The presence of oxygen functional groups is detrimental to the capacitive performance of porous carbon electrode in organic electrolyte. In this regards, hydrogen thermal reduction has been demonstrated effective appr...The presence of oxygen functional groups is detrimental to the capacitive performance of porous carbon electrode in organic electrolyte. In this regards, hydrogen thermal reduction has been demonstrated effective approach in removing the unstable surface oxygen while maintaining the high porosity of carbon matrix. However, the exact evolution mechanism of various oxygen species during this process, as well as the correlation with electrochemical properties, is still under development. Herein, biomass-based porous carbon is adopted as the model material to trace its structure evolution of oxygen removal under hydrogen thermal reduction process with the temperature range of 400–800 °C. The optimum microstructure with low oxygen content of 0.90% and proper pore size distribution was achieved at 700°C. XPS, TPRMS and Boehm titration results indicate that the oxygen elimination undergoes three distinctive stages(intermolecular dehydration, hydrogenation and decomposition reactions). The optimum microstructure with low oxygen content of 0.90% and proper pore size distribution was achieved at 700 °C. Benefiting from the stable electrochemical interface and the optimized porous structure, the as-obtained HAC-700 exhibit significantly suppressed self-discharge and leak current, with improved cycling stability, which is attributable to the stabilization of electrochemical interface between carbon surface and electrolyte. The result provides insights for rational design of surface chemistry for high-performance carbon electrode towards advanced energy storage.展开更多
Hydrogen sulfide(H_2S)has been found to be the third most important endogenous gaseous signaling molecule after nitric oxide(NO)and carbonic oxide(CO)and plays crucial roles in living organisms and biological systems....Hydrogen sulfide(H_2S)has been found to be the third most important endogenous gaseous signaling molecule after nitric oxide(NO)and carbonic oxide(CO)and plays crucial roles in living organisms and biological systems.Here we use aggregation-induced emission(AIE)of a small organic molecule(TPE-indo)to detect H_2S in both solution and living cells.TPE-indo can target mitochondria and aggregate to fluoresce,which can serve as a sensor for monitoring H_2S in the mitochondria.We regulate the fluorescence of AIE molecules by tuning the viscosity of the solution to form TPE-indo nanoparticles,constructing a probe for H_2S with good selectivity and high sensitivity.The nucleophilic addition of HS-to the TPE-indo is crucial for the rapid H_2S detection.The imaging and analysis of H_2S in mitochondria of living cells with the probe demonstrate potential biological applications.展开更多
基金National Science Foundation for Excellent Young Scholars of China (21922815)Key Research and Development (R&D) Projects of Shanxi Province (201903D121007)+3 种基金Natural Science Foundations of Shanxi Province (201801D221156)DNL Cooperation Fund of CAS (DNL180308)Science and Technology Service Network Initiative of CAS (KFJ-STS-ZDTP-068)Youth Innovation Promotion Association of CAS。
文摘The presence of oxygen functional groups is detrimental to the capacitive performance of porous carbon electrode in organic electrolyte. In this regards, hydrogen thermal reduction has been demonstrated effective approach in removing the unstable surface oxygen while maintaining the high porosity of carbon matrix. However, the exact evolution mechanism of various oxygen species during this process, as well as the correlation with electrochemical properties, is still under development. Herein, biomass-based porous carbon is adopted as the model material to trace its structure evolution of oxygen removal under hydrogen thermal reduction process with the temperature range of 400–800 °C. The optimum microstructure with low oxygen content of 0.90% and proper pore size distribution was achieved at 700°C. XPS, TPRMS and Boehm titration results indicate that the oxygen elimination undergoes three distinctive stages(intermolecular dehydration, hydrogenation and decomposition reactions). The optimum microstructure with low oxygen content of 0.90% and proper pore size distribution was achieved at 700 °C. Benefiting from the stable electrochemical interface and the optimized porous structure, the as-obtained HAC-700 exhibit significantly suppressed self-discharge and leak current, with improved cycling stability, which is attributable to the stabilization of electrochemical interface between carbon surface and electrolyte. The result provides insights for rational design of surface chemistry for high-performance carbon electrode towards advanced energy storage.
基金the National Basic Research Program of China(2011CB933201,2012AA022703)the National Natural Science Foundation of China(21222502,91213305)+1 种基金Youth Innovation Promotion Association(CAS),the CAS/SAFEA International Partnership Program for Creative Research Teamsthe“Strategic Priority Research Program”of the Chinese Academy of Sciences(XDA09030305)
文摘Hydrogen sulfide(H_2S)has been found to be the third most important endogenous gaseous signaling molecule after nitric oxide(NO)and carbonic oxide(CO)and plays crucial roles in living organisms and biological systems.Here we use aggregation-induced emission(AIE)of a small organic molecule(TPE-indo)to detect H_2S in both solution and living cells.TPE-indo can target mitochondria and aggregate to fluoresce,which can serve as a sensor for monitoring H_2S in the mitochondria.We regulate the fluorescence of AIE molecules by tuning the viscosity of the solution to form TPE-indo nanoparticles,constructing a probe for H_2S with good selectivity and high sensitivity.The nucleophilic addition of HS-to the TPE-indo is crucial for the rapid H_2S detection.The imaging and analysis of H_2S in mitochondria of living cells with the probe demonstrate potential biological applications.
