This paper reports for the first time the electrogenerated chemiluminescence (ECL) behavior of graphite-like carbon nitride (g-C(3)N(4)) with K(2)S(2)O(8) as the coreactant. The possible ECL reaction mechanisms are proposed. The spectral features of the ECL emission and photoluminescence (PL) of g-C(3)N(4) are compared, and their resemblance demonstrates that the excited states of g-C(3)N(4) from both ECL and photoexcitation are the same. The effects of K(2)S(2)O(8) concentration, pH, g-C(3)N(4)/carbon powder ratio, and scan rate on the ECL intensity have been studied in detail. Furthermore, it is observed that the ECL intensity is efficiently quenched by trace amounts of Cu(2+). g-C(3)N(4) is thus employed to fabricate an ECL sensor which shows high selectivity to Cu(2+) determination. The limit of detection is determined as 0.9 nM. It is anticipated that g-C(3)N(4) could be a new class of promising material for fabricating ECL sensors.

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A novel facile and template-free method to prepare a nanoball-like NiO x material has been developed. The preparation involves the synthesis of an a-Ni(OH) 2 precursor by microwave heating and calcination of the precursor. The NiO x material possesses a nanoball-like structure with a large surface area. The pseudo-capacitive properties of the NiO x material were evaluated by cyclic voltammetry and electro-chemical impedance spectroscopy in 6 M KOH solution. The specific capacitances were 951, 796, 713 and 650 F g À1 , corresponding to the scan rates of 2.0, 5.0, 10 and 20 mV s À1 , respectively. The NiO x material also showed excellent cycling stability and maintained 92% of its maximum specific capacitance after 1000 cycles. The hybrid supercapacitor based on this NiO x material exhibited moderate energy density and power density.

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Reverse-phase high-performance liquid chromatographic (RP-HPLC) separation and analysis of polydisperse water-soluble gold nanoclusters (AuNCs) stabilised with N,N'-dimethylformamide (DMF) were investigated. Under optimal elution gradient conditions, the separation of DMF-AuNCs was monitored by absorption and fluorescence spectroscopy. The UV-vis spectral characteristics of the separated DMF-AuNCs have been captured and they do not possess distinct surface plasmon resonance bands, indicating that all DMF-AuNCs are small AuNCs. The photoluminescence emission spectra of the separated DMF-AuNCs are in the blue-light region. Moreover, cationic DMF-AuNCs are for the first time identified by ion chromatography. Our proposed RP-HPLC methodology has been successfully applied to separate AuNCs of various Au atoms as well as DMF-stabilised ligands. Finally, the composition of the separated DMF-AuNCs was confirmed by matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry and electrospray ionisation mass spectrometry, proving that the as-synthesised DMF-AuNCs product consists of Au₁₀⁺, Au₁₀, Au₁₁, Au₁₂, Au₁₃, and Au₁₄ NCs stabilised with various numbers of DMF ligands.