journal article·2025-07-14

Dual-Armed N-Methoxy Triphenyl-Aminated Phenothiazine-Linked Benzodithiophene Hole Transport and Interface Passivation Materials for Perovskite Solar Cells

Ravikumar Gurusamy, Vidya Sudhakaran Menon, Ananthan Alagumalai, Sivasankar Parameshwaran, Arya Kamal, Gowri Chandran Chandrakumar Veena, Sai Athmeeya G Shet, V N Ravi Kishore Vutukuri, Gurusamy Thangavelu Senthil Andavan, Ananthanarayanan Krishnamoorthy

ACS Applied Energy Materials· Volume 8· Issue 13
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Abstract

The efficient and stable operation of perovskite solar cells (PSCs) under ambient conditions remains a key challenge for their commercialization, with surface defects and interfacial instability being major performance bottlenecks. This study introduces two organic molecules, RK1 and RK4, designed to function as both interfacial passivation agents and hole transport materials (HTMs), to address these challenges through a unified dual-role approach. These molecules were synthesized via N -methoxy triphenyl-aminated phenothiazine units, coupled with sulfur-rich methoxy benzodithiophene units in donor−π–donor (D 1 –π–D 2 ) and donor−π–donor−π–donor (D 1 –π–D 2 –π–D 1 ) configurations and named as RK1 and RK4, respectively. As evidenced by steady-state photoluminescence (PL) and time-resolved photoluminescence (TRPL) studies, these molecules enable efficient hole extraction, and as confirmed by X-ray photoelectron spectroscopy (XPS) studies, they effectively passivate defects such as undercoordinated Pb 2+ ions by coordination interaction. Devices employing RK1 and RK4 as interfacial layers achieved power conversion efficiencies (PCEs) of 17.28 and 18.52%, respectively, with RK4 as a standalone HTM reaching a PCE of 16.82%. In addition to the superior performance, RK1- and RK4-passivated devices exhibited better stability with unencapsulated devices retaining up to 78% of their initial PCE after 888 h and up to 58% after 1536 h, compared to the spiro-OMeTAD devices, which degraded rapidly just within 216 h. The durability and better device performance is attributed to the enhanced hydrophobicity of RK1 and RK4, which minimizes moisture ingress and ion migration, coupled with their ability to improve crystallinity and suppress nonradiative recombination. By integrating multisite defect passivation, optimized energy level engineering, enhanced hole mobility, and hydrophobicity, this work offers a promising strategy for dual-role organic materials, advancing PSCs toward scalable and commercially viable solutions.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Perovskite Materials and Applications · Conducting polymers and applications · Organic Electronics and Photovoltaics

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Organic and Perovskite Photovoltaics Laboratory (OPPV), Department of Chemistry

SRM Institute of Science and Technology

Department of Chemistry

Sri Sathya Sai Institute of Higher Learning

Funding

Department of Science and Technology, Ministry of Science and Technology, India · SRM Institute of Science and Technology

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