Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 217

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Visible/Near-Infrared-Light-Induced H2 Production over g-C3N4 Co-sensitized by Organic Dye and Zinc Phthalocyanine Derivative

Zhang, Xiaohu, Peng, Tianyou, Yu, Lijuan, Li, Renjie, Li, Qianqian, Li, Zhen·2015·ACS Catalysis

Abstract

A new route is carried out to achieve broad spectral responsive photocatalytic H 2 production over g-C 3 N 4 co-sensitized by an indole-based D-π-A organic dye (LI-4) and an asymmetric zinc phthalocyanine derivative (Zn-tri-PcNc) with complementary absorption spectra. Experimental results indicate that both LI-4 and Zn-tri-PcNc are efficient photosensitizers of g-C 3 N 4 for H 2 production, and their co-sensitized g-C 3 N 4 (LI-4/g-C 3 N 4 /Zn-tri-PcNc) exhibits an extremely high H 2 production activity (371.4 μmol h –1 ) under visible/near-infrared (NIR) light (λ ≥ 420 nm) irradiation, which approximates the summation of the H 2 production activity of LI-4/g-C 3 N 4 (233.8 μmol h –1 ) and Zn-tri-PcNc/g-C 3 N 4 (132.3 μmol h –1 ), although LI-4 and Zn-tri-PcNc can just absorb the light in the range of 400–600 and 600–750 nm, respectively. Moreover, the co-sensitized catalyst shows a broad visible/NIR light responsive range (400–800 nm) with impressively high apparent quantum yields (AQY) of 16.3, 7.7, and 1.75% at 420, 500, and 700 nm monochromatic light irradiation, respectively. The present work gives a new advance toward panchromatic light responsive photocatalytic application by combining the photosensitization of two different dyes with complementary absorption spectra on one kind of semiconductor.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1021/cs5016468

Cites

5 of 5 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 5 references

Cited by

Metadata

Authors
Zhang, X., Peng, T., Yu, L., Li, R., Li, Q., & Li, Z.
Venue
ACS Catalysis
Published
2014-12-22
Volume
5
Issue
2
Pages
504-510
ISSN
2155-5435 (ISSN-L)
OpenAlex
W2325556079
Cited by
217
References
5
FWCI
5.13
Type
journal article
Language
en
Open access
closed

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.