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Updated: Jan 3, 2026

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
An energy band compactable B-rGO/PbTiO3 p-n junction: a highly dynamic and durable photocatalyst for enhanced
Lekha Paramanik1, K Hemalata Reddy, K M Parida
1Centre for Nanoscience and Nanotechnology, SOA (Deemed to be University), Bhubaneswar 751030, Odisha, India. paridakulamani@yahoo.com kulamaniparida@soa.ac.in.
Abstract:
Reduced graphene oxide (rGO) intentionally doped with boron atoms is a promising tactic to extract bandgap energy and p-type semiconducting behavior from graphene-based materials. Moreover, the integration of p-type boron-doped rGO with an n-type material through a heterojunction interface exhibits complementary properties to restrict the fast recombination of charge carriers and enhance the photoreaction towards energy applications. Herein, we have prepared boron-doped rGO/PbTiO3 p-n heterojunctions via a hydrothermal method. The successful formation of an excellent p-n heterojunction was demonstrated by TEM, XPS and Raman analysis. The constructed boron-doped rGO/PbTiO3 p-n heterojunctions exhibit dramatic increases in photoelectrochemical and photocatalytic performance due to the presence of a space charge region at the interface of the two materials. The scenario also revealed the double-edge sword functions of B-rGO: the material itself (i) acts as a visible light active photocatalyst with a band gap energy of 2.7 eV and (ii) participates in enhanced charge transfer via the band edge alignment between B-rGO and PbTiO3, as elucidated from photoluminescence and electrochemical impedance studies. Furthermore, the optimal 2B-rGO/PT p-n heterojunction possesses outstanding repeatability and exhibited the highest rate of hydrogen evolution, i.e. 293.79 μmol h-1 under visible light irradiation. The results for these materials may provide advanced insight into the design of next-generation high-efficiency black graphene-based heterojunctions.
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