Boron nanosheets induced microstructure and charge transfer tailoring in carbon nanofibrous mats towards highly efficient water splitting

• Main Authors: Li, Hongling, Ren, Bohua, Liu, Wenwen, Jing, Lin, Tay, Roland Yingjie, Tsang, Siu Hon, Ricardez–Sandoval, Luis, Yu, Aiping, Teo, Edwin Hang Tong
• Other Authors: School of Electrical and Electronic Engineering
• Format: Article
• Language: English
• Published: 2022
• Subjects: Engineering::Materials; Boron Carbon Oxynitride Nanofibrous Mat; Oxygen Evolution Reaction
• Online Access: https://hdl.handle.net/10356/159889
• Institution: Nanyang Technological University

Development of metal-free carbon-based electrocatalysts with high-efficiency and excellent durability towards both oxygen and hydrogen evolution reactions (OER and HER) in a single electrolyte system is crucial yet challenging for sustainable energy generation. In this work, we report a facile and scalable strategy for fabricating self-supporting boron carbon oxynitride nanofibrous (BCNONF) mats with controllable boron contents via electrospinning and subsequent thermal treatment. Notably, the optimal BCNONF mat affords outstanding OER performance in alkaline electrolyte with low overpotential of 403 mV at 10 mA·cm−2, small Tafel slop of 72.9 mV·dec−1, and high stability (88.1% current density retention after 10 h), outperforming the commercial Ir/C benchmark. Moreover, it can serve as a remarkable HER catalyst with better stability than that of the commercial Pt/C counterpart in the same electrolyte, indicating its bifunctional characteristics. When employed as both anode and cathode of an electrolyzer, the self-supporting BCNONF mats exhibit superior activities with a potential of only 1.79 V at 10 mA·cm−2 and high long-term durability (90.6% current density retention after 50 h) for overall water splitting. Furthermore, density functional theory (DFT) calculations reveal that the remarkable OER and HER bifunctional performance of the BCNONF catalyst are originated from the reduced adsorption strength of O atom and the stronger H* adsorption on the BCNO surface as compared to those on CNO surface, which in turn facilitate efficient interfacial charge transfer between the electrocatalytic intermediates and the BCNONF catalyst.