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| 1 | Bi/Bi2O3 nanoparticles supported on N-doped reduced graphene oxide for highly efficient CO2 electroreduction to formate显示文摘Electrocatalytic CO2 reduction(CO2 ER)into formate is a desirable route to achieve efficient transformation of CO2 to value-added chemicals,however,it still suffers from limited catalytic activity and poor selectivity.Herein,we develop a hybrid electrocatalyst composed of bismuth and bismuth oxide nanoparticles(NPs)supported on nitrogen-doped reduced graphene oxide(Bi/Bi2 O3/NrGO)nanosheets prepared by a combined hydrothermal with calcination treatment.Thanks to the combination of undercoordinated sites and strong synergistic effect between Bi and Bi2 O3,Bi/Bi2 O3/NrGO-700 hybrid displays a promoted CO2 ER catalytic performance and selectivity for formate production,as featured by a small onset potential of-0.5 V,a high current density of-18 mA/cm2,the maximum Faradaic efficiency of85%at-0.9 V,and a low Tafel slope of 166 mV/dec.Experimental results reveal that the higher CO2 ER performance of Bi/Bi2 O3/NrGO-700 than that of Bi NPs supported on NrGO(Bi/NrGO)can be due to the partial reduction of Bi2 O3 NPs into Bi,which significantly increases undercoordinated active sites on Bi NPs surface,thus boosting its CO2 ER performance.Furthermore,a two-electrode device with Ir/C anode and Bi/Bi2 O3/NrGO-700 cathode could be integrated with two alkaline batteries or a planar solar cell to achieve highly active water splitting and CO2 ER. | Junjie Sun Wanzhen Zheng Siliu Lyu Feng He Bin Yang Zhongjian Li Lecheng Lei Yang Hou | 2020 | Chinese Chemical Letters2020，31，6： | 4 |
| 2 | A Universal Principle to Accurately Synthesize Atomically Dispersed Metal–N_4 Sites for CO_2 Electroreduction显示文摘Atomically dispersed metal-nitrogen sites-anchored carbon materials have been developed as effective catalysts for CO2 electroreduction(CO2 ER),but they still suffer from the imprecisely control of type and coordination number of N atoms bonded with central metal.Herein,we develop a family of single metal atom bonded by N atoms anchored on carbons(SAs-M-N-C,M=Fe,Co,Ni,Cu)for CO2 ER,which composed of accurate pyrrole-type M-N4 structures with isolated metal atom coordinated by four pyrrolic N atoms.Benefitting from atomically coordinated environment and specific selectivity of M-N4 centers,SAs-Ni-N-C exhibits superior CO2 ER performance with onset potential of-0.3 V,CO Faradaic efficiency(F.E.) of 98.5%at-0.7 V,along with low Tafel slope of 115 mV dec-1 and superior stability of 50 h,exceeding all the previously reported M-N-C electrocatalysts for CO2-to-CO conversion.Experimental results manifest that the different intrinsic activities of M-N4 structures in SAs-M-N-C result in the corresponding sequence of Ni> Fe> Cu> Co for CO2 ER performance.An integrated Zn-CO2 battery with Zn foil and SAs-Ni-N-C is constructed to simultaneously achieve CO2-to-CO conversion and electric energy output,which delivers a peak power density of 1.4 mW cm-2 and maximum CO F.E.of 93.3%. | Wanzhen Zheng Feng Chen Qi Zeng Zhongjian Li Bin Yang Lecheng Lei Qinghua Zhang Feng He Xilin Wu Yang Hou | 2020 | Nano-Micro Letters2020，12，9： | 2 |
| 3 | Correction to: A Universal Principle to Accurately Synthesize Atomically Dispersed Metal-N4 Sites for CO2 Electroreduction显示文摘In the original publication,the author name was incorrectly published as Xilin Wu.The correct author name should be Xi-Lin Wu,which is provided in this correction.Open Access This article is licensed under a Creative Commons Attribution 4.0 International License,which permits use,sharing,adaptation,distribution and reproduction in any medium or format,as long as you give appropriate credit to the original author(s)and the source,provide a link to the Creative Commons licence,and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons licence,unless indicated otherwise in a credit line to the material. | Wanzhen Zheng Feng Chen Qi Zeng Zhongjian Li Bin Yang Lecheng Lei Qinghua Zhang Feng He Xi‑Lin Wu Yang Hou | 2020 | Nano-Micro Letters2020，12，10： | 0 |
| 4 | Distinctive phosphorylation pattern during mitotic exit network(MEN)regulation is important for the development and pathogenicity of Magnaporthe oryzae显示文摘The mitotic exit network(MEN)pathway is a vital kinase cascade regulating the timely and correct progress of cell division.In the rice blast fungus Magnaporthe oryzae,the MEN pathway,consisting of conserved protein kinases MoSep1 and MoMob1-MoDbf2,is important in the development and pathogenicity of the fungus.We found that deletion of MoSEP1 affects the phosphorylation of MoMob1,but not MoDbf2,in contrast to what was found in the buddy yeast Saccharomyces cerevisiae,and verified this finding by in vitro phosphorylation assay and mass spectrom-etry(MS)analysis.We also found that S43 residue is the critical phosphor-site of MoMob1 by MoSep1,and proved that MoSep1-dependent MoMob1 phosphorylation is essential for cell division during the development of M.oryzae.We further provided evidence demonstrating that MoSep1 phosphorylates MoMob1 to maintain the cell cycle during vegetative growth and infection.Taken together,our results revealed that the MEN pathway has both distinct and conservative functions in regulating the cell cycle during the development and pathogenesis of M.oryzae. | Wanzhen Feng Jiansheng Wang Xinyu Liu Haowen Wu Muxing Liu Haifeng Zhang Xiaobo Zheng Ping Wang Zhengguang Zhang | 2022 | Stress Biology2022，2，1： | 0 |
| 5 | BaTiO_(3)@Au nanoheterostructure suppresses triple-negative breast cancer by persistently disrupting mitochondrial energy metabolism显示文摘Abnormal metabolism has become a potential target for highly malignant and invasive triple-negative breast cancer(TNBC)due to its relatively low response to traditional therapeutics.The existing metabolic interventions demonstrated unsatisfactory therapeutic outcomes and potential systemic toxicity,resulting from the metabolic instability and limited targeting ability of inhibitors as well as complex tumor microenvironment.To address these limitations,here we developed a robust pyroelectric BaTiO_(3)@Au core–shell nanostructure(BTO@Au)to selectively and persistently block energy generation of tumor cells.Stimulated by near-infrared(NIR)laser,the Au shell could generate heat to activate the BaTiO_(3)core to produce reactive oxygen species(ROS)regardless of the constrained microenvironment,thus prominently inhibits mitochondrial oxidative phosphorylation(OXPHOS)and reduces ATP production to induce TNBC cell apoptosis.The therapeutic effects have been well demonstrated in vitro and in vivo,paving a new way for the development of metabolic interventions. | Yanlin Feng Jianlin Wang Xin Ning Aiyun Li Qing You Wanzhen Su Deping Wang Jianyun Shi Lan Zhou Fangfang Cao Xiaoyuan Chen Jimin Cao | 2023 | Nano Research2023，16，2： | 0 |
| 6 | Molecular Design Strategy for Practical Singlet Fission Materials:The Charm of Donor/Acceptor Decorated Quinoidal Structure显示文摘Singlet fission(SF)has attracted much attention on account of its great potential for applications in high efficiency solar energy conversion.The major roadblock to realize this potential is rooted in the limited availability of practical SF material with strong absorption,suitable triplet energy level,an efficient SF process,and good chemical stability.Quinoidal structures feature an innate diradical character,which endows these skeletons with SF potential yet results in some structural instability. | Long Wang Xiaomei Shi Shishi Feng WanZhen Liang Hongbing Fu Jiannian Yao | 2022 | CCS Chemistry2022，4，8： | 0 |
| 7 | One-step synthesis of site-specific antibody-drug conjugates by reprograming IgG glycoengineering with LacNAc-based substrates显示文摘Glycosite-specific antibody-drug conjugatess(gsADCs), harnessing Asn297 N-glycan of IgG Fc as the conjugation site for drug payloads, usually require multi-step glycoengineering with two or more enzymes, which limits the substrate diversification and complicates the preparation process.Herein, we report a series of novel disaccharide-based substrates, which reprogram the IgG glycoengineering to one-step synthesis of gsADCs, catalyzed by an endo-N-acetylglucosaminidase(ENGase) of Endo-S2. IgG glycoengineering via ENGases usually has two steps: deglycosylation by wild-type(WT) ENGases and transglycosylation by mutated ENGases. But in the current method, we have found that disaccharide LacNAc oxazoline can be efficiently assembled onto IgG by WT Endo-S2 without hydrolysis of the product, which enables the one-step glycoengineering directly from native antibodies.Further studies on substrate specificity revealed that this approach has excellent tolerance on various modification of 6-Gal motif of LacNAc. Within 1 h, one-step synthesis of gsADC was achieved using the LacNAc-toxin substrates including structures free of bioorthogonal groups. These gsADCs demonstrated good homogeneity, buffer stability, in vitro and in vivo anti-tumor activity. This work presents a novel strategy using LacNAc-based substrates to reprogram the multi-step IgG glycoengineering to a one-step manner for highly efficient synthesis of gsADCs. | Wei Shi Wanzhen Li Jianxin Zhang Tiehai Li Yakai Song Yue Zeng Qian Dong Zeng Lin Likun Gong Shuquan Fan Feng Tang Wei Huang | 2022 | Acta Pharmaceutica Sinica B2022，12，5： | 0 |
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