The development of efficient, highly stable photocatalysts is essential to address the two challenges of environmental remediation and renewable energy. Structurally strong Zeolitic Imidazolate Framework-8 (ZIF-8) has intrinsic drawbacks, including a large bandgap and fast charge-carrier recombination. This paper presents a highly efficient approach to designing the optoelectronic behaviour of ZIF-8 via controlled nickel doping. Ni(x)-ZIF-8 (0, 2.5, 5, 7.5, and 10 mol, x), and bimetallic metal–organic frameworks were prepared via a simple room-temperature process. Through adequate characterization, the incorporation of Ni2+ into the ZIF-8 lattice has been demonstrated to be successful, resulting in substantial structural and electronic changes. Framework integrity was confirmed using XRD and FTIR analysis, which revealed increased microstrain and the formation of Ni-N bonds. Most importantly, UV-Vis spectrophotometry and electrochemical studies indicated that the bandgap was systematically narrowed: a pristine ZIF-8 had a high bandgap of 3.65 eV, and a Ni(10)-ZIF-8 had a low bandgap of 3.23 eV, while charge-transfer resistance was reduced significantly. All these synergies led to high photocatalytic performance. The best Ni(2.5)-ZIF-8 catalyst achieved a desirable result, degrading methylene blue to more than 98.5%, which was far superior to that of the pure framework. Moreover, the hydrogen evolution reaction (HER) showed higher electrocatalytic activity, with a significantly lower overpotential and higher current density. This article defines Ni doping as an effective route to convert ZIF-8 into a high-performance, dual-functional photocatalyst. It opens the door to implementing solar-powered environmental remediation and hydrogen generation using ZIF-8.
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AbdelAll et al. (2025) studied this question.
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