This research demonstrates enhanced nitrogen fixation efficiency in a novel schottky junction, indicating new avenues for photocatalytic design.
The development of efficient photocatalytic systems for nitrogen fixation hinges on the precise regulation of charge separation and electron transfer kinetics. Here, we present a chemically bonded Schottky junction, CuTi0.25-NC/BiOBr, in which a nitrogen-doped carbon (NC) layer protects the embedded transition metals from overoxidation. In a sacrificial-agent-free aqueous environment, the CuTi0.25-NC/BOB heterojunction achieves an ammonia production rate of 764.1 μmol g⁻¹ h⁻¹ under simulated solar irradiation. This performance represents a 10-fold enhancement relative to pristine BOB and substantially surpasses that of metal-free NC/BOB and single-metal control systems. Mechanistic studies reveal that CuTi0.25-NC and BiOBr form Cu/Ti-O-Bi chemical bonds through d-p orbital interactions, which increase the electron density at the active Bi sites. This coupled modulation precisely tunes the p-band center of Bi, promoting N₂ activation while enhancing interfacial stability and providing an atomic-level pathway for charge transfer. Our findings underscore the critical role of interfacial orbital coupling in heterostructure design and establish a strategic paradigm for constructing high-performance nitrogen fixation systems that transcend conventional heterojunction engineering.
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Yang et al. (2026) studied this question.
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