Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Theoretical studies, anticancer activity, and photovoltaic performance of newly synthesized carbazole-based dyes
Mohamed R. Elmorsy, Ehab Abdel‐Latif, Hatem E. Gaffer, et al.
Journal of Molecular Structure (2022) Vol. 1255, pp. 132404-132404
Closed Access | Times Cited: 17

Showing 17 citing articles:

Significant improvement of dye-sensitized solar cell performance using low-band-gap chromophores based on triphenylamine and carbazole as strong donors
Mohamed R. Elmorsy, Safa A. Badawy, Ehab Abdel‐Latif, et al.
Dyes and Pigments (2023) Vol. 214, pp. 111206-111206
Closed Access | Times Cited: 33
Innovating dye-sensitized solar cells: Thiazole-based Co-sensitizers for enhanced photovoltaic performance with theoretical insights
Ahmed S. Radwan, Mohamed R. Elmorsy, Ehab Abdel‐Latif, et al.
Optical Materials (2023) Vol. 140, pp. 113914-113914
Closed Access | Times Cited: 23
Synthesis and biological evaluation of novel [1,2,3]triazolo-pyrrolo[1,2-a]pyrido[4,3-d]pyrimidines as EGFR targeting anticancer agents
Sandhya Rani Bandi, Natte Kavitha, Satheesh Kumar Nukala, et al.
Journal of Molecular Structure (2022) Vol. 1274, pp. 134378-134378
Closed Access | Times Cited: 28
Hydrazonothiazole dyes for enhanced dye-sensitized solar cells in greenhouse applications: Achieving high power conversion efficiency and long-term stability
Safa A. Badawy, Ehab Abdel‐Latif, Mohammed A. Assiri, et al.
Dyes and Pigments (2023) Vol. 217, pp. 111447-111447
Closed Access | Times Cited: 19
Computational design and experimental investigation of novel thiophene-based organic dyes with N,N-dimethylaminophenyl and morpholinophenyl donors for dye-sensitized solar cells
Mohamed R. Elmorsy, Fatma H. Abdelhamed, Arwa sultan Alqahtani, et al.
Optical Materials (2024) Vol. 151, pp. 115386-115386
Closed Access | Times Cited: 5
The 9H-carbazole based derivative dyes for dye-sensitized solar cells technology
Ismail Abubakari
Computational and Theoretical Chemistry (2025), pp. 115165-115165
Closed Access
Synthesis of innovative triphenylamine-functionalized organic photosensitizers outperformed the benchmark dye N719 for high-efficiency dye-sensitized solar cells
Safa A. Badawy, Ehab Abdel‐Latif, Ahmed A. Fadda, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 25
Synthesis of efficient bi-anchoring bifuran/biphenyl derivatives for dye-sensitized solar cell applications
Heba M. El‐Shafeai, Safa A. Badawy, Mohamed A. Ismail, et al.
RSC Advances (2023) Vol. 13, Iss. 14, pp. 9720-9731
Open Access | Times Cited: 12
Tandem dye-sensitized solar cells achieve 12.89% efficiency using novel organic sensitizers
Safa A. Badawy, Ehab Abdel‐Latif, Mohamed R. Elmorsy
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 3
Amplifying performance through co-sensitization of Acrylamide/2-Pyridone dyes in DSSCs
Amal Mostafa, Safa A. Badawy, Ehab Abdel‐Latif, et al.
Journal of Photochemistry and Photobiology A Chemistry (2024) Vol. 450, pp. 115478-115478
Closed Access | Times Cited: 2
Unleashing synergistic co-sensitization of BOA dyes and Ru(ii) complexes for dye-sensitized solar cells: achieving remarkable efficiency exceeding 10% through comprehensive characterization, advanced modeling, and performance analysis
Safa A. Badawy, Ehab Abdel‐Latif, Walid H. Mohamed, et al.
RSC Advances (2024) Vol. 14, Iss. 35, pp. 25549-25560
Open Access | Times Cited: 2
Synthesis of phenylthiourea-based pyrazole, thiazole and/or pyran compounds: molecular modeling and biological activity
Ahmad Fawzi Qarah, Kahdr Alatawi, Adel I. Alalawy, et al.
Journal of Taibah University for Science (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 6
دراسة الفعالية الكيميائية للأسبرين باستخدام نظرية الدالة الوظيفية للكثافة: تاثير المجاميع المعوضة
Halah T. Mohammed, Ahmed M. Kamil, Abbas A-Ali Drea, et al.
Baghdad Science Journal (2024) Vol. 21, Iss. 11, pp. 3379-3388
Open Access | Times Cited: 1
Synthesis, Computational Analysis, and Anti-Proliferative Evaluation of Novel Bithienylbenzamidine Derivatives: Towards Cytostatic Cancer Therapeutics
Fatma H. Abdelhamed, Mohamed R. Elmorsy, Mohamed M. Hammouda, et al.
Journal of Molecular Structure (2024), pp. 140421-140421
Closed Access | Times Cited: 1
Exploring the potential of heterocyclic carbazole-derived dyes for DSSCs
Nainamalai Devarajan, Praveen Naik, Demudu Babu Gorle
Journal of Photochemistry and Photobiology A Chemistry (2024), pp. 116177-116177
Closed Access | Times Cited: 1
Simple organic dyes containing multiple anchors as effective co‐sensitizers for DSSCs loaded with Ru (II) complex N‐719
Ameen M. Aldusi, Ahmed A. Fadda, Mohamed A. Ismail, et al.
Applied Organometallic Chemistry (2022) Vol. 36, Iss. 12
Closed Access | Times Cited: 8
Design of N-heterocycle based-phthalonitrile/metal phthalocyanine–silver nanoconjugates for cancer therapies
Özlem İpsiz Öney, H. Yasemin Yenilmez, Dilek Bahar, et al.
Dalton Transactions (2023) Vol. 52, Iss. 37, pp. 13119-13128
Closed Access | Times Cited: 1
Page 1

Scroll to top