Kar, AshishAshishKarSingh, ManjeetManjeetSinghPaital, DiptiranjanDiptiranjanPaitalKhatua, SaumyakantiSaumyakantiKhatua2025-08-312025-08-312021-11-0410.1021/acs.jpcc.1c065502-s2.0-85118773986https://d8.irins.org/handle/IITG2025/25224Here, we show that nanoparticles’ surface charge is a key factor that determines their tip-specificity in a covalently linked assembly of anisotropic plasmonic nanoparticles. We developed a strategy to controllably tune the surface charge of gold nanoparticles over a broad ζ potential range between −5 and −35 mV using simple acid-base chemistry and showed that dithiol-driven, end-to-end linked dimers of gold nanorods were formed reproducibly within a ζ potential range between −10 and −17 mV in acetonitrile medium. Below this ζ potential range, nanoparticles collapse together to form large clusters without any tip-specificity. For ζ potentials above this range, electrostatic repulsion prevents them from binding to each other. Our approach of using the surface charge of nanoparticles as a key control parameter for achieving tip-specificity is quite versatile and works for different anisotropic nanoparticles including gold nanorods of different aspect ratios and gold nanobipyramids.falseEstablishing Surface Charge as a Key Control Parameter for Linker-Driven Tip-Specific Ordering of Anisotropic Gold NanoparticlesArticle1932745523895-239034 November 20215arJournal4WOS:000716453300033