Gupta, SurajSurajGuptaPrapaitrakool, ChayathornChayathornPrapaitrakoolBhagat, Brajesh RajeshBrajesh RajeshBhagatYeh, Chun LinChun LinYehDashora, AlpaAlpaDashoraSirisuk, AkawatAkawatSirisukPatel, NaineshNaineshPatelDaneu, NinaNinaDaneuKocjan, AndražAndražKocjanSpreitzer, MatjažMatjažSpreitzerJEFFREY CHI-SHENG WUKržmanc, Marjeta MačekMarjeta MačekKržmanc2024-03-272024-03-272024-03-2203603199https://scholars.lib.ntu.edu.tw/handle/123456789/641395Despite being one of the most widely studied metal-free semiconductors, graphitic carbon-nitride (gC3N4) shows meaningful photocatalytic activities only when loaded with noble-metal co-catalysts. The present work reports an alternative to noble metals in the form of cobalt boride (CoB) co-catalyst that can be easily integrated within the gC3N4 framework with facile fabrication strategies. The optimized CoB-gC3N4 composite showed ∼60 times higher hydrogen generation rate compared to bare gC3N4 nanosheets, with good stability. Detailed morphological, structural, chemical, electrochemical and spectroscopic investigations revealed the key aspects of CoB-gC3N4 composite that unanimously led to higher photocatalytic activity. Computational investigations not only corroborated the experimental results but also established that the surface Co and B sites in CoB provided the most energetically favoured sites for hydrogen evolution reaction. Based on the experimental and computational investigations, a generic reaction mechanism was formulated that will prove as a guiding light for future studies on similar photocatalytic systems.Graphitic carbon nitride | Hydrogen evolution reaction | Non-noble co-catalyst | Photocatalysis | Transition-metal boride[SDGs]SDG7journal article10.1016/j.ijhydene.2024.02.2612-s2.0-85186410539https://api.elsevier.com/content/abstract/scopus_id/85186410539