RESUMEN
A multicomponent covalent organic framework (COF-Tfp-BpyDaaq) integrating bipyridine with diaminoanthraquinone through a triformylphoroglucinol linkage was synthesized for the first time as a photocatalyst for overall H2O2 photosynthesis. It exhibits enhanced photo-charge separation and H2O2 production rate over its two-component counterparts, demonstrating the pivotal role of multicomponent synthesis in designing efficient photocatalysts.
RESUMEN
Photocatalytic water oxidation is a key half-reaction for various solar-to-fuel conversion systems but requires simultaneous water affinity and hole accumulation at the photocatalytic site. Here, we present the rational design and synthesis of an ionic-type covalent organic framework (COF) named tetraphenylporphyrin cobalt and cobalt bipyridine complex (CoTPP-CoBpy3) COF, combining cobalt porphyrin and cobalt bipyridine building blocks as a photocatalyst for water oxidation. The good dispersibility of porous large-size (>2 micrometers) COF nanosheets (≈1.45 nanometers) facilitates local water collection; the ultrafast triplet-state charge transfer (1.8 picoseconds) and prolonged charge separation (1.2 nanoseconds) further contribute to the efficient accumulation of holes in the CoTPP moiety, leading to a photocatalytic dioxygen production rate of 7323 micromoles per gram per hour. Moreover, we have identified an end-on superoxide radical (O2·) intermediate at the active site of the CoTPP moiety and proposed an electron-intermediate cascade mechanism that elucidates the synergistic coupling of electron relay (S1-T1-T1') and intermediate evolution during the photocatalytic process.
RESUMEN
Hydrogen generation via electrochemical splitting plays an important role to achieve hydrogen economy. However, the large-scale application is highly limited by high cost and low efficiency. Herein, a new type of rechargeable Zn-hydrazine (Zn-Hz) battery is proposed and realized by a bifunctional electrocatalyst based on two separate cathodic reactions of hydrogen evolution (discharge: 2H2 O + 2e- â H2 + 2OH- ) and hydrazine oxidation (charge: 1 / 2 N 2 H 4 + 2 OH - â 1 / 2 N 2 + 2 H 2 O + 2 e - $1{\rm{/}}2\,{{\rm{N}}_2}{{\rm{H}}_4}{\bm{ + }}2{\rm{O}}{{\rm{H}}^{\bm{ - }}}{\bm{ \to }}1{\rm{/}}2\,{{\rm{N}}_2}{\bm{ + }}2{{\rm{H}}_2}{\rm{O}}{\bm{ + }}2{e^{\bm{ - }}}$ ). This Zn-Hz battery, driven by temporally decoupled electrochemical hydrazine splitting on the cathode during discharge and charge processes, can generate separated hydrogen without purification. When the highly active bifunctional cathode of 3D Mo2 C/Ni@C/CS is paired with Zn foil, the Zn-Hz battery can achieve efficient hydrogen generation with a low energy input of less than 0.4 V (77.2 kJ mol-1 ) and high energy efficiency of 96%. Remarkably, this battery exhibits outstanding long-term stability for 600 cycles (200 h), achieving continuous hydrogen production on demand, which presents great potential for practical application.