Abstract: An electronic device includes a fuel cell providing a fuel voltage, a first switch, a rechargeable battery providing a battery voltage, a second switch, a relay, a driving circuit, and a controller. The first switch provides the fuel voltage to a first node according to a first control signal. The second switch is coupled to the first node, and charges the rechargeable battery with the fuel voltage according to a second control signal. The relay provides a voltage of the first node to the load according to the third control signal. The driving circuit generates the first control signal, the second control signal, and the third control signal according to a driving signal. The controller generates the driving signal according to the fuel voltage and the battery voltage.

Abstract: An electronic device includes a fuel cell, a first switch, a rechargeable battery, a second switch, and a relay. The fuel cell provides a fuel voltage. The first switch provides the fuel voltage to a first node according to a first control signal. The rechargeable battery provides a battery voltage. The second switch is coupled to the first node and charges the rechargeable battery with the fuel voltage according to a second control signal. The relay provides a voltage of the first node to the load according to the third control signal.

Abstract: The present invention provides a phosphorescent tris-chelated transition metal complex having one carbon-nitrogen (C^N) or nitrogen-nitrogen (N^N) chromophoric ligand forming a coordination sphere thereof with a transition metal, and two identical carbon-phosphorus (C^P) chelates being incorporated into the coordination sphere, wherein the metal is iridium, platinum, osmium or ruthenium, and the chromophoric ligands possess a relatively lower energy gap in comparison with that of the non-chromophoric chelate, the latter afforded an effective barrier for inhibiting the ligand-to-ligand charge transfer process, so that bright phosphorescence can be observed. The architecture and energy gap of the present molecular designs are suitable for generation of high efficiency blue, green and even red emissions.

Abstract: The present invention provides a series of phosphorescent transition metal complexes having a facially arranged, carbon-phosphorus-carbon (C^P^C) tridentate chelate, alone with one monoanionic bidentate chromophoric chelate (either C^N or A^N) and one arbitrary charge neutral chelate (L), or with one charge neutral bidentate chromophoric chelate (N^N) and one arbitrary anionic ligand (X); all of them can be used to generate high efficiency photo-induced phosphorescence at room temperature, as well as bright electroluminescence upon employment of these materials in the fabrication of organic light-emitting devices.

Abstract: The present invention provides a phosphorescent tris-chelated transition metal complex having one carbon-nitrogen (C?N) or nitrogen-nitrogen (N?N) chromophoric ligand forming a coordination sphere thereof with a transition metal, and two identical carbon-phosphorus (C?P) chelates being incorporated into the coordination sphere, wherein the metal is iridium, platinum, osmium or ruthenium, and the chromophoric ligands possess a relatively lower energy gap in comparison with that of the non-chromophoric chelate, the latter afforded an effective barrier for inhibiting the ligand-to-ligand charge transfer process, so that bright phosphorescence can be observed. The architecture and energy gap of the present molecular designs are suitable for generation of high efficiency blue, green and even red emissions.

Abstract: The present invention discloses a phosphorescent tris-chelated transition metal complex comprising i) two identical carbon-nitrogen (C^N) or nitrogen-nitrogen (N^N) chromophoric ligands being incorporated into a coordination sphere thereof with a transition metal, and one carbon-phosphorus (C^P) chelate being incorporated into the coordination sphere; or ii) one carbon-nitrogen (C^N) or nitrogen-nitrogen (N^N) chromophoric ligand forming a coordination sphere thereof with a transition metal, and two identical carbon-phosphorus (C^P) chelates being incorporated into the coordination sphere, wherein the metal is iridium, platinum, osmium or ruthenium, and the chromophoric ligands possess a relatively lower energy gap in comparison with that of the non-chromophoric chelate, the latter afforded an effective barrier for inhibiting the ligand-to-ligand charge transfer process, so that bright phosphorescence can be observed.

Abstract: The present invention provides a series of phosphorescent transition metal complexes having a facially arranged, carbon-phosphorus-carbon (C?P?C) tridentate chelate, alone with one monoanionic bidentate chromophoric chelate (either C?N or A?N) and one arbitrary charge neutral chelate (L), or with one charge neutral bidentate chromophoric chelate (N?N) and one arbitrary anionic ligand (X); all of them can be used to generate high efficiency photo-induced phosphorescence at room temperature, as well as bright electroluminescence upon employment of these materials in the fabrication of organic light-emitting devices.

Abstract: The present invention discloses a phosphorescent tris-chelated transition metal complex comprising i) two identical carbon-nitrogen (C?N) or nitrogen-nitrogen (N?N) chromophoric ligands being incorporated into a coordination sphere thereof with a transition metal, and one carbon-phosphorus (C?P) chelate being incorporated into the coordination sphere; or ii) one carbon-nitrogen (C?N) or nitrogen-nitrogen (N?N) chromophoric ligand forming a coordination sphere thereof with a transition metal, and two identical carbon-phosphorus (C?P) chelates being incorporated into the coordination sphere, wherein the metal is iridium, platinum, osmium or ruthenium, and the chromophoric ligands possess a relatively lower energy gap in comparison with that of the non-chromophoric chelate, the latter afforded an effective barrier for inhibiting the ligand-to-ligand charge transfer process, so that bright phosphorescence can be observed.