conjugated Polymer ◽  
Apparent Quantum Yield ◽  
High Hydrogen ◽  
Photocatalytic Hydrogen Evolution ◽  
Efficient Charge ◽  
Donor Acceptor

A library of 237 organic binary/ternary nanohybrids consisting of conjugated polymers donors and both fullerene and non-fullerene molecular acceptors was prepared and screened for sacrificial photocatalytic hydrogen evolution. These donor-acceptor nanohybrids (DANHs) showed significantly enhanced hydrogen evolution rates compared with the parent donor or acceptor compounds. DANHs of <a></a><a>a polycarbazole</a>-based donor combined with a methanofullerene acceptor (PCDTBT/PC<sub>60</sub>BM) showed a high hydrogen evolution rate of 105.2 mmol g<sup>-1</sup> h<sup>-1</sup> under visible light (λ > 420 nm). This DANH photocatalyst produced 5.9 times more hydrogen than a sulfone-containing polymer (P10) under the same conditions, which is one of the most efficient organic photocatalysts reported so far. An apparent quantum yield of hydrogen evolution of 3.0 % at 595 nm was measured for this DANH. The photocatalytic activity of the DANHs, which in optimized cases reached 179.0 mmol g<sup>-1</sup> h<sup>-1</sup>, is attributed to efficient charge transfer at the polymer donor/molecular acceptor interface. We also show that ternary donor<sub>A</sub>-donor<sub>B</sub>-acceptor nanohybrids can give higher activities than binary donor-acceptor hybrids in some cases.

Significant improvement of photocatalytic hydrogen evolution of diketopyrrolopyrrole-based donor–acceptor conjugated polymers through side-chain engineering

2019 ◽  
Vol 10 (47) ◽  
pp. 6473-6480 ◽  
Author(s):  
Ruimin Diao ◽  
Haonan Ye ◽  
Zhicheng Yang ◽  
Shicong Zhang ◽  
Kangyi Kong ◽  
...  
Keyword(s):  
Absorption Spectrum ◽  
Conjugated Polymers ◽  
Hydrogen Evolution ◽  
Evolution Rate ◽  
Side Chain ◽  
Photocatalytic Hydrogen Evolution ◽  
Hydrogen Evolution Rate ◽  
Donor Acceptor

The hydrogen evolution rate of PDPP3B-O4 with butoxy chain was 5.53 mmol h−1 g−1 with 1% Pt loading (λ > 400 nm), increased 110 times than PDPP3B-C8 with octyl chain due to wider absorption spectrum and better wettability via side chain engineering.

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