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| 1 | Oxygen-vacancy-rich TiO_(2)enables highly active and durable water electrolysis of urchin-like RuO_(2)catalyst显示文摘The material innovation is prerequisite to accelerating sluggish oxygen evolution reaction(OER)kinetics,thus promoting the realization of hydrogen energy community.Herein,we develop an oxygen-vacancy-rich TiO_(2)supported RuO_(2)catalyst(RuO_(2)@r-TiO_(2))towards improved OER activity and stability.The oxygen vacancy on TiO_(2)not only supplies electrons to produce lower valence Ru,but also provides sufficient anchoring site for the deposition of RuO_(2)nanocrystal.Beyond that,it can generate strong electronic interaction between TiO_(2)and supported RuO_(2),and thereby tailors the intermediates’adsorption energy on the RuO_(2)surface.As a result,the derived RuO_(2)@r-TiO_(2)catalyst exhibits superior OER activity and stability with the overpotential of 211 mV at a current density of 10 mA cm^(−2)and negligible activity degradation after 6 h operation,outperforming the non-oxygen-vacancy counterpart(223.3 mV,12.75%activity loss)and RuO_(2)catalyst(234.6 mV,42.86%activity loss). | GAO HongMei XIAO MeiLing LI GuoQiang GAO LiQin MENG QingLei LUO ZhaoYan LUO ErGui LIU ChangPeng JIN Zhao GE JunJie XING Wei | 2022 | Science China(Technological Sciences)2022，65，10： | 3 |
| 2 | Accelerated oxygen reduction on Fe/N/C catalysts derived from precisely-designed ZIF precursors显示文摘Fe/N/C material is the most competitive alternative to precious-metal catalysts for oxygen reduction.In view of the present consensus on active centers,further effort is directed at maximizing the density of single Fe atoms.Here,the imperfections in commonly used doping strategy of Fe for the synthesis of zeolitic imidazolateframework(ZIF)-derived Fe/N/C catalysts are revealed.More importantly,a strikingly improved catalyst is obtained by a‘second pyrolysis’method and delivers a half-wave potential of 0.825 V(vs.RHE)in acidic media.The strong confinement effect of carbonaceous host accounts for the formation of dense single-atom sites and thus the high activity.Our findings will potentially facilitate future improvement of M/N/C catalysts. | Ergui Luo Chen Wang Yang Li Xian Wang Liyuan Gong Tuo Zhao Zhao Jin Junjie Ge Changpeng Liu Wei Xing | 2020 | Nano Research2020，13，9： | 2 |
| 3 | Fe,Cu-codoped metal-nitrogen-carbon catalysts with high selectivity and stability for the oxygen reduction reaction显示文摘Metal-nitrogen-carbon materials(M-N-C) are non-noble-metal-based alternatives to platinum-based catalysts and have attracted tremendous attention due to their low-cost,high abundance,and efficient catalytic performance towards the oxygen reduction reaction(ORR).Among them,Fe-based materials show remarkable ORR activity,but they are limited by low selectivity and low stability.To address these issues,herein,we have synthesized FeCu-based M-N-C catalysts,inspired by the bimetal center of cytochrome c oxidase(CcO).In acidic media,the selectivity was notably improved compared with Febased materials,with peroxide yields less than 1.2%(<1/3 of the hydrogen peroxide yields of Fe-N-C catalysts).In addition to Cu-N-C catalysts which can catalytically reduce hydrogen peroxide,the reduction current of hydrogen peroxide using FeCu-N-C-20 exceeded that of Fe-N-C by about 6% when the potential was greater than 0.4 V.Furthermore,FeCu-based M-N-C catalysts suffered from only a15 mV attenuation in their half-wave potentials after 10,000 cycles of accelerated degradation tests(ADT),while there was a 30 mV negative shift for Fe-N-C.Therefore,we propose that the H_(2)O_(2) released from Fe-Nx sites or N-doped carbon sites would be reduced by adjacent Cu-Nx sites,re sulting in low H_(2)O_(2) yields and high stability. | Yuemin Wang Ergui Luo Xian Wang Qinglei Meng Junjie Ge Changpeng Liu Wei Xing | 2021 | Chinese Chemical Letters2021，32，1： | 0 |
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