Zhenan Bao, Ph.D

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Zhenan Bao, Ph.D. Department of Chemical Engineering Tel: (650)-723-2419 Stanford University Fax: (650)-723-9780 443 Via Ortega, Room 307 E-mail: [email protected] Stanford, CA 94305 Abstract: "Sensors for robotic applications and implantable electronics" Skin is the body’s largest organ, and is responsible for the transduction of a vast amount of information. This conformable, stretchable, self-healable and biodegradable material simultaneously collects signals from external stimuli that translate into information such as pressure, pain, and temperature. The development of electronic materials, inspired by the complexity of this organ is a tremendous, unrealized materials challenge. However, the advent of organic-based electronic materials may offer a potential solution to this longstanding problem. In this talk, I will describe the design of skin-inspired sensors and their applications in robotics and implantable applications Bio: Prior to joining Stanford in 2004, Zhenan Bao was a Distinguished Member of Technical Staff in Bell Labs, Lucent Technologies. She received her Ph.D in Chemistry from the University of Chicago in 1995. She has over 500 refereed publications and over 65 US patents with a Google Scholar H-Index >160. She pioneered a number of molecular design concepts for organic electronic materials. Her work has enabled flexible electronic circuits and displays. In the past ten years, she pioneered the field of skin-inspired organic electronic materials, which resulted in unprecedented performance or functions in medical devices, energy storage and environmental applications. Bao is a member of the National Academy of Engineering and the National Academy of Inventors. Bao was selected as Nature’s Ten people who mattered in 2015 as a “Master of Materials” for her work on artificial electronic skin. She was awarded the inaugural ACS Central Science Disruptor and Innovator Prize in 2020, the Wilhelm Exner Medal by Austrian Federal Minister of Science 2018, ACS Award on Applied Polymer Science 2017, the L'Oréal- UNESCO For Women in Science Award in the Physical Sciences 2017, the AICHE Andreas Acrivos Award for Professional Progress in Chemical Engineering in 2014. .

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Zhenan Bao K
Zhenan Bao K. K. Lee Professor, Senior Fellow at the Precourt Institute for Energy and Professor, by courtesy, of Materials Science and Engineering and of Chemistry Chemical Engineering Curriculum Vitae available Online CONTACT INFORMATION • Administrative Contact Kumiko Jacobs Email [email protected] Tel 650-723-7503 Bio BIO Zhenan Bao joined Stanford University in 2004. She is currently a K.K. Lee Professor in Chemical Engineering, and with courtesy appointments in Chemistry and Material Science and Engineering. She is the Department Chair of Chemical Engineering from 2018. She is a member of the National Academy of Engineering, the American Academy of Arts and Sciences and the National Academy of Inventors. She founded the Stanford Wearable Electronics Initiative (eWEAR) and is the current faculty director. She is also an affiliated faculty member of Precourt Institute, Woods Institute, ChEM-H and Bio-X. Professor Bao received her Ph.D. degree in Chemistry from The University of Chicago in 1995 and joined the Materials Research Department of Bell Labs, Lucent Technologies. She became a Distinguished Member of Technical Staff in 2001. Professor Bao currently has more than 600 refereed publications and more than 100 US patents. She served as a member of Executive Board of Directors for the Materials Research Society and Executive Committee Member for the Polymer Materials Science and Engineering division of the American Chemical Society. She was an Associate Editor for the Royal Society of Chemistry journal Chemical Science, Polymer Reviews and Synthetic Metals. She serves on the international advisory board for Advanced Materials, Advanced Energy Materials, ACS Nano, Accounts of Chemical Reviews, Advanced Functional Materials, Chemistry of Materials, Chemical Communications, Journal of American Chemical Society, Nature Asian Materials, Materials Horizon and Materials Today.
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CACS 2021 Spring Virtual Program Inaugural CACS 40Th Anniversary Keynote
Chinese American Chemical Society Aagend CACS 2021 Spring Virtual Program Inaugural CACS 40th Anniversary Keynote In concurrence with the 2021 ACS Spring Conference Cost: Free, Donations Welcome Registration Required: Register Here Tuesday, April 20th, 2021 7:30pm - 9:00pm EDT/4:30pm - 6:00pm PDT Inaugural CACS 40th Anniversary Keynote Address: Zhenan Bao, Ph.D. Stanford University Skin-Inspired Organic Electronics (see following page for bio and abstract) 4:30 PM (PDT): CACS Overview (Dr. Marinda Wu, CACS Board Chair; Dr. Lei Li, CACS President) 4:45 PM (PDT): Introduction of CACS Keynote Speaker (Dr. Jasmine Lu, CACS Vice President) 4:50 PM (PDT): Keynote Address (Professor Zhenan Bao, Stanford) 5:35 PM (PDT): Q&A Session 6:00 PM (PDT): Plaque Presentation (Dr. Marinda Wu, CACS Board Chair) Thanks to our sponsors: Click here to register | Visit cacshq.org for more information Keynote Address: Skin-Inspired Organic Electronics Chinese American Chemical Society Zhenan Bao, Ph.D. K.K. Lee Professor and Department Chair in the Department of Chemical Engineering Stanford University Director of Stanford Wearable Electronics Initiative (eWEAR) AbstractBiography Zhenan Bao is Department Skin is the body’s largest organ, and is responsible Chair and K.K. Lee Professor for the transduction of a vast amount of information. of Chemical Engineering, and by This conformable, stretchable, self-healable and courtesy, a Professor of biodegradable material simultaneously collects Chemistry and a Professor of signals from external stimuli that translate into Material Science and Engineering information such as pressure, pain, and temperature. at Stanford University. Bao The development of electronic materials, inspired by founded the Stanford Wearable the complexity of this organ is a tremendous, Electronics Initiate (eWEAR) in unrealized materials challenge.
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Zhenan Bao, Ph.D
Zhenan Bao, Ph.D. Department of Chemical Engineering Tel: (650)-723-2419 Stanford University Fax: (650)-723-9780 443 Via Ortega, Room 307 E-mail: [email protected] Stanford, CA 94305 H-INDEX: 155; TOTAL CITATION: >93,500 (Data from Google Scholar) PROFESSIONAL APPOINTMENTS & EDUCATION: Department of Chemical Engineering, Stanford University • Department Chair, 2018-present Department of Chemical Engineering, Stanford University • K.K. Lee Professorship, 2016-present Stanford Wearable Electronics Initiative (eWEAR) • Founder and Director, 2016-present Department of Chemical Engineering, Stanford University • Professor, 2012-present Department of Chemistry, Stanford University • Professor by courtesy, 2012-present Department of Materials Science and Engineering, Stanford University • Professor by courtesy, 2012-present Department of Chemical Engineering, Stanford University • Associate Professor, 2004-2012 PyrAmes, Stanford, California • Founder, Board of Directors, 2016-present C3 Nano Co., Hayward, California • Founder, Board of Directors, 2010-present Bell Labs, Lucent Technologies, Murray Hill, NJ. • Distinguished Member of Technical Staff, Materials Research Department, 2001-2004. Zhenan Bao CV 1 • Member of Technical Staff, Polymer and Organic Materials Research Department, 1995-2001. University of Chicago, Chicago, IL. • Ph.D., Chemistry, 1995 • MS, Chemistry, 1993 University of Illinois, Chicago, IL. • Chemistry Major, 1991. Nanjing University, Nanjing, China. • Chemistry Major, 1987-1990. HONORS AND AWARDS: 1. Gibbs Medal, by America Chemical Society Chicago section, 2020. 2. ALumni Achievement Award, University of Chicago, Department of Chemistry, 2020. 3. ACS Nano Lectureship Award, by America Chemical Society ACS Nano, 2018. 4. WiLheLm Exner Medal presented by Austrian Federal Minister of Science, 2018. 5. American Chemical Society (ACS) AppLied Polymer Science Award, 2017. 6. L’Oreal UNESCO Women in Science Award in Physical Science, 2017.
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Professor Locklin's Curriculum Vitae
Dr. Jason Locklin Curriculum Vita 4A. ACADEMIC HISTORY Name: Jason Locklin Present Rank: Professor, University of Georgia Assignment: 0.48-EFT Research, 0.25-EFT Instruction, 0.03 Administration Tenure Status: Tenured Administrative Title: Director, New Materials Institute; Director Integrated Bioscience and Nanotechnology Cleanroom Graduate Faculty Status: Appointed to Graduate Faculty in January 2007 Education Ph.D. in Chemistry, University of Houston, Houston, TX, 2004 M.S. in Chemistry, University of Alabama at Birmingham, Birmingham, AL, 2002 B.S. in Chemistry, Millsaps College, Jackson, MS, 1999 Positions Held July 2018-present: Professor, Department of Chemistry and College of Engineering, University of Georgia, Athens, GA (promotion approved, November 2017, starts with fiscal year of university) July 2012-June 2018: Associate Professor, Department of Chemistry and College of Engineering, University of Georgia, Athens, GA January 2007-June 2012: Assistant Professor, Department of Chemistry and Faculty of Engineering, University of Georgia, Athens, GA September 2011-present: Director Integrated Bioscience and Nanotechnology Cleanroom September 2016-present: Director of the New Materials Institute December 2004-December 2006: Postdoctoral Scholar, Department of Chemical Engineering, Stanford University, Stanford, CA, (Research Advisor: Zhenan Bao) August 2002-December 2004: Graduate Research Associate, University of Houston, Houston, TX (Research Advisor: Rigoberto Advincula) January 2000-August 2002: Graduate Research Associate, University of Alabama Birmingham, Birmingham, AL (Research Advisor: Rigoberto Advincula) Post-Graduate Awards National Science Foundation Faculty Early Career Development Award (2010-2015) Intelligence Community Young Investigator Award (2007-2009) NE Georgia Section ACS Chemist of the Year for Research (2010) Atlanta Magazine: Groundbreaker Award for Germ Free Textiles (2011) 4B.
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Lei Fang CV 201902
Dr. Lei Fang / Texas A&M University Curriculum Vitae Lei Fang Department of Chemistry, Texas A&M University 3255 TAMU, College Station, TX 77843, USA Phone: +1-979-845-3186 / E-mail: [email protected] http://www.chem.tamu.edu/rgroup/fang/ Experience and Education Assistant Professor of Chemistry / Texas A&M University Department of Chemistry (Primary Appointment) 2013–Present Department of Materials Science and Engineering (Affiliated Appointment) 2014–Present Postdoctoral Scholar / Stanford University 2011–2013 Department of Chemical Engineering Mentor: Professor Zhenan Bao PhD / Northwestern University 2008–2010 Department of Chemistry Mentor: Professor Fraser Stoddart (Nobel Laureate 2016) Thesis Title “Expanding the Scope on Mechanically Interlocked Molecules” Graduate Student / University of California, Los Angeles 2006–2007 Department of Chemistry & Biochemistry Mentor: Professor Fraser Stoddart (Nobel Laureate 2016) MS / Wuhan University & Hong Kong Baptist University 2003–2006 Department of Chemistry Mentor: Professor Yong-Bing He & Professor Wing-Hong Chan Thesis Title “Study on the Synthesis and Application of Molecular Fluorescent Sensor” BS / Wuhan University 1999–2003 Department of Chemistry Honors, Awards and Memberships Thieme Chemistry Journal Award Thieme Chemistry 2019 Polymers Young Investigator Award MDPI 2018 Polymer Chemistry Emerging Investigator Royal Society of Chemistry 2018 Montague-Center for Teaching Excellence Scholar Texas A&M University 2017 NSF CAREER Award National Science Foundation 2017 ACS PMSE Young
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Skin-Inspired Electronics: an Emerging Paradigm
Article Cite This: Acc. Chem. Res. 2018, 51, 1033−1045 pubs.acs.org/accounts Skin-Inspired Electronics: An Emerging Paradigm Published as part of the Accounts of Chemical Research special issue “The Interface of Biology with Nanoscience and Electronics”. † § † ‡ § † § † † Sihong Wang, , Jin Young Oh, , , Jie Xu, , Helen Tran, and Zhenan Bao*, † Department of Chemical Engineering, Stanford University, Stanford, California 94305, United States ‡ Department of Chemical Engineering, Kyung Hee University, Yongin 17104, Republic of Korea CONSPECTUS: Future electronics will take on more important roles in people’s lives. They need to allow more intimate contact with human beings to enable advanced health monitoring, disease detection, medical therapies, and human− machine interfacing. However, current electronics are rigid, nondegradable and cannot self-repair, while the human body is soft, dynamic, stretchable, biodegradable, and self-healing. Therefore, it is critical to develop a new class of electronic materials that incorporate skinlike properties, including stretchability for conformable integration, minimal discomfort and suppressed invasive reactions; self-healing for long-term durability under harsh mechanical conditions; and biodegrad- ability for reducing environmental impact and obviating the need for secondary device removal for medical implants. These demands have fueled the development of a new generation of electronic materials, primarily composed of polymers and polymer composites with both high electrical performance and skinlike properties, and consequently led to a new paradigm of electronics, termed “skin-inspired electronics”. This Account covers recent important advances in skin-inspired electronics, from basic material developments to device components and proof-of-concept demonstrations for integrated bioelectronics applications. To date, stretchability has been the most prominent focus in this ﬁeld.
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Molecular Design for Electrolyte Solvents Enabling Energy-Dense and Long-Cycling Lithium Metal Batteries
ARTICLES https://doi.org/10.1038/s41560-020-0634-5 Molecular design for electrolyte solvents enabling energy-dense and long-cycling lithium metal batteries Zhiao Yu 1,2,6, Hansen Wang 3,6, Xian Kong 1, William Huang 3, Yuchi Tsao1,2,3, David G. Mackanic 1, Kecheng Wang3, Xinchang Wang4, Wenxiao Huang3, Snehashis Choudhury 1, Yu Zheng1,2, Chibueze V. Amanchukwu1, Samantha T. Hung 2, Yuting Ma1, Eder G. Lomeli3, Jian Qin 1, Yi Cui 3,5 ✉ and Zhenan Bao 1 ✉ Electrolyte engineering is critical for developing Li metal batteries. While recent works improved Li metal cyclability, a methodol- ogy for rational electrolyte design remains lacking. Herein, we propose a design strategy for electrolytes that enable anode-free Li metal batteries with single-solvent single-salt formations at standard concentrations. Rational incorporation of –CF2– units yields fluorinated 1,4-dimethoxylbutane as the electrolyte solvent. Paired with 1 M lithium bis(fluorosulfonyl)imide, this elec- trolyte possesses unique Li–F binding and high anion/solvent ratio in the solvation sheath, leading to excellent compatibility with both Li metal anodes (Coulombic efficiency ~ 99.52% and fast activation within five cycles) and high-voltage cathodes (~6 V stability). Fifty-μm-thick Li|NMC batteries retain 90% capacity after 420 cycles with an average Coulombic efficiency of 99.98%. Industrial anode-free pouch cells achieve ~325 Wh kg−1 single-cell energy density and 80% capacity retention after 100 cycles. Our design concept for electrolytes provides a promising path to high-energy, long-cycling Li metal batteries. i-ion batteries have made a great impact on society, recognized of fluorinated diluent molecules were further developed to form recently by the Nobel Prize in Chemistry1,2.
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A Stiff and Healable Polymer Based on Dynamic‐Covalent Boroxine Bonds
www.advmat.de www.MaterialsViews.com A Stiff and Healable Polymer Based on Dynamic-Covalent COMMUNICATION Boroxine Bonds Jian-Cheng Lai , Jin-Feng Mei , Xiao-Yong Jia , Cheng-Hui Li , * Xiao-Zeng You , * and Zhenan Bao * The ability to spontaneously repair damage, which is termed properties. Speciﬁ cally, we use dynamic-covalent boroxine bond as self-healing, is an important survival feature in nature. Syn- to crosslink the poly(dimethylsiloxane) (PDMS) chain into 3D thetic self-healing materials are highly desirable because this networks. The as-prepared sample is very strong and stiff, and can lead to extension of materials’ lifetime and reduction of can bear a load of more than 450 times of its weight. Upon wet- waste. [ 1 ] So far, two types of self-healing materials have been ting, the equilibrium of surface-exposed boroxine was shifted reported: (i) extrinsic self-healing materials in which a healing toward the disassociated state so that abundant free boronic agent has to be pre-embedded (in microcapsules [ 2 ] or microvas- acid were generated and the PDMS chains were decrosslinked, cular [ 3 ] networks), and (ii) intrinsic self-healing materials that resulting in increased molecular segments mobility ( Figure 1 ). are able to heal cracks by utilizing reversible covalent bonds This process was reversed by removing water. Therefore, the (such as alkoxyamine, [ 4 ] disulﬁ de, [ 5 ] Diels–Alder reaction, [ 6 ] polymer can be completely healed upon heating after wetting. radical dimerization reaction, [ 7 ] and cycloaddition reaction [ 8 ] ) or Such stiff and healable property combined into a synthetic dynamic interactions (such as hydrogen bonds, [ 9 ] π–π stacking polymer has never been realized before.
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Organic Electronics
Organic Electronics DISTINGUISHED SPEAKERS Dr. Campbell Scott, IBM Almaden Research Center Professor Peter Peumans, Stanford University Professor Zhenan Bao, Stanford University Dr. Robert Jan Visser, Chief Technology Officer, Vitex Systems Inc. MODERATOR & EVENT CHAIR Anthony Waitz (Quantum Insight) VENUE Frances C. Arrillaga Alumni Center, Stanford University Apr 22, 2005 6:00-9:00 pm SPONSORS www.mitstanfordberkeleynano.org AGENDA 6:00 – 6:50 pm Registration, Refreshments and Networking 7:00 – 7:05 pm Introduction Anthony Waitz, Event Moderator and Chair 7:05 – 8:30 pm Speaker presentations 8:30 – 9:00 pm Session close ABSTRACT Imagine next generation electronic devices that are printed onto flexible substrates like plastic. This is the promise of the emerging field of flexible electronics where the active materials are deposited in ultra-thin layers onto non-traditional substrates. This new technology movement is significantly enabled by the use of organic materials. The success of OLED's (organic light emitting diodes) has opened the way for consideration of organic materials in many new applications. Organic electronics on flexible substrates promises to be disruptive to a number of large markets, such as electronics, displays, and solar energy. Because of the size of the opportunity, large corporations as well as new technology startups are pursuing the creation of low cost and high performance organic electronic and optoelectronic devices. SPEAKER BIOS Dr. Campbell Scott Research Staff Member, IBM Almaden Research Center J. Campbell Scott received his BSc in physics from St. Andrews University in Scotland and his PhD from the University of Pennsylvania. He was an Assistant Professor of Physics at Cornell University before joining the IBM San Jose Research Laboratory (now the Almaden Research Center) as a Research Staff Member.
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第十一届中美华人纳米论坛程序册 the 11Th Sino-US Nano Forum
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Batteries: Now and Future
Batteries: Now and Future Yi Cui Department of Materials Science and Engineering Stanford University Stanford Institute for Materials and Energy Sciences SLAC National Accelerator Laboratory Mobile Phone Evolution Battery in iphone 6 plus Drone Electrical Vehicles Stationary Storage CA, ~60 GWh World ~10 TWh ~85,000Wh ~70Wh ~10 Wh 1 billion pieces/yr How far can battery technology go? - Energy density (Wh/kg, Wh/L) - Cost ($/kWh) - Safety - Cycle life - Charge rate Lithium Ion Battery Cells: Now and Future Goals Cell level (goal) System level (goal) Energy ~200 (600) ~100 (300) (Wh/kg) Cost 150-200 (70) 300-500 (150) ($/kWh) Cycle life 3000 (10,000 for grid) Safety High energy density (weight/volume) -Range increase -Lower cost Revolution in Transportation, Grid, Renewable How do We Store Electrons? e− + M + ←⎯→M e− + M + + Host←⎯→MHost M atomic weight M maximum voltage M cost ($/kg) Pb2+/4+ (207) + Li (<4.5V) Li (40)* 2+ Zn (65) + Na (<4.2V) Na (1) Al3+ (27) 2+ Mg2+ (25) Mg (<~3.8V) Mg (2) Na+ (23) Al3+ (<~3.1V) Al (2) 2+ Li+ (7) Zn (<~2.2V) Zn (2) 2+/4+ H+ (1) Pb (<2.1V) Pb (2) + H (<~1.5V) H (nearly free) *The cost of Li in Li ion batteries is only ~3%. Battery Operation: Li Ion Batteries (Courtesy of Venkat Srinivasan) Materials issues of batteries - Electron transport in solid - Ionic diffusion in liquid and solid - Structure/volume change: strain - Solid electrolyte intephase (SEI) 9 High Energy Lithium Batteries Negative electrodes Graphite (2D): 370 mAh/g Silicon: 4200 mAh/g 10X Li (3860 mAh/g) P (2600 mAh/g) Positive electrodes LiMn2O4 (3D): LiCoO2(2D) LiFePO4 (1D) Sulfur 150 mAh/g 150mAh/g 170mAh/g ~1670 mAh/g 10X Theoretical Specific Energy 6000 4500 Cathode LiCoO2 Layer oxide 3000 Li2S6X or S Air 1500 3X Theoretical Specific energy (wh/kg) energy Specific Theoretical 0 C anode Si anode Li anode Grid-Scale Storage Technology Semi-solid flow batteries Liquid metal batteries Y.M Chiang, C.
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(London Time) Wednesday 19Th September
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